TY - JOUR
T1 - Anti-ergotypic T cells in naïve rats
AU - Mimran, Avishai
AU - Mor, Felix
AU - Quintana, Francisco J.
AU - Cohen, Irun R.
PY - 2005/5
Y1 - 2005/5
N2 - T regulatory cells play an important role in regulating T cell responses. Anti-ergotypic T cells are a subset of regulatory T cells that proliferate in response to activation markers, ergotopes, expressed on activated, and not on resting syngeneic T cells. Here we report the presence of anti-ergotypic T cells in lymph nodes, spleens and thymuses of naïve rats. The development of anti-ergotypic T cells appeared to be independent of antigen priming, as thymocytes from one-day old rats exhibited significant anti-ergotypic proliferative responses. The anti-ergotypic T cells were found to be of the CD8+ phenotype, and included both TCRα/β+ and TCRγ/δ+ T cells. The TCRγ/δ+ anti-ergotypic T cells secreted IFNγ and TNFα in response to activated T cells; the TCRα/β+ T cells proliferated but did not secret detectable cytokines. We found that the interaction between the anti-ergotypic T cells and stimulator T cells required cell-to-cell contact between the T cells. Professional APCs were not needed. The response of the TCRα/β+CD8+ anti-ergotypic T cells was MHC-I restricted and B7-CD28 dependent; the response of the TCRγ/δ + anti-ergotypic T cells was B7-CD28 dependent, but was not inhibited by antibodies to classical MHC-I or MHC-II molecules. The existence of anti-ergotypic T cells in naïve animals suggests that these cells might have a role in the regulation and maintenance of the immune system.
AB - T regulatory cells play an important role in regulating T cell responses. Anti-ergotypic T cells are a subset of regulatory T cells that proliferate in response to activation markers, ergotopes, expressed on activated, and not on resting syngeneic T cells. Here we report the presence of anti-ergotypic T cells in lymph nodes, spleens and thymuses of naïve rats. The development of anti-ergotypic T cells appeared to be independent of antigen priming, as thymocytes from one-day old rats exhibited significant anti-ergotypic proliferative responses. The anti-ergotypic T cells were found to be of the CD8+ phenotype, and included both TCRα/β+ and TCRγ/δ+ T cells. The TCRγ/δ+ anti-ergotypic T cells secreted IFNγ and TNFα in response to activated T cells; the TCRα/β+ T cells proliferated but did not secret detectable cytokines. We found that the interaction between the anti-ergotypic T cells and stimulator T cells required cell-to-cell contact between the T cells. Professional APCs were not needed. The response of the TCRα/β+CD8+ anti-ergotypic T cells was MHC-I restricted and B7-CD28 dependent; the response of the TCRγ/δ + anti-ergotypic T cells was B7-CD28 dependent, but was not inhibited by antibodies to classical MHC-I or MHC-II molecules. The existence of anti-ergotypic T cells in naïve animals suggests that these cells might have a role in the regulation and maintenance of the immune system.
KW - Autoimmune diseases
KW - Lymph nodes and thymus
KW - Regulatory T cells
KW - Spleen
KW - T lymphocytes
UR - http://www.scopus.com/inward/record.url?scp=17444368987&partnerID=8YFLogxK
U2 - 10.1016/j.jaut.2004.12.002
DO - 10.1016/j.jaut.2004.12.002
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C2 - 15848041
AN - SCOPUS:17444368987
SN - 0896-8411
VL - 24
SP - 191
EP - 201
JO - Journal of Autoimmunity
JF - Journal of Autoimmunity
IS - 3
ER -