eoe sub articles

EoE Sub Articles

1. Generation and validation of single chain Fab antibody (scFab)-CARs.
NOTE: CARs typically contain 3 critical domains&#8212;an antigen-targeting domain, a spacer/transmembrane domain, and a cytoplasmic signaling domain. The precise design of each CAR depends on the intended target, and so, apart from the key features of the construct relevant to the generation of the retrovirus, will not be described in detail in this protocol. The overall design of the CARs used for the studies described below is shown in Figure 1. In brief, the targeting domain comprises the entire light chain and variable and CH1 domain of the heavy chain from the parent monoclonal antibody linked by a semi-rigid linker. The spacer/transmembrane domain is from mouse CD28, and the signaling domain is a fusion containing elements from mouse CD28, CD137 (4-1BB), and CD247 (CD3&#950;). These elements are assembled by standard molecular biology procedures such as splice overlap polymerase chain reaction (PCR), or the synthesis of an appropriate &#34;gene block&#34;. Details of the generation of the mAB287 CAR are contained in Zhang et al. The cDNA sequences can be obtained from the authors upon request.
<ol>
	<li>Assembling the CAR construct&#8203;
	<ol>
		<li>Synthesize the targeting single chain Fab antibody (scFab) and combined spacer/signaling domains separately, and use a &#34;3 point&#34; ligation technique to assemble the final construct (Figure 1). 
		&#8203;NOTE: The key requirement for the CAR insert is that it should contain flanking restriction endonuclease sites allowing ligation into the retroviral expression vector pMSCV-IRES-GFP II (pMIG II), or a related derivative are also appropriate.</li>
	</ol>
	</li>
	<li>Validation of CAR surface expression
	<ol>
		<li>Transduce the hybridoma cells using pMIG II derived retroviral particles generated by a standard protocol (e.g., Holst et al.).</li>
		<li>Run flow cytometry analysis to detect the expression of GFP from the CAR vector.</li>
		<li>Stain surface expression of the CAR of the transduced hybridomas using labeled antibodies against the mouse &#954; chain (e.g., clone RMK-45).</li>
	</ol>
	</li>
	<li>Validation of CAR specificity
	<ol>
		<li>Stimulate the transduced hybridoma cells with appropriate plate-bound or cellular antigens. After overnight co-culture collect supernatants and secreted cytokines, and assayed by enzyme-linked immunosorbent assay (ELISA). 
		NOTE: Ideally, each CAR should be independently validated before being used for transduction. At this step, the experiment may be paused and restarted later.</li>
	</ol>
	</li>
</ol>
2. Transfection of viral producer cells (day - 4 to day 3)
NOTE: Retrovirus is produced using Phoenix-ECO cells (see the Table of Materials). Use appropriate precautions for the generation of potentially infectious agents (preferably including a designated Biosafety level 2 (BSL-2) cabinet and separate incubator for culturing transfected/transduced cells).
<ol>
	<li>Thawing Phoenix cells (Day -4)
	<ol>
		<li>Thaw 2 x 106 Phoenix-Eco cells. Scale up the number of Phoenix cells if multiple transductions are planned.</li>
		<li>Plate them in a 10 cm tissue culture dish with 10 mL of medium (Dulbecco&#39;s modified Eagle medium (DMEM) containing 10% fetal calf serum (FCS)).</li>
	</ol>
	</li>
	<li>Passage Phoenix cells (Day -3)
