Abstract
Spleen cells from mice injected intravenously with syngeneic male germ cells exhibited reduced immune functions as determined by natural killer cell activity, mixed lymphocyte reactivity and cytotoxic lymphocyte (CTL) function. The decrease in CTL responses to trinitrophenyl-modified self (TNP-self) was detected as early as 4 d after sperm injection and was observed to H-2 alloantigens 3 wk after injection. Radiosensitive suppressor T cells were found to suppress the CTL response to TNP-self. Suppression lasted for a period of at least 7 wk after a single inoculation of the germ cells. Some variability in immune suppression capability was observed using different preparations of germ cells which are not yet completely understood. Sperm were more effective in inducing suppression than testicular cells derived from the seminiferous tubules. Furthermore, sperm from older animals were more effective than those from younger mice. These findings are discussed with respect to possible regulatory influences of germ cells on the immune system when the blood-testes barrier is broken.
Full Text
The Full Text of this article is available as a PDF (801.4 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Alexander N. J., Anderson D. J. Vasectomy: consequences of autoimmunity to sperm antigens. Fertil Steril. 1979 Sep;32(3):253–260. doi: 10.1016/s0015-0282(16)44228-7. [DOI] [PubMed] [Google Scholar]
- Alexander N. J., Clarkson T. B. Vasectomy increases the severity of diet-induced atherosclerosis in Macaca fascicularis. Science. 1978 Aug 11;201(4355):538–541. doi: 10.1126/science.96532. [DOI] [PubMed] [Google Scholar]
- Anderson D. J., Alexander N. J. Antisperm antibody titres, immune complex deposition and immunocompetence in long-term vasectomized mice. Clin Exp Immunol. 1981 Jan;43(1):99–108. [PMC free article] [PubMed] [Google Scholar]
- 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]
- Bluestone J. A., Lopez C., Hurtenbach U. Mixed lymphocyte reactivity in spleen cells from F-9 tumor-bearing ice. I. Suppressor cell induction and characterization. Cell Immunol. 1981 Aug;62(2):334–340. doi: 10.1016/0008-8749(81)90334-8. [DOI] [PubMed] [Google Scholar]
- Caulfield M. J., Cerny J. Cell interactions in leukemia-associated immunosuppression: suppression of thymus-independent antibody responses by leukemia spleen cells (Moloney) in vitro is mediated by normal T cells. J Immunol. 1980 Jan;124(1):255–260. [PubMed] [Google Scholar]
- 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]
- Gachelin G., Fellous M., Guenet J. L., Jacob F. Developmental expression of an early embryonic antigen common to mouse spermatozoa and cleavage embryos, and to human spermatozoa: its expression during spermatogenesis. Dev Biol. 1976 Jun;50(2):310–320. doi: 10.1016/0012-1606(76)90154-8. [DOI] [PubMed] [Google Scholar]
- Globerson A., Umiel T. Ontogeny of suppressor cells. II. Suppression of graft-versus-host and mixed leukocyte culture responses by embryonic cells. Transplantation. 1978 Dec;26(6):438–442. doi: 10.1097/00007890-197812000-00016. [DOI] [PubMed] [Google Scholar]
- Gottlieb M. S., Schroff R., Schanker H. M., Weisman J. D., Fan P. T., Wolf R. A., Saxon A. Pneumocystis carinii pneumonia and mucosal candidiasis in previously healthy homosexual men: evidence of a new acquired cellular immunodeficiency. N Engl J Med. 1981 Dec 10;305(24):1425–1431. doi: 10.1056/NEJM198112103052401. [DOI] [PubMed] [Google Scholar]
- Hurtenbach U., Morgenstern F., Bennett D. Induction of tolerance in vitro by autologous murine testicular cells. J Exp Med. 1980 Apr 1;151(4):827–838. doi: 10.1084/jem.151.4.827. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Law H. Y., Bodmer W. F., Mathews J. D., Skegg D. C. The immune response to vasectomy and its relation to the HLA system. Tissue Antigens. 1979 Aug;14(2):115–139. doi: 10.1111/j.1399-0039.1979.tb00830.x. [DOI] [PubMed] [Google Scholar]
