Abstract
The administration of soluble mouse thyroglobulin (MTg) in conjunction with bacterial lipopolysaccharide (LPS) led to the termination of natural tolerance to MTg in mice. The extent of autoimmunity correlated with responsiveness to MTg, previously shown by the injection of MTg in complete Freund's adjuvant (CFA) to be dependent upon the H-2 haplotype. In good responder B10.BR (H-2k) mice given MTg either with LPS or in CFA, high antibody levels to MTg and extensive mononuclear cell infiltration in the thyroid were observed. In contrast, congenic poor responder B10.D2 (H-2d) mice given MTg plus LPS showed low levels of antibody to MTg, compared to those receiving MTg in CFA, and insignificant cellular infiltration of the thyroid. In no instance did autoimmunity develop in either good or poor responder strain given MTg, LPS, or CFA along although LPS was antigenic in both of these congenic strains. Since the genetic difference in responsiveness to MTg is known to be T-cell based, the involvement of T cells in LPS-treated mice was suspected. This was further ascertained by the use of athymic poor responder (BALB/c) mice and thymectomized, irradiated, and bone marrow- reconstituted B10.BR mice. Antibodies to MTg were detected only in heterozygous (nu/+) mice and good responder mice reconstituted with both thymus and bone marrow cells. In addition, significant cellular infiltration in the thyroid occurred only in fully reconstituted good responder mice. Thus, the adjuvant effect of LPS on responsiveness to MTg required T cells. Since unmodified MTg and LPS abrogated selftolerance to MTg, the need for cross-reactive T cells could be excluded. These observations suggest the presence of self-reactive T cells.
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- Allison A. C., Davies A. J. Requirement of thymus-dependent lymphocytes for potentiation by adjuvants of antibody formation. Nature. 1971 Oct 1;233(5318):330–332. doi: 10.1038/233330a0. [DOI] [PubMed] [Google Scholar]
- Allison A. C. Self-tolerance and autoimmunity in the thyroid. N Engl J Med. 1976 Oct 7;295(15):821–827. doi: 10.1056/NEJM197610072951508. [DOI] [PubMed] [Google Scholar]
- Allison A. C. Unresponsiveness to self antigens. Lancet. 1971 Dec 25;2(7739):1401–1403. doi: 10.1016/s0140-6736(71)90673-8. [DOI] [PubMed] [Google Scholar]
- Armerding D., Katz D. H. Activation of T and B lymphocytes in vitro. I. Regulatory influence of bacterial lipopolysaccharide (LPS) on specific T-cell helper function. J Exp Med. 1974 Jan 1;139(1):24–43. doi: 10.1084/jem.139.1.24. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Capanna S. L., Kong Y. M. Further studies on the prevention of tolerance induction by poly A:U. Immunology. 1974 Oct;27(4):647–653. [PMC free article] [PubMed] [Google Scholar]
- Clagett J. A., Weigle W. O. Roles of T and B lymphocytes in the termination of unresponsiveness to autologous thyroglobulin in mice. J Exp Med. 1974 Mar 1;139(3):643–660. doi: 10.1084/jem.139.3.643. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Coutinho A., Möller G. Thymus-independent B-cell induction and paralysis. Adv Immunol. 1975;21:113–236. doi: 10.1016/s0065-2776(08)60220-5. [DOI] [PubMed] [Google Scholar]
- Geyer J. W., Kong Y. C. Tolerance induction to a thymus-dependent antigen in vitro: treatment of nonadherent cells with tolerogen biologically filtered in vitro. Cell Immunol. 1974 Sep;13(3):447–458. doi: 10.1016/0008-8749(74)90264-0. [DOI] [PubMed] [Google Scholar]
