The authors acknowledge funding from the European Commission GLYCOTwinning GA 101079417 and EJPRD/0001/2020 EU 825575; the Funda&#231;&#227;o para a Ci&#234;ncia e Tecnologia (FCT) Portugal, under&#160;grants FCT 2022.04607.PTDC, UIDP/04378/2020, UIDB/04378/2020 (UCIBIO), and LA/P/0140/2020 (i4HB). FCT-NOVA. and Stemmatters were also funded by the Fundo Europeu de Desenvolvimento Regional (FEDER), through the Programa Operacional Regional do Norte (Norte 2020) for the SI I&#38;amp;DT DCMatters project (NORTE-01-0247-FEDER-047212). We acknowledge Biolabs facility at FCT-NOVA and GLYCOVID NOVA Saude.

De-Sialylated Monocyte-Derived-DCs from Isolated PBMCs Using Sialidase Treatment

The authors declare no competing financial interests or other conflicts of interest.

Monocyte isolation 
This manuscript describes a protocol to generate mo-DCs from human-isolated monocytes CD14+ (Figure 1A), followed by performing a sialidase treatment to reduce the sialic acid content on the surface of these cells.
There are different ways to obtain human DCs, such as directly from peripheral blood or tissues or through differentiation from precursors such as stem cells or monocytes. Obtaining DCs differentiated from monocytes isolated from peripheral blood is far more straightforward due to the ease of obtaining high quantities of monocytes compared to other DC sources41. Still, to obtain a high percentage of isolated monocytes, all the protocol steps must be carefully followed. For instance, the density gradient medium may be toxic to the cells, and to prevent cell death, one must avoid prolonged cell contact with the density gradient medium and wash the cells thoroughly. Cell manipulation must be done as quickly as possible to avoid the loss of cell viability. From PBMCs, monocytes can be isolated through positive selection using the magnetic-activated cell sorting (MACS) method, which is a suitable technology for yielding a high number of monocytes. In addition, compared with other monocyte selection methods, mo-DCs derived from MACS-isolated monocytes possess a greater ability to stimulate anti-tumour T-cell activity42. In this protocol, once isolated, the monocytes were incubated with IL-4 and GM-CSF for a period of 5-6 days to achieve the differentiation into immature mo-DCs (Figure 1). The results showed that morphologically (Figure 1A) and phenotypically (Figure 1B), the isolated monocytes differentiated into immature mo-DCs. Moreover, throughout the differentiation, the mo-DCs lost the expression of CD14 markers and gained the expression of CD1a and MHC-II (Figure 1B), which are required for antigen presentation to T-cells.
This isolation and differentiation of monocytes into mo-DCs are limitations to this protocol. The isolation process is a sensitive step that must be carefully and swiftly executed to avoid cell death, and this step must also be done every time mo-DCs are needed for a new experiment. The differentiation process takes 5-6 days which poses a difficulty in terms of employing this method for high-throughput analyses. Nonetheless, the isolation method and using cytokines to differentiate mo-DCs are useful for generating a high number of functional mo-DCs in vitro for experimentation purposes. The mo-DCs generated in this protocol are able to undergo sialidase treatment, flow cytometry, ELISA, confocal microscopy, and so on, thus emphasizing the importance and usefulness of this method30.
Immature mo-DCs and sialidase treatment 
Sialidases are essential in sialylation regulation and are responsible for removing sialic acids from the cell surface glycans. In mo-DCs, sialic acid removal by sialidase leads to the maturation of these cells, which increases antigen-cross presentation and subsequent T-cell activation and anti-tumor activity30.
Immature human mo-DCs display a high content of cell surface &#945;(2,6)- and &#945;(2,3)-linked sialic acids27 compared to mature mo-DCs31,43. Furthermore, removing sialic acids by treating mo-DCs with sialidase improves the maturation of the DCs28,30,31. The sialidase selected for this experiment was from the bacterium Clostridium perfringens. Still, other organisms also produce sialidases, such as the bacteria Streptococcus pneumoniae, Vibrio cholerae, or Salmonella typhimurium44, the leech Macrobdella decora45, and even Homo sapiens46, and sialidases from these organisms are also used experimentally. However, each sialidase has different substrate specificities. Additionally, using the sialidase enzyme can have its limitations; for example, the manipulation of mo-DCs during the treatment can further stimulate these cells. Furthermore, the amount of sialidase and the incubation times must be optimized based on the type of cells being used and their sialic acid composition. The sialic acid removal is not a permanent effect but rather a transient phenomenon, because the cell will restore its cell surface sialic acid content. Besides sialidase, there are other methods to reduce the sialic acid molecules at the surface of cells, such as using sialyltransferase inhibitors, gene knockouts of sialyltransferase genes, or metabolic blockade of sialic acid using sialic acid mimetics47,48,49. Nonetheless, these methods may present distinct effects on cells, and besides desialylation, the cell viability must be considered. The sialidase enzyme treatment is a practical method for effectively and transiently removing cell surface sialic acids while maintaining the cell viability.
In this work, sialidase was added to the immature mo-DCs at the concentration of 500 mU/5 x 106 cells/mL, and the cells were incubated at 37 &#176;C for 60 min. The treatment was performed using RPMI-1640 without serum to preserve the cell viability and avoid any interaction between the sialylated molecules present in the serum30. Sialidase treatment can be performed with other buffers besides RPMI, such as 50 mM sodium acetate, pH 5.1 (in the case of C. perfingens sialidase), or PBS50,51,52. Nonetheless, RPMI-1640 is the most common culture medium for DCs as it maintains constant experimental conditions during the procedure, avoids inducing maturation, and reduces any stress that may be caused by sialidase buffers or PBS53,54,55,56. After incubation with sialidase, it is critical to wash the cells thoroughly with a serum-supplemented medium to guarantee that the enzyme reaction has stopped. The presence of sialylated molecules in the serum will compete as substrates for sialidase, thus assuring a rapid reaction stop.
Surface marker characterization by flow cytometry and confocal microscopy 
For the determination of the sialic acid profile, in protocol section 3, we utilized lectin staining followed by flow cytometry and confocal laser scanning microscopy. For the cell staining procedure, in both cases, the lectin concentrations and incubation conditions were optimized to avoid cell agglutination and death. It is critical to perform the incubation at 4 &#176;C in buffers containing at least 2% of either FBS or BSA to avoid non-specific binding of the lectins. In this protocol, RPMI-1640 containing 10% FBS was used to maintain constant experimental conditions and avoid cell stress. Regarding confocal microscopy, fixation of the cells prior to staining is essential to preserve the morphology, prevent autolysis, and maintain antigenicity.
The analysis of the mo-DC phenotype by flow cytometry showed that sialidase-treated mo-DCs had a significantly higher amount of PNA lectin bound to the cell surface compared to MMA and SNA lectins, which decreased after the sialidase treatment (Figure 2A). As expected, PNA staining increased, since PNA recognizes non-sialylated antigens, in contrast to MAA and SNA, which bind directly to &#945;2,3- and &#945;2,6-sialic acids, respectively30. This staining confirms the effective removal of sialic acids from the cell surface using this protocol. Another method that can be used to validate the treatment and analyze the cell surface sialic acid content is lectin staining followed by confocal microscopy, as exemplified in Figure 2B.
Besides the former examples, alternative approaches exist to evaluate and characterize sialic acid content, such as lectin probing by western blotting. Alternative sialic acid-specific lectins are also available, such as Siglecs, a group of lectins that have a distinct preference for sialic acid types and linkages57. Besides using lectins in either technique (flow cytometry, microscopy, or western blot), it is also possible to characterize the sialic acid content using antibodies; for instance, &#945;2,8-sialic acids can be assessed by antibodies such as clone 735, which is specific for polysialic acid58. In addition, after sialidase treatment, cells can be functionally tested for their biological or therapeutic efficiency by evaluating their phenotype and ability to activate T-cells40. In fact, as shown in the examples provided, sialidase-treated mo-DCs showed higher maturation phenotype, as well as an elevated expression of antigen-presenting and co-stimulatory molecules.
Furthermore, sialidase-treated mo-DCs can be loaded with antigens and co-cultured with T-cells or other cells and then can be studied regarding the phenotype, cytokine secretion profile, or other features. In the example provided, the data show that sialidase-treated mo-DCs can be loaded with tumor antigens and then used to activate T-cells. In fact, the resulting T-cells showed increased IFN-&#947; secretion, which is in agreement with previous reports on the effect of sialic acid shortage on boosting the capacity of mo-DCs to activate T-cells27,28,29,30,31.
In conclusion, this protocol shows a feasible, viable, and practical method to generate mo-DCs for sialic acid content manipulation by treatment with sialidase. This protocol presents a methodology that can serve different purposes and applications. This method can not only have a crucial role in understanding the role of sialic acids in the maturation and response of immune cells but can also be used as an immunomodulatory tool.

