Skip to main content
The Journal of Experimental Medicine logoLink to The Journal of Experimental Medicine
. 1993 Aug 1;178(2):559–566. doi: 10.1084/jem.178.2.559

Acquired tolerance to experimental autoimmune encephalomyelitis by intrathymic injection of myelin basic protein or its major encephalitogenic peptide

PMCID: PMC2191104  PMID: 7688026

Abstract

Experimental autoimmune encephalomyelitis (EAE) is an inflammatory disease of the central nervous system that can be induced in a number of species by immunization with myelin basic protein (MBP) in adjuvant, and serves as an experimental model for the study of multiple sclerosis. The role of the thymus in acquired tolerance in autoimmune models has not been thoroughly investigated. In this study, we examined the effects of intrathymic injection of MBP or its major encephalitogenic peptide on the course of EAE in Lewis rats. A single intrathymic injection of MBP 48 h pre- but not postimmunization protects animals from actively induced EAE. An intact MBP-primed thymus was required up to 10 d postimmunization, as thymectomy on days 1, 2, and 7 postimmunization abrogated the protective effect, whereas thymectomy on day 10 did not. The proliferative response of primed lymphocytes was significantly reduced in animals that were intrathymically injected with MBP. Protection against clinical EAE was induced by thymic injection of the major encephalitogenic region (residues 71-90) but not a nonencephalitogenic (21-40) MBP epitope. Immunohistologic examination of the brain from rats intrathymically injected with encephalitogenic peptide showed markedly reduced cellular infiltrate and virtual absence of activation and inflammatory cytokines as compared with rats intrathymically injected with the nonencephalitogenic peptide. These results indicate that the thymus may play an active role in acquired systemic immunologic tolerance in T cell-mediated experimental autoimmune diseases. This effect may be mediated by a process of clonal inactivation of autoreactive T cell clones circulating through the thymus.

