[en] The injection of semi-allogeneic F1 spleen cells into newborn mice of a parental strain induces a state of immune tolerance characterized by anti-donor CTL unresponsiveness and the appearance of a transient SLE-like autoimmune syndrome associating autoantibody production, hypergammaglobulinemia, splenomegaly and glomerulonephritis. Our previous experiments have demonstrated that host Th2-like CD4+ T lymphocytes activate donor F1 B cells persisting in the host to produce autoantibodies, and that this cellular interaction relies on the presence of alloMHC class II molecules on donor B cells. In order to investigate the role and the involvement of MHC alloantigens in the cellular T(host)-B(donor) interaction, newborn C57BL/6 (B6) mice were injected with F1 spleen cells differing from the host at the level of defined portions of the MHC class I (K) or class II (I-A and I-E) molecules. B6 mice injected at birth with spleen cells from different F1 strains were tolerant to each alloantigen (alloAg) tested, as assessed by specific anti-donor CTL unresponsiveness. However, the SLE-like autoimmune syndrome only developed in B6 mice injected at birth with F1 spleen cells differing at the level of MHC class II I-A or I-E molecules. Autoantibodies appeared later in B6 mice neonatally tolerized to I-E alloAg than those detected in B6 mice neonatally tolerized to I-A alloAg. These results show that the SLE-like autoimmune disease that develops concomitantly to neonatally-induced tolerance to alloAg is the consequence of cognate T host-B donor cellular interactions triggered by even minute differences in the MHC class II I-A or MHC class II I-E molecules
Kramar, G.; World Health Organization-Immunology Research and Training Center, Department of Pathology, CMU, 1211 Geneva 4,
Schurmans, Stéphane ; Université Libre de Bruxelles - ULB > Institut de Recherche Interdisciplinaire en Biologie Humaine et Nucléaire, Institut de Biologie et de Médecine Moléculaire
Berney, M.; World Health Organization-Immunology Research and Training Center, Department of Pathology, CMU, 1211 Geneva 4,
Izui, S.; World Health Organization-Immunology Research and Training Center, Department of Pathology, CMU, 1211 Geneva 4,
del Giudice, G.; Institute of Biochemistry, University of Lausanne, 1066 Epalinges, Switzerland
Lambert, P. H.
Language :
English
Title :
Autoimmunity following neonatal tolerance to alloantigens: role of donor I-A and I-E molecules
Billingham, R. E., L. Brent, and P. B. Medawar. 1953 Actively acquired tolerance to foreign cells. Nature 172: 603.
Billingham, R. E. and L. Brent. 1959. Quantitative studies on tissue transplantation immunity. IV Induction of tolerance in newborn mice and studies on the phenomenon of runt disease. Phil. Trans. R. Soc. Lond. (Biol). 242: 439.
Feng, H. M., A. L. Glasebrook, H. D. Engers, and J. Louis. 1983. Clonal analysis of T cell unresponsiveness to alloantigens induced by neonatal injection of F1 spleen cells into parental mice. J. Immunol. 131: 2165.
Goldman, M., H. Feng, H. Engers, A. Hochmann, J. Louis, and P. H. Lambert. 1983. Autoimmunity and immune complex disease after neonatal induction of transplantation tolerance in mice. J. Immunol. 131: 251.
Kramar, G., T. Aguado, J. Louis, G. Del Giudice, and P. H. Lambert. 1993. Characterization of host CD4+ T lymphocytes in mice neonatally tolerized to alloantigens. Eur. J. Immunol. 23: 2551.
Luzuy, S., J. Merino, H. Engers, S. Izui, and P. H. Lambert. 1986. Autoimmunity after induction of neonatal tolerance to alloantigens: role of B cell chimerism and F1 donor B cell activation. J. Immunol. 136: 4420.
Merino, J., S. Schurmans, S. Luzuy, S. Izui, P. Vassali, and P. H. Lambert. 1987. Autoimmune syndrome after induction of neonatal tolerance to alloantigens. Effects of in vivo treatment with anti-T cell subset monoclonal antibodies. J. Immunol. 139: 1426.
Merino, J., J. L. Alonso, A. Ramos, A. Gonzalez, V. Rodriguez-Valverde, and M. De la Hera. 1991. Depletion of CD8+ T cells does not modify the evolution of the autoimmune syndrome observed in mice neonatally tolerized to alloantigens. Allerg. Immunol. 9: 227.
