The NSW Health Statewide Biobank gratefully acknowledges support from NSW Health Pathology, the NSW Office for Health and Medical Research, and the Sydney Local Health District. Additionally, the authors gratefully acknowledge Omico and other research studies supported by the NSW Health Statewide Biobank for granting permission to publish in-house generated data and to use unused specimens for research purposes. The authors thank Professor Jennifer Bryne (NSW Health Pathology, University of Sydney) for critical leadership and discussions. Figure 1 was created with BioRender.com.

Quality control blood specimens and in-house generated data (such as cell count, viability and&#160;age of specimen at processing) were obtained from consented research studies at the NSW Health Statewide Biobank, Royal Prince Alfred Hospital (HREC approval: 2019/ETH06776). Processed (i.e., plasma depleted), unscreened, and de-identified adult human blood samples were collected in EDTA tubes. These quality control blood specimens were processed less than 72 h after collection and were used for PBMC isolation experiments comparing the density gradient and bead-based methods. For the density gradient separation method used in the representative results, see the procedure in Supplementary File 1. The details of the reagents and the equipment used for this study are listed in the Table of Materials.
1. Whole blood preparation
<ol>
	<li>Gently invert 10 mL whole blood tubes (coated with ethylenediaminetetraacetic acid [EDTA], acid-citrate-dextrose [ACD], or lithium heparin) 10 times at room temperature.</li>
	<li>Optional:&#160;If whole blood is to be stored, aliquot into cryotubes for -80 &#176;C storage.</li>
	<li>Centrifuge the tubes using a swinging-bucket rotor at 800 x g for 10 min at 22 &#176;C with the brake ON (9 acceleration/ 9 deceleration).</li>
</ol>
2. Buffy coat collection
<ol>
	<li>After centrifugation, place the samples in a biological safety cabinet and check for the three distinct layers (as shown in Figure 1). 
	NOTE: RBCs are found in the lower dark red layer of the centrifuge tube. A white opaque layer containing white blood cells and platelets is located above the RBC layer, known as the buffy coat. The top yellow layer contains plasma.</li>
	<li>Optional: If plasma is to be stored, aliquot plasma into cryotubes for -80 &#176;C storage.</li>
	<li>Pipette 1 mL of buffy coat (starting material) from a 10 mL blood tube and transfer to the tube specified and labeled in step 3.1 and step 4.1 for the manual and automated methods, respectively. Swirl the buffy coat (white opaque layer) using the pipette tip and collect the buffy coat by aspirating. 
	NOTE: Less than 100 &#181;L of plasma and RBCs are acceptable during aspiration. If multiple blood tubes are collected for one participant, buffy coats can be pooled; however, this may affect platelet concentration13.</li>
	<li>For manual processing, proceed to section&#160;3. For automated processing, proceed to section 4.</li>
	<li>Optional: If RBCs are to be stored, aliquot RBCs into cryotubes for -80 &#176;C storage.</li>
</ol>
3. PBMC purification - Manual method
NOTE: Up to 8 samples per magnet holder can be processed by a single operator.
<ol>
	<li>Label 3 x 5 mL polystyrene tubes with letters A-C. 
	NOTE: Use sequential numbering if performing more than one sample, i.e., 1A, 1B, 1C, 2A, 2B, 2C.</li>
	<li>Add 60 &#181;L of 0.1 M EDTA (for a final EDTA concentration of 6 mM, pH 8.0, see Supplementary File 2 for the recipe) to tube A containing the buffy coat transferred in step 2.3.</li>
	<li>Add 50 &#181;L of the&#160;cocktail mix tube (see Table of Materials) to tube A, mix by pipetting up and down at least 3 times, and incubate for 5 min at room temperature.</li>
	<li>Add 890 &#181;L of PBS to tube A and mix by pipetting up and down at least 3 times.</li>
	<li>Vortex the&#160;magnetic bead tube (see&#160;Table of Materials)&#160;for 30 s.</li>
	<li>Add 50 &#181;L of the magnetic beads to tube A and mix by pipetting up and down at least 3 times.</li>
	<li>Immediately place tube A into the magnet stand and incubate for 5 min at room temperature.</li>
	<li>Carefully pipette the enriched cell suspension into tube B, collecting the clear fraction with no/minimal (&#60;100 &#181;L) RBCs for optimal PBMC recovery. 
	NOTE: Do not disturb the beads bound to the magnet. A transfer pipette is recommended.</li>
	<li>Remove tube A from the magnet stand and dispose.</li>
	<li>Add 50 &#181;L magnetic beads to cell suspension in tube B and mix by pipetting up and down at least 3 times.</li>
	<li>Immediately place tube B into the magnet stand and incubate for 5 min at room temperature.</li>
	<li>Carefully pipette the enriched cell suspension into tube C, collecting only the clear fraction. 
	NOTE: Do not disturb the beads bound to the magnet. A transfer pipette is recommended.</li>
	<li>Remove tube B from the magnet stand and dispose.</li>
	<li>Immediately place tube C into the magnet stand and incubate for 5 min at room temperature.</li>
	<li>Carefully pipette the enriched cell suspension into a labeled centrifuge tube and top up to 2 mL with PBS.</li>
	<li>Transfer 50 &#181;L of the cell suspension to a sample cup of the automated cell counter. For a 1:10 dilution cell count, add 450 &#181;L of PBS. Proceed to section 5 for cell counting steps.</li>
</ol>
4. PBMC purification - Automated method
NOTE: Up to 4 samples can be processed by a single automated PBMC instrument.&#160;Multiple instruments can be run in parallel by a single operator.
<ol>
	<li>Label 2 x 14 mL tubes with letters A and B, 1 x 50 mL centrifuge tube with letter C, and 1 x 50 mL centrifuge tube with &#34;waste&#34;. 
	NOTE: Only one waste container is required for every run on the automated PBMC instrument. Use sequential numbering if performing more than one sample, i.e., 1A, 1B, 1C, 2A, 2B, 2C.</li>
	<li>Add 60 &#181;L of 0.1 M EDTA (for a final EDTA concentration of 6 mM) to tube A containing the buffy coat transferred in step 2.3.</li>
	<li>Vortex the magnetic bead tube (see&#160;Table of Materials)&#160;for 30 s.</li>
	<li>Turn on the automated PBMC instrument by switching the power on at the front of the instrument.</li>
	<li>On the automated PBMC instrument home screen, select profile and select the desired protocol. 
	NOTE: EasySep Direct Human PBMC isolation 19654 - buffy coat was the protocol profile selected for this PBMC isolation. See the manufacture&#39;s standard procedure for this profile in protocol report14.</li>
	<li>Enter the starting volume (the amount of buffy coat aspirated into tube A), and repeat for each sample.</li>
	<li>Select all the quadrants that will use the same reagent kit. 
	NOTE: If the same protocol is used for more than one quadrant, the automated PBMC instrument will suggest using the same reagent kit for all quadrants14.</li>
	<li>Load the instrument&#39;s carousel with labeled consumables, filter tips and buffer container. The reagent kit containing the magnetic bead tube and cocktail mix tube are to be loaded into quadrant 1. 
	NOTE: The instrument will ask if the user wishes to use 1 reagent kit for all quadrants. Select &#39;yes&#39; and highlight all quadrants using the reagent kit.</li>
	<li>Once loading is complete, remove lids from consumables and reagents and select run on the instrument screen.</li>
	<li>When the run is complete, select unload and remove samples (containing PBMC suspension labeled in tube C) from the instrument&#39;s carousel. Store the magnetic bead tube, cocktail mix tube, and buffer container at 4 &#176;C. Discard tubes labeled as A, B, and waste (see step 4.1) and filter tips. 
	NOTE: No top-up with PBS is necessary for the automated method, as the PBMC suspension produces a final volume of 7 mL.</li>
	<li>Transfer 500 &#181;L of the cells to a sample cup for a no-dilution cell count. Proceed to section 5 for cell counting.</li>
</ol>
5. Cell counting
<ol>
	<li>Perform cell counting and viability using the trypan blue dye exclusion method following the manufacturer&#39;s instructions15. 
	NOTE: For the author&#39;s internal processes, cell analysis is performed using an automated cell counter with the following settings to acquire the PBMCs. 
	Dilution factor = 10 (for manual protocol, if cell suspension is in a low volume) or 1 (for automated protocol) 
	Cell type: PBMC 
	Concentration range = 5 x 104 to 1 x 107 cells/mL 
	Size range (diameter) = 8 &#181;m to 50 &#181;m 
	Number of Images = 50</li>
</ol>
6. Cryopreservation preparation
<ol>
	<li>Centrifuge (using a swinging bucket rotor) the sample tubes at 300 x g for 8 min at 22 &#176;C with the brake ON (9 acceleration/ 9 deceleration).</li>
	<li>After centrifugation, place the samples back in the biological safety cabinet.</li>
	<li>Using a pipette, carefully remove the supernatant. A small amount of supernatant can be left with the PBMC pellet to ensure it is not disturbed.</li>
	<li>Resuspend the pellet in 3 mL of cold cryopreservation medium. Slowly and gently mix the suspension up and down until homogenous. 
	NOTE: The volume of the cyropreservation medium can be adjusted based on the desired final PBMC concentration.</li>
	<li>Dispense&#160;1 mL of the resuspended PBMC into a pre-assigned cryotube and place it inside a control rate freezing container for a minimum of 4 h at -80 &#176;C. 
	NOTE: The volume of PBMCs aliquoted to each cryotube can be adjusted based on the investigator&#39;s preference.</li>
	<li>After storing cryotubes at -80 &#176;C for a minimum of 4 h, transfer the cryotubes to a liquid nitrogen vapor phase tank&#160;for long-term storage.</li>
</ol>
7. Statistical data analysis
<ol>
	<li>Representative result data was analyzed using statistical and graphing software as specified in Supplementary File 3.</li>
</ol>

