Abstract
The graft-vs.-host reaction (GVHR) results in damage to the epithelial and lymphoid compartments of the thymus and thus in abnormal maturation and function of thymocytes in mice undergoing GVHR. In this report, the effects of GVHR on thymic T cell receptor (TCR) expression and usage have been investigated. GVHR was induced in unirradiated F1 hybrid mice by the intravenous transfer of parental lymphoid cells. Expression of the CD3/TCR complex on thymocyte subsets defined by CD4 and CD8 was studied by three-color flow cytometry. The level of CD3/TCR was decreased on CD4+CD8-, but not CD4-CD8+, mature thymocytes. The lack of upregulation of CD3/TCR on CD4 single-positive thymocytes, but not on their CD8+ counterparts, suggested an abnormality of class II major histocompatibility complex (MHC) expression in the thymuses of mice undergoing GVHR. Immunofluorescence staining of thymic frozen sections revealed that MHC class II expression was dramatically decreased in GVH- reactive mice. GVHR-induced changes in positive and negative selection were evaluated by determining the incidence of specific V beta TCR segment usage in the thymus. In normal mice, thymocyte usage of any given V beta segment was highly consistent between individuals of the same strain and age; however, a marked divergence in the incidence of TCR V beta 6hi and V beta 8hi cells between GVH-reactive littermate mice was observed, suggesting that thymic positive selection had become disregulated in these animals. Furthermore, negative selection was defective; the incidence of phenotypically self-reactive V beta 6hi T cells was significantly greater in the thymuses of GVH-reactive mice bearing the endogenous superantigen Mls-1a than in untreated controls. Thus, mice undergoing GVHR showed defective TCR upregulation on CD4+CD8- thymocytes and changes in TCR usage reflecting aberrant thymic selection, in conjunction with decreased expression of MHC class II. Most abnormalities of TCR expression and usage on CD4+ thymocytes observed in GVH-reactive mice were analogous to those of class II knockout mice.
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Selected References
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- Berg L. J., Frank G. D., Davis M. M. The effects of MHC gene dosage and allelic variation on T cell receptor selection. Cell. 1990 Mar 23;60(6):1043–1053. doi: 10.1016/0092-8674(90)90352-f. [DOI] [PubMed] [Google Scholar]
- Beschorner W. E., Di Gennaro K. A., Hess A. D., Santos G. W. Cyclosporine and the thymus: influence of irradiation and age on thymic immunopathology and recovery. Cell Immunol. 1987 Dec;110(2):350–364. doi: 10.1016/0008-8749(87)90128-6. [DOI] [PubMed] [Google Scholar]
- Beschorner W. E., Shinn C. A., Fischer A. C., Santos G. W., Hess A. D. Cyclosporine-induced pseudo-graft-versus-host disease in the early post-cyclosporine period. Transplantation. 1988 Aug;46(2 Suppl):112S–117S. doi: 10.1097/00007890-198808001-00021. [DOI] [PubMed] [Google Scholar]
- Bill J., Palmer E. Positive selection of CD4+ T cells mediated by MHC class II-bearing stromal cell in the thymic cortex. Nature. 1989 Oct 19;341(6243):649–651. doi: 10.1038/341649a0. [DOI] [PubMed] [Google Scholar]
- Charley M. R., Bangert J. L., Hamilton B. L., Gilliam J. N., Sontheimer R. D. Murine graft-versus-host skin disease: a chronologic and quantitative analysis of two histologic patterns. J Invest Dermatol. 1983 Nov;81(5):412–417. doi: 10.1111/1523-1747.ep12522551. [DOI] [PubMed] [Google Scholar]
- Cosgrove D., Gray D., Dierich A., Kaufman J., Lemeur M., Benoist C., Mathis D. Mice lacking MHC class II molecules. Cell. 1991 Sep 6;66(5):1051–1066. doi: 10.1016/0092-8674(91)90448-8. [DOI] [PubMed] [Google Scholar]
- Cunningham A. J., Szenberg A. Further improvements in the plaque technique for detecting single antibody-forming cells. Immunology. 1968 Apr;14(4):599–600. [PMC free article] [PubMed] [Google Scholar]