Sialic acid-carrying glycans (sialoglycans) have gained significant interest due to their immunomodulatory role. The monosaccharide sialic acid, which is most prevalent in humans in the form of N-acetylneuraminic acid, presents fundamental ligands for lectins with a recognized role in immunology, such as Selectins and Siglecs. These lectins recognize sialoglycans either on the same cell (cis) or on different cells (trans) and play a significant role in host-pathogen interactions and various physiological and pathological cellular activities1,2,3. Furthermore, since sialic acid occupies the terminal positions of cell surface glycoconjugates, it can conceal the underlying structures, thus inhibiting cell-to-cell contact via non-specific repulsive effects or by obstructing detection by other lectins4. The activity of a variety of sialyltransferases (that transfer sialic acids) and of sialidases (that cleave sialic acid bonds) within the cell determines the amount of sialic acid present at the surface. In addition, soluble sialyltransferases and sialidases expressed by the host or pathogens can extrinsically modify the amount of sialic acid on the cell surface5,6.
Aberrant sialylation is a feature of several pathological conditions. In autoimmune diseases, hyposialylation can contribute to unrestrained immune activation and organ damage, since sialic acid helps to discriminate self-antigens and regulate inflammatory responses7. Conversely, hypersialylation results in the over-expression of sialoglycans, such as sialyl-Tn, sialyl-Lewis antigens, polysialic acid, and gangliosides, which constitutes a hallmark of some cancers8,9. Hypersialylation also depends on increased expression of specific enzymes such as N-acetylglucosaminyltransferase (GNT-V), which generates hypersialylated tri- and/or tetra-antennary N-linked glycans, which have been associated with cancer growth and metastasis10. The sialic acid content also regulates protein stability and function, which are key for the role of relevant oncogenic players11. Therefore, increased sialylation can facilitate tumor development, metastasis, drug resistance, and immune evasion. Moreover, the upregulation of sialoglycans enables tumors to interact with inhibitory Siglec receptors on immune cells and avoid immune surveillance. For that reason, sialoglycans are now considered to be glyco-immune checkpoints and attractive therapeutic targets. For instance, inhibitors of the Siglec-immune axis are already in early clinical trials, since the immune cell receptor Siglec (sialic-acid-binding ImmunoGlobulin-like LECtin) plays an immune-inhibitory role12.
Enzymes have been used to modulate the glycan profile as tools for study or for therapeutic strategies13,14. Sialidase has been employed to alter cancer cell malignancy since sialylated glycans such as sialyl Lewis X are critical for cell migration and cancer metastasis15. At the same time, sialidase inhibitors, which impede sialic acid cleavage, have reached clinics for treating sialic acid-dependent viral infections16. Recently, sialic acid modulation has gained further interest due to the critical role of sialic acids as ligands in the Siglec-immune axis, meaning they offer novel means to reduce cancer escape from immune responses. This interest was further strengthened by the 2022 Nobel laureate Bertozzi and her team&#39;s contribution of several strategies that selectively cleave diverse sialoglycans and improve anti-cancer immune responses17. Thus, sialidase-based strategies represent a promising modality for glyco-immune checkpoint therapy. The glycophenotype of cells of the immune system is dependent on the type of cell and their activation status. Regarding T-cells, glycans have a key role in the pathophysiological steps of T-cell development and thymocyte selection, T-cell activity, differentiation, and proliferation18. For instance, polylactosamine on glycoproteins influences basal levels of B lymphocytes and T lymphocytes and macrophage activation19. In macrophages, distinct glycan expression patterns have an important role in macrophage recruitment to the tumor microenvironment (TME)20. Hence, the expression of O-linked and N-linked glycans by immune cells could be used as potential glycobiomarkers for therapeutic approaches in the treatment of cancer and autoimmune diseases.
Dendritic cells (DCs) are specific antigen-presenting cells with a unique capacity to trigger immune responses, such as anti-cancer immunity21. DCs must undergo an upregulation of their antigen-presenting MHC molecules to present antigens to T-cells (signal 1), co-stimulatory molecules to activate T-cells (signal 2) and pro-inflammatory cytokines, such as IL-12, to trigger type 1 helper T-cell proliferation (signal 3)22. The resulting immune profile is tightly regulated, and checkpoints are essential for preventing healthy cells from being attacked. Since DCs can stimulate various immune responses against tumor cells, they are used as cell-based vaccines, and a sizable number of clinical studies have demonstrated their potential benefits23,24. After the FDA approved the first DC-based vaccine in 201025,26, many other DC-based vaccines have been developed. DC-based vaccines are mainly produced ex vivo and administered to patients to elicit immune responses against tumors. However, insufficient or brief maturation is currently one of the factors limiting the clinical efficacy of DCs and means expensive cytokine cocktails must be used. Without adequate maturation, DCs cannot activate T-cells in clinical circumstances. Instead, the DCs express immune checkpoints and trigger a tolerogenic immune response that prevents cytotoxic T-cells from acting against tumor cells.
Human DCs have heavily sialylated surfaces, and this sialylation decreases upon maturation and during an overall immune response27. The maturation of DCs can be induced by eliminating these sialic acids with sialidase. Desialylation greatly upregulates various cytokines, including IL-12, due to the translocation of the NF-kB transcription factor to the nucleus6,28. In addition, desialylation improves antigen cross-presentation through MHC-I and anti-tumour immune responses29,30. Accordingly, the knockout of the sialyltransferases ST3Gal.l and ST6Gal.l, which have a major role in DC sialylation, generates a more mature phenotype in murine DCs31.
Sialidase treatment provides a method for stimulating all aspects of DC maturation, including increased antigen presentation, increased expression of co-stimulatory molecules, and increased cytokine production, to address the shortcomings mentioned above and enable DCs to elicit effective responses. This article presents a procedure to obtain viable desialylated human DCs through the use of a bacterial sialidase. De-sialylated DCs show an improved maturation profile and can be used as cell models to boost anti-tumour immune responses in vitro. The DCs are obtained from blood monocytes, which are then differentiated in vitro in the presence of the cytokine interleukin-4 (IL-4) and granulocyte macrophage colony-stimulating factor (GM-CSF). This work also describes lectin-based methods to analyze sialic acid at the cell surface and methods to immunophenotype the DC maturation level. The procedure described here can be used to desialylate other cell types, thus providing an approach to investigate the role of sialoglycans, which are vital glyco-immune checkpoints and relevant in immunomodulation.