High-Throughput PBMC Isolation Using Immunomagnetic Beads

<ol><li>Alexovic, M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Human+peripheral+blood+mononuclear+cells%3A+A+review+of+recent+proteomic+applications%5BTitle%5D)+AND+%22Proteomics%22%5BJournal%5D)">Human peripheral blood mononuclear cells: A review of recent proteomic applications.</a> Proteomics. 22 (15-16), e2200026(2022).</li>
<li>Zhang, M., Huang, B. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((The+multi-differentiation+potential+of+peripheral+blood+mononuclear+cells%5BTitle%5D)+AND+%22Stem+Cell+Res+Ther%22%5BJournal%5D)">The multi-differentiation potential of peripheral blood mononuclear cells.</a> Stem Cell Res Ther. 3 (6), 48(2012).</li>
<li>Arimilli, S., Damratoski, B. E., Chen, P., Jones, B. A., Prasad, G. L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Rapid+isolation+of+leukocyte+subsets+from+fresh+and+cryopreserved+peripheral+blood+mononuclear+cells+in+clinical+research%5BTitle%5D)+AND+%22Cryo+Lett%22%5BJournal%5D)">Rapid isolation of leukocyte subsets from fresh and cryopreserved peripheral blood mononuclear cells in clinical research.</a> Cryo Lett. 33 (5), 376-384 (2012).</li>
<li>Kleeberger, C. A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Viability+and+recovery+of+peripheral+blood+mononuclear+cells+cryopreserved+for+up+to+12+years+in+a+multicenter+study%5BTitle%5D)+AND+%22Clin+Diagn+Lab+Immunol%22%5BJournal%5D)">Viability and recovery of peripheral blood mononuclear cells cryopreserved for up to 12 years in a multicenter study.</a> Clin Diagn Lab Immunol. 6 (1), 14-19 (1999).</li>
<li>Ulmer, A. J., Scholz, W., Ernst, M., Brandt, E., Flad, H. D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Isolation+and+subfractionation+of+human+peripheral+blood+mononuclear+cells+%28PBMC%29+by+density+gradient+centrifugation+on+percoll%5BTitle%5D)+AND+%22Immunobiology%22%5BJournal%5D)">Isolation and subfractionation of human peripheral blood mononuclear cells (PBMC) by density gradient centrifugation on percoll.</a> Immunobiology. 166 (3), 238-250 (1984).</li>
<li>Fuss, I. J., Kanof, M. E., Smith, P. D., Zola, H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Isolation+of+whole+mononuclear+cells+from+peripheral+blood+and+cord+blood%5BTitle%5D)+AND+%22Curr+Protoc+Immunol%22%5BJournal%5D)">Isolation of whole mononuclear cells from peripheral blood and cord blood.</a> Curr Protoc Immunol. 7, 711-718 (2009).</li>
<li>Gautam, A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Investigating+gene+expression+profiles+of+whole+blood+and+peripheral+blood+mononuclear+cells+using+multiple+collection+and+processing+methods%5BTitle%5D)+AND+%22PLoS+One%22%5BJournal%5D)">Investigating gene expression profiles of whole blood and peripheral blood mononuclear cells using multiple collection and processing methods.</a> PLoS One. 14 (12), e0225137(2019).</li>
<li>Hamot, G., Ammerlaan, W., Mathay, C., Kofanova, O., Betsou, F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Method+validation+for+automated+isolation+of+viable+peripheral+blood+mononuclear+cells%5BTitle%5D)+AND+%22Biopreserv+Biobank%22%5BJournal%5D)">Method validation for automated isolation of viable peripheral blood mononuclear cells.</a> Biopreserv Biobank. 13 (3), 152-163 (2015).</li>
<li>Coppola, L., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Purification+of+viable+peripheral+blood+mononuclear+cells+for+biobanking+using+a+robotized+liquid+handling+workstation%5BTitle%5D)+AND+%22J+Transl+Med%22%5BJournal%5D)">Purification of viable peripheral blood mononuclear cells for biobanking using a robotized liquid handling workstation.</a> J Transl Med. 17 (1), 371(2019).</li>
<li> Stemcell Technologies. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Vol.+27156%5BTitle%5D)+AND+%22STEMCELL+TECHNOLOGIES%22%5BJournal%5D)">Vol. 27156.</a> STEMCELL TECHNOLOGIES. , 1-4 (2020).</li>
<li>Hornschuh, M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Negative+magnetic+sorting+preserves+the+functionality+of+ex+vivo+cultivated+non-adherent+human+monocytes%5BTitle%5D)+AND+%22Biology+%28Basel%29%22%5BJournal%5D)">Negative magnetic sorting preserves the functionality of ex vivo cultivated non-adherent human monocytes.</a> Biology (Basel). 11 (11), 1583(2022).</li>
<li>Bhattacharjee, J., Das, B., Mishra, A., Sahay, P., Upadhyay, P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Monocytes+isolated+by+positive+and+negative+magnetic+sorting+techniques+show+different+molecular+characteristics+and+immunophenotypic+behaviour%5BTitle%5D)+AND+%22F1000Res%22%5BJournal%5D)">Monocytes isolated by positive and negative magnetic sorting techniques show different molecular characteristics and immunophenotypic behaviour.</a> F1000Res. 6, 2045(2017).</li>