- JOHNSON A. G., GAINES S., LANDY M. Studies on the O antigen of Salmonella typhosa. V. Enhancement of antibody response to protein antigens by the purified lipopolysaccharide. J Exp Med. 1956 Feb 1;103(2):225–246. doi: 10.1084/jem.103.2.225. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jones J. M., Kind P. D. Enhancing effect of bacterial endotoxins on bone marrow cells in the immune response to SRBC. J Immunol. 1972 May;108(5):1453–1455. [PubMed] [Google Scholar]
- Kagnoff M. F., Billings P., Cohn M. Functional characteristics of Peyer's patch lymphoid cells. II. Lipopolysaccharide is thymus dependent. J Exp Med. 1974 Feb 1;139(2):407–413. doi: 10.1084/jem.139.2.407. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kong Y. M., Capanna S. L. Interference with tolerance induction in mice by poly A:U. Cell Immunol. 1974 Mar 30;11(1-3):488–492. doi: 10.1016/0008-8749(74)90047-1. [DOI] [PubMed] [Google Scholar]
- Lagrange P. H., Mackaness G. B. Effects of bacterial lipopolysaccharide on the induction and expression of cell-mediated immunity. II. Stimulation of the efferent arc. J Immunol. 1975 Jan;114(1 Pt 2):447–451. [PubMed] [Google Scholar]
- Lightbody J. J., Kong Y. M. Mitogen-stimulated glutaraldehyde-fixed spleen cells: ability to stimulate in the mixed lymphocyte reaction and generate effector cells in cell-mediated lympholysis. J Immunol. 1976 Oct;117(4):1336–1339. [PubMed] [Google Scholar]
- Louis J. A., Chiller J. M., Weigle W. O. The ability of bacterial lipopolysaccharide to modulate the induction of unresponsiveness to a state of immunity. Cellular parameters. J Exp Med. 1973 Dec 1;138(6):1481–1495. doi: 10.1084/jem.138.6.1481. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Möller G., Gronowicz E., Persson U., Coutinho A., Möller E., Hammarström L., Smith E. Spleen cells from animals tolerant to a thymus-dependent antigen can be activated by lipopolysaccharide to synthesize antibodies against the tolerogen. J Exp Med. 1976 Jun 1;143(6):1429–1438. doi: 10.1084/jem.143.6.1429. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Orgad S., Cohen I. R. Autoimmune encephalomyelitis: activation of thymus lymphocytes against syngeneic brain antigens in vitro. Science. 1974 Mar 15;183(4129):1083–1085. doi: 10.1126/science.183.4129.1083. [DOI] [PubMed] [Google Scholar]
- Poston R. N. A buffered chromic chloride method of attaching antigens to red cells: use in haemagglutination. J Immunol Methods. 1974 May;5(1):91–96. doi: 10.1016/0022-1759(74)90050-7. [DOI] [PubMed] [Google Scholar]
- RIBI E., MILNER K. C., PERRINE T. D. Endotoxic and antigenic fractions from the cell wall of Salmonella enteritidis; methods for separation and some biologic activities. J Immunol. 1959 Jan;82(1):75–84. [PubMed] [Google Scholar]
- Rose N. R. Differing responses of inbred rat strains in experimental autoimmune thyrioditis. Cell Immunol. 1975 Aug;18(2):360–364. doi: 10.1016/0008-8749(75)90064-7. [DOI] [PubMed] [Google Scholar]
- Rose N. R., Kite J. H., Jr, Doebbler T. K., Spier R., Skelton F. R., Witebsky E. Studies on experimental thyroiditis. Ann N Y Acad Sci. 1965 Jun 30;124(1):201–230. doi: 10.1111/j.1749-6632.1965.tb18957.x. [DOI] [PubMed] [Google Scholar]
- Rose N. R., Stylos W. A. Splitting of human thyroglobulin. I. Reduction and alkylation. Clin Exp Immunol. 1969 Jul;5(1):129–140. [PMC free article] [PubMed] [Google Scholar]
