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Alteration of CD39+Foxp3+ CD4 T cell and cytokine levels in EAE/MS following anti-CD52 treatment.
- Source :
-
Journal of neuroimmunology [J Neuroimmunol] 2017 Feb 15; Vol. 303, pp. 22-30. Date of Electronic Publication: 2016 Dec 21. - Publication Year :
- 2017
-
Abstract
- While examining the therapeutic value of anti-CD52 antibody against EAE/MS, we identified a unique subset of CD39+ Tregs in repopulating GALT tissues, a major lymphoid reservoir, which was accompanied by amelioration of disease. Furthermore, anti-CD52 treatment leads to increased expression of BDNF, IL-10, and SMAD3 in the brains of EAE mice. This condition is associated with suppression of IL-17, a critical inflammatory factor in EAE/MS progression. Additionally, we found elevated levels of CD4+CD39+ Tregs in PBMCs of RRMS patients treated with humanized anti-CD52 mAb. Thus, anti-CD52 can affect multiple immune mediated pathways involved in the pathogenesis of EAE/MS.<br /> (Copyright © 2016. Published by Elsevier B.V.)
- Subjects :
- Animals
Antibodies, Monoclonal pharmacology
Antigens, CD immunology
Antigens, Neoplasm immunology
Apyrase immunology
CD4-Positive T-Lymphocytes drug effects
CD4-Positive T-Lymphocytes immunology
CD52 Antigen
Cytokines immunology
Encephalomyelitis, Autoimmune, Experimental drug therapy
Encephalomyelitis, Autoimmune, Experimental immunology
Forkhead Transcription Factors immunology
Glycoproteins antagonists & inhibitors
Glycoproteins immunology
Humans
Mice
Mice, Inbred C57BL
Multiple Sclerosis drug therapy
Multiple Sclerosis immunology
Multiple Sclerosis metabolism
Treatment Outcome
Antibodies, Monoclonal therapeutic use
Antigens, CD metabolism
Antigens, Neoplasm metabolism
Apyrase metabolism
CD4-Positive T-Lymphocytes metabolism
Cytokines metabolism
Encephalomyelitis, Autoimmune, Experimental metabolism
Forkhead Transcription Factors metabolism
Glycoproteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1872-8421
- Volume :
- 303
- Database :
- MEDLINE
- Journal :
- Journal of neuroimmunology
- Publication Type :
- Academic Journal
- Accession number :
- 28087077
- Full Text :
- https://doi.org/10.1016/j.jneuroim.2016.12.010