<li>Ohlsson, S., Diedrich, B., Uhlin, M., Sandgren, P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Optimized+processing+for+pathogen+inactivation+of+double-dose+buffy-coat+platelet+concentrates%3A+Maintained+in+vitro+quality+over+7-day+storage%5BTitle%5D)+AND+%22Vox+Sang%22%5BJournal%5D)">Optimized processing for pathogen inactivation of double-dose buffy-coat platelet concentrates: Maintained in vitro quality over 7-day storage.</a> Vox Sang. 113 (7), 611-621 (2018).</li>
<li>Easysep direct human PBMC isolation kit for processing 100 mL buffy coat. Stemcell Technologies. , Available from: 
 <a target="_blank" href="https://www.stemcell.com/products/brands/easysep-cell-separation.html">https://www.stemcell.com/products/brands/easysep-cell-separation.html</a> (2022).</li>
<li>Vi-cell XR cell viability analyzer instructions for use. Beckman Coulter. , Available from: 
 <a target="_blank" href="https://mbcbiolabs.com/wp-content/uploads/2022/08/Beckman-Coulter-ViCell-Manual.pdf">https://mbcbiolabs.com/wp-content/uploads/2022/08/Beckman-Coulter-ViCell-Manual.pdf</a> (2017).</li>
<li>Fuchs, Y. F., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Next-generation+biobanking%3A+Employing+a+robotic+system+for+automated+mononuclear+cell+isolation%5BTitle%5D)+AND+%22Biopreserv+Biobank%22%5BJournal%5D)">Next-generation biobanking: Employing a robotic system for automated mononuclear cell isolation.</a> Biopreserv Biobank. 21 (1), 106-110 (2023).</li>
<li>Tigner, A., Ibrahim, S. A., Murray, I. V. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Histology%2C+white+blood+cell%5BTitle%5D)+AND+%22StatPearls+Publishing%22%5BJournal%5D)">Histology, white blood cell.</a> StatPearls Publishing. , (2024).</li>
<li>Mathay, C., Ammerlaan, W., Betsou, F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Automatic+buffy+coat+extract+on%3A+Methodology%2C+feasibility%2C+optimization%2C+and+validation+study%5BTitle%5D)+AND+%22Biopreserv+Biobank%22%5BJournal%5D)">Automatic buffy coat extract on: Methodology, feasibility, optimization, and validation study.</a> Biopreserv Biobank. 10 (6), 543-547 (2012).</li>
<li>Golke, T., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Delays+during+PBMC+isolation+have+a+moderate+effect+on+yield%2C+but+severly+compromise+cell+viability%5BTitle%5D)+AND+%22Clin+Chem+Lab+Med%22%5BJournal%5D)">Delays during PBMC isolation have a moderate effect on yield, but severly compromise cell viability.</a> Clin Chem Lab Med. 60 (5), 701-706 (2022).</li>
<li>Yi, P. C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Impact+of+delayed+PBMC+processing+on+functional+and+genomic+assays%5BTitle%5D)+AND+%22J+Immunol+Methods%22%5BJournal%5D)">Impact of delayed PBMC processing on functional and genomic assays.</a> J Immunol Methods. 519, 113514(2023).</li>
<li>Mckenna, K. C., Beatty, K. M., Vicetti Miguel, R., Bilonick, R. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Delayed+processing+of+blood+increases+the+frequency+of+activated+CD11b%2B+CD15%2B+granulocytes+which+inhibit+t-cell+function%5BTitle%5D)+AND+%22J+Immunol+Methods%22%5BJournal%5D)">Delayed processing of blood increases the frequency of activated CD11b+ CD15+ granulocytes which inhibit t-cell function.</a> J Immunol Methods. 341 (1-2), 68-75 (2009).</li>
<li>Mallone, R., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Isolation+and+preservation+of+peripheral+blood+mononuclear+cells+for+analysis+of+islet+antigen-reactive+t-cell+responses%3A+Position+statement+of+the+t-cell+workshop+committee+of+the+immunology+of+diabetes+society%5BTitle%5D)+AND+%22Clin+Exp+Immunol%22%5BJournal%5D)">Isolation and preservation of peripheral blood mononuclear cells for analysis of islet antigen-reactive t-cell responses: Position statement of the t-cell workshop committee of the immunology of diabetes society.</a> Clin Exp Immunol. 163 (1), 33-49 (2011).</li>
<li>Betsou, F., Gaignaux, A., Ammerlaan, W., Norris, P. J., Stone, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Biospecimen+science+of+blood+for+peripheral+blood+mononuclear+cell+%28PBMC%29+functional+applications%5BTitle%5D)+AND+%22Curr+Pathobiol+Rep%22%5BJournal%5D)">Biospecimen science of blood for peripheral blood mononuclear cell (PBMC) functional applications.</a> Curr Pathobiol Rep. 7 (2), 17-27 (2019).</li>
</ol>

The authors declare no conflicts of interest.