Merino, J., S. Schurmans, M. Duchosal, S. Izui, and P. H. Lambert. 1989. Autoimmune syndrome after induction of neonatal tolerance to alloantigens: CD4+ T cells from the tolerant host activate autoreactive F1 B cells. J. Immunol. 143: 2202.
Schurmans, S., H. Heusser, H.-Y. Qin, J. Merino, G. Brighouse, and P. H. Lambert. 1990. In vivo e ect of anti-IL-4 monoclonal antibody on neonatal induction of tolerance and on associated autoimmune syndrome. J. Immunol. 145: 2465.
Kramar, G., S. Schurmans, T. Aguado, S. Izui, G. Del Giudice, and P. H. Lambert. 1993. Anti-Ia treatment prevents lupus-like autoimmune syndrome in mice neonatally tolerized to alloantigens. J. Autoimmun. 1: 27.
Schurmans, S., G. Brighhouse, G. Kramar, L. Wen, S. Izui, J. Merino, and P. H. Lambert. 1991. Transient T and B cell activation after neonatal induction of tolerance to MHC class II or MIs alloantigens. J. Immunol. 146: 2152.
Hansen, T. H., R. Melvold, J. S. Arn, and D. H. Sachs. 1980. Evidence for mutation in an I-A gene. Nature 285: 340.
Morgan, G. M., I. F. C. McKenzie, and W. Melvold. 1980. The definition of a new Ia antigenic specifity using the B6.C-H-2bm12 I-region mutant strain. Immunogenetics 11: 1.
Sandrin, M. S., I. F. C. McKenzie, R. W. Melvold, and J. Hämmerling. 1982. Serological analysis of B6.C-H-2bm12 (I-A mutant). Eur. J. Immunol. 12: 205.
Yamamura, K., H. Kukutani, V. Folsom, L. K. Clayton, M. Kimoto, S. Akira, S. Kashiwamura, S. Tonegawa, and T. Kishimoto. 1985. Functional expression of a microinjected Ead gene in C57BL/6 transgenic mice. Nature 316: 67.
Nathenson, S. G., J. Geliebter, G. M. Pfa enbach, and R. A. Ze. 1986. Murine major histocompatibility complex class-I mutants: Molecular analysis and structure-function implications. Ann. Rev. Immunol. 4: 471.
McCarthy, S. A. and F. H. Bach. 1983. A comparison of the neonatal tolerance-inducing capacities of H-2 class I and class II antigens. J. Immunol. 131: 1676.
McCarthy, S. A. and F. H. Bach. 1983. The cellular mechanism of maintenance of neonatally induced tolerance to H-2 class I antigens. J. Immunol. 131: 1676.
De Waal, L. P., C. J. M. Melief, and R. W. Melvold. 1981. Cytotoxic T lymphocytes generated across an I-Ab mutant difference are directed against a molecule bearing Ia antigens. Eur. J. Immunol. 11: 258.
Lerner, E. A., L. A. Matis, C. A. Janeway, Jr., P. P. Jones, R. H. Schwartz, and D. B. Murphy. 1980. Monoclonal antibody against an Ir gene product? J. Exp. Med. 152: 1085.
Dialinas, D. P., Z. S. Quan, K. A. Wall, A. Pierres, J. Quistaux, M. R. Lohen, M. Pierres, and F. W. Fitch. 1983. Characterization of the murine T cell surface molecule designated L3T4 identified by monoclonal antibody G.K 1.5 similarly of L3T4 to the human Leu-3/T4. J. Immunol. 131: 2445.
Pierres, M., C. Goridis, and P. Goldstein. 1982. Inhibition of murine T cell-mediated cytolysis and T cell proliferation by a rat monoclonal antibody immunoprecipitating lymphoid cell surface polypeptides of 94.000 and 180.000 molecular weight. Eur. J. Immunol. 12: 60.
Bill, J., O. Kanagawa, D. L. Woodland, and E. Palmer. 1980. The MHC molecule I-E is necessary but not su cient for the clonal deletion of Vß11-bearing T cells. J. Exp. Med. 169: 1405.
Palmer, E., D. L. Woodland, M. P. Happ, J. Bill, and O. Kanagawa. 1989. A third set of genes regulates thymic selection. Cold Spring Harb. Symp. Quant. Biol. 54: 135.
Melief, C. J. M., R. F. Schwartz, H. I. Kohn, and R. W. Melvold. 1975. Dermal histocompatibility and in vitro lymphocytes reactions of three new H-2 mutants. Immunogenetics 2: 337.