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>15 mL conical tube</td>
			<td>AstiK&#8217;s</td>
			<td>CTGP-E15-050</td>
			<td>Obtaining Monocyte-derived Dendritic Cells; Treatment of Cells with Sialidase</td>
		</tr>
		<tr>
			<td>24-well plate</td>
			<td>Greiner Bio-one</td>
			<td>662 160</td>
			<td>Obtaining Monocyte-derived Dendritic Cells; Treatment of Cells with Sialidase</td>
		</tr>
		<tr>
			<td>50 mL conical tube</td>
			<td>AstiK&#8217;s</td>
			<td>CTGP-E50-050</td>
			<td>Obtaining Monocyte-derived Dendritic Cells</td>
		</tr>
		<tr>
			<td>7-Aminoactinomycin D (7-AAD)</td>
			<td>BioLegend</td>
			<td>420404</td>
			<td>Obtaining Monocyte-derived Dendritic Cells</td>
		</tr>
		<tr>
			<td>Annexin V</td>
			<td>Immunotools</td>
			<td>31490013</td>
			<td>Obtaining Monocyte-derived Dendritic Cells</td>
		</tr>
		<tr>
			<td>Attune Acoustic Focusing Flow Cytometer</td>
			<td>Thermo Fisher Scientific&#160;</td>
			<td></td>
			<td>Determination of Sialic Acid Profile; Maturation Profiling of mo-DCs</td>
		</tr>
		<tr>
			<td>BSA</td>
			<td>Sigma - Aldrich</td>
			<td>A3294-100G</td>
			<td>Obtaining Monocyte-derived Dendritic Cells; Determination of Sialic Acid Profile</td>
		</tr>
		<tr>
			<td>CD14 (Monoclonal T&#220;K4)</td>
			<td>Miltenyi Biotec</td>
			<td>130-080-701</td>
			<td>Obtaining Monocyte-derived Dendritic Cells</td>
		</tr>
		<tr>
			<td>CD80</td>
			<td>Immunotools</td>
			<td>21270803</td>
			<td>Maturation Profiling of mo-DCs</td>
		</tr>
		<tr>
			<td>CD86</td>
			<td>Immunotools</td>
			<td>21480863</td>
			<td>Maturation Profiling of mo-DCs</td>
		</tr>
		<tr>
			<td>Cell counting slides and trypan blue</td>
			<td>EVE</td>
			<td>EVS-050</td>
			<td>Obtaining Monocyte-derived Dendritic Cells</td>
		</tr>
		<tr>
			<td>Centrifuge</td>
			<td>Eppendorf</td>
			<td>5430 R</td>
			<td>Obtaining Monocyte-derived Dendritic Cells; Treatment of Cells with Sialidase; Determination of Sialic Acid Profile; Maturation Profiling of mo-DCs</td>
		</tr>
		<tr>
			<td>Density gradient medium (Histopaque)</td>
			<td>Sigma - Aldrich</td>
			<td>10771-100ML</td>
			<td>Obtaining Monocyte-derived Dendritic Cells</td>
		</tr>
		<tr>
			<td>EDTA</td>
			<td>Gibco, ThermoFisher</td>
			<td>15400054</td>
			<td>Obtaining Monocyte-derived Dendritic Cells</td>
		</tr>
		<tr>
			<td>Elisa kit (IFN-&#947;)</td>
			<td>Immunotools</td>
			<td>31673539</td>
			<td>Maturation Profiling of mo-DCs</td>
		</tr>
		<tr>
			<td>EVE automated cell count</td>
			<td>NanoEntek</td>
			<td>10027-452</td>
			<td>Obtaining Monocyte-derived Dendritic Cells</td>
		</tr>
		<tr>
			<td>Fetal bovine serum (FBS)</td>
			<td>Gibco</td>
			<td>10500064</td>
			<td>Obtaining Monocyte-derived Dendritic Cells; Treatment of Cells with Sialidase; Determination of Sialic Acid Profile</td>
		</tr>
		<tr>
			<td>Granulocyte-macrophage colony-stimulating factor (GM-CSF)</td>
			<td>Miltenyi Biotec</td>
			<td>&#160; 130-093-864</td>
			<td>Obtaining Monocyte-derived Dendritic Cells</td>
		</tr>
		<tr>
			<td>Human CD14 microbeads (Immunomagnetic beads)</td>
			<td>Miltenyi Biotec</td>
			<td>130-050-201</td>
			<td>Obtaining Monocyte-derived Dendritic Cells</td>
		</tr>
		<tr>
			<td>Interleukin (IL)-1&#946;</td>
			<td>Sigma - Aldrich</td>
			<td>I9401</td>
			<td>Obtaining Monocyte-derived Dendritic Cells</td>
		</tr>
		<tr>
			<td>Interleukin (IL)-4</td>
			<td>Miltenyi Biotec</td>
			<td>130-093-919</td>
			<td>Obtaining Monocyte-derived Dendritic Cells</td>
		</tr>
		<tr>
			<td>Interleukin (IL)-6</td>
			<td>Sigma - Aldrich</td>
			<td>SRP3096</td>
			<td>Obtaining Monocyte-derived Dendritic Cells</td>
		</tr>
		<tr>
			<td>L-glutamine</td>
			<td>Gibco</td>
			<td>A2916801</td>
			<td>Obtaining Monocyte-derived Dendritic Cells</td>
		</tr>
		<tr>
			<td>LS column and plunger</td>
			<td>Miltenyi Biotec</td>
			<td>130-042-401</td>