Human PBMCs are versatile cell types used for numerous assays; however, isolation throughput is often a limitation in many laboratories, including biobanks16. Previously, the NSW Health Statewide Biobank isolated PBMCs using the density gradient method. Automation was investigated for the density gradient separation method to increase processing capacity, but barriers to implementation were identified, including (i) the cost of a liquid handler with a centrifugation unit to be fully automated, with the&#160;added&#160;requirement for a HEPA unit to produce a sterile product, (ii) trained personnel for programming, and (iii) time required for protocol testing. Therefore, this study explored alternative methods and identified the commercially obtained Human PBMC kit that could be used for manual and automated processing. Sterility is ensured as the equipment required for processing fits within a standard (length of 1.2 m) biological safety cabinet. This paper details modifications made to the manufacturer&#39;s recommended protocol14, to increase efficiency and lower reagent costs without sacrificing quality. Additionally, the manufacturer&#39;s protocol was extended to detail steps to biobank specimens for future research, including whole blood (step 1.2), plasma (step 2.2), and RBC (step 2.5) aliquoting from the original blood tube, as well as cell counting and cryopreservation.
In this study, three PBMC isolation protocols were compared: density gradient separation, manual, and automated bead-based isolation. Modifications to the manufacturer&#39;s manual bead-based protocol were made, including the removal of buffy coat dilution prior to PBMC isolation, and elimination of the requirement for break OFF for centrifugations, allowing investigators to follow an adaptable, cost-effective, and high throughput PBMC isolation protocol. First, eight matched whole blood samples were used to isolate PBMCs to compare the density gradient separation and manual bead-based technique. Importantly, cell population distributions, cell viability, and recovery of PBMCs were not significantly different between the two methods compared, as shown in Figure 2A-F, Figure 3A, and Supplementary Figure 1, respectively. In the representative data, cell counts were higher for the density gradient separation method using the trypan blue exclusion method but not when a hematology cell analyzer was used. The PBMC cell type settings on the cell counter employed a cell diameter range of 8-50 &#181;m, and therefore, counts will include PBMCs as well as granulocytes (approximately 12-15 &#181;m in diameter) when using the trypan blue exclusion method17. While the hematological cell counter offered higher specificity than the trypan blue exclusion method, some recovery calculations were higher than 100%, reflecting the instrument&#39;s margin of error (see Supplementary Figure 1). It is, therefore, recommended that investigators apply a combination of cell counting techniques when comparing the yields from PBMC isolation protocols, as most techniques do not offer both specific and highly sensitive differential cell counts. Further, assays were not performed to compare the functional activity of PBMCs yielded from either technique, which is a limitation of our analysis.
Next, the manual and automated bead-based methods were compared, and no significant differences between PBMC yield or viability were identified from 8 matched samples (Figure 4A,B). Cell populations were not individually compared, as the same antibody isolation cocktail was used for both methods. Importantly, the hands-on time to process 8 samples was reduced from 43 min to 22 min using the automated protocol&#160;(Figure 4C). While throughput, prevention of technician burnout, and consistency of specimen processing are ensured using automation, the cost of reagents and consumables are significantly higher at 3-4 fold more than the manual bead-based method. This is after making modifications to the manufacture&#39;s protocol to use 1 mL of buffy coat (from a whole blood volume of 10 mL) instead of the recommended range of 2-5 mL (from a whole blood volume of 10 mL and/or greater). If budget is a limitation, opting for the manual method can reduce processing time by ~25% while maintaining reagent and consumable costs comparable to those of the density separation method. It is recommended&#160;to process no more than 8 samples at a time per technician to ensure adequate staggering of samples (~30 s/sample) within the 5 min incubation periods (steps 3.7, 3.11, and 3.14).
In both the manual and automated bead-based methods, the removal of the buffy coat is a critical step to ensure optimal PBMC isolation. It is important to note that a buffy coat rather than whole blood is used in this protocol as the volume of reagents are&#160;based on starting material volumes10. Effectively removing the entire buffy coat volume can be technically challenging. Initially, this method detailed removing 0.5 mL buffy coat, however it was increased to 1 mL to improve recovery. To ensure adequate and consistent recovery of buffy coat, detailing this process is important in protocol documentation and training. It is recommended to swirl a pipette tip whilst aspirating the buffy coat while taking care not to aspirate too many RBCs from the layer below (step 2.3). It is important not to saturate the antibody cocktail that binds unwanted cells (i.e., granulocytes and red blood cells), which can impact yield and purity10. To minimize RBCs collected during the buffy coat extraction, the pipette tip should be inbetween the plasma and buffy coat layer. The volume of the buffy coat can be increased from 1 mL; however, care must be taken as described above to ensure that no more than 10% of the collected volume contains RBCs. Alternatively, an automated liquid handler can be used to collect buffy coats consistently18. However, the dedicated hours required to calibrate and troubleshoot liquid handling instrument protocols, especially considering the expense, may not be feasible for most laboratories.
The transition and application of the automation bead-based protocol was essential given the NSW Health Statewide Biobank&#39;s aim to process 23,000 PBMCs over the next 3 years. Here, it was demonstrated that PBMCs can be isolated from ACD tubes up to 9 days from collection with mean viabilities &#62;70%. While yields were optimal 24 h post-collection, processing within this timeframe is not always feasible as samples may need to be transported. It was shown that PBMCs isolated with either the manual or automated bead-based method may have yields of &#62;3 x 105 cells/mL whole blood when isolated within 4 days of collection and &#62;1 x 105 cells/mL whole blood when isolated within 10 days of collection. Low&#160;numbers for samples over 5 days are noted as a limitation of this analysis. Further, data was not separated based on participant ages, genders, and clinical history, as this information was not made available. Although a comparative analysis is needed to examine the effects of delays in processing times for both methods, it has previously been reported that delays in PBMC isolation using the density gradient method decrease cell quality and significantly increase RBC contamination19,20. In addition, granulocyte proportions increase if processing is delayed, and hence, specimens of similar &#34;ages&#34; should be grouped for downstream analyses20,21,22. Of note, this experiment was performed using blood anticoagulated with acid citric dextrose (i.e., trisodium citrate, citric acid, and dextrose); however, yield and/or proportion of cell types may vary if other anticoagulants are used23; therefore investigators are advised to choose an appropriate anticoagulant based on the intended downstream PBMC analyses.
In summary, a protocol for PBMC isolation using magnetic beads that is adaptable to high throughput workflows is detailed to fulfill the requirements for scaling without compromising cell viability. Both the manual and automated methods can be optimized to produce specific cell concentrations by changing starting and resuspension volumes. The NSW Health Statewide Biobank has transitioned from extracting ~60 PBMCs per month using the traditional density gradient separation technique to ~300 PBMCs per month using this automation-compatible bead-based method. The authors&#39; next aim is to use the automated platform to process up to 1200 PBMCs per month and further compare PBMCs isolated by both magnetic bead-based (manual and automated) and density gradient techniques to guide the implementation of this technique to other laboratories with a particular focus on biobanks.

Peripheral blood mononuclear cell (PBMC) isolation is a technique that separates and isolates lymphocytes and monocytes from other whole blood constituents. PBMCs are a versatile cell type used for numerous applications including, but not limited to, immunotherapy, vaccine development, target or biomarker identification, and antibody/small molecule drug development1,2. These cells may be isolated from healthy or diseased individuals and can be used immediately in downstream processes or cryopreserved for future research3. In some instances, the downstream purpose is known, while in others, as is common in biobanking, PBMCs are isolated and stored for future unspecified applications4.
Density gradient centrifugation is the traditional technique for isolating PBMCs5,6,7 from whole blood, utilizing the differential separation of the constituent cell types based on cell density during centrifugation. While there may be some variation in this method, whole blood is generally diluted with phosphate-buffered saline (PBS), layered over a density gradient medium in a specialized or standard centrifuge tube, and then spun. Four distinct layers result: the top plasma layer is enriched with platelets, a thin PBMC layer is above the density gradient medium, and finally, the bottom layer consists of red blood cells (RBCs) and granulocytes. Although this method has previously been termed &#39;the gold standard&#39;8, there are limitations for scale-up, such as lengthy processing time, centrifuge capacity, difficulty in aliquoting other blood products (i.e., plasma and RBCs), and being laborious to automate. While automation is possible for this method9, it does require comprehensive programming of a liquid handler (with a centrifugation module to be fully automated) and would remain a lengthy process.
Henceforth, an alternate workflow that uses immunomagnetic bead separation with either an eight-holder magnet for manual processing or an instrument for fully automated processing is presented. This method utilizes an antibody cocktail that is added to cells and binds unwanted cell populations, in this case, platelets, granulocytes, and RBCs. These unwanted populations are subsequently removed by magnetic separation, leaving monocyte and lymphocyte populations in the negative fraction that are ready for downstream processing10. This negative selection method is faster than positive selection methods which require additional steps to remove the antibody and magnetic bead complex from the PBMCs. Negative selection is additionally advantageous as it has been described as a way to preserve cell functionality11,12.