	<ol>
		<li>Remove medium, and wash with 5 mL of Dulbecco&#39;s phosphate-buffered saline (DPBS).</li>
		<li>Add 3 mL of 0.25% trypsin and incubate at 37 &#176;C under 10% CO2 atmosphere for 3 min.</li>
		<li>Harvest the cells then pellet by centrifugation for 3 min at 200 x g. Re-plate cells with 10 mL fresh medium and incubate at 37 &#176;C.</li>
	</ol>
	</li>
	<li>Irradiation of Phoenix cells (Day -1 afternoon)
	<ol>
		<li>To minimize further cell division, collect Phoenix cells as described in step 2.2, resuspend in 5 mL of medium, and gamma irradiate cells on ice (1000 rad). 
		NOTE: Caution should be used for radiation work to avoid personnel exposure.</li>
		<li>Centrifuge the irradiated cells, resuspend in fresh medium, plate at 2 x 106 cells (in 10 mL of medium)/plate/CAR, and incubate.</li>
	</ol>
	</li>
	<li>Transfection (Day 0 - morning)
	<ol>
		<li>Aspirate the supernatant from the Phoenix cells, wash with 5 mL of phosphate-buffered saline (PBS), and carefully add 7 mL of reduced serum medium (e.g., Opti-MEM) dropwise to the sidewall of the plate to avoid disturbing the monolayer. Transfer cells back to incubator.</li>
		<li>Take two 14 mL round bottom polypropylene tubes, and add 1.5 mL of reduced serum medium to each. To one tube, add 40 &#181;L of transfection reagent (see the Table of Materials).</li>
		<li>To the other tube, add 15 &#181;g of Ab-CAR-plasmid (generated in step 1) and 5 &#181;g of envelope and packaging plasmid (5 &#181;g pCL-Eco). Incubate tubes at room temperature for 5 min.</li>
		<li>Add the transfection reagent mixture from step 2.4.2 dropwise to the second tube without contacting the tube sides, and mix by pipetting the solution up and down gently 3 times. Incubate at room temperature for at least 20 min.</li>
		<li>Add 3 mL of the mixture dropwise to the Phoenix cells, and place in a tissue culture incubator.</li>
		<li>After 4&#8211;5 h add 1 mL of FCS. Culture cells overnight at 37 &#176;C.</li>
	</ol>
	</li>
	<li>Medium change (Day 1)&#8203;
	<ol>
		<li>Remove the supernatant containing the plasmid/transfection reagent complexes and dispose of them in accordance with institutional procedures for handling infectious material. Add 4 mL of fresh, pre-warmed culture medium to the cells.</li>
	</ol>
	</li>
	<li>Harvest virus for Transduction (Day 2)
	<ol>
		<li>Collect the virus-containing medium from the Phoenix cells with a sterile syringe, filter (0.45 &#181;m) to remove residual cell debris, and collect in a new tube.</li>
		<li>Add recombinant human interleukin-2 (rhIL-2) stock to a final concentration of 200 international unit (IU)/mL. Use the virus immediately for transduction (step 5.3). Add 4 mL of fresh medium to the Phoenix cells and place in the incubator.</li>
	</ol>
	</li>
	<li>Repeat virus collection (Day 3)
	<ol>
		<li>Repeat step 2.6, but discard Phoenix cells as infectious waste instead of adding fresh medium. This supernatant is used in step 5.4.</li>
	</ol>
	</li>
</ol>
3. Primary CD8 T cell isolation and activation (day -1 to day 0)
NOTE: Previously, collect CD8 T cells from female nonobese diabetic (NOD) mice at 4&#8211;5 weeks, a time point before islet inflammation starts. Handle all the mice following Institutional Animal Care &#38; Use Committee (IACUC) approved protocols. CD8 T cells are enriched from splenocytes using a commercial negative selection kit.
<ol>
