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. 1973 Jul;32(4):283–293. doi: 10.1136/ard.32.4.283

Mechanisms of tolerance and autoimmunity.

A C Allison
PMCID: PMC1006104  PMID: 4131672

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Selected References

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

  1. Ada G. L. Antigen binding cells in tolerance and immunity. Transplant Rev. 1970;5:105–129. doi: 10.1111/j.1600-065x.1970.tb00358.x. [DOI] [PubMed] [Google Scholar]
  2. Allison A. C., Denman A. M., Barnes R. D. Cooperating and controlling functions of thymus-derived lymphocytes in relation to autoimmunity. Lancet. 1971 Jul 17;2(7716):135–140. doi: 10.1016/s0140-6736(71)92306-3. [DOI] [PubMed] [Google Scholar]
  3. Asherson G. L., Zembala M., Barnes R. M. The mechanism of immunological unresponsiveness to picryl chloride and the possible role of antibody mediated depression. Clin Exp Immunol. 1971 Jul;9(1):111–121. [PMC free article] [PubMed] [Google Scholar]
  4. Bankhurst A. D., Torrigiani G., Allison A. C. Lymphocytes binding human thyroglobulin in healthy people and its relevance to tolerance for autoantigens. Lancet. 1973 Feb 3;1(7797):226–230. doi: 10.1016/s0140-6736(73)90066-4. [DOI] [PubMed] [Google Scholar]
  5. Cannat A., Seligmann M. Induction by isoniazid and hydrallazine of antinuclear factors in mice. Clin Exp Immunol. 1968 Jan;3(1):99–105. [PMC free article] [PubMed] [Google Scholar]
  6. Chiller J. M., Habicht G. S., Weigle W. O. Kinetic differences in unresponsiveness of thymus and bone marrow cells. Science. 1971 Feb 26;171(3973):813–815. doi: 10.1126/science.171.3973.813. [DOI] [PubMed] [Google Scholar]
  7. Cole G. A., Nathanson N., Prendergast R. A. Requirement for theta-bearing cells in lymphocytic choriomeningitis virus-induced central nervous system disease. Nature. 1972 Aug 11;238(5363):335–337. doi: 10.1038/238335a0. [DOI] [PubMed] [Google Scholar]
  8. Denman A. M., Russell A. S., Denman E. J. Adoptive transfer of the diseases of New Zealand black mice to normal mouse strains. Clin Exp Immunol. 1969 Dec;5(6):567–595. [PMC free article] [PubMed] [Google Scholar]
  9. Dresser D. W., Mitchison N. A. The mechanism of immunological paralysis. Adv Immunol. 1968;8:129–181. doi: 10.1016/s0065-2776(08)60466-6. [DOI] [PubMed] [Google Scholar]
  10. Feldmann M., Nossal G. J. Tolerance, enhancement and the regulation of interactions between T cells, B cells and macrophages. Transplant Rev. 1972;13:3–34. doi: 10.1111/j.1600-065x.1972.tb00058.x. [DOI] [PubMed] [Google Scholar]
  11. Fialkow P. J., Gilchrist C., Allison A. C. Autoimmunity in chronic graft-versus-host disease. Clin Exp Immunol. 1973 Apr;13(4):479–486. [PMC free article] [PubMed] [Google Scholar]
  12. Gershon R. K., Cohen P., Hencin R., Liebhaber S. A. Suppressor T cells. J Immunol. 1972 Mar;108(3):586–590. [PubMed] [Google Scholar]
  13. Gershon R. K., Kondo K. Infectious immunological tolerance. Immunology. 1971 Dec;21(6):903–914. [PMC free article] [PubMed] [Google Scholar]
  14. Hannestad K., Kao M. S., Eisen H. N. Cell-bound myeloma proteins on the surface of myeloma cells: potential targets for the immune system. Proc Natl Acad Sci U S A. 1972 Aug;69(8):2295–2299. doi: 10.1073/pnas.69.8.2295. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Hirsch M. S., Allison A. C., Harvey J. J. Immune complexes in mice infected neonatally with Moloney leukaemogenic and murine sarcoma viruses. Nature. 1969 Aug 16;223(5207):739–740. doi: 10.1038/223739a0. [DOI] [PubMed] [Google Scholar]
  16. Iverson G. M. Ability of CBA mice to produce anti-idiotypic sera to 5563 myeloma protein. Nature. 1970 Jul 18;227(5255):273–274. doi: 10.1038/227273a0. [DOI] [PubMed] [Google Scholar]