Full Text

The Full Text of this article is available as a PDF (2.8 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Agus D. B., Surh C. D., Sprent J. Reentry of T cells to the adult thymus is restricted to activated T cells. J Exp Med. 1991 May 1;173(5):1039–1046. doi: 10.1084/jem.173.5.1039. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Chou C. H., Fritz R. B., Chou F. C., Kibler R. F. The immune response of Lewis rats to peptide 68-88 of guinea pig myelin basic protein. I. T cell determinants. J Immunol. 1979 Oct;123(4):1540–1543. [PubMed] [Google Scholar]
  3. Dau P. C., Peterson R. D. Transformation of rodent lymphoid cells by an encephalitogen of human origin. Int Arch Allergy Appl Immunol. 1969;35(4):353–368. doi: 10.1159/000230188. [DOI] [PubMed] [Google Scholar]
  4. Ellison G. W., Waksman B. H. Role of the thymus in tolerance. IX. Inhibition of experimental autoallergic encephalomyelitis by intrathymic injection of encephalitogen. J Immunol. 1970 Aug;105(2):322–326. [PubMed] [Google Scholar]
  5. Eylar E. H., Brostoff S., Hashim G., Caccam J., Burnett P. Basic A1 protein of the myelin membrane. The complete amino acid sequence. J Biol Chem. 1971 Sep 25;246(18):5770–5784. [PubMed] [Google Scholar]
  6. Eylar E. H., Caccam J., Jackson J. J., Westall F. C., Robinson A. B. Experimental allergic encephalomyelitis: synthesis of disease-inducing site of the basic protein. Science. 1970 Jun 5;168(3936):1220–1223. doi: 10.1126/science.168.3936.1220. [DOI] [PubMed] [Google Scholar]
  7. Gerling I. C., Serreze D. V., Christianson S. W., Leiter E. H. Intrathymic islet cell transplantation reduces beta-cell autoimmunity and prevents diabetes in NOD/Lt mice. Diabetes. 1992 Dec;41(12):1672–1676. doi: 10.2337/diab.41.12.1672. [DOI] [PubMed] [Google Scholar]
  8. Higgins P. J., Weiner H. L. Suppression of experimental autoimmune encephalomyelitis by oral administration of myelin basic protein and its fragments. J Immunol. 1988 Jan 15;140(2):440–445. [PubMed] [Google Scholar]
  9. Inaba M., Inaba K., Hosono M., Kumamoto T., Ishida T., Muramatsu S., Masuda T., Ikehara S. Distinct mechanisms of neonatal tolerance induced by dendritic cells and thymic B cells. J Exp Med. 1991 Mar 1;173(3):549–559. doi: 10.1084/jem.173.3.549. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Jayaraman S., Luo Y., Dorf M. E. Tolerance induction in T helper (Th1) cells by thymic macrophages. J Immunol. 1992 May 1;148(9):2672–2681. [PubMed] [Google Scholar]
  11. Jones L. A., Chin L. T., Kruisbeek A. M. Acquisition of self-tolerance in T cells is achieved by different mechanisms, operating both inside and outside the thymus. Thymus. 1990 Nov-Dec;16(3-4):195–206. [PubMed] [Google Scholar]
  12. 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]
  13. Khoury S. J., Hancock W. W., Weiner H. L. Oral tolerance to myelin basic protein and natural recovery from experimental autoimmune encephalomyelitis are associated with downregulation of inflammatory cytokines and differential upregulation of transforming growth factor beta, interleukin 4, and prostaglandin E expression in the brain. J Exp Med. 1992 Nov 1;176(5):1355–1364. doi: 10.1084/jem.176.5.1355. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Khoury S. J., Lider O., al-Sabbagh A., Weiner H. L. Suppression of experimental autoimmune encephalomyelitis by oral administration of myelin basic protein. III. Synergistic effect of lipopolysaccharide. Cell Immunol. 1990 Dec;131(2):302–310. doi: 10.1016/0008-8749(90)90256-q. [DOI] [PubMed] [Google Scholar]
  15. Koevary S. B., Blomberg M. Prevention of diabetes in BB/Wor rats by intrathymic islet injection. J Clin Invest. 1992 Feb;89(2):512–516. doi: 10.1172/JCI115614. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. LAATSCH R. H., KIES M. W., GORDON S., ALVORD E. C., Jr The encephalomyelitic activity of myelin isolated by ultracentrifugation. J Exp Med. 1962 Apr 1;115:777–788. doi: 10.1084/jem.115.4.777. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Mueller D. L., Jenkins M. K., Schwartz R. H. Clonal expansion versus functional clonal inactivation: a costimulatory signalling pathway determines the outcome of T cell antigen receptor occupancy. Annu Rev Immunol. 1989;7:445–480. doi: 10.1146/annurev.iy.07.040189.002305. [DOI] [PubMed] [Google Scholar]
  18. Offner H., Hashim G., Vandenbark A. A. Response of rat encephalitogenic T lymphocyte lines to synthetic peptides of myelin basic protein. J Neurosci Res. 1987;17(4):344–348. doi: 10.1002/jnr.490170404. [DOI] [PubMed] [Google Scholar]
  19. Ohzato H., Monaco A. P. Induction of specific unresponsiveness (tolerance) to skin allografts by intrathymic donor-specific splenocyte injection in antilymphocyte serum-treated mice. Transplantation. 1992 Dec;54(6):1090–1095. doi: 10.1097/00007890-199212000-00026. [DOI] [PubMed] [Google Scholar]
  20. Posselt A. M., Barker C. F., Friedman A. L., Naji A. Prevention of autoimmune diabetes in the BB rat by intrathymic islet transplantation at birth. Science. 1992 May 29;256(5061):1321–1324. doi: 10.1126/science.1598576. [DOI] [PubMed] [Google Scholar]
  21. Remuzzi G., Rossini M., Imberti O., Perico N. Kidney graft survival in rats without immunosuppressants after intrathymic glomerular transplantation. Lancet. 1991 Mar 30;337(8744):750–752. doi: 10.1016/0140-6736(91)91368-5. [DOI] [PubMed] [Google Scholar]
  22. 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]
  23. Sprent J., Lo D., Gao E. K., Ron Y. T cell selection in the thymus. Immunol Rev. 1988 Jan;101:173–190. doi: 10.1111/j.1600-065x.1988.tb00737.x. [DOI] [PubMed] [Google Scholar]
  24. Tanaka K., Tilney N. L., Kupiec-Weglinski J. W. Maturing thymocytes in accelerated rejection of cardiac allografts in presensitized rats. Transplantation. 1992 Sep;54(3):515–519. doi: 10.1097/00007890-199209000-00024. [DOI] [PubMed] [Google Scholar]
  25. Traugott U., Scheinberg L. C., Raine C. S. On the presence of Ia-positive endothelial cells and astrocytes in multiple sclerosis lesions and its relevance to antigen presentation. J Neuroimmunol. 1985 Apr;8(1):1–14. doi: 10.1016/s0165-5728(85)80043-6. [DOI] [PubMed] [Google Scholar]
  26. Zamvil S. S., Mitchell D. J., Powell M. B., Sakai K., Rothbard J. B., Steinman L. Multiple discrete encephalitogenic epitopes of the autoantigen myelin basic protein include a determinant for I-E class II-restricted T cells. J Exp Med. 1988 Sep 1;168(3):1181–1186. doi: 10.1084/jem.168.3.1181. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from The Journal of Experimental Medicine are provided here courtesy of The Rockefeller University Press

RESOURCES