			<td>Obtaining Monocyte-derived Dendritic Cells</td>
		</tr>
		<tr>
			<td>Maackia amurensis&#160;(MAA) lectin (MAA lectin - Biotinylated)</td>
			<td>Vector labs</td>
			<td>B-1265-1</td>
			<td>Determination of Sialic Acid Profile</td>
		</tr>
		<tr>
			<td>MHC-I (HLA-ABC)</td>
			<td>Immunotools</td>
			<td>21159033</td>
			<td>Maturation Profiling of mo-DCs</td>
		</tr>
		<tr>
			<td>MHC-II (HLA-DR)</td>
			<td>Immunostep</td>
			<td>HLADRA-100T</td>
			<td>Maturation Profiling of mo-DCs</td>
		</tr>
		<tr>
			<td>Microtubes</td>
			<td>AstiK&#8217;s</td>
			<td>PCRP-E015-500</td>
			<td>Obtaining Monocyte-derived Dendritic Cells; Treatment of Cells with Sialidase; Determination of Sialic Acid Profile; Maturation Profiling of mo-DCs</td>
		</tr>
		<tr>
			<td>Neuraminidase (Sialidase)</td>
			<td>Roche</td>
			<td>11585886001</td>
			<td>Treatment of Cells with Sialidase</td>
		</tr>
		<tr>
			<td>Non-essential amino acids (NEAA)</td>
			<td>Gibco</td>
			<td>11140-050</td>
			<td>Obtaining Monocyte-derived Dendritic Cells</td>
		</tr>
		<tr>
			<td>Paraformaldehyde (PFA 2%)</td>
			<td>Polysciences Europe</td>
			<td>25085-1</td>
			<td>Determination of Sialic Acid Profile; Maturation Profiling of mo-DCs</td>
		</tr>
		<tr>
			<td>Paraformaldehyde (PFA 4%)</td>
			<td>Biotium</td>
			<td>22023</td>
			<td>Determination of Sialic Acid Profile</td>
		</tr>
		<tr>
			<td>Pasteur pipettes</td>
			<td>Labbox</td>
			<td>PIPP-003-500</td>
			<td>Obtaining Monocyte-derived Dendritic Cells</td>
		</tr>
		<tr>
			<td>Peanut (Arachis hypogaea) Agglutinin&#160;(PNA) lectin (PNA lectin - FITC)</td>
			<td>Vector labs</td>
			<td>FL-1071</td>
			<td>Determination of Sialic Acid Profile</td>
		</tr>
		<tr>
			<td>Penicillin/streptomycin</td>
			<td>Gibco</td>
			<td>15140163</td>
			<td>Obtaining Monocyte-derived Dendritic Cells</td>
		</tr>
		<tr>
			<td>Phosphate Buffered Saline (PBS)</td>
			<td>NZYTech</td>
			<td>&#160; MB18201</td>
			<td>Obtaining Monocyte-derived Dendritic Cells; Treatment of Cells with Sialidase; Determination of Sialic Acid Profile; Maturation Profiling of mo-DCs</td>
		</tr>
		<tr>
			<td>Prostaglandin E2 (PGE2)</td>
			<td>Sigma - Aldrich</td>
			<td>P0409</td>
			<td>Obtaining Monocyte-derived Dendritic Cells</td>
		</tr>
		<tr>
			<td>RBC lysis buffer</td>
			<td>BioLegend</td>
			<td>420302</td>
			<td>Obtaining Monocyte-derived Dendritic Cells</td>
		</tr>
		<tr>
			<td>RPMI-1640 medium&#160;(containing 11.1 mM glucose)</td>
			<td>Gibco</td>
			<td>31870074</td>
			<td>Obtaining Monocyte-derived Dendritic Cells; Treatment of Cells with Sialidase; Determination of Sialic Acid Profile</td>
		</tr>
		<tr>
			<td>Sambucus nigra lectin (SNA lectin - Biotinylated)</td>
			<td>Vector labs</td>
			<td>&#160; B-1305-2</td>
			<td>Determination of Sialic Acid Profile</td>
		</tr>
		<tr>
			<td>Sambucus nigra lectin (SNA lectin - FITC)</td>
			<td>Vector labs</td>
			<td>FL-1301-2</td>
			<td>Determination of Sialic Acid Profile</td>
		</tr>
		<tr>
			<td>Sodium pyruvate</td>
			<td>Thermofisher</td>
			<td>11360-070</td>
			<td>Obtaining Monocyte-derived Dendritic Cells</td>
		</tr>
		<tr>
			<td>SpectroMax190</td>
			<td>Molecular Devices</td>
			<td></td>
			<td>Maturation Profiling of mo-DCs</td>
		</tr>
		<tr>
			<td>Streptavidin-PE</td>
			<td>BioLegend</td>
			<td>&#160; 405203</td>
			<td>Determination of Sialic Acid Profile; Maturation Profiling of mo-DCs</td>
		</tr>
		<tr>
			<td>Tetramethylbenzidine (TMB)</td>
			<td>Sigma - Aldrich</td>
			<td>T0440</td>
			<td>Maturation Profiling of mo-DCs</td>
		</tr>
		<tr>
			<td>Tumour necrosis factor-&#945; (TNF-&#945;)</td>
			<td>Sigma - Aldrich</td>
			<td>H8916</td>
			<td>Obtaining Monocyte-derived Dendritic Cells</td>
		</tr>
		<tr>
			<td>Zeiss LSM710 confocal microscope</td>
			<td>Zeiss</td>
			<td></td>
			<td>Determination of Sialic Acid Profile</td>
		</tr>
	</tbody>
</table>