	<li>Coating plates with CD3/CD28 antibodies (Day -1)
	<ol>
		<li>Add 1 mL of a mixture of anti-mouse CD3 and CD28 antibodies (both at 1 &#181;g/mL in PBS) to each well of a 24-well plate, and incubate at 4 &#176;C overnight.</li>
		<li>The next day, wash the plates with 1 mL of sterile PBS 3 times before adding the murine CD8 T cells (step 4.1). 
		&#8203;NOTE: The number of wells to be coated will vary for each experiment, depending on the total number of activated CD8 T cells required.</li>
	</ol>
	</li>
	<li>Collection of splenocytes (Day 0)
	<ol>
		<li>Euthanize two NOD female mice aged 4&#8211;5 weeks using CO2 inhalation followed by decapitation. Harvest the spleens and put them onto a cell strainer soaking in 10 mL PBS in a cell culture dish on the ice.</li>
		<li>In a cell culture hood, cut each spleen into 3&#8211;5 pieces, press tissues with a sterile plunger of a 3 or 5 mL syringe to force spleen fragments apart and allow cells to pass through the wire mesh.</li>
		<li>Gently remove red blood cells by resuspending splenocytes in 1:4 diluted red cell lysis buffer (1 mL of lysis buffer in 3 mL of PBS for one spleen), and incubating for 5 min at room temperature.</li>
		<li>Then, dilute 10 &#956;L of the cell suspension with trypan blue dye solution for counting cells with a hemocytometer, and pellet the rest of the cells by centrifugation at 350 x g for 7 min.</li>
	</ol>
	</li>
	<li>Enrichment of CD8 T cells (Day 0)
	<ol>
		<li>Enrich CD8 T cells by negative selection using a mouse CD8 T cell isolation kit, following the manufacturer&#39;s instructions. 
		NOTE: To ensure high purity always round up the cell numbers when calculating the volume of biotinylated-antibody to be added (e.g., use the volume of reagents suggested for 108 cells for a calculated 9.1 x 107 cells).</li>
		<li>Suspend cell pellets in 400 &#181;L of buffer and 100 &#181;L of biotin-antibody cocktail per 1 x 108 cells, mix well and incubate for 5 min in the refrigerator (4 &#176;C) to allow antibody binding.</li>
		<li>Add 300 &#181;L of labeling buffer and 200 &#181;L of anti-biotin micro-beads per 1 x 108 cells, mix well and incubate for 10 min at 4 &#176;C.</li>
		<li>While waiting for the micro-bead binding, set up the separation column onto the separator. Wash column by rinsing with 3 mL of labeling buffer.</li>
		<li>Pass 1000 &#181;L of bead/cell mixture through a 40 &#181;m cell strainer before loading onto the separation column to remove cell aggregates. Collect the column flow-through into a pre-chilled 15 mL tube.</li>
		<li>Wash the column as instructed by the manufacturer, collecting all the effluent into the same tube. Determine the cell number (same as step 3.2.4) and collect by centrifugation at 350 x g for 5 min. Wash the cells by resuspending in 2 mL of complete T cell medium (RPMI-1640 containing FCS, 2-mercaptoethanol, rhIL-2 (200 U/mL), mouse Interleukin-7 (mIL-7, 0.5 ng/mL), ITS, 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid (HEPES) and penicillin-streptomycin) and centrifuging at 350 x g for 5 min.</li>
		<li>Resuspend the cells in pre-warmed (37 &#176;C) complete T cell medium at a concentration of 0.25&#8211;0.5 x 106/mL.</li>
	</ol>
	</li>
</ol>
4. T cell activation (Day 0 to 2)
<ol>
	<li>Add 2 mL of the cell suspension (0.25&#8211;0.5 x 106/mL) to each coated well of the CD3/CD28 antibody coated 24-well plate from step 3.1.2. Use a swirling motion to dispense the cells evenly. 