- Einsele H., Ehninger G., Schneider E. M., Krüger G. F., Vallbracht A., Dopfer R., Schmidt H., Waller H. D., Müller C. A. High frequency of graft-versus-host-like syndromes following syngeneic bone marrow transplantation. Transplantation. 1988 Mar;45(3):579–585. doi: 10.1097/00007890-198803000-00016. [DOI] [PubMed] [Google Scholar]
- Fischer A. C., Laulis M. K., Horwitz L., Beschorner W. E., Hess A. Host resistance to cyclosporine induced syngeneic graft-versus-host disease. Requirement for two distinct lymphocyte subsets. J Immunol. 1989 Aug 1;143(3):827–832. [PubMed] [Google Scholar]
- Fukushi N., Arase H., Wang B., Ogasawara K., Gotohda T., Good R. A., Onoé K. Thymus: a direct target tissue in graft-versus-host reaction after allogeneic bone marrow transplantation that results in abrogation of induction of self-tolerance. Proc Natl Acad Sci U S A. 1990 Aug;87(16):6301–6305. doi: 10.1073/pnas.87.16.6301. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fukuzawa M., Via C. S., Shearer G. M. Defective thymic education of L3T4+ T helper cell function in graft-vs-host mice. J Immunol. 1988 Jul 15;141(2):430–439. [PubMed] [Google Scholar]
- Fung-Leung W. P., Schilham M. W., Rahemtulla A., Kündig T. M., Vollenweider M., Potter J., van Ewijk W., Mak T. W. CD8 is needed for development of cytotoxic T cells but not helper T cells. Cell. 1991 May 3;65(3):443–449. doi: 10.1016/0092-8674(91)90462-8. [DOI] [PubMed] [Google Scholar]
- Galy A. H., Spits H. IL-1, IL-4, and IFN-gamma differentially regulate cytokine production and cell surface molecule expression in cultured human thymic epithelial cells. J Immunol. 1991 Dec 1;147(11):3823–3830. [PubMed] [Google Scholar]
- Gao E. K., Lo D., Cheney R., Kanagawa O., Sprent J. Abnormal differentiation of thymocytes in mice treated with cyclosporin A. Nature. 1988 Nov 10;336(6195):176–179. doi: 10.1038/336176a0. [DOI] [PubMed] [Google Scholar]
- Gratama J. W., Fibbe W. E., Naipal A. M., Slats J., Stijnen T., D'Amaro J., Bolhuis R. L., The T. H., Janssen J. Cytomegalovirus immunity and T lymphocytes in bone marrow donors and acute graft-versus-host disease. Bone Marrow Transplant. 1986 Dec;1(2):141–146. [PubMed] [Google Scholar]
- Grusby M. J., Johnson R. S., Papaioannou V. E., Glimcher L. H. Depletion of CD4+ T cells in major histocompatibility complex class II-deficient mice. Science. 1991 Sep 20;253(5026):1417–1420. doi: 10.1126/science.1910207. [DOI] [PubMed] [Google Scholar]
- Guy-Grand D., Vassalli P. Gut injury in mouse graft-versus-host reaction (GVHR). Adv Exp Med Biol. 1987;216A:661–671. doi: 10.1007/978-1-4684-5344-7_78. [DOI] [PubMed] [Google Scholar]
- Guy-Grand D., Vassalli P. Gut injury in mouse graft-versus-host reaction (GVHR). Adv Exp Med Biol. 1987;216A:661–671. doi: 10.1007/978-1-4684-5344-7_78. [DOI] [PubMed] [Google Scholar]
- Happ M. P., Woodland D. L., Palmer E. A third T-cell receptor beta-chain variable region gene encodes reactivity to Mls-1a gene products. Proc Natl Acad Sci U S A. 1989 Aug;86(16):6293–6296. doi: 10.1073/pnas.86.16.6293. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Haskins K., Hannum C., White J., Roehm N., Kubo R., Kappler J., Marrack P. The antigen-specific, major histocompatibility complex-restricted receptor on T cells. VI. An antibody to a receptor allotype. J Exp Med. 1984 Aug 1;160(2):452–471. doi: 10.1084/jem.160.2.452. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kanagawa O., Palmer E., Bill J. The T cell receptor V beta 6 domain imparts reactivity to the Mls-1a antigen. Cell Immunol. 1989 Apr 1;119(2):412–426. doi: 10.1016/0008-8749(89)90255-4. [DOI] [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]
- Khairallah M., Spach C., Maitre F., Motta R. Endocrine involvement in minor (non-H-2) graft versus host reaction in mice: dissociated effect on corticosterone and aldosterone plasma levels. Endocrinology. 1988 Oct;123(4):1949–1954. doi: 10.1210/endo-123-4-1949. [DOI] [PubMed] [Google Scholar]
- Koller B. H., Marrack P., Kappler J. W., Smithies O. Normal development of mice deficient in beta 2M, MHC class I proteins, and CD8+ T cells. Science. 1990 Jun 8;248(4960):1227–1230. doi: 10.1126/science.2112266. [DOI] [PubMed] [Google Scholar]