generation of monocyte-derived dendritic cells with differing sialylated phenotypes

Sialic acids are negatively charged monosaccharides typically found at the termini of cell surface glycans. Due to their hydrophilicity and biophysical characteristics, they are involved in numerous biological processes, such as modulation of the immune response, recognition of self and non-self antigens, carbohydrate-protein interactions, etc. The cellular content of sialic acid is regulated by sialidase, which catalyzes the removal of sialic acid residues. Several studies have shown that sialo-glycans are critical in monitoring immune surveillance by engaging with cis and trans inhibitory Siglec receptors on immune cells. Likewise, glyco-immune checkpoints in cancer are becoming crucial targets for developing immunotherapies. Additionally, dendritic cells (DCs) are envisioned as an important component in immunotherapies, especially in cancer research, due to their unique role as professional antigen-presenting cells (APC) and their capacity to trigger adaptive immune responses and generate immunologic memory. Nevertheless, the function of DCs is dependent on their full maturation. Immature DCs have an opposing function to mature DCs and a high sialic acid content, which further dampens their maturation level. This downregulates the ability of immature DCs to activate T-cells, leading to a compromised immune response. Consequently, removing sialic acid from the cell surface of human DCs induces their maturation, thus increasing the expression of MHC molecules and antigen presentation. In addition, it can restore the expression of co-stimulatory molecules and IL-12, resulting in DCs having a higher ability to polarize T-cells toward a Th1 phenotype and specifically activate cytotoxic T-cells to kill tumor cells. Therefore, sialic acid has emerged as a key modulator of DCs and is being used as a novel target to advance their therapeutic use. This study provides a unique approach to treat in vitro monocyte-derived DCs with sialidase, aimed at generating DC populations with different cell surface sialic acid phenotypes and tailored maturation and co-stimulatory profiles.