	NOTE: Add the cells using a swirling motion to distribute them evenly and minimize edge effects. If the cells cluster along the edge of the wells, both the transduction rate and cell viability will be decreased.</li>
	<li>As a control, plate the same number of CD8 T cells into a single non-coated well of the plate. Incubate the cells at 37 &#176;C using a 10% CO2 gassed incubator for 48 h. 
	NOTE: After 48 h, activation can be confirmed using a microscope; the activated cells will be larger than the cells that did not encounter anti-CD3/CD28 antibodies.</li>
</ol>
5. Transduction of activated CD8 T cells (days 1 to 3)
NOTE: This protocol uses a spin-transduction method. A centrifuge with a swing-out rotor and tissue culture plate adaptors that is capable of maintaining an internal temperature of 37 &#176;C is required. To ensure maximum efficiency, on the day of transduction pre-warm the centrifuge to 37 &#176;C before collecting the virus.
<ol>
	<li>Preparation of human fibronectin fragment coated plates (Day 1 to day 2)&#8203;
	<ol>
		<li>On day 1, add 0.5 mL of fibronectin (50 &#181;g/mL in PBS) to the wells of a 24-well plate, and incubate overnight at 4 &#176;C. 
		&#8203;NOTE: Typically, two fibronectin-coated wells are required per plate of transfected Phoenix cells.</li>
		<li>On day 2 remove the fibronectin solution, and replace with 1 mL of 2% bovine serum albumin (BSA) in PBS. Incubate at room temperature for 30 min to &#34;block&#34; non-specific binding sites.</li>
		<li>Wash the treated wells with 1 mL of sterile PBS. After removing the wash solution, the plate is ready for use; or, can be sealed and stored at 4 &#176;C for up to one week.</li>
	</ol>
	</li>
	<li>Collection of activated CD8 T cells (Day 2)&#8203;
	<ol>
		<li>Harvest the activated CD8 T cells, count and calculate cell viability using trypan blue or a suitable automated instrument.</li>
		<li>Collect cells by centrifugation and resuspend at 5 x 106 viable cells/mL for transduction. Maintain a small aliquot of cells in culture in the complete T cell medium in the CO2 incubator to provide a control for subsequent fluorescence activated cell sorting of the transduced cells (step 6). 
		NOTE: After activation for 48 h, the total number of cells should have increased by approximately 1.5 fold, and have a viability greater than 95%.</li>
	</ol>
	</li>
	<li>Transduction (Day 2)
	<ol>
		<li>Add 100 &#181;L of activated CD8 cell suspension per well (0.5 x 106 cells) to the fibronectin coated plate. Then add 1.5&#8211;2 mL of virus-containing medium (from step 2.6) to each well. Mix using a swirling motion to dispense the cells evenly (Figure 2).</li>
		<li>Place the plate in a zip-lock plastic bag and seal (to provide secondary containment). Centrifuge at 2000 x g for 90 min at 37 &#176;C.</li>
		<li>Remove the plate from the centrifuge. In the biological safety, cabinet carefully remove the plastic bag and ensure that the outside of the plate is not contaminated with any medium.</li>
		<li>Then transfer the plate to the dedicated 37 &#176;C CO2 incubator. After 4 h, remove 1 mL of the medium from each well and replace with 1 mL of pre-warmed complete T cell medium. Replace the plate in the CO2 incubator. 
		NOTE: Handle all media from the transduced cells as infectious waste.</li>
	</ol>
	</li>
</ol>

