TOLERANCE OF CD8+ T-CELLS DEVELOPING IN PARENT -] F1-CHIMERAS PREPARED WITH SUPRALETHAL IRRADIATION - STEP-WISE INDUCTION OF TOLERANCE IN THE INTRATHYMIC AND EXTRATHYMIC ENVIRONMENTS

被引:30
作者
KOSAKA, H [1 ]
SPRENT, J [1 ]
机构
[1] Scripps Res Inst, DEPT IMMUNOL, IMM4A, 10666 N TORREY PINES RD, LA JOLLA, CA 92037 USA
关键词
D O I
10.1084/jem.177.2.367
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Tolerance of CD8+ cells was examined in parent --> F1 bone marrow chimeras (BMC) prepared with supralethal irradiation; host class I expression in the chimeras was limited to non-BM-derived cells. In terms of helper-independent proliferative responses in vitro and induction of graft-vs.-host disease on adoptive transfer, CD8+ cells from long-term chimeras showed profound tolerance to host antigens irrespective of whether the cells were prepared from the thymus or from spleen or lymph nodes. By limiting dilution analysis, cytotoxic T lymphocyte (CTL) precursors specific for host antigens were rare in the extrathymic lymphoid tissues. In the thymus, by contrast, host-specific CTL precursors were only slightly less frequent than in normal parental strain mice. These host-specific CD8+ cells survived when BMC thymocytes were transferred intravenously to a neutral environment, i.e., to donor strain mice. When transferred to further BMC hosts, however, most of the host-reactive cells disappeared. Collectively, the data suggest that tolerance of CD8+ cells in BMC hosts occurs in both the intrathymic and extrathymic environments. In the thymus, contact with host antigens on thymic epithelial cells deletes CD8+ cells controlling helper-independent proliferative responses and in vivo effector functions but spares typical helper-dependent CTL precursors. After export from the thymus, most of the CTL precursors are eliminated after contacting host antigens on stromal cells in the extrathymic environment.
引用
收藏
页码:367 / 378
页数:12
相关论文
共 38 条
[1]   MOUSE LEUKEMIA - THERAPY WITH MONOCLONAL-ANTIBODIES AGAINST A THYMUS DIFFERENTIATION ANTIGEN [J].
BERNSTEIN, ID ;
TAM, MR ;
NOWINSKI, RC .
SCIENCE, 1980, 207 (4426) :68-71
[2]   CHARACTERIZATION OF MURINE THYMOCYTES WITH CD3-ASSOCIATED T-CELL RECEPTOR STRUCTURES [J].
BLUESTONE, JA ;
PARDOLL, D ;
SHARROW, SO ;
FOWLKES, BJ .
NATURE, 1987, 326 (6108) :82-84
[3]   CYTO-TOXIC LYMPHOCYTE-T RESPONSES IN ALLOGENEIC RADIATION BONE-MARROW CHIMERAS - THE CHIMERIC HOST STRICTLY DICTATES THE SELF-REPERTOIRE OF IA-RESTRICTED T-CELLS BUT NOT H-2K D-RESTRICTED T-CELLS [J].
BRADLEY, SM ;
KRUISBEEK, AM ;
SINGER, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1982, 156 (06) :1650-1664
[4]  
BRUCE J, 1981, J IMMUNOL, V127, P2496
[5]   EXPRESSION OF INTERLEUKIN-2 RECEPTORS AS A DIFFERENTIATION MARKER ON INTRATHYMIC STEM-CELLS [J].
CEREDIG, R ;
LOWENTHAL, JW ;
NABHOLZ, M ;
MACDONALD, HR .
NATURE, 1985, 314 (6006) :98-100
[6]   CHARACTERIZATION OF THE MURINE ANTIGENIC DETERMINANT, DESIGNATED L3T4A, RECOGNIZED BY MONOCLONAL-ANTIBODY GK1.5 - EXPRESSION OF L3T4A BY FUNCTIONAL T-CELL CLONES APPEARS TO CORRELATE PRIMARILY WITH CLASS II MHC ANTIGEN-REACTIVITY [J].
DIALYNAS, DP ;
WILDE, DB ;
MARRACK, P ;
PIERRES, A ;
WALL, KA ;
HAVRAN, W ;
OTTEN, G ;
LOKEN, MR ;
PIERRES, M ;
KAPPLER, J ;
FITCH, FW .
IMMUNOLOGICAL REVIEWS, 1983, 74 :29-56
[7]   THYMIC CYTO-TOXIC LYMPHOCYTES-T ARE PRIMED INVIVO TO MINOR HISTOCOMPATIBILITY ANTIGENS [J].
FINK, PJ ;
BEVAN, MJ ;
WEISSMAN, IL .
JOURNAL OF EXPERIMENTAL MEDICINE, 1984, 159 (02) :436-451
[8]   IMMUNE-RESPONSES OF THYMUS LYMPHOCYTE EMBRYONIC CHIMERAS - STUDIES ON TOLERANCE AND MAJOR HISTOCOMPATIBILITY COMPLEX RESTRICTION IN XENOPUS [J].
FLAJNIK, MF ;
DUPASQUIER, L ;
COHEN, N .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1985, 15 (06) :540-547
[9]   STRONG T-CELL TOLERANCE IN PARENT-]F1 BONE-MARROW CHIMERAS PREPARED WITH SUPRALETHAL IRRADIATION - EVIDENCE FOR CLONAL DELETION AND ANERGY [J].
GAO, EK ;
LO, D ;
SPRENT, J .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 171 (04) :1101-1121
[10]   T-CELL CONTACT WITH IA ANTIGENS ON NONHEMOPOIETIC CELLS INVIVO CAN LEAD TO IMMUNITY RATHER THAN TOLERANCE [J].
GAO, EK ;
KOSAKA, H ;
SURH, CD ;
SPRENT, J .
JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 174 (02) :435-446