Woodland, D., M. P. Happ, J. Bill, and E. Palmer. 1990. Requirement for cotolerogenic gene products in the clonal deletion of aß T cells. Science 247: 964.
Woodland, D., M. P. Happ, K. J. Gollub, and E. Palmer. 1991. An endogenous retrovirus mediating deletion of aß T cells? Nature 349: 529.
Woodland, D., F. E. Lund, M. P. Happ, M. A. Blackman, E. Palmer, and R. B. Corley. 1991. Endogenous superantigen expression is controlled by mouse mammary tumor proviral loci. J. Exp. Med. 174: 1255.
Salaün, J., A. Bandeira, I. Khazaal, O. Burlen-Defranoux, V. Thomas-Vaslin, M. Coltey, N. M. Le Douarin, and A. Couthino. 1992. Transplantation tolerance is unrelated to super-antigen dependent deletion and anergy. Proc. Natl. Acad. Sci. USA 89: 10420.
Schönrich, G., F. Momburg, M. Malissen, A. Schmidt-Verhulst, B. Malissen, G. H. Hämmerling, and B. Arnold. 1992. Distinct mechanisms of extrathymic T cell tolerance due to di erential expression of self antigen. Int. Immunol. 4: 581.
Hansen, T. H. and H. Y. Tse. 1987. Insights into immune-response gene function using an Ia mutant mouse strain. Crit. Rev. Immunol. 7: 169.
Del Giudice, G., J. A. Cooper, J. Merino, A. S. Verdini, A. Pessi, A. R. Togna, H. D. Engers, G. Corradin, and P. H. Lambert. 1987. The antibody response in mice to carrier-free synthetic polymers of Plasmodium Falciparum circumsporozoite repetitive epitope is I-Ab-restricted: possible implications for malaria vaccines. J. Immunol. 137: 2952.
Infante, A. J., P. A. Thompson, K. A. Krolick, and K. A. Waal. Determinant selection in murine experimental autoimmune myasthenia gravis. 1991. E ect of the bm12 mutation on T cell recognition of acetylcholine receptor epitopes. J. Immunol. 146: 2977.
Bellone, M., N. Ostile, S. Lei, X.-D. Wu, and B. M. Conti-Tronconi. 1991. The I-Abm12 mutation which confers resistance to experimental myasthenia gravis, drastically affects the epitope repertoire of murine CD4+ cells sensitized to nicotin acetylcholine receptor. J. Immunol. 147: 1484.
Chiang, B.-L., E. Bearer, A. Ansari, K. Dorshkind, and M. E. Gershwin, 1990. The bm12 mutation and autoantibodies to dsDNA in NZB.H-2bm12 mice. J. Immunol. 145: 94.
De la Hera, M., A. de la Hera, A. Ramos, L. Buella, J. L. Alfonso, V. Rodriguez-Valverde, and J. Merino. 1992. Self-limited autoimmune disease related to transient donor B cell activation in mice neonatally injected with semi-allogeneic F1 cells. Int. Immunol. 4: 67.
Gonzalez A. L., C. Conde, C. Revilla, A. Ramos, B. Renedo, and J. Merino. 1993. Autoimmune syndrome after induction of neonatal tolerance to I-E antigens. Eur. J. Immunol. 23: 2353.
Hutchings, P., O. Kanagawa, H. Nishimoto, H. Kikutani, K.-I. Yamamura, and T. Kishimoto. 1987. Prevention of autoimmune insulitis in NOD mice. Nature 328: 432.
Merino, R., M. Iwamoto, L. Fossati, P. Muniesa, K. Araki, S. Takahashi, J. Huarte, K.-I. Yamamura, J.-D. Vassalli, and S. Izui. 1993. Prevention of systemic lupus erythematosus in autoimmune BXSB mice by a transgene encoding I-E a-chain. J. Exp. Med. 178: 1189.
Podolin, P. L., A. Pressey, N. H. DeLarato, P. A. Fischer, L. B. Peterson, and L. S. Wicker. 1993. I-E+ Nonobese diabetic mice develop insulitis and diabetes. J. Exp. Med. 178: 793.
Kelner, G. A., M. K. Jenkins, and R. Jamerson. 1993. A single amino acid substitution in cytochrome c T cell stimulatory peptide changes the MHC restriction element from one isotype (I-Ak) to another (I-Ek). Mol. Immunol. 30: 569.