Abstract
Graft-versus-host reaction (GVHR) following allogeneic bone marrow (BM) transplantation was investigated by analyzing expression of antigen receptors on T cells specific for recipient antigens. GVHR chimeras were prepared by transplanting mixtures of splenic T cells and T-cell-depleted BM cells from B10 (I-E-, Mls-1b) or B10.AQR (I-E+, Mls-1b) mice into lethally irradiated AKR/J (I-E+, Mls-1a) recipients. Increased proportions of V beta 6+ T cells reactive to recipient antigens (I-E and Mls-1a) were observed in thymuses from such chimeras 1 or 5 wk after BM transplantation. V beta 6+ T cells observed 1 wk after BM transplantation were derived from mature T cells that had been inoculated into recipients. These cells responded to recipient antigens expressed in the thymus. After 5 wk, thymocytes brightly positive for V beta 6+ were shown not to descend from mature T cells but to differentiate from precursor cells present in the BM inocula. Since V beta 6+ T cells were eliminated in thymuses from non-GVHR chimeras 5 wk after BM transplantation using T-cell-depleted BM cells alone, it appears that GVHR occurring in the thymus at an early stage abrogates thymic stromal functions essential to induction of self-tolerance in the T-cell repertoire. These findings propose a mechanism (autoimmunity) to explain in part the pathogenesis of chronic GVHR.
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- Elkins W. L., Kavathas P., Bach F. H. Activation of T cells by H-2 factors in the graft-vs-host reaction. Transplant Proc. 1973 Dec;5(4):1759–1762. [PubMed] [Google Scholar]
- Gale R. P. Graft-versus-host disease. Immunol Rev. 1985 Dec;88:193–214. doi: 10.1111/j.1600-065x.1985.tb01159.x. [DOI] [PubMed] [Google Scholar]
- Good R. A., Kapoor N., Reisner Y. Bone marrow transplantation--an expanding approach to treatment of many diseases. Cell Immunol. 1983 Nov;82(1):36–54. doi: 10.1016/0008-8749(83)90139-9. [DOI] [PubMed] [Google Scholar]
- Good R. A. Toward safer marrow transplantation. N Engl J Med. 1982 Feb 18;306(7):421–423. doi: 10.1056/NEJM198202183060710. [DOI] [PubMed] [Google Scholar]
- Heim L. R., Martinez C., Good R. A. Cause of homologous disease. Nature. 1967 Apr 1;214(5083):26–29. doi: 10.1038/214026a0. [DOI] [PubMed] [Google Scholar]
- Hengartner H., Odermatt B., Schneider R., Schreyer M., Wälle G., MacDonald H. R., Zinkernagel R. M. Deletion of self-reactive T cells before entry into the thymus medulla. Nature. 1988 Nov 24;336(6197):388–390. doi: 10.1038/336388a0. [DOI] [PubMed] [Google Scholar]
- Iwabuchi K., Ogasawara K., Ogasawara M., Yasumizu R., Noguchi M., Geng L., Fujita M., Good R. A., Onoé K. A study on proliferative responses to host Ia antigens in allogeneic bone marrow chimera in mice: sequential analysis of the reactivity and characterization of the cells involved in the responses. J Immunol. 1987 Jan 1;138(1):18–25. [PubMed] [Google Scholar]
- Kappler J. W., Roehm N., Marrack P. T cell tolerance by clonal elimination in the thymus. Cell. 1987 Apr 24;49(2):273–280. doi: 10.1016/0092-8674(87)90568-x. [DOI] [PubMed] [Google Scholar]
- Kappler J. W., Staerz U., White J., Marrack P. C. Self-tolerance eliminates T cells specific for Mls-modified products of the major histocompatibility complex. Nature. 1988 Mar 3;332(6159):35–40. doi: 10.1038/332035a0. [DOI] [PubMed] [Google Scholar]
