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Triggering of CD99 on monocytes by a specific monoclonal antibody regulates T cell activation
- Source :
- Cellular Immunology. 335:51-58
- Publication Year :
- 2019
- Publisher :
- Elsevier BV, 2019.
-
Abstract
- CD99, a leukocyte surface glycoprotein, has been implicated in many cellular processes including cell adhesion, cell migration and T cell activation. Our previous study demonstrated the anti-CD99 monoclonal antibody (mAb) clone MT99/3 inhibited T cell activation; however, the mechanism is unclear. In this study, we demonstrated that CD99 expressed on monocytes played a role in the inhibition of T cell activation. Anti-CD99 mAb MT99/3 downregulated the expression of costimulatory molecule CD86, but upregulated IL-6, IL-10 and TNF-α production by monocytes. The inhibitory effect of mAb MT99/3 required cell to cell contact between monocytes and lymphocytes. The soluble mediators produced by monocytes alone were insufficient to induce hypo-function of T lymphocytes. In summary, we demonstrated that ligation of CD99 on monocytes by anti-CD99 mAb MT99/3 could mediate T cell hypo-responsiveness. These findings provide the first evidence of the role of CD99 on monocytes that contributes to T cell activation.
- Subjects :
- 0301 basic medicine
medicine.drug_class
T-Lymphocytes
T cell
Primary Cell Culture
Immunology
Cell
Epitopes, T-Lymphocyte
12E7 Antigen
Biology
Lymphocyte Activation
Monoclonal antibody
Monocytes
03 medical and health sciences
0302 clinical medicine
Antigens, CD
Cell Movement
Cell Adhesion
Leukocytes
medicine
Humans
Cell adhesion
CD86
Membrane Glycoproteins
Interleukin-6
Tumor Necrosis Factor-alpha
Monocyte
Antibodies, Monoclonal
Cell migration
Healthy Volunteers
Interleukin-10
Cell biology
030104 developmental biology
medicine.anatomical_structure
Clone (B-cell biology)
Cell Adhesion Molecules
030215 immunology
Subjects
Details
- ISSN :
- 00088749
- Volume :
- 335
- Database :
- OpenAIRE
- Journal :
- Cellular Immunology
- Accession number :
- edsair.doi.dedup.....a478ce9b752b255364123ae6e0b03190
- Full Text :
- https://doi.org/10.1016/j.cellimm.2018.10.012