Skip to main content
The Journal of Experimental Medicine logoLink to The Journal of Experimental Medicine
. 1981 Oct 1;154(4):1016–1032. doi: 10.1084/jem.154.4.1016

The black mink (Mustela vison). A natural model of immunologic male infertility

PMCID: PMC2186489  PMID: 6116740

Abstract

Breeding for fine black fur has generated a colony of mink wherein 20- 30% of the males are infertile. Two clinical groups are distinguishable: one being infertile from the start (primary infertility), and the other infertile after one or more years of fertility (secondary fertility). Although the etiology of primary infertility is unknown, the available data indicate that secondary infertility is associated with an autoimmune disease of the testis. Thus, male mink with secondary infertility have (a) higher prevalence and levels of anti-sperm antibody when compared with animals with primary infertility, and the antibody prevalence varies with fur color; (b) severe monocytic orchitis (47%) and/or aspermatogenesis (75%) with negative cultures for bacterial, fungal, mumps, or Coxsackie B viral organisms; (c) massive and extensive granular deposits of mink IgG and/or C3 (71%), typical of immune complexes, along the basal lamina of seminiferous tubules; (d) testes that when eluted with buffer or low pH yielded IgG that was 10-fold enriched in anti-sperm antibody activity as compared with serum IgG; and (e) no immunopathologic evidence of Aleutian mink disease. Although the sperm antigen-antibody complexes in the testis may be important as a pathogenetic mechanism of the testicular disease, there is no correlation between fluorescent anti- sperm antibody detection in the serum and the infertile state. The infertile black mink is a new model of infertility associated with naturally occurring autoimmune disease of the testis.

Full Text

The Full Text of this article is available as a PDF (2.6 MB).