- Kisielow P., Blüthmann H., Staerz U. D., Steinmetz M., von Boehmer H. Tolerance in T-cell-receptor transgenic mice involves deletion of nonmature CD4+8+ thymocytes. Nature. 1988 Jun 23;333(6175):742–746. doi: 10.1038/333742a0. [DOI] [PubMed] [Google Scholar]
- Korngold R., Sprent J. Lethal graft-versus-host disease after bone marrow transplantation across minor histocompatibility barriers in mice. Prevention by removing mature T cells from marrow. J Exp Med. 1978 Dec 1;148(6):1687–1698. doi: 10.1084/jem.148.6.1687. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Krown S. E., Coico R., Scheid M. P., Fernandes G., Good R. A. Immune function in fully allogeneic mouse bone marrow chimeras. Clin Immunol Immunopathol. 1981 May;19(2):268–283. doi: 10.1016/0090-1229(81)90069-6. [DOI] [PubMed] [Google Scholar]
- O'Reilly R. J. Allogenic bone marrow transplantation: current status and future directions. Blood. 1983 Nov;62(5):941–964. [PubMed] [Google Scholar]
- Ogasawara M., Iwabuchi K., Good R. A., Onoe K. Bone marrow cells from allogeneic bone marrow chimeras inhibit the generation of cytotoxic lymphocyte responses against both donor and recipient cells. J Immunol. 1988 Nov 15;141(10):3306–3312. [PubMed] [Google Scholar]
- Onoé K., Fernandes G., Good R. A. Humoral and cell-mediated immune responses in fully allogeneic bone marrow chimera in mice. J Exp Med. 1980 Jan 1;151(1):115–132. doi: 10.1084/jem.151.1.115. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Onoé K., Fernandes G., Shen F. W., Good R. A. Sequential changes of thymocyte surface antigens with presence or absence of graft-vs-host reaction following allogeneic bone marrow transplantation. Cell Immunol. 1982 Apr;68(2):207–219. doi: 10.1016/0008-8749(82)90106-x. [DOI] [PubMed] [Google Scholar]
- Onoé K., Iwabuchi K., Iwabuchi C., Arase H., Hatakeyama S., Wambua P. P., Fukushi N., Negishi I., Good R. A., Ogasawara K. Donor and recipient specific tolerance in cells from semi-allogeneic, H-2 subregion compatible or fully allogeneic bone marrow chimeras attributable to clonal deletion. Immunobiology. 1989 Jun;179(2-3):172–189. doi: 10.1016/s0171-2985(89)80015-4. [DOI] [PubMed] [Google Scholar]
- Onoé K., Iwabuchi K., Katsume C., Gotohda T., Arase A., Hatakeyama S., Mishima M., Good R. A., Ogasawara K. A study on graft-versus-host reaction (GVHR) by Simonsen's splenomegaly assay. Cells and antigen systems involved in induction of GVHR. Acta Pathol Jpn. 1989 Feb;39(2):101–110. doi: 10.1111/j.1440-1827.1989.tb01487.x. [DOI] [PubMed] [Google Scholar]
- Payne J., Huber B. T., Cannon N. A., Schneider R., Schilham M. W., Acha-Orbea H., MacDonald H. R., Hengartner H. Two monoclonal rat antibodies with specificity for the beta-chain variable region V beta 6 of the murine T-cell receptor. Proc Natl Acad Sci U S A. 1988 Oct;85(20):7695–7698. doi: 10.1073/pnas.85.20.7695. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Piguet P. F. GVHR elicited by products of class I or class II loci of the MHC: analysis of the response of mouse T lymphocytes to products of class I and class II loci of the MHC in correlation with GVHR-induced mortality, medullary aplasia, and enteropathy. J Immunol. 1985 Sep;135(3):1637–1643. [PubMed] [Google Scholar]