- Rose N. R., Twarog F. J., Crowle A. J. Murine thyroiditis: importance of adjuvant and mouse strain for the induction of thyroid lesions. J Immunol. 1971 Mar;106(3):698–704. [PubMed] [Google Scholar]
- Rudbach J. A. Molecular immunogenicity of bacterial lipopolysaccharide antigens: establishing a quantitative system. J Immunol. 1971 Apr;106(4):993–1001. [PubMed] [Google Scholar]
- SHAW C. M., ALVORD E. C., Jr, FAHLBERG W. J., KIES M. W. SUBSTITUTES FOR THE MYCOBACTERIA IN FREUND'S ADJUVANTS IN THE PRODUCTION OF EXPERIMENTAL "ALLERGIC" ENCEPHALOMYELITIS IN THE GUINEA PIG. J Immunol. 1964 Jan;92:28–40. [PubMed] [Google Scholar]
- Schmidtke J. R., Dixon F. J. Immune response to a hapten coupled to a nonimmunogenic carrier. Influence of lipopolysaccharide. J Exp Med. 1972 Aug 1;136(2):392–397. doi: 10.1084/jem.136.2.392. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schrader J. W. The role of T cells in IgG production; thymus-dependent antigens induce B cell memory in the absence of T cells. J Immunol. 1975 Jun;114(6):1665–1669. [PubMed] [Google Scholar]
- Skidmore B. J., Chiller J. M., Morrison D. C., Weigle W. O. Immunologic properties of bacterial lipopolysaccharide (LPS): correlation between the mitogenic, adjuvant, and immunogenic activities. J Immunol. 1975 Feb;114(2 Pt 2):770–775. [PubMed] [Google Scholar]
- Small M., Trainin N. Control of autoreactivity by a humoral factor of the thymus (THF). Cell Immunol. 1975 Nov;20(1):1–11. doi: 10.1016/0008-8749(75)90078-7. [DOI] [PubMed] [Google Scholar]
- Torrigiani G., Doniach D., Roitt I. M. Serum thyroglobulin levels in healthy subjects and in patients with thyroid disease. J Clin Endocrinol Metab. 1969 Mar;29(3):305–314. doi: 10.1210/jcem-29-3-305. [DOI] [PubMed] [Google Scholar]
- Twarog F. J., Kenney E., Rose N. R. Adjuvants for the production of autoimmune thyroiditis in the rat. Proc Soc Exp Biol Med. 1970 Jan;133(1):185–189. doi: 10.3181/00379727-133-34437. [DOI] [PubMed] [Google Scholar]
- Vladutiu A. O., Rose N. R. Autoimmune murine thyroiditis relation to histocompatibility (H-2) type. Science. 1971 Dec 10;174(4014):1137–1139. doi: 10.1126/science.174.4014.1137. [DOI] [PubMed] [Google Scholar]
- Vladutiu A. O., Rose N. R. Cellular basis of the genetic control of immune responsiveness to murine thyroglobulin in mice. Cell Immunol. 1975 May;17(1):106–113. doi: 10.1016/s0008-8749(75)80010-4. [DOI] [PubMed] [Google Scholar]
- Vladutiu A. O., Rose N. R. Murine thyroiditis. 3. Influence of syngeneic and allogeneic thyroid antigen on induction of the disease. Clin Exp Immunol. 1972 Jun;11(2):245–254. [PMC free article] [PubMed] [Google Scholar]
- WEIGLE W. O. THE INDUCTION OF AUTOIMMUNITY IN RABBITS FOLLOWING INJECTION OF HETEROLOGOUS OR ALTERED HOMOLOGOUS THYROGLOBULIN. J Exp Med. 1965 Feb 1;121:289–308. doi: 10.1084/jem.121.2.289. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Watson J., Trenkner E., Cohn M. The use of bacterial lipopolysaccharides to show that two signals are required for the induction of antibody synthesis. J Exp Med. 1973 Sep 1;138(3):699–714. doi: 10.1084/jem.138.3.699. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Weigle W. O., High G. J., Nakamura R. M. The role of mycobacteria and the effect of proteolytic degradation of thyroglobulin on the production of autoimmune thyroiditis. J Exp Med. 1969 Aug 1;130(2):243–262. doi: 10.1084/jem.130.2.243. [DOI] [PMC free article] [PubMed] [Google Scholar]