Selected References

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

  1. Alexander N. J., Wilson B. J., Patterson G. D. Vasectomy: immunologic effects in rhesus monkeys and men. Fertil Steril. 1974 Feb;25(2):149–156. [PubMed] [Google Scholar]
  2. Ansbacher R. Vasectomy: sperm antibodies. Fertil Steril. 1973 Oct;24(10):788–792. doi: 10.1016/s0015-0282(16)39974-5. [DOI] [PubMed] [Google Scholar]
  3. Bell E. B., McLaren A. Reduction of fertility in female mice iso-immunized with a sub-cellular sperm fraction. J Reprod Fertil. 1970 Jul;22(2):345–356. doi: 10.1530/jrf.0.0220345. [DOI] [PubMed] [Google Scholar]
  4. Bigazzi P. E., Kosuda L. L., Hsu K. C., Andres G. A. Immune complex orchitis in vasectomized rabbits. J Exp Med. 1976 Feb 1;143(2):382–404. doi: 10.1084/jem.143.2.382. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. CLARK H. F., SHEPARD C. C. A DIALYSIS TECHNIQUE FOR PREPARING FLUORESCENT ANTIBODY. Virology. 1963 Aug;20:642–644. doi: 10.1016/0042-6822(63)90292-7. [DOI] [PubMed] [Google Scholar]
  6. Dym M., Fawcett D. W. The blood-testis barrier in the rat and the physiological compartmentation of the seminiferous epithelium. Biol Reprod. 1970 Dec;3(3):308–326. doi: 10.1093/biolreprod/3.3.308. [DOI] [PubMed] [Google Scholar]
  7. FREUND J., LIPTON M. M., THOMPSON G. E. Aspermatogenesis in the guinea pig induced by testicular tissue and adjuvants. J Exp Med. 1953 May;97(5):711–726. doi: 10.1084/jem.97.5.711. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Fritz T. E., Lombard S. A., Tyler S. A., Norris W. P. Pathology and familial incidence of orchitis and its relation to thyroiditis in a closed beagle colony. Exp Mol Pathol. 1976 Apr;24(2):142–158. doi: 10.1016/0014-4800(76)90002-2. [DOI] [PubMed] [Google Scholar]
  9. Haas G. G., Jr, Cines D. B., Schreiber A. D. Immunologic infertility: identification of patients with antisperm antibody. N Engl J Med. 1980 Sep 25;303(13):722–727. doi: 10.1056/NEJM198009253031303. [DOI] [PubMed] [Google Scholar]
  10. KATSH S. Infertility in female guinea pigs induced by injection of homologous sperm. Am J Obstet Gynecol. 1959 Aug;78(2):276–278. doi: 10.1016/0002-9378(59)90172-3. [DOI] [PubMed] [Google Scholar]
  11. Kunz H. W., Gill T. J., 3rd, Dixon B. D., Taylor F. H., Greiner D. L. Growth and reproduction complex in the rat. Genes linked to the major histocompatibility complex that affect development. J Exp Med. 1980 Dec 1;152(6):1506–1518. doi: 10.1084/jem.152.6.1506. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Linnet L., Hjort T., Fogh-Andersen P. Association between failure to impregnate after vasovasostomy and sperm agglutinins in semen. Lancet. 1981 Jan 17;1(8212):117–119. doi: 10.1016/s0140-6736(81)90708-x. [DOI] [PubMed] [Google Scholar]
  13. MINTZ B., RUSSELL E. S. Gene-induced embryological modifications of primordial germ cells in the mouse. J Exp Zool. 1957 Mar;134(2):207–237. doi: 10.1002/jez.1401340202. [DOI] [PubMed] [Google Scholar]
  14. Menge A. C. Effects of isoimmunization and isoantisera against seminal antigens on fertility process in female rabbits. Biol Reprod. 1971 Apr;4(2):137–144. doi: 10.1093/biolreprod/4.2.137. [DOI] [PubMed] [Google Scholar]
  15. Porter D. D., Larsen A. E., Porter H. G. Aleutian disease of mink. Adv Immunol. 1980;29:261–286. doi: 10.1016/s0065-2776(08)60046-2. [DOI] [PubMed] [Google Scholar]
  16. Shulman S., Mininberg D. T., Davis J. E. Significant immunologic factors in male infertility. J Urol. 1978 Feb;119(2):231–234. doi: 10.1016/s0022-5347(17)57442-x. [DOI] [PubMed] [Google Scholar]
  17. Shulman S., Zappi E., Ahmed U., Davis J. E. Immunologic consequences of vasectomy. Contraception. 1972 Apr;5(4):269–278. doi: 10.1016/0010-7824(72)90066-2. [DOI] [PubMed] [Google Scholar]
  18. Sundick R. S., Wick G. Increased 131I uptake by the thyroid glands of Obese strain (OS) chickens derived from non-Protamone-supplemented hens. Clin Exp Immunol. 1974 Sep;18(1):127–139. [PMC free article] [PubMed] [Google Scholar]
  19. Tung K. S., Alexander N. J. Immunopathologic studies on vasectomized guinea pigs. Biol Reprod. 1977 Sep;17(2):241–254. doi: 10.1095/biolreprod17.2.241. [DOI] [PubMed] [Google Scholar]
  20. Tung K. S. Allergic orchitis lesions are adoptively transferred from vasoligated guinea pigs to syngeneic recipients. Science. 1978 Sep 1;201(4358):833–835. doi: 10.1126/science.684410. [DOI] [PubMed] [Google Scholar]
  21. 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]
  22. 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]
  23. Tung K. S., Okada A., Yanagimachi R. Sperm autoantigens and fertilization. I. Effects of antisperm autoantibodies on Rouleaux formation, viability, and acrosome reaction of guinea pig spermatozoa. Biol Reprod. 1980 Nov;23(4):877–886. doi: 10.1095/biolreprod23.4.877. [DOI] [PubMed] [Google Scholar]
  24. Tung K. S., Unanue E. R., Dixon F. J. Pathogenesis of experimental allergic orchitis. II. The role of antibody. J Immunol. 1971 Jun;106(6):1463–1472. [PubMed] [Google Scholar]
  25. Tung K. S., Woodroffe A. J. Immunopathology of experimental allergic orchitis in the rabbit. J Immunol. 1978 Jan;120(1):320–328. [PubMed] [Google Scholar]
  26. Yanagimachi R., Okada A., Tung K. S. Sperm autoantigens and fertilization: II. Effects of anti-guinea pig sperm autoantibodies on sperm-ovum interactions. Biol Reprod. 1981 Apr;24(3):512–518. doi: 10.1095/biolreprod24.3.512. [DOI] [PubMed] [Google Scholar]

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

RESOURCES