Peripheral expression of self-MHC-II influences the reactivity and self-tolerance of mature CD4+ T cells:: Evidence from a lymphopenic T cell model

被引:81
作者
Bhandoola, A
Tai, XG
Eckhaus, M
Auchincloss, H
Mason, K
Rubin, SA
Carbone, KM
Grossman, Z
Rosenberg, AS
Singer, A
机构
[1] NCI, Expt Immunol Branch, Bethesda, MD 20892 USA
[2] NIH, Vet Resources Program, Bethesda, MD 20892 USA
[3] Massachusetts Gen Hosp, Transplantat Unit, Boston, MA 02114 USA
[4] US FDA, Div Therapeut Prot, Bethesda, MD 20892 USA
[5] US FDA, Lab Pediat & Resp Viral Dis, Bethesda, MD 20892 USA
[6] Tel Aviv Univ, Dept Physiol & Pharmacol, IL-69978 Tel Aviv, Israel
[7] NIAID, Immunol Lab, Bethesda, MD 20892 USA
关键词
D O I
10.1016/S1074-7613(02)00417-X
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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").
引用
收藏
页码:425 / 436
页数:12
相关论文
共 40 条
  • [1] Auchincloss Hugh Jr., 1993, P1099
  • [2] Mouse CD1-specific NK1 T cells: Development, specificity, and function
    Bendelac, A
    Rivera, MN
    Park, SH
    Roark, JH
    [J]. ANNUAL REVIEW OF IMMUNOLOGY, 1997, 15 : 535 - 562
  • [3] Survival and homeostatic proliferation of naive peripheral CD4+ T cells in the absence of self peptide:MHC complexes
    Clarke, SRM
    Rudensky, AY
    [J]. JOURNAL OF IMMUNOLOGY, 2000, 165 (05) : 2458 - 2464
  • [4] MICE LACKING MHC CLASS-II MOLECULES
    COSGROVE, D
    GRAY, D
    DIERICH, A
    KAUFMAN, J
    LEMEUR, M
    BENOIST, C
    MATHIS, D
    [J]. CELL, 1991, 66 (05) : 1051 - 1066
  • [5] Tuning antigen receptor signaling by CD22: Integrating cues from antigens and the microenvironment
    Cyster, JG
    Goodnow, CC
    [J]. IMMUNITY, 1997, 6 (05) : 509 - 517
  • [6] CD4+ T cell survival is not directly linked to self-MHC-induced TCR signaling
    Dorfman, JR
    Stefanová, I
    Yasutomo, K
    Germain, RN
    [J]. NATURE IMMUNOLOGY, 2000, 1 (04) : 329 - 335
  • [7] The peptide ligands mediating positive selection in the thymus control T cell survival and homeostatic proliferation in the periphery
    Ernst, B
    Lee, DS
    Chang, JM
    Sprent, J
    Surh, CD
    [J]. IMMUNITY, 1999, 11 (02) : 173 - 181
  • [8] H-2 ANTIGENS OF THYMUS DETERMINE LYMPHOCYTE SPECIFICITY
    FINK, PJ
    BEVAN, MJ
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1978, 148 (03) : 766 - 775
  • [9] Homeostasis and anergy of CD4+CD25+ suppressor T cells in vivo
    Gavin, MA
    Clarke, SR
    Negrou, E
    Gallegos, A
    Rudensky, A
    [J]. NATURE IMMUNOLOGY, 2002, 3 (01) : 33 - 41
  • [10] Tuning of activation thresholds explains flexibility in the selection and development of T cells in the thymus
    Grossman, Z
    Singer, A
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (25) : 14747 - 14752