TY - JOUR
T1 - Peripheral expression of self-MHC-II influences the reactivity and self-tolerance of mature CD4+ T cells
T2 - Evidence from a lymphopenic T cell model
AU - Bhandoola, Avinash
AU - Tai, Xuguang
AU - Eckhaus, Michael
AU - Auchincloss, Hugh
AU - Mason, Karen
AU - Rubin, Steven A.
AU - Carbone, Kathryn M.
AU - Grossman, Zvi
AU - Rosenberg, Amy S.
AU - Singer, Alfred
PY - 2002/10/1
Y1 - 2002/10/1
N2 - While intrathymic MHC expression influences the specificity of developing thymocytes, we considered that peripheral MHC expression might influence the reactivity of postthymic T cells. We now report for CD4+ T cells that peripheral MHC-II expression does influence their reactivity and self-tolerance. Upon transfer into MHC-II-deficient lymphopenic hosts, mature CD4+ T cells were found to acquire an activated memory phenotype and to become: (1) autoreactive against syngeneic MHC-II+ skin grafts, (2) hyperreactive against third-party MHC-II+ skin grafts, and (3) functionally dysregulated, resulting in a lymphoproliferative disorder characterized by intraepithelial infiltrations. Peripheral MHC-II expression appeared to influence CD4+ T cell reactivity by two complementary mechanisms: maintenance of CD4+CD25+ regulatory T cells ("suppression") and direct dampening of CD4+ T cell reactivity ("tuning").
AB - While intrathymic MHC expression influences the specificity of developing thymocytes, we considered that peripheral MHC expression might influence the reactivity of postthymic T cells. We now report for CD4+ T cells that peripheral MHC-II expression does influence their reactivity and self-tolerance. Upon transfer into MHC-II-deficient lymphopenic hosts, mature CD4+ T cells were found to acquire an activated memory phenotype and to become: (1) autoreactive against syngeneic MHC-II+ skin grafts, (2) hyperreactive against third-party MHC-II+ skin grafts, and (3) functionally dysregulated, resulting in a lymphoproliferative disorder characterized by intraepithelial infiltrations. Peripheral MHC-II expression appeared to influence CD4+ T cell reactivity by two complementary mechanisms: maintenance of CD4+CD25+ regulatory T cells ("suppression") and direct dampening of CD4+ T cell reactivity ("tuning").
UR - http://www.scopus.com/inward/record.url?scp=18644365981&partnerID=8YFLogxK
U2 - 10.1016/S1074-7613(02)00417-X
DO - 10.1016/S1074-7613(02)00417-X
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AN - SCOPUS:18644365981
SN - 1074-7613
VL - 17
SP - 425
EP - 436
JO - Immunity
JF - Immunity
IS - 4
ER -