  17. Jacobson E. B., Herzenberg L. A. Active suppression of immunoglobulin allotype synthesis. I. Chronic suppression after perinatal exposure to maternal antibody to paternal allotype in (SJL x BALB-c)F 1 mice. J Exp Med. 1972 May 1;135(5):1151–1162. doi: 10.1084/jem.135.5.1151. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Katz D. H. The allogeneic effect on immune responses: model for regulatory influences of T lymphocytes on the immune system. Transplant Rev. 1972;12:141–179. doi: 10.1111/j.1600-065x.1972.tb00055.x. [DOI] [PubMed] [Google Scholar]
  19. Lindenmann J., Klein P. A. Viral oncolysis: increased immunogenicity of host cell antigen associated with influenza virus. J Exp Med. 1967 Jul 1;126(1):93–108. doi: 10.1084/jem.126.1.93. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. McCullagh P. J. The transfer of immunological competence to rats tolerant of sheep erythrocytes with lymphocytes from normal rats. Aust J Exp Biol Med Sci. 1970 Aug;48(4):351–367. doi: 10.1038/icb.1970.38. [DOI] [PubMed] [Google Scholar]
  21. Miller J. F., Mitchell G. F. Thymus and antigen-reactive cells. Transplant Rev. 1969;1:3–42. doi: 10.1111/j.1600-065x.1969.tb00135.x. [DOI] [PubMed] [Google Scholar]
  22. Naor D., Sulitzeanu D. Binding of 125I-BSA to lymphoid cells of tolerant mice. Int Arch Allergy Appl Immunol. 1969;36(1):112–113. doi: 10.1159/000230728. [DOI] [PubMed] [Google Scholar]
  23. OUDIN J., MICHEL M. [A new allotype form of rabbit serum gamma-globulins, apparently associated with antibody function and specificity]. C R Hebd Seances Acad Sci. 1963 Jul 17;257:805–808. [PubMed] [Google Scholar]
  24. Oldstone M. B., Dixon F. J. Pathogenesis of chronic disease associated with persistent lymphocytic choriomeningitis viral infection. I. Relationship of antibody production to disease in neonatally infected mice. J Exp Med. 1969 Mar 1;129(3):483–505. doi: 10.1084/jem.129.3.483. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Penn I., Starzl T. E. Malignant tumors arising de novo in immunosuppressed organ transplant recipients. Transplantation. 1972 Oct;14(4):407–417. doi: 10.1097/00007890-197210000-00001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Ramseier H., Lindenmann J. F1 hybrid animals: reactivity against recognition structures of parental strain lymphoid cells. Pathol Microbiol (Basel) 1969;34(6):379–387. doi: 10.1159/000162189. [DOI] [PubMed] [Google Scholar]
  27. Roitt I. M., Greaves M. F., Torrigiani G., Brostoff J., Playfair J. H. The cellular basis of immunological responses. A synthesis of some current views. Lancet. 1969 Aug 16;2(7616):367–371. doi: 10.1016/s0140-6736(69)92712-3. [DOI] [PubMed] [Google Scholar]
  28. Teague P. O., Friou G. J. Antinuclear antibodies in mice. II. Transmission with spleen cells; inhibition or prevention with thymus or spleen cells. Immunology. 1969 Nov;17(5):665–675. [PMC free article] [PubMed] [Google Scholar]
  29. Tonietti G., Oldstone M. B., Dixon F. J. The effect of induced chronic viral infections on the immunologic diseases of New Zealand mice. J Exp Med. 1970 Jul 1;132(1):89–109. doi: 10.1084/jem.132.1.89. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. 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]
  31. Uhr J. W., Möller G. Regulatory effect of antibody on the immune response. Adv Immunol. 1968;8:81–127. doi: 10.1016/s0065-2776(08)60465-4. [DOI] [PubMed] [Google Scholar]
  32. Unanue E. R. Antigen-binding cells. I. Their idenification and role in the immune response. J Immunol. 1971 Oct;107(4):1168–1174. [PubMed] [Google Scholar]
  33. Volkert M., Larsen J. H. Immunological tolerance to viruses. Prog Med Virol. 1965;7:160–207. [PubMed] [Google Scholar]
  34. Weigle W. O. Recent observations and concepts in immunological unresponsiveness and autoimmunity. Clin Exp Immunol. 1971 Oct;9(4):437–447. [PMC free article] [PubMed] [Google Scholar]
  35. Wick G., Kite J. H., Jr, Witebsky E. Spontaneous thyroiditis in the obese strain of chickens. IV. The effect of thymectomy and thymo-bursectomy on the development of the disease. J Immunol. 1970 Jan;104(1):54–62. [PubMed] [Google Scholar]

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