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>2-Mercaptoethanol (50mM)</td>
			<td>Gibco</td>
			<td>21985-023</td>
			<td>50 uM</td>
		</tr>
		<tr>
			<td>5&#39; RACE PCR</td>
			<td>Clontech</td>
			<td>634859</td>
			<td></td>
		</tr>
		<tr>
			<td>anti-mouse CD28 antibodies</td>
			<td>eBioscience</td>
			<td>14-0281-86</td>
			<td>final concentration at 1&#181;g/ml</td>
		</tr>
		<tr>
			<td>anti-mouse CD3e antibody</td>
			<td>eBioscience</td>
			<td>145-2C11</td>
			<td>final concentration at 1&#181;g/ml</td>
		</tr>
		<tr>
			<td>Biotin Rat Anti-Mouse IFN-&#947;</td>
			<td>BD Biosciences</td>
			<td>554410</td>
			<td>Working concentration at 0.5 &#181;g/ml</td>
		</tr>
		<tr>
			<td>BSA</td>
			<td>Sigma</td>
			<td>A7030</td>
			<td></td>
		</tr>
		<tr>
			<td>Endo-free Maxi-Prep kit</td>
			<td>Qiagen</td>
			<td>12362</td>
			<td></td>
		</tr>
		<tr>
			<td>Gentamicin</td>
			<td>Gibco</td>
			<td>15750-060</td>
			<td>Final 50 &#181;g/ml.</td>
		</tr>
		<tr>
			<td>Heat inactivated FCS</td>
			<td>Hyclone</td>
			<td>SH30087.03</td>
			<td>Final 10% FCS</td>
		</tr>
		<tr>
			<td>HEPES (100X)</td>
			<td>Gibco</td>
			<td>15630-080</td>
			<td>1X</td>
		</tr>
		<tr>
			<td>Insulin-Transferrin-Selenium-Ethanolamine (ITS 100x)</td>
			<td>ThermoFisher</td>
			<td>51500056</td>
			<td>Final concentraion is 1x</td>
		</tr>
		<tr>
			<td>Lipofectamine 2000</td>
			<td>Invitrogen</td>
			<td>11668019</td>
			<td></td>
		</tr>
		<tr>
			<td>LS Columns</td>
			<td>Miltenyi Biotec</td>
			<td>130-042-401</td>
			<td></td>
		</tr>
		<tr>
			<td>MACS Separation Buffer</td>
			<td>Miltenyi Biotec</td>
			<td>130-091-221</td>
			<td></td>
		</tr>
		<tr>
			<td>Mouse CD8a+ T Cell Isolation Kit</td>
			<td>Miletenyi Biotec Inc</td>
			<td>130-104-075</td>
			<td></td>
		</tr>
		<tr>
			<td>Mouse CD8a+ T Cell Isolation Kit</td>
			<td>Miltenyi Biotec</td>
			<td>130-104-075</td>
			<td></td>
		</tr>
		<tr>
			<td>Opti-MEM medium</td>
			<td>ThermoFisher</td>
			<td>31985070</td>
			<td></td>
		</tr>
		<tr>
			<td>Penicillin-Streptomycin (5000U/ml)</td>
			<td>ThermoFisher</td>
			<td>15070063</td>
			<td>50 U/ml</td>
		</tr>
		<tr>
			<td>Phoenix-ECO cells</td>
			<td>ATCC</td>
			<td>CRL-3214</td>
			<td></td>
		</tr>
		<tr>
			<td>Phosphate-buffered saline (PBS)</td>
			<td>Gibco</td>
			<td>10010-023</td>
			<td></td>
		</tr>
		<tr>
			<td>pMIG II</td>
			<td>Addgene</td>
			<td>52107</td>
			<td></td>
		</tr>
		<tr>
			<td>pMSCV-IRES-GFP II</td>
			<td>Addgene</td>
			<td>52107</td>
			<td></td>
		</tr>
		<tr>
			<td>Red cell lysis buffer</td>
			<td>Sigma</td>
			<td>R7767</td>
			<td></td>
		</tr>
		<tr>
			<td>RetroNectin</td>
			<td>Takara</td>
			<td>T100A</td>
			<td>Working concentration at 50 &#181;g/ml in PBS</td>
		</tr>
		<tr>
			<td>rhIL-2 (stock concentration 105 IU/ul)</td>
			<td>Peprotech</td>
			<td>200-02</td>
			<td>Final concentration at 200 IU/ml</td>
		</tr>
		<tr>
			<td>rmIL-7 ( stock concentration 50ng/ul)</td>
			<td>R&#38;D</td>
			<td>407-ML-005</td>
			<td>Final concentration at 0.5ng/ml</td>
		</tr>
		<tr>
			<td>RPMI-1640</td>
			<td>Gibco</td>
			<td>11875-093</td>
			<td></td>
		</tr>
		<tr>
			<td>Sterile Cell Strainers</td>
			<td>Fisher Scientific</td>
			<td>22-363-548</td>
			<td></td>
		</tr>
		<tr>
			<td>Tryple</td>
			<td>Gibco</td>
			<td>12605-028</td>
			<td></td>
		</tr>
	</tbody>
</table>