- Kornbluth M., You-Ten E., Desbarats J., Gamache S., Xenocostas A., Lapp W. S. T cell subsets in the thymus of graft-versus-host immunosuppressed mice. Sensitivity of the L3T4+Lyt-2- subset to cortisone. Transplantation. 1991 Jan;51(1):262–267. doi: 10.1097/00007890-199101000-00044. [DOI] [PubMed] [Google Scholar]
- Kruisbeek A. M., Mond J. J., Fowlkes B. J., Carmen J. A., Bridges S., Longo D. L. Absence of the Lyt-2-,L3T4+ lineage of T cells in mice treated neonatally with anti-I-A correlates with absence of intrathymic I-A-bearing antigen-presenting cell function. J Exp Med. 1985 May 1;161(5):1029–1047. doi: 10.1084/jem.161.5.1029. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lapp W. S., Ghayur T., Mendes M., Seddik M., Seemayer T. A. The functional and histological basis for graft-versus-host-induced immunosuppression. Immunol Rev. 1985 Dec;88:107–133. doi: 10.1111/j.1600-065x.1985.tb01155.x. [DOI] [PubMed] [Google Scholar]
- Leist T. P., Heuchel R., Zinkernagel R. M. Increased bactericidal macrophage activity induced by immunological stimuli is dependent on interferon (IFN)-gamma. Interference of anti-IFN-gamma but not anti-IFN-alpha/beta with modulation of macrophage activity caused by lymphocytic choriomeningitis virus infection or systemic graft-vs.-host reactions. Eur J Immunol. 1988 Aug;18(8):1295–1298. doi: 10.1002/eji.1830180822. [DOI] [PubMed] [Google Scholar]
- Levy R. B., Jones M., Cray C. Isolated peripheral T cells from GvHR recipients exhibit defective IL-2R expression, IL-2 production, and proliferation in response to activation stimuli. J Immunol. 1990 Dec 15;145(12):3998–4005. [PubMed] [Google Scholar]
- MacDonald H. R., Hengartner H., Pedrazzini T. Intrathymic deletion of self-reactive cells prevented by neonatal anti-CD4 antibody treatment. Nature. 1988 Sep 8;335(6186):174–176. doi: 10.1038/335174a0. [DOI] [PubMed] [Google Scholar]
- Matsuzaki G., Yoshikai Y., Ogimoto M., Kishihara K., Nomoto K. Clonal deletion of self-reactive T cells at the early stage of T cell development in thymus of radiation bone marrow chimeras. J Immunol. 1990 Jul 1;145(1):46–51. [PubMed] [Google Scholar]
- Mendes M. L., Rode H., Peres A., Kongshavn P. A., Lapp W. S. Interleukin-1 and interleukin-2 defects associated with murine graft-versus-host-induced immunodeficiency. Transplantation. 1985 Apr;39(4):418–424. doi: 10.1097/00007890-198504000-00016. [DOI] [PubMed] [Google Scholar]
- Morris S. C., Cheek R. L., Cohen P. L., Eisenberg R. A. Autoantibodies in chronic graft versus host result from cognate T-B interactions. J Exp Med. 1990 Feb 1;171(2):503–517. doi: 10.1084/jem.171.2.503. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mowat A. M., Felstein M. V. Experimental studies of immunologically mediated enteropathy. V. Destructive enteropathy during an acute graft-versus-host reaction in adult BDF1 mice. Clin Exp Immunol. 1990 Feb;79(2):279–284. doi: 10.1111/j.1365-2249.1990.tb05191.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Murphy K. M., Heimberger A. B., Loh D. Y. Induction by antigen of intrathymic apoptosis of CD4+CD8+TCRlo thymocytes in vivo. Science. 1990 Dec 21;250(4988):1720–1723. doi: 10.1126/science.2125367. [DOI] [PubMed] [Google Scholar]
- Nestel F. P., Price K. S., Seemayer T. A., Lapp W. S. Macrophage priming and lipopolysaccharide-triggered release of tumor necrosis factor alpha during graft-versus-host disease. J Exp Med. 1992 Feb 1;175(2):405–413. doi: 10.1084/jem.175.2.405. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Okada C. Y., Holzmann B., Guidos C., Palmer E., Weissman I. L. Characterization of a rat monoclonal antibody specific for a determinant encoded by the V beta 7 gene segment. Depletion of V beta 7+ T cells in mice with Mls-1a haplotype. J Immunol. 1990 May 1;144(9):3473–3477. [PubMed] [Google Scholar]
- Parthenais E., Lapp W. S. Evidence for two types of non-specific suppressor cells activated by the graft-versus-host reaction in mice. Scand J Immunol. 1978 Mar;7(3):215–220. doi: 10.1111/j.1365-3083.1978.tb00446.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]