<table><tbody><tr><td>Cell cryopreservation media CS10, 100 mL (CRYOSTOR)</td><td>StemCell&lt;sup&gt;TM&lt;/sup&gt; Technologies</td><td>07930</td><td></td></tr><tr><td>Class II Biological Safety Cabinet</td><td>Thermo Scientififc&lt;sup&gt;TM&lt;/sup&gt;</td><td>51033311</td><td></td></tr><tr><td>CoolCell 1 mL FX</td><td>BioTools</td><td>BCS-407P</td><td>This is the control rate freezing container used.</td></tr><tr><td>Distilled Water&amp;nbsp;</td><td>Bacto Laboratories</td><td>561832</td><td></td></tr><tr><td>DxH 500 Hematology Analyzer&amp;nbsp;</td><td>Beckman Coulter Life Sciences</td><td>B40601</td><td>Referred to as external automated cell counter.</td></tr><tr><td>EasyEights&lt;sup&gt;TM&lt;/sup&gt; EasySep&lt;sup&gt;TM&lt;/sup&gt; Magnet</td><td>StemCell&lt;sup&gt;TM&lt;/sup&gt; Technologies</td><td>18103</td><td></td></tr><tr><td>EasySep&lt;sup&gt;TM&lt;/sup&gt; Direct Human PBMC Isolation Kit</td><td>StemCell&lt;sup&gt;TM&lt;/sup&gt; Technologies</td><td>19654</td><td>Kit includes the magnetic bead tube and the cocktail mix tube</td></tr><tr><td>Ethylenediaminetetraacetic acid</td><td>Sigma-Aldrich Pty Ltd</td><td>E6758-500G</td><td>Instructions to make 0.1M EDTA solution from EDTA salt is located in supplemental file 2.</td></tr><tr><td>Lymphoprep&lt;sup&gt;TM&lt;/sup&gt; Density Gradient Medium</td><td>StemCell&lt;sup&gt;TM&lt;/sup&gt; Technologies</td><td>7851</td><td></td></tr><tr><td>Megafuge ST4 Plus Centrifuge</td><td>Thermo Scientififc&lt;sup&gt;TM&lt;/sup&gt;</td><td>THR75009903</td><td></td></tr><tr><td>Orion Star A211 pH meter electrode</td><td>Thermo Scientififc&lt;sup&gt;TM&lt;/sup&gt;</td><td>STARA2110</td><td></td></tr><tr><td>Orion&amp;trade; ROSS Ultra&amp;trade; Glass Triode&amp;trade; pH/ATC Combination Electrodes</td><td>Thermo Scientififc&lt;sup&gt;TM&lt;/sup&gt;</td><td>8302BNURCA</td><td></td></tr><tr><td>Phosphate buffered saline (PBS), solution, 1X, 500ml</td><td>Life Technologies Australia Pty Ltd</td><td>10010023</td><td></td></tr><tr><td>Prism</td><td>GraphPad</td><td></td><td></td></tr><tr><td>RoboSep&lt;sup&gt;TM&lt;/sup&gt; Buffer 1X</td><td>StemCell&lt;sup&gt;TM&lt;/sup&gt; Technologies</td><td>20104</td><td>Software used for statistical analysis.</td></tr><tr><td>RoboSep&lt;sup&gt;TM&lt;/sup&gt;-S</td><td>StemCell&lt;sup&gt;TM&lt;/sup&gt; Technologies</td><td>21000</td><td>Fully automated cell separator instrument.</td></tr><tr><td>RoboSep&amp;trade; Filter Tips</td><td>StemCell&lt;sup&gt;TM&lt;/sup&gt; Technologies</td><td>20125</td><td></td></tr><tr><td>SepMate&lt;sup&gt;TM&lt;/sup&gt;-50 (IVD) tubes</td><td>StemCell&lt;sup&gt;TM&lt;/sup&gt; Technologies</td><td>85460</td><td>IVD - In vitro diagnostics. Also known as SepMate&lt;sup&gt;TM&lt;/sup&gt;-50 tubes</td></tr><tr><td>Vi-CELL XR Cell Anlayzer</td><td>Beckman Coulter Life Sciences</td><td></td><td>Internal automated cell counter. Instrument obsolete and no longer available for purchase (as of December 31, 2022). Alternative instrument is the ViCell BLU Cell Viability Analyzer (Product no. C19196).</td></tr><tr><td>Vi-CELL XR Quad Pack Reagent Kit</td><td>Beckman Coulter Life Sciences</td><td>383722</td><td></td></tr></tbody></table>

isolating human peripheral blood mononuclear cells from buffy coats via high throughput immunomagnetic bead separation

Peripheral blood mononuclear cells (PBMCs) are a heterogeneous population of monocytes and lymphocytes. Cryopreserved PBMCs have stable viability in long-term storage, making them an ideal cell type for many downstream research purposes, including flow cytometry, immunoassays, and genome sequencing. Typically, PBMCs are isolated via&#160;density gradient centrifugation, however, it is a low-throughput workflow that is difficult and costly to scale. This article presents a high-throughput workflow using a magnetic bead-based PBMC isolation method that is quick to implement. Total cell concentration, viability, and population distribution with PBMCs obtained using density gradient isolation were compared, and cell viability and proportion of cell types were comparable for both techniques. Isolated PBMCs demonstrated over 70% viability up to 9 days after blood collection, although yield decreased by half after 5 days compared to PBMCs processed within 24 h of collection. In summary, this article describes a PBMC protocol that utilizes a bead-based approach to adapt to a high throughput workflow and demonstrates that both manual and automated bead-based methods can increase processing capacity and provide flexibility for various budgets.