- Lerner R. A., Wilson C. B., Villano B. C., McConahey P. J., Dixon F. J. Endogenous oncornaviral gene expression in adult and fetal mice: quantitative, histologic, and physiologic studies of the major viral glycorprotein, gp70. J Exp Med. 1976 Jan 1;143(1):151–166. doi: 10.1084/jem.143.1.151. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lord E. M., Sensabaugh G. F., Stites D. P. Immunosuppressive activity of human seminal plasma. I. Inhibition of in vitro lymphocyte activation. J Immunol. 1977 May;118(5):1704–1711. [PubMed] [Google Scholar]
- Marcus Z. H., Freisheim J. H., Houk J. L., Herman J. H., Hess E. V. In vitro studies in reproductive immunology. 1. Suppression of cell-mediated immune response by human spermatozoa and fractions isolated from human seminal plasma. Clin Immunol Immunopathol. 1978 Mar;9(3):318–326. doi: 10.1016/0090-1229(78)90103-4. [DOI] [PubMed] [Google Scholar]
- Masur H., Michelis M. A., Greene J. B., Onorato I., Stouwe R. A., Holzman R. S., Wormser G., Brettman L., Lange M., Murray H. W. An outbreak of community-acquired Pneumocystis carinii pneumonia: initial manifestation of cellular immune dysfunction. N Engl J Med. 1981 Dec 10;305(24):1431–1438. doi: 10.1056/NEJM198112103052402. [DOI] [PubMed] [Google Scholar]
- Muir V. Y., Turk J. L. Immunological unresponsiveness during induction of experimental autoimmune orchitis in guinea-pigs: studies in vivo and in vitro. Immunology. 1979 Jan;36(1):95–102. [PMC free article] [PubMed] [Google Scholar]
- Murgita R. A., Andersson L. C., Sherman M. S., Bennich H., Wigzell H. Effects of human alpha-foetoprotein on human B and T lymphocyte proliferation in vitro. Clin Exp Immunol. 1978 Aug;33(2):347–356. [PMC free article] [PubMed] [Google Scholar]
- Reinherz E. L., O'Brien C., Rosenthal P., Schlossman S. F. The cellular basis for viral-induced immunodeficiency: analysis by monoclonal antibodies. J Immunol. 1980 Sep;125(3):1269–1274. [PubMed] [Google Scholar]
- Romrell L. J., Bellvé A. R., Fawcett D. W. Separation of mouse spermatogenic cells by sedimentation velocity. A morphological characterization. Dev Biol. 1976 Mar;49(1):119–131. doi: 10.1016/0012-1606(76)90262-1. [DOI] [PubMed] [Google Scholar]
- Schmitt-Verhulst A. M., Pettinelli C. B., Henkart P. A., Lunney J. K., Shearer G. M. H-2-restricted cytotoxic effectors generated in vitro by the addition of trinitrophenyl-conjugated soluble proteins. J Exp Med. 1978 Feb 1;147(2):352–368. doi: 10.1084/jem.147.2.352. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Shearer G. M., Polisson R. P. Mutual recognition of parental and F1 lymphocytes. Selective abrogation of cytotoxic potential of F1 lymphocytes by parental lymphocytes. J Exp Med. 1980 Jan 1;151(1):20–31. doi: 10.1084/jem.151.1.20. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Siegal F. P., Lopez C., Hammer G. S., Brown A. E., Kornfeld S. J., Gold J., Hassett J., Hirschman S. Z., Cunningham-Rundles C., Adelsberg B. R. Severe acquired immunodeficiency in male homosexuals, manifested by chronic perianal ulcerative herpes simplex lesions. N Engl J Med. 1981 Dec 10;305(24):1439–1444. doi: 10.1056/NEJM198112103052403. [DOI] [PubMed] [Google Scholar]
- Stites D. P., Erickson R. P. Suppressive effect of seminal plasma on lymphocyte activation. Nature. 1975 Feb 27;253(5494):727–729. doi: 10.1038/253727a0. [DOI] [PubMed] [Google Scholar]
- Wilson B. J., Porter G., Goldstein A. Reduced T cell reactivity in vasectomized rhesus monkeys: association with histocompatibility type. Fertil Steril. 1979 Apr;31(4):434–440. [PubMed] [Google Scholar]