Author Spotlight: Dendritic Cells Maturation Using Sialidases-Based Enzymatic Treatment of the Cell Surface 

Generation of Monocyte-Derived Dendritic Cells with Differing Sialylated Phenotypes

The scope of the glycoimmunology group research is studying the role of glycan immunology in human health and disease. This research aims to disentangle biological mechanisms modulated by glycosylations, and to discover novel glycan-based therapies for cancer and congenital disorders of glycosylation. Our focus has been on sialylated glycans that affect the function of relevant molecules, particularly during response.We developed technologies to alter sialic acid contents and a multimodal platform for high-throughput dissolvement of glycan binding proteins with potential clinical applications. To advance the research in the field, we use several technologies such as glycan profiling, selecting or antibody staining, mass spectrometry, and immunohistochemistry, in vitro assays with cell lines as disease models, sialic acid content manipulations through enzymatic and metabolic engineering. The current experimental challenges relate to understanding the complex interactions between sialylated glycans and lectins.There are mechanisms and functional consequences in several immune responses. The sialic acid modulates the potency of dendritic cells and MHC1 turnover. This discovery pinpointed new biological and pathological mechanisms and developed innovative therapies.It also identified novel immune pathways and approaches for their therapeutic modulation. One of the issues in ex vivo production of human monocyte derived dendritic cells for therapeutic uses is their inability to mature fully. This protocol shows that DCs maturation can be achieved by enzymatically treating the cell surface with sialidases while maintaining cell viability.This method is cost effective and time saving. Compared to sialic acid metabolic inhibitors, sialidase treatment offers a rapid effective and method of removing cell surface sialic acids while maintaining cell viability. Understanding the role of sialic acid content in glycans generates some precedent awareness of the importance of this glycan in cancer and will foster the identification of new disease mechanisms and neuropath strategies.

Monocyte isolation and monocyte differentiation into mo-DCs 
In accordance with the protocol, human PBMCs were isolated from the buffy coat using density gradient separation with density gradient medium and thoroughly washed. Trypan blue was used to perform viable cell counting on the day of isolation, as described previously in step 1.4.1. Subsequently, CD14+ monocyte isolation was carried out through positive selection. To achieve this, PBMCs were incubated with magnetic beads containing an antibody that recognizes the CD14 antigen. The selected CD14+ monocytes were cultured in a medium supplemented with GM-CSF and IL-4 for 5-6 days27 to differentiate into immature mo-DCs (Figure 1A). The maturation of mo-DCs can be obtained by applying a cocktail of cytokines, including IL-6, IL-1&#946;, TNF-&#945;, and PGE235 (Figure 1A).
During the differentiation process, as a result of IL-4 and GMCSF stimulation, the cell phenotype is expected to change. Data shows that mo-DCs lose expression of surface marker CD14, mainly expressed by monocytes (Figure 1B), and gain significant expression of CD1a, a marker expressed by human DCs36,37. mo-DCs also obtain higher MHC-II (HLA-DR) expression, an antigen-presenting molecule expressed by human DCs and other antigen-presenting cells38 (Figure 1B).
Cell surface sialic acid content 
The treatment of mo-DCs with sialidase reduces the sialic acid content on the surface of mo-DCs, which can be confirmed by staining with lectins, which are proteins capable of binding to carbohydrates39. Since the enzyme used removes both &#945;2,3 and &#945;2,6-linked sialic acids from the cell surface, mo-DCs were stained with PNA, which recognizes T antigen-Gal&#946;1-3GalNAc&#945;1-Ser/Thr, as well as MAA and SNA lectins, which bind to &#945;2,3- and &#945;2,6-sialic, respectively. The effectiveness of the sialidase treatment was evaluated by flow cytometry and by confocal microscopy (Figure 2). As shown in Figure 2A, sialidase treatment significantly decreased MAA and SNA binding while increasing PNA staining. The decrease in SNA staining after sialidase treatment was further confirmed by confocal microscopy analysis showing a significantly reduced SNA staining at the cell surface (Figure 2B).
Functional characterization of sialidase-treated mo-DCs 
To evaluate how sialidase treatment affects mo-DC functions, the maturation level of mo-DCs was assessed after sialidase treatment. As shown in Figure 3A, the sialidase treatment leads to a significant increase in the expression of the antigen-presenting molecules MHC I and MHC II and the expression of the CD80 and CD86 co-stimulatory molecules. To assess the effect of sialic acid removal on the ability of mo-DCs to induce T-cell responses, sialidase-treated mo-DCs loaded with tumor cell lysates were used to prime autologous T-cells (Figure 3). Next, the profile of the resulting T-cells was characterized based on their capacity to secrete the Th1 cytokine IFN-&#947;. As shown in Figure 3B, when compared with T-cells primed by fully sialylated mo-DCs, the T-cells primed by sialidase-treated mo-DCs secreted significantly higher levels of IFN-&#947;. These results suggest that sialidase-treated mo-DCs have improved capacity to prime autologous T-cells.
Cell viability 