The proportions of lymphocytes, monocytes, neutrophils, eosinophils, and basophils pre- (i.e., in whole blood) and post-PBMC isolation were measured when PBMCs were isolated using the bead-based or density gradient separation method. Proportions of lymphocytes and monocytes were significantly enriched by both methods (Figure 2A,B). Additionally, proportions of neutrophils, eosinophils, and basophils (i.e., granulocytes) were significantly decreased in PBMCs isolated by the bead-based method (Figure 2C-F). There were no significant differences in the proportions of lymphocytes, monocytes, neutrophils, eosinophils, basophils, and granulocytes between the density gradient and bead-based methods (Figure 2). Percentage recovery was additionally calculated for the cell types listed above (see Supplementary Figure 1). Mean cell viabilities were over 95% for both methods, and were not significantly different (Figure 3A). PBMCs were also counted using a size range (diameter) of 8 µm to 50 µm, where the density gradient separation method produced approximately two times higher total cell counts (Figure 3B). 
Next, the automated bead-based method was compared to the manual method. No significant differences were identified for cell viability (Figure 4A) or total cell counts (Figure 4B) using the manual or automated method. The time to process these 8 samples was compared, including hands-off time requiring no human intervention. The total processing time of 8 samples was 43 min vs. 57 min for the manual vs. the automated method. The automated method included 35 min of hands-off processing (Figure 4C).
The bead-based workflow of PBMC isolation (with whole blood and plasma aliquoting) was piloted over 9 months, whereby 1410 PBMC samples were isolated from unscreened human blood using the manual platform for the first 820 participants and then using the automated method for the next 590 participants. Processing was performed either on the same day or up to 10 days post-collection as per the study acceptance criteria, with delays in processing largely due to sample transit times. With either the manual or automated method, PBMCs processed within 24 h of the collection had the highest viability and recovery (Figure 5). Mean cell viability was &gt;90% for PBMCs processed within 5 days and &gt;70% for PBMCs processed within 10 days (Figure 5A). Mean PBMC yields decreased by 50% after 5 days compared to specimens processed within 24 h (Figure 5B).
<img alt="Blood cell isolation and cryopreservation process diagram; centrifuge, magnetic beads, cryotubes." class="xfigimg" src="/files/ftp_upload/66887/66887fig01.jpg" data-altupdatedat="1747911167000" data-alt="Figure 1"> 
Figure 1: Schematic workflow of the bead-based PBMC isolation protocol from buffy coat. <a href="https://www.jove.com/files/ftp_upload/66887/66887fig01large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Cell isolation method comparison; graphs show percentages of lymphocytes, monocytes, other cells." class="xfigimg" src="/files/ftp_upload/66887/66887fig02.jpg" data-altupdatedat="1747911167000" data-alt="Figure 2"> 
Figure 2: Proportions of lymphocytes, monocytes, neutrophils, eosinophils, basophils, and granulocytes in whole blood pre- and post-PBMC isolation by density gradient and bead-based methods. Percentage of lymphocytes (A), monocytes (B), neutrophils (C), eosinophils (D), basophils (E), and granulocytes (F) in matched whole blood pre-PBMC isolation (squares) and in PBMCs post isolation via the density gradient (open circles) or bead-based (closed circles) method (n = 8). ns = not significant, and *p &lt; 0.05 as determined by One-Way ANOVA (A and B) or Friedman's test (C-F). <a href="https://www.jove.com/files/ftp_upload/66887/66887fig02large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Cell viability and count comparison chart; density gradient vs. bead-based method." class="xfigimg" src="/files/ftp_upload/66887/66887fig03.jpg" data-altupdatedat="1747911167000" data-alt="Figure 3"> 
Figure 3: Viability and total cell count of PBMC isolated by density gradient and bead-based methods. (A) Mean (± SD) cell viability for samples processed using density gradient (squares, dark bar) vs. bead-based (circles, open bar) methods for 8 paired samples. ns = not significant by paired t-test. (B) Total cell count for samples processed using density gradient (squares, dark bar) vs. bead-based (circles, open bar) methods for 8 paired samples. *p &lt; 0.05 determined using a paired t-test. <a href="https://www.jove.com/files/ftp_upload/66887/66887fig03large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Cell viability, count, and processing time comparison using trypan blue method; charts show manual vs automated results." class="xfigimg" src="/files/ftp_upload/66887/66887fig04.jpg" data-altupdatedat="1747911167000" data-alt="Figure 4"> 
Figure 4: Comparison of manual and automated bead-based methods. (A) Mean (± SD) cell viability for samples processed using manual (squares, dark bar) vs. automated (circles, open bar) bead-based methods for 8 paired samples. ns = not significant by Mann-Whitney test. (B) Total cell count for samples processed using manual (squares) vs. automated (circles) bead-based methods for 8 paired samples. ns = not significant by paired t-test. (C) Processing time for 8 samples processed using manual vs. automated methods, including hands-on (light bar) and hands-off time periods (dark bar). <a href="https://www.jove.com/files/ftp_upload/66887/66887fig04large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Bar graphs of cell viability and yield; manual vs automated processes over 10 days; statistics shown." class="xfigimg" src="/files/ftp_upload/66887/66887fig05.jpg" data-altupdatedat="1747911167000" data-alt="Figure 5"> 
Figure 5: Viability and yield of PBMC isolated from the bead-based method either manually or using automation according to the time between sample collection and PBMC storage. (A) Mean (± 95% CI) cell viability for participant samples processed using manual (dark bar) vs. automated (open bar) bead-based methods. Table detailing participant numbers. ns = not significant. na = not applicable. *p &lt; 0.05 by Tukey's multiple comparison's test. (B) Total cell count for participant samples processed using manual (dark bar) vs. automated (open bar) bead-based methods. Table detailing participant numbers. ns = not significant. na = not applicable. *p &lt; 0.05 by Tukey's multiple comparison's test. No value for Automated Day 10 due to the replicate number being lower than 3. <a href="https://www.jove.com/files/ftp_upload/66887/66887fig05large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
Supplementary Figure 1: Figure of differential cell percentage recovery with the density gradient and bead-based methods. The percentage was calculated using absolute cell counts pre-isolation in whole blood and post-isolation cell suspension using the density gradient method (squares, dark bar) and bead-based method (circles, open bar) (n = 8). ns = not significant, and *p &lt; 0.05 as determined by unpaired t-test. <a href="https://www.jove.com/files/ftp_upload/66887/Supplementary%20Figure%201.zip" target="_blank">Please click here to download this File.</a>
Supplementary File 1: Density gradient protocol. <a href="https://www.jove.com/files/ftp_upload/66887/Supplementary%20File%201_editedv2.zip" target="_blank">Please click here to download this File.</a>
Supplementary File 2: Preparation of 0.1 M EDTA, pH 8.0 in PBS. <a href="https://www.jove.com/files/ftp_upload/66887/Supplementary%20File%202_editedv2.zip" target="_blank">Please click here to download this File.</a>
Supplementary File 3: Detailed procedures performed to generate the representative data. <a href="https://www.jove.com/files/ftp_upload/66887/Supplementary%20File%203_editedv2.zip" target="_blank">Please click here to download this File.</a>

Author Spotlight: Advancements in PBMC Isolation &#8211; Enhancing Throughput and Consistency in Research

This protocol details a high-throughput automation-compatible method to isolate human peripheral blood mononuclear cells for biobanking and other purposes.

Isolating Human Peripheral Blood Mononuclear Cells from Buffy Coats via High Throughput Immunomagnetic Bead Separation

Peripheral blood mononuclear cells (PBMCs) are a heterogeneous population of monocytes and lymphocytes. Cryopreserved PBMCs have stable viability in ...

isolating-human-peripheral-blood-mononuclear-cells-from-buffy-coats

Research

JoVE Journal

Biology

3.0K Views.  New South Wales Health Pathology. Het isoleren van perifere mononucleaire bloedcellen, ook wel PBMC's genoemd, is doorgaans een langdurig en handmatig proces. We zagen een alternatieve methode die snel te implementeren zou zijn en in staat zou zijn om grote aantallen monsters te verwerken. Ons protocol biedt een geautomatiseerde methode met hoge doorvoer, waardoor consistentie wordt gegarandeerd en burn-out van technici wordt voorkomen.We beschrijven ook onze automatiseringscompatibele...

