Skip to main content
The American Journal of Pathology logoLink to The American Journal of Pathology
. 1987 Feb;126(2):303–314.

Murine autoimmune oophoritis, epididymoorchitis, and gastritis induced by day 3 thymectomy. Autoantibodies.

K S Tung, S Smith, P Matzner, K Kasai, J Oliver, F Feuchter, R E Anderson
PMCID: PMC1899563  PMID: 3826296

Abstract

In adult mice thymectomized at age 3 days (D3TX), increased incidences and/or levels of organ-specific antibodies to oocytes and/or zona pellucida, to testicular cell-sperm-differentiation antigens (TSDA), and to gastric parietal cells were detected, and these correlated significantly with oophoritis, orchitis (not epididymovasitis), and gastritis, respectively. The autoantibodies occurred in mice with the corresponding endogenous antigens. Thus, anti-oocyte/zona antibodies were detected in female, anti-TSDA antibodies in male, and anti-parietal cell antibodies in both sexes. Anti-oocyte/zona antibodies were first detected at age 5-6 weeks and were absent by 25 weeks. Serum antizona antibodies, but not anti-oocyte antibodies, inhibited mouse fertilization in vitro. In contrast, antibodies to sperm acrosome and antibodies to sperm surface did not correlate with testicular or epididymal disease. Moreover, both male and female mice had increased levels of anti-sperm surface antibodies, indicating that the sperm antigens detected may not be organ-specific. In addition, sera from 5-10% of D3TX mice reacted with a wide spectrum of epididymal and testicular antigens with defined cellular locations but of yet unknown specificity. Although the incidence of antibodies to cytoskeletal antigens was not significantly elevated after D3TX, anti-nuclear antibodies were more frequently detected in (SWR/J X A/J) F1 (SWRAF1) and (C57 BL/6J X A/J) F1 (B6AF1) mice after D3TX.

Full text

PDF
303

Images in this article

Selected References

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

  1. Coulam C. B., Ryan R. J. Premature menopause. I. Etiology. Am J Obstet Gynecol. 1979 Mar 15;133(6):639–643. doi: 10.1016/0002-9378(79)90011-5. [DOI] [PubMed] [Google Scholar]
  2. Han L. P., Tung K. S. A quantitative assay for antibodies to surface antigens of guinea pig testicular cells and spermatozoa. Biol Reprod. 1979 Aug;21(1):99–107. doi: 10.1095/biolreprod21.1.99. [DOI] [PubMed] [Google Scholar]
  3. Kohno S., Munoz J. A., Williams T. M., Teuscher C., Bernard C. C., Tung K. S. Immunopathology of murine experimental allergic orchitis. J Immunol. 1983 Jun;130(6):2675–2682. [PubMed] [Google Scholar]
  4. Mahi C. A., Yanagimachi R. Prevention of in vitro fertilization of canine oocytes by anti-ovary antisera: a potential approach to fertility control in the bitch. J Exp Zool. 1979 Oct;210(1):129–135. doi: 10.1002/jez.1402100114. [DOI] [PubMed] [Google Scholar]
  5. Sakaguchi S., Takahashi T., Nishizuka Y. Study on cellular events in post-thymectomy autoimmune oophoritis in mice. II. Requirement of Lyt-1 cells in normal female mice for the prevention of oophoritis. J Exp Med. 1982 Dec 1;156(6):1577–1586. doi: 10.1084/jem.156.6.1577. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Sakaguchi S., Takahashi T., Nishizuka Y. Study on cellular events in postthymectomy autoimmune oophoritis in mice. I. Requirement of Lyt-1 effector cells for oocytes damage after adoptive transfer. J Exp Med. 1982 Dec 1;156(6):1565–1576. doi: 10.1084/jem.156.6.1565. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Taguchi O., Nishizuka Y. Autoimmune oophoritis in thymectomized mice: T cell requirement in adoptive cell transfer. Clin Exp Immunol. 1980 Nov;42(2):324–331. [PMC free article] [PubMed] [Google Scholar]
  8. Taguchi O., Nishizuka Y. Experimental autoimmune orchitis after neonatal thymectomy in the mouse. Clin Exp Immunol. 1981 Nov;46(2):425–434. [PMC free article] [PubMed] [Google Scholar]
  9. Taguchi O., Nishizuka Y., Sakakura T., Kojima A. Autoimmune oophoritis in thymectomized mice: detection of circulating antibodies against oocytes. Clin Exp Immunol. 1980 Jun;40(3):540–553. [PMC free article] [PubMed] [Google Scholar]
  10. Theofilopoulos A. N., Dixon F. J. Murine models of systemic lupus erythematosus. Adv Immunol. 1985;37:269–390. doi: 10.1016/s0065-2776(08)60342-9. [DOI] [PubMed] [Google Scholar]
  11. 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]
  12. Tung K. S., Goldberg E. H., Goldberg E. Immunobiological consequence of immunization of female mice with homologous spermatozoa: induction of infertility. J Reprod Immunol. 1979 Oct;1(3):145–158. doi: 10.1016/0165-0378(79)90015-9. [DOI] [PubMed] [Google Scholar]
  13. Tung K. S. Human sperm antigens and antisperm antibodies I. Studies on vasectomy patients. Clin Exp Immunol. 1975 Apr;20(1):93–104. [PMC free article] [PubMed] [Google Scholar]
  14. Tung K. S., Smith S., Teuscher C., Cook C., Anderson R. E. Murine autoimmune oophoritis, epididymoorchitis, and gastritis induced by day 3 thymectomy. Immunopathology. Am J Pathol. 1987 Feb;126(2):293–302. [PMC free article] [PubMed] [Google Scholar]

Articles from The American Journal of Pathology are provided here courtesy of American Society for Investigative Pathology

RESOURCES