- Rammensee H. G., Kroschewski R., Frangoulis B. Clonal anergy induced in mature V beta 6+ T lymphocytes on immunizing Mls-1b mice with Mls-1a expressing cells. Nature. 1989 Jun 15;339(6225):541–544. doi: 10.1038/339541a0. [DOI] [PubMed] [Google Scholar]
- Ramsdell F., Lantz T., Fowlkes B. J. A nondeletional mechanism of thymic self tolerance. Science. 1989 Nov 24;246(4933):1038–1041. doi: 10.1126/science.2511629. [DOI] [PubMed] [Google Scholar]
- Rolink A. G., Pals S. T., Gleichmann E. Allosuppressor and allohelper T cells in acute and chronic graft-vs.-host disease. II. F1 recipients carrying mutations at H-2K and/or I-A. J Exp Med. 1983 Feb 1;157(2):755–771. doi: 10.1084/jem.157.2.755. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Speiser D. E., Schneider R., Hengartner H., MacDonald H. R., Zinkernagel R. M. Clonal deletion of self-reactive T cells in irradiation bone marrow chimeras and neonatally tolerant mice. Evidence for intercellular transfer of Mlsa. J Exp Med. 1989 Aug 1;170(2):595–600. doi: 10.1084/jem.170.2.595. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sprent J., Schaefer M., Gao E. K., Korngold R. Role of T cell subsets in lethal graft-versus-host disease (GVHD) directed to class I versus class II H-2 differences. I. L3T4+ cells can either augment or retard GVHD elicited by Lyt-2+ cells in class I different hosts. J Exp Med. 1988 Feb 1;167(2):556–569. doi: 10.1084/jem.167.2.556. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sprent J., Schaefer M., Lo D., Korngold R. Functions of purified L3T4+ and Lyt-2+ cells in vitro and in vivo. Immunol Rev. 1986 Jun;91:195–218. doi: 10.1111/j.1600-065x.1986.tb01489.x. [DOI] [PubMed] [Google Scholar]
- Storb R., Thomas E. D. Allogeneic bone-marrow transplantation. Immunol Rev. 1983;71:77–102. doi: 10.1111/j.1600-065x.1983.tb01069.x. [DOI] [PubMed] [Google Scholar]
- Sykes M., Sheard M., Sachs D. H. Effects of T cell depletion in radiation bone marrow chimeras. I. Evidence for a donor cell population which increases allogeneic chimerism but which lacks the potential to produce GVHD. J Immunol. 1988 Oct 1;141(7):2282–2288. [PubMed] [Google Scholar]
- Truitt R. L., Shih C. Y., Lefever A. V., Tempelis L. D., Andreani M., Bortin M. M. Characterization of alloimmunization-induced T lymphocytes reactive against AKR leukemia in vitro and correlation with graft-vs-leukemia activity in vivo. J Immunol. 1983 Oct;131(4):2050–2058. [PubMed] [Google Scholar]
- Van Ewijk W., Rouse R. V., Weissman I. L. Distribution of H-2 microenvironments in the mouse thymus. Immunoelectron microscopic identification of I-A and H-2K bearing cells. J Histochem Cytochem. 1980 Oct;28(10):1089–1099. doi: 10.1177/28.10.6999083. [DOI] [PubMed] [Google Scholar]
- Yoshikai Y., Ogimoto M., Matsumoto K., Sakumoto M., Matsuzaki G., Nomoto K. Deletion of Mls-reactive T cells in H-2-compatible but Mls-incompatible bone marrow chimeras. Eur J Immunol. 1989 Jun;19(6):1009–1013. doi: 10.1002/eji.1830190609. [DOI] [PubMed] [Google Scholar]
- van Rappard-Van der Veen F. M., Kiesel U., Poels L., Schuler W., Melief C. J., Landegent J., Gleichmann E. Further evidence against random polyclonal antibody formation in mice with lupus-like graft-vs-host disease. J Immunol. 1984 Apr;132(4):1814–1820. [PubMed] [Google Scholar]