Video: Auteur in de schijnwerpers: Vooruitgang in PBMC-isolatie - Verbetering van de doorvoer en consistentie in onderzoek

Generation of Induced Pluripotent Stem Cells from Frozen Buffy Coats using Non-integrating Episomal Plasmids

Somatic cells can be reprogrammed into induced pluripotent stem cells (iPSCs) by forcing the expression of four transcription factors (Oct-4, Sox-2, Klf-4, and c-Myc), typically expressed by human embryonic stem cells (hESCs). Due to their similarity with hESCs, iPSCs have become an important tool for potential patient-specific regenerative medicine, avoiding ethical issues associated with hESCs. In order to obtain cells suitable for clinical application, transgene-free iPSCs need to be generated to avoid transgene reactivation, altered gene expression and misguided differentiation. Moreover, a highly efficient and inexpensive reprogramming method is necessary to derive sufficient iPSCs for therapeutic purposes. Given this need, an efficient non-integrating episomal plasmid approach is the preferable choice for iPSC derivation. Currently the most common cell type used for reprogramming purposes are fibroblasts, the isolation of which requires tissue biopsy, an invasive surgical procedure for the patient. Therefore, human peripheral blood represents the most accessible and least invasive tissue for iPSC generation.
In this study, a cost-effective and viral-free protocol using non-integrating episomal plasmids is reported for the generation of iPSCs from human peripheral blood mononuclear cells (PBMNCs) obtained from frozen buffy coats after whole blood centrifugation and without density gradient separation.

Induced pluripotent stem cells (iPSCs) represent a source of patient-specific tissues for clinical applications and basic research. Here, we present a detailed protocol to reprogram human peripheral blood mononuclear cells (PBMNCs) obtained from frozen buffy coats into viral-free iPSCs using non-integrating episomal plasmids.

Somatic cells can be reprogrammed into induced pluripotent stem cells (iPSCs) by forcing the expression of four transcription factors (Oct-4, Sox-2, ...

Developmental Biology

Isolating Human Peripheral Blood Mononuclear Cells and CD4+ T cells from S&#233;zary Syndrome Patients for Transcriptomic Profiling

Cutaneous T-cell lymphomas (CTCL) are derived from the transformation and uncontrolled proliferation of mature skin-homing T cells, and mycosis fungoides (MF) and S&#233;zary syndrome (SS) represent the most common subtypes. Despite a number of studies on characterizing gene expression, genetic alterations, and epigenetic abnormalities of CTCL, the molecular pathogenesis of MF/SS remains unclear. MF refers to the more common CTCL with a skin-predominance, and is usually limited to skin, whereas&#160;SS is an aggressive leukemic variant of CTCL with widespread skin involvement and is characterized by neoplastic distribution mainly involving blood, skin, and lymph node. Focusing on clinical practice, the identification of gene expression biomarkers has&#160;enormous potential to improve diagnosis and treatment of MF/SS. Indeed, recent transcriptomic studies have identified potential diagnostic biomarkers from differences in gene expression between normal and malignant T cells, which may improve our understanding of SS biology, and reveal potential therapeutic targets. This manuscript describes a detailed reproducible protocol for the isolation of peripheral blood mononuclear cells from fresh whole blood from patients diagnosed with SS, selection of CD4+ memory T cells (CD4+CD45RO+ T cells), chemical stimulation, and preparation of RNA suitable for transcriptomic profiling to discover novel prognostic molecular markers to gain additional insight in disease etiology. The stimulation using chemical agonist to activate nuclear regulation provides more specific assessment for pathways important in the dynamic transcription regulation and gene expression and eliminates confounding defects that may arise from upstream signaling defects arising from TCR antigen loss at the cell membrane. The data obtained from comparison of transcriptome of unstimulated to stimulated SS T cells unmasks functional regulatory gene expression defects not evident from analysis of quiescent unstimulated cells. Furthermore, the method outlined from this approach can be adapted for studying T cell gene expression defects in other T cell immune diseases.

We present a simple protocol for the isolation of peripheral blood mononuclear cells from whole blood obtained from patients diagnosed with S&#233;zary Syndrome, followed by selection of CD4+ T cells, their stimulation with phorbol12-myristate13-acetate and A23187 ionophore, and preparation of RNA for transcriptomic profiling.

Cutaneous T-cell lymphomas (CTCL) are derived from the transformation and uncontrolled proliferation of mature skin-homing T cells, and mycosis fungoides ...

Cancer Research

Generation of Human Monocyte-derived Dendritic Cells from Whole Blood

Dendritic cells (DCs) recognize foreign structures of different pathogens, such as viruses, bacteria, and fungi, via a variety of pattern recognition receptors (PRRs) expressed on their cell surface and thereby activate and regulate immunity. 
The major function of DCs is the induction of adaptive immunity in the lymph nodes by presenting antigens via MHC I and MHC II molecules to na&#239;ve T lymphocytes. Therefore, DCs have to migrate from the periphery to the lymph nodes after the recognition of pathogens at the sites of infection. For in vitro experiments or DC vaccination strategies, monocyte-derived DCs are routinely used. These cells show similarities in physiology, morphology, and function to conventional myeloid dendritic cells. They are generated by interleukin 4 (IL-4) and granulocyte-macrophage colony-stimulating factor (GM-CSF) stimulation of monocytes isolated from healthy donors. Here, we demonstrate how monocytes are isolated and stimulated from anti-coagulated human blood after peripheral blood mononuclear cell (PBMC) enrichment by density gradient centrifugation. Human monocytes are differentiated into immature DCs and are ready for experimental procedures in a non-clinical setting after 5 days of incubation.

Here, we demonstrate how monocytes are isolated by magnetic bead separation from peripheral blood mononuclear cells after density gradient centrifugation of human anti-coagulated blood. Following incubation for 5 days, human monocytes are differentiated into immature dendritic cells and are ready for experimental procedures in a non-clinical setting.

Dendritic cells (DCs) recognize foreign structures of different pathogens, such as viruses, bacteria, and fungi, via a variety of pattern recognition ...

Immunology and Infection

Separation of Immune Cell Subpopulations in Peripheral Blood Samples from Children with Infectious Mononucleosis

Infectious mononucleosis (IM) is an acute syndrome mostly associated with primary Epstein&#8211;Barr virus (EBV) infection. The main clinical symptoms include irregular fever, lymphadenopathy, and significantly increased lymphocytes in peripheral blood. The pathogenic mechanism of IM is still unclear; there is no effective treatment method for it, with mainly symptomatic therapies being available. The main question in EBV immunobiology is why only a small subset of infected individuals shows severe clinical symptoms and even develop EBV-associated malignancies, whilemost individuals are asymptomatic for life with the virus.
B cells are first involved in IM because EBV receptors are presented on their surface. Natural killer (NK) cells are cytotoxic innate lymphocytes that are important for killing EBV-infected cells. The proportion of CD4+ T cells decreases while that of CD8+ T cells expands dramatically during acute EBV infection, and the persistence of CD8+ T cells is important for lifelong control of IM. Those immune cells play important roles in IM, and their functions need to be identified separately. For this purpose, monocytes are separated first from peripheral blood mononuclear cells (PBMCs) of IM individuals using CD14 microbeads, a column, and a magnetic separator.
The remaining PBMCs are stained with peridinin-chlorophyll-protein (PerCP)/Cyanine 5.5 anti-CD3, allophycocyanin (APC)/Cyanine 7 anti-CD4, phycoerythrin (PE) anti-CD8, fluorescein isothiocyanate (FITC) anti-CD19, APC anti-CD56, and APC anti-CD16 antibodies to sort CD4+ T cells, CD8+ T cells, B cells, and NK cells using a flow cytometer. Furthermore, transcriptome sequencing of five subpopulations was performed to explore their functions and pathogenic mechanisms in IM.