a technique for the generation of antigen-specific car t cells

Source: Davidson, H. W., et al. <a href="https://app.jove.com/v/59985">High-Efficiency Generation of Antigen-Specific Primary Mouse Cytotoxic T Cells for Functional Testing in an Autoimmune Diabetes Model.</a> J. Vis. Exp. (2019).
This video demonstrates a technique for generating antigen-specific chimeric antigen receptor (CAR) T cells through retroviral transduction. Activated murine CD8+ T cells are added to a microwell plate coated with recombinant fibronectin fragments. Retroviral vectors containing transgenic RNA encoding an antigen-specific chimeric antigen receptor (CAR) are then introduced, and the plate is centrifuged to facilitate transduction. After incubation, the transduced cells express antigen-specific CARs on their surface.

<img alt="Figure 1" src="/files/ftp_upload/22263/22263_Figure1.jpg" /> 
Figure 1: Schematic of the CAR retroviral construct. The CAR comprises a targeting domain derived from the Fab fragment of a suitable mouse monoclonal antibody, and a spacer/ membrane anchor/ signaling domain from mouse CD28, CD137 and CD247. The synthetic cDNA is inserted into the pMIG-II retroviral expression vector. Restriction endonuclease sites used for generating the mAb287-CAR are shown.</...

A Technique for the Generation of Antigen-Specific CAR T Cells

1. Generation and validation of single chain Fab antibody (scFab)-CARs.
NOTE: CARs typically contain 3 critical domains&#8212;an antigen-targeting domain, ...

Take a microwell plate coated with recombinant fibronectin fragments and add activated murine CD8-positive T cells.
Introduce retroviral vectors containing a transgenic RNA that encodes a chimeric antigen receptor or CAR.
Cover the plate and seal it in a bag to avoid contamination. Centrifuge the plate at a low speed to facilitate virus-cell interaction.
Fibronectin binds to the virus and the cell, colocalizing them to enhance virus-mediated gene transfer.
Post-centrifugation, remove the sealed bag and incubate the plate under physiological conditions.
The envelope of the viral vector fuses with the cell membrane, releasing the viral RNA and enzymes.
The viral enzymes reverse-transcribe the released RNA and integrate the resulting DNA into the host genome, enabling the cells to express surface-bound CARs.
The CAR comprises an antigen-binding domain specific to the target antigen and signaling domains for T cell activation.
The antigen-specific CAR T cells are ready for downstream assays.

a-technique-for-the-generation-of-antigen-specific-car-t-cells

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Immunology

Immunotherapy

Cellular Immunotherapy

151 次观看. 来源:Davidson， H. W. et al.高效生成抗原特异性原代小鼠细胞毒性 T 细胞，用于自身免疫性糖尿病模型中的功能测试。J. Vis. Exp. （2019 年）。 该视频演示了一种通过逆转录病毒转导生成抗原特异性嵌合抗原受体 （CAR） T 细胞的技术。将活化的小鼠 CD8+ T 细胞加入到包被有重组纤连蛋白片段的微孔板中。然后引入含有编码抗原特异性嵌合抗原受体 （CAR） 的转基因 RNA 的逆转录病毒?...

视频: 一种生成抗原特异性 CAR T 细胞的技术 - 概念

A Syngeneic Mouse B-Cell Lymphoma Model for Pre-Clinical Evaluation of CD19 CAR T Cells

The astonishing clinical success of CD19 chimeric antigen receptor (CAR) T-cell therapy has led to the approval of two second generation chimeric antigen receptors (CARs) for acute lymphoblastic leukemia (ALL) andnon-Hodgkin lymphoma (NHL). The focus of the field is now on emulating these successes in other hematological malignancies where less impressive complete response rates are observed. Further engineering of CAR T cells or co-administration of other treatment modalities may successfully overcome obstacles to successful therapy in other cancer settings.
We therefore present a model in which others can conduct pre-clinical testing of CD19 CAR T cells. Results in this well tested B-cell lymphoma model are likely to be informative CAR T-cell therapy in general.
This protocol allows the reproducible production of mouse CAR T cells through calcium phosphate transfection of Plat-E producer cells with MP71 retroviral constructs and pCL-Eco packaging plasmid followed by collection of secreted retroviral particles and transduction using recombinant human fibronectin fragment and centrifugation. Validation of retroviral transduction, and confirmation of the ability of CAR T cells to kill target lymphoma cells ex vivo, through the use of flow cytometry, luminometry and enzyme-linked immunosorbent assay (ELISA), is also described.
Protocols for testing CAR T cells in vivo in lymphoreplete and lymphodepleted syngeneic mice, bearing established, systemic lymphoma are described. Anti-cancer activity is monitored by in vivo bioluminescence and disease progression. We show typical results of eradication of established B-cell lymphoma when utilizing 1st or 2nd generation CARs in combination with lymphodepleting pre-conditioning and a minority of mice achieving long term remissions when utilizing CAR T cells expressing IL-12 in lymphoreplete mice.
These protocols can be used to evaluate CD19 CAR T cells with different additional modification, combinations of CAR T cells and other therapeutic agents or adapted for the use of CAR T cells against different target antigens.