After sialidase treatment, a viability assay was performed to ensure the treatment was not cytotoxic to the cells. Following treatment, mo-DCs were stained with 7-AAD and Annexin V, to detect nonviable and apoptotic cells, and analyzed by flow cytometry (Figure 4). Data shows no significant difference in cell viability between untreated (Figure 4, left panel) and sialidase-treated cells (Figure 4, right panel).
<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/65525/65525fig01.jpg" /> 
Figure 1: Differentiation of isolated monocytes into mo-DCs. (A) CD14+ monocytes were isolated from buffy coats and cultured at a concentration of 1.3 x 106 cells/mL at 37 &#176;C. The monocytes were differentiated in medium supplemented with 750 U/mL of IL-4 and 1,000 U/mL of GM-CSF. Microscopic analysis of the morphology of monocytes isolated from human buffy coat at day 0 (top image). Immature mo-DCs; cells were differentiated during a period of 5 days using IL-4 and GM-CSF (middle image). Matured mo-DCs were obtained by using IL-6, IL-1&#946;, TNF-&#945;, and PGE2 cytokines for 24 h (bottom image). Scale bars: 100 &#181;m. (B) The cells were analyzed at day 0, day 2, and day 5 throughout the differentiation period using flow cytometry. The following antibodies were used to characterize cell surface markers: (a-c) CD14; (d-f) CD1a, and (g-i) HLA-DR (MHC class II). The figure shows representative histograms of at least three independent assays. Panel (B) has been modified from Videira et al.40, patent WO2017002045A1. <a href="https://www.jove.com/files/ftp_upload/65525/65525fig01large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 2" class="xfigimg" src="/files/ftp_upload/65525/65525fig02.jpg" /> 
Figure 2: Sialidase treatment of human mo-DCs to remove &#945;2,6- and &#945;2,3-linked sialic acids from the cell surface. (A) Analysis of mo-DCs by flow cytometry using lectin staining to test the efficacy of sialidase treatment. Human mo-DCs were treated with sialidase (grey bars) or left untreated (white bars) and stained with SNA lectin (recognizing [2,6]-sialic acids), MAA lectin (recognizing [2,3]-sialic acids), and PNA lectin (recognizing T antigen-Gal&#946;1-3GalNAc&#945;1-Ser/Thr). The values represent the mean fluorescence intensity (MFI) of at least three independent assays. Statistical significance was determined using a two-tailed paired t-test (*P &#60; 0.05 or ***P &#60; 0.0001), referring to the difference between the untreated and sialidase-treated DCs. Sialidase treatment decreased MAA binding and increased PNA staining in human mo-DCs, resulting from the removal of &#945;(2,3)-linked sialic acids; the removal of &#945;(2,6)-linked sialic acids after sialidase treatment was detected by a decrease in SNA staining. (B) Confocal microscopy of mo-DCs treated with sialidase and prepared on coverslips for observation. A range of z-stack images was collected from different cells and processed to include the mean staining intensity. Scale bars: 20 &#181;m. Panel (A) has been modified from Silva et al.30; panel (B) has been modified from Silva et al.29. <a href="https://www.jove.com/files/ftp_upload/65525/65525fig02large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 3" class="xfigimg" src="/files/ftp_upload/65525/65525fig03.jpg" /> 
Figure 3: Sialidase treatment of mo-DCs inducing a higher expression of maturation markers. (A) mo-DCs treated with sialidase showed a higher maturation phenotype than fully sialylated mo-DCs. Flow cytometry was used to evaluate the expression of several maturation markers. The mo-DCs were treated with sialidase for 1 h at 37 &#176;C; the graph values represent the mean fluorescence intensity (MFI) (average &#177; SEM) of at least three independent assays. Statistically significant differences were calculated using a t-test (*P &#60; 0.05, **P &#60; 0.01), referring to the difference between the untreated and sialidase-treated conditions. (B) Desialylated human mo-DCs loaded with whole tumor antigens induced specific T-cell responses. The mo-DCs were treated with sialidase for 1 h at 37 &#176;C or left untreated, followed by loading with MCF-7 lysates (TL) as a source of whole tumor cell antigens. Co-culture between mo-DCs and autologous T-cells was performed for 4-8 days in the presence of IL-2 (10 U/mL). T-cells primed with desialylated mo-DCs showed significantly higher secretion of the Th1 cytokine, IFN-&#947;. Following T-cell stimulation with mo-DCs, the cytokines secreted into the co-culture supernatants were measured by ELISA (n = 7). The graph values represent the concentration (pg/mL) (average &#177; SEM). Statistically significant differences were calculated using a t-test (*P &#60; 0.05). The figure has been modified from Silva et al.30. <a href="https://www.jove.com/files/ftp_upload/65525/65525fig03large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 4" class="xfigimg" src="/files/ftp_upload/65525/65525fig04.jpg" /> 
Figure 4: Lack of impact of sialidase treatment on the viability of human mo-DCs. Untreated mo-DCs (left panel) and sialidase-treated mo-DCs (right panel) were subjected to dual staining with annexin V and 7-AAD, and the staining was analyzed by flow cytometry. The data showed no significant difference in cell viability between the untreated and sialidase-treated cells, suggesting that mo-DCs can tolerate sialidase treatment and remain viable to exert their immunologic function. The figure has been modified from Silva et al.30. <a href="https://www.jove.com/files/ftp_upload/65525/65525fig04large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>