We describe a method combining immunomagnetic beads and fluorescence-activated cell sorting to isolate and analyze defined immune cell subpopulations of peripheral blood mononuclear cells (monocytes, CD4+ T cells, CD8+ T cells, B cells, and natural killer cells). Using this method, magnetic and fluorescently labeled cells can be purified and analyzed.

Infectious mononucleosis (IM) is an acute syndrome mostly associated with primary Epstein&#8211;Barr virus (EBV) infection. The main clinical symptoms ...

Isolation of Human Neutrophils from Whole Blood and Buffy Coats

Neutrophils (PMNs) are the most abundant leukocytes in human circulation, ranging from 40 to 70% of total blood leukocytes. They are the first cells recruited at the site of inflammation via rapid extravasation through vessels. There, neutrophils perform an array of functions to kill invading pathogens and mediate immune signaling. Freshly purified neutrophils from human blood are the model of choice for study, as no cell line fully replicates PMN functions and biology. However, neutrophils are short-lived, terminally differentiated cells and are highly susceptible to activation in response to physical (temperature, centrifugation speed) and biological (endotoxin, chemo- and cytokines) stimuli. Therefore, it is crucial to follow a standardized, reliable, and fast method to obtain pure and non-activated cells. This protocol presents an updated protocol combining density gradient centrifugation, red blood cell (RBC) sedimentation, and RBC lysis to obtain high PMN purity and minimize cell activation. Furthermore, methods to assess neutrophil isolation quality, viability, and purity are also discussed.

This protocol details a method for the isolation of neutrophils from whole blood, buffy coats, or leukapheresis membranes, achieving good yield, high purity, and minimal cell activation. We utilize gradient purification, red blood cell (RBC) sedimentation, and RBC lysis to obtain a high-quality/purity neutrophil preparation.

Neutrophils (PMNs) are the most abundant leukocytes in human circulation, ranging from 40 to 70% of total blood leukocytes. They are the first cells ...

Isolation and Cryopreservation of Highly Viable Human Peripheral Blood Mononuclear Cells From Whole Blood: A Guide for Beginners

Peripheral blood mononuclear cells (PBMCs) are commonly used in biomedical research on the immune system and its response to disease and pathogens. This detailed protocol describes the equipment, supplies, and steps for isolating, cryopreserving, and thawing high-quality and highly viable PBMCs from whole blood cells suitable for downstream applications such as flow cytometry and RNA-sequencing. Protocols for processing plasma and buffy coat from the whole blood in parallel and concurrently with PBMCs are also described. This easy-to-follow step-by-step protocol, which utilizes density gradient centrifugation to isolate PBMCs, is accompanied by a checklist of supplies, equipment, and preparation steps. This protocol is suitable for individuals with any prior experience with laboratory techniques and can be implemented in clinical or research laboratories. High-quality cell viability and RNA sequencing resulted from PBMCs collected by operators with no prior laboratory experience using this protocol.

This protocol presents an accessible guide for collecting, storing, and thawing peripheral blood mononuclear cells suitable for downstream analyses and workflows like flow cytometry and RNA sequencing. Plasma and buffy coat collections are also demonstrated.

Peripheral blood mononuclear cells (PBMCs) are commonly used in biomedical research on the immune system and its response to disease and pathogens. This ...

Medicine

Isolation of Monocytes from Whole Blood by Immunomagnetic Negative Selection

Source: Plaisance-Bonstaff, K., et al. <a href="https://app.jove.com/v/59967">Isolation, Transfection, and Culture of Primary Human Monocytes.</a> J. Vis. Exp. (2019)
In this video, we demonstrate the isolation of monocytes from whole human blood by immunomagnetic negative separation. The isolated monocytes can be used for further downstream analysis.

Source: Plaisance-Bonstaff, K., et al. Isolation, Transfection, and Culture of Primary Human Monocytes. J. Vis. Exp. (2019)
In this video, we demonstrate ...

JoVE Encyclopedia of Experiments

Immunology

Immune Systems and Components

Cell Isolation and Culture

Isolating Cord Blood Hematopoietic Stem Cells to Generate Human Immune System Mice

Source: Lanis, J. M., et al. <a href="https://app.jove.com/v/64606">Testing Cancer Immunotherapeutics in a Humanized Mouse Model Bearing Human Tumors.</a> J. Vis. Exp. (2022)
This video demonstrates a technique for generating human immune system (HIS) mice. CD34+ hematopoietic stem cells (HSCs) are isolated from human cord blood buffy coat cells using antibody-coated magnetic beads. The CD34+ HSCs are expanded in a growth medium enriched with cytokines and cryopreserved. Finally, the thawed HSCs are injected into an immunodeficient mouse pup to establish the HIS mouse model.

All procedures involving sample collection have been performed in accordance with the institute&#39;s IRB guidelines. All procedures involving animal ...

Immunotherapy

Model Development and Disease Study

Isolation and Purification of B Cells from Human Peripheral Blood

Source: Tzeng, S. J. <a href="https://app.jove.com/v/54582">The Isolation, Differentiation, and Quantification of Human Antibody-secreting B Cells from Blood: ELISpot as a Functional Readout of Humoral Immunity.</a> J. Vis. Exp. (2016)
In this video, we demonstrate the isolation of B cells from human peripheral blood using biotinylated antibodies specific for non-B cells and streptavidin-conjugated magnetic microbeads.

Source: Tzeng, S. J. The Isolation, Differentiation, and Quantification of Human Antibody-secreting B Cells from Blood: ELISpot as a Functional Readout of ...

Negative Immunomagnetic Selection: A Method to Purify B-cells from Peripheral Blood Mononuclear Cells

Source: Serra S. et al. <a href="https://www.jove.com/t/54124">HPLC-based Assay to Monitor Extracellular Nucleotide/Nucleoside Metabolism in Human Chronic Lymphocytic Leukemia Cells.</a> J. Vis. Exp. (2016)
The video explains a way to purify B-cells by immunomagnetic targeting and separation from peripheral blood mononuclear cells suspension. The method involve labeling unwanted cell types with specific antibodies or ligands (linked to magnetic particles) targeting specific cell surface proteins, to be depleted from the heterogenous cell suspension by magnetic separation.

Source: Serra S. et al. HPLC-based Assay to Monitor Extracellular Nucleotide/Nucleoside Metabolism in Human Chronic Lymphocytic Leukemia Cells. J. Vis. ...

Isolating Human Peripheral Blood Mononuclear Cells from Buffy Coats via High Throughput Immunomagnetic Bead Separation

Samenvatting

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