Here, we present a protocol for the production and pre-clinical testing of murine CD19 CAR T cells by retroviral transduction and utilization as a therapy against established syngeneic A20 B-cell lymphoma in BALB/c mice with or without lymphodepleting pre-conditioning.

同源小鼠 B 细胞淋巴瘤模型对 CD19 轿车 T 细胞的临床前评价

The astonishing clinical success of CD19 chimeric antigen receptor (CAR) T-cell therapy has led to the approval of two second generation chimeric antigen ...

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JoVE Journal

癌症研究

Using CRISPR/Cas9 to Knock Out GM-CSF in CAR-T Cells

Chimeric antigen receptor T (CAR-T) cell therapy is a cutting edge and potentially revolutionary new treatment option for cancer. However, there are significant limitations to its widespread use in the treatment of cancer. These limitations include the development of unique toxicities such as cytokine release syndrome (CRS) and neurotoxicity (NT) and limited expansion, effector functions, and anti-tumor activity in solid tumors. One strategy to enhance CAR-T efficacy and/or control toxicities of CAR-T cells is to edit the genome of the CAR-T cells themselves during CAR-T cell manufacturing. Here, we describe the use of CRISPR/Cas9 gene editing in CAR-T cells via transduction with a lentiviral construct containing a guide RNA to granulocyte macrophage colony-stimulating factor (GM-CSF) and Cas9. As an example, we describe CRISPR/Cas9 mediated knockout of GM-CSF. We have shown that these GM-CSFk/o CAR-T cells effectively produce less GM-CSF while maintaining critical T cell function and result in enhanced anti-tumor activity in vivo compared to wild type CAR-T cells.

Here, we present a protocol to genetically edit CAR-T cells via a CRISPR/Cas9 system.

使用 CRISPR/Cas9 在 CAR-T 电池中敲除 GM-CSF

Chimeric antigen receptor T (CAR-T) cell therapy is a cutting edge and potentially revolutionary new treatment option for cancer. However, there are ...

Production of Human CRISPR-Engineered CAR-T Cells

Adoptive cell therapies using chimeric antigen receptor T cells (CAR-T cells) have demonstrated remarkable clinical efficacy in patients with hematological malignancies and are currently being investigated for various solid tumors. CAR-T cells are generated by removing T cells from a patient's blood and engineering them to express a synthetic immune receptor that redirects the T-cells to recognize and eliminate target tumor cells. Gene editing of CAR-T cells has the potential to improve safety of current CAR-T cell therapies and further increase the efficacy of CAR-T cells. Here, we describe methods for the activation, expansion, and characterization of human CRISPR-engineered CD19 directed CAR-T cells. This comprises transduction of the CAR lentiviral vector and use of single guide RNA (sgRNA) and Cas9 endonuclease to target genes of interest in T cells. The methods described in this protocol can be universally applied to other CAR constructs and target genes beyond the ones used for this study. Furthermore, this protocol discusses strategies for gRNA design, lead gRNA selection and target gene knockout validation to reproducibly achieve high-efficiency, multiplex CRISPR-Cas9 engineering of clinical grade human T cells.

Here, we present a protocol for gene editing in primary human T cells using CRISPR Cas Technology to modify CAR-T cells.

A Technique for the Generation of Antigen-Specific CAR T Cells

成績單

A Technique for the Generation of Antigen-Specific CAR T Cells