- Petrie H. T., Hugo P., Scollay R., Shortman K. Lineage relationships and developmental kinetics of immature thymocytes: CD3, CD4, and CD8 acquisition in vivo and in vitro. J Exp Med. 1990 Dec 1;172(6):1583–1588. doi: 10.1084/jem.172.6.1583. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Piguet P. F., Janin-Mercier A., Vassalli P., Saurat J. H. Epidermal lesions of the GVHR: evaluation of the role of different MHC and non MHC loci and of the Ly-2+ and L3T4+ T lymphocytes. J Immunol. 1987 Jul 15;139(2):406–410. [PubMed] [Google Scholar]
- Rahemtulla A., Fung-Leung W. P., Schilham M. W., Kündig T. M., Sambhara S. R., Narendran A., Arabian A., Wakeham A., Paige C. J., Zinkernagel R. M. Normal development and function of CD8+ cells but markedly decreased helper cell activity in mice lacking CD4. Nature. 1991 Sep 12;353(6340):180–184. doi: 10.1038/353180a0. [DOI] [PubMed] [Google Scholar]
- Roberts J. L., Sharrow S. O., Singer A. Clonal deletion and clonal anergy in the thymus induced by cellular elements with different radiation sensitivities. J Exp Med. 1990 Mar 1;171(3):935–940. doi: 10.1084/jem.171.3.935. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Salaün J., Bandeira A., Khazaal I., Calman F., Coltey M., Coutinho A., Le Douarin N. M. Thymic epithelium tolerizes for histocompatibility antigens. Science. 1990 Mar 23;247(4949 Pt 1):1471–1474. doi: 10.1126/science.247.4949.1471. [DOI] [PubMed] [Google Scholar]
- Seddik M., Seemayer T. A., Lapp W. S. The graft-versus-host reaction and immune function. I. T helper cell immunodeficiency associated with graft-versus-host-induced thymic epithelial cell damage. Transplantation. 1984 Mar;37(3):281–286. doi: 10.1097/00007890-198403000-00013. [DOI] [PubMed] [Google Scholar]
- Seemayer T. A., Lapp W. S., Bolande R. P. Thymic epithelial injury in graft-versus-host reactions following adrenalectomy. Am J Pathol. 1978 Nov;93(2):325–338. [PMC free article] [PubMed] [Google Scholar]
- Seemayer T. A., Lapp W. S., Bolande R. P. Thymic involution in murine graft-versus-host reaction. Epithelial injury mimicking human thymic dysplasia. Am J Pathol. 1977 Jul;88(1):119–134. [PMC free article] [PubMed] [Google Scholar]
- Vandekerckhove B. A., Baccala R., Jones D., Kono D. H., Theofilopoulos A. N., Roncarolo M. G. Thymic selection of the human T cell receptor V beta repertoire in SCID-hu mice. J Exp Med. 1992 Dec 1;176(6):1619–1624. doi: 10.1084/jem.176.6.1619. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Xenocostas A., Osmond D. G., Lapp W. S. The effect of the graft-versus-host reaction on B lymphocyte production in bone marrow of mice. Depressed genesis of early progenitors prior to mu heavy chain expression. Transplantation. 1991 May;51(5):1089–1096. doi: 10.1097/00007890-199105000-00031. [DOI] [PubMed] [Google Scholar]
- Yoshikai Y., Ogimoto M., Matsuzaki G., Nomoto K. Bone marrow-derived cells are essential for intrathymic deletion of self-reactive T cells in both the host- and donor-derived thymocytes of fully allogeneic bone marrow chimeras. J Immunol. 1990 Jul 15;145(2):505–509. [PubMed] [Google Scholar]
- Zijlstra M., Bix M., Simister N. E., Loring J. M., Raulet D. H., Jaenisch R. Beta 2-microglobulin deficient mice lack CD4-8+ cytolytic T cells. Nature. 1990 Apr 19;344(6268):742–746. doi: 10.1038/344742a0. [DOI] [PubMed] [Google Scholar]
- Zúiga-Pflücker J. C., Jones L. A., Longo D. L., Kruisbeek A. M. CD8 is required during positive selection of CD4-/CD8+ T cells. J Exp Med. 1990 Feb 1;171(2):427–437. doi: 10.1084/jem.171.2.427. [DOI] [PMC free article] [PubMed] [Google Scholar]
- van Ewijk W., Ron Y., Monaco J., Kappler J., Marrack P., Le Meur M., Gerlinger P., Durand B., Benoist C., Mathis D. Compartmentalization of MHC class II gene expression in transgenic mice. Cell. 1988 May 6;53(3):357–370. doi: 10.1016/0092-8674(88)90156-0. [DOI] [PubMed] [Google Scholar]
- von Boehmer H., Kirberg J., Rocha B. An unusual lineage of alpha/beta T cells that contains autoreactive cells. J Exp Med. 1991 Nov 1;174(5):1001–1008. doi: 10.1084/jem.174.5.1001. [DOI] [PMC free article] [PubMed] [Google Scholar]