Abstract
By interacting with CD26 on the CD4+ T cell surface and with the AdoR A2B on the DC surface, ADA triggers a costimulatory signal for human T cells. The aim of this study was to know whether ADA-mediated costimulation plays a role in the differentiation of T cells. The results show that irrespective of its enzymatic activity and dependent on TNF-α, IFN-γ, and IL-6 action, ADA enhanced the differentiation of CD4 +CD45RA+CD45RO-naïve T cells toward CD4 +CD25+CD45RO+ Teffs and CD4+CD45RA- CD45RO+ memory T cells. Furthermore, ADA potentiated generation of CD4+CD25highFoxp3+ Tregs by a mechanism that seems to be mainly dependent on the enzymatic activity of ADA. Interestingly, an ADA-mediated increase on Teff, memory T cell, and Treg generation occurred, not only in cocultures from healthy individuals but also from HIV-infected patients. These data suggest that ADA is a relevant modulator of CD4+ T cell differentiation, even in cells from immunologically compromised individuals.
Original language | English |
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Pages (from-to) | 127-136 |
Number of pages | 10 |
Journal | Journal of Leukocyte Biology |
Volume | 89 |
Issue number | 1 |
DOIs | |
Publication status | Published - Jan 2011 |
Keywords
- CD26
- CD45RA/CD45RO
- Dendritic cells
- Foxp3
- T cell activation
- Th1
ASJC Scopus subject areas
- Immunology and Allergy
- Immunology
- Cell Biology