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A unique, comprehensive protocol to generate de-sialylated human monocyte-derived dendritic cells (mo-DCs) from isolated peripheral blood mononuclear cells (PBMCs) using a sialidase treatment is presented. Further, methods to assess the phenotypic and functional characterization of mo-DCs and evaluate how sialidase treatment improves the maturation level of mo-DCs are described.

Sialic acids are negatively charged monosaccharides typically found at the termini of cell surface glycans. Due to their hydrophilicity and biophysical ...

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JoVE Journal

Immunology and Infection

Monocyte Isolation and Monocyte Differentiation into Monocyte-Derived Dendritic Cells

Begin isolating peripheral blood mononuclear cells by accessing the human buffy coat and transferring seven milliliters into a sterile 15 milliliters conical tube. Add six milliliters of PBS solution for a preliminary wash. Centrifuge the tube for 10 minutes at 1, 100 G in a centrifuge with a swing rotor, and brake off at room temperature.Collect the leukocyte suspension using a Pasture pipette and transfer it to a new sterile 15 milliliter conical tube. Add PBS solution to the leukocyte suspension until it reaches 10 milliliters and mix it gently by pipetting up and down. Next prepare the density gradient solution by placing three milliliters of density gradient medium into a new sterile 15 milliliters conical tube.Allow it to reach room temperature. Slowly add five milliliters of diluted leukocyte suspension on the conical tube walls containing the density gradient medium to create a five to three density gradient separation. Avoid disturbing the medium.Proceed to gradient separation by centrifuging the suspension present in the density gradient medium using a centrifuge with a swing rotor and the brake off. Next carefully transfer up to 25 milliliters of the thin layer of PBMCs to a new 50 milliliters conical tube filled with PBS using a Pasture pipette and mix it well to remove residual cells and debris, centrifuge the samples at room temperature for 10 minutes at 600 G with a normal brake. Discard the supernatant and fill the sample to 10 milliliters using PBS.Take an aliquot to count the cells. To remove the platelets, centrifuge them with a normal brake and carefully invert the tube to discard the supernatant. For monocyte CD14 positive isolation using magnetic activated cell sorting, resuspend the cell pellet in the microbeads buffer and CD14 immuno magnetic beads.Incubate the cell suspension for 15 minutes at four degrees Celsius. To remove the unbound beads, add one to two milliliters of microbeads buffer per one times 10 to the seventh cells before centrifuging the suspension at room temperature for 10 minutes at 600 G.Then carefully invert the tube to discard the supernatant. Prepare the LS column and place it on the magnet before use.Rinse it with three milliliters of microbeads buffer and immediately resuspend the cell pellet in 500 microliters of microbeads buffer per one times 10 to the eighth cells. Add the cell suspension to the LS column inlet and collect the negative cell fraction in a 15 milliliter conical tube below the column outlet. Wash the column three times with three milliliters of microbead buffer.After the final wash, remove the column from the magnet and place it on a sterile 15 milliliter conical tube. Pipette five milliliters of microbeads buffer into the column inlet. Immediately insert the syringe plunger filled with the target cells into the column inlet and dispense the cells in the column.Then centrifuge CD14 negative and CD14 positive cell fractions and discard the supernatant. For monocyte differentiation into human monocyte derived dendritic cells, prepare a cell suspension containing 1.3 times 10 to the sixth cells per milliliter by adding the appropriate volume of differentiation medium to the CD14 positive cells. Resuspend the monocytes by pipetting with a Pasture pipette.After plating the 1.3 times 10 to the sixth cells per milliliter suspension per well of a 24 well plate, incubate in a culture incubator at 37 degrees Celsius with 5%carbon dioxide. Change the culture medium and supplement it with fresh cytokines every two to three days. To collect the differentiated cells, transfer the entire cell suspension to a sterile conical tube using a micro pipette and wash the culture flask twice with PBS.After centrifuging the conical tubes at room temperature for 10 minutes at 180 G, resuspend the pellet in the appropriate media or buffer for the experimental setup. During the monocyte differentiation, interleukin four and granulocyte macrophage colony stimulating factor stimulation changed the cell phenotype. Data showed that human monocyte derived dendritic cells lost the expression of surface marker CD14, mainly expressed by monocytes and gained significant expression of CD1A.a marker expressed by human dendritic cells. Human monocyte derived dendritic cells also obtain higher expression of MHC2 HLA-DR, an antigen presenting molecule expressed by human dendritic cells and other antigen presenting cells.

Treatment of the Monocyte-Derived Dendritic Cells (mo-DCs) with Sialidase

Treatment of the Monocyte-Derived Dendritic Cells (Mo-DCs) with Sialidase  

Collect approximately 10 times 10 to the sixth human monocyte derived dendritic cells differentiated from the monocytes. From the 10 wells of the 24 well plate having 1.3 times 10 to the sixth cells per well, transfer them to a new sterile 15 milliliter conical tube. After centrifuging the cells at 300G for five to seven minutes at room temperature, using the normal break, discard the supernatant to remove dead cells and debris.Add 10 milliliters of RPMI 1640 medium containing 11.1 millimolar glucose to the tube. After centrifuging at room temperature for four minutes at 300G, using the normal break, discard the supernatant again. Add two milliliters of RPMI 1640 medium to the cell pellet and divide one milliliter of the cell suspension into two new sterile micro tubes labeled as number one and number two.To micro tube one, add 500 milli units of Sialidase from Clostridium perfringens. Incubate both tubes for 60 minutes at 37 degrees celsius. After incubation, transfer the cells from both micro tubes into corresponding new 15 milliliter conical tubes labeled as number one and number two.Then add approximately four milliliters of complete RPMI 1640 medium containing 10%FBS to each conical tube. Centrifuge the tubes at room temperature for four minutes at 300G using the normal break and add five milliliters of complete RPMI 1640 medium to the pellet. Plate one milliliter cells per well.The effectiveness of Sailidase treatment for reducing the sialic acid content down the surface of human monocyte derived dendritic cells was evaluated by flow cytometry and confocal microscopy. Sailidase treatment significantly decreased Maackia Amurensis lectin and Sambucus nigra lectin binding while increasing Peanut agglutinin lectin staining. The decrease in Sambucus nigra lectin staining after Sailidase treatment showed a significantly reduced Sambucus nigra lectin staining at the cell's surface.

Maturation Profiling of Human Monocyte-Derived Dendritic Cells (mo-DCs)

Maturation Profiling of Human Monocyte-Derived Dendritic Cells (Mo-DCs)  

Begin collecting a new sample of the cells of interest for antibody staining by washing the cells at room temperature for five minutes at 300 G with normal break. Distribute the cells into micro tubes. To perform the staining using the desired antibodies, incubate the fluorescence conjugated antibodies in the dark for 15 minutes at room temperature.Wash the cells with one milliliter of PBS before centrifuging for five minutes at 300 G at room temperature. Add up to 100 microliters of PBS to all the micro tubes. Then resuspend the cells in 300 microliters of 2%paraformaldehyde, and store the tubes in the dark at four degrees Celsius until flow cytometry.A significant increase was observed in the expression of the antigen presenting molecules MHC-I and MHC-II, and the expression of the CD80 and CD86 co-stimulatory molecules due to sialidase treatment.

1.6K Views.  Universidade NOVA de Lisboa.  A unique, comprehensive protocol to generate de-sialylated human monocyte-derived dendritic cells (mo-DCs) from isolated peripheral blood mononuclear cells (PBMCs) using a sialidase treatment is presented. Further, methods to assess the phenotypic and functional characterization of mo-DCs and evaluate how sialidase treatment improves the maturation level of mo-DCs are described.

De-Sialylated Monocyte-Derived-DCs from Isolated PBMCs Using Sialidase Treatment

Summary