4.6 Article

Multiple Lesions Contribute to Infertility in Males Lacking Autoimmune Regulator

Journal

AMERICAN JOURNAL OF PATHOLOGY
Volume 191, Issue 9, Pages 1592-1609

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.ajpath.2021.05.021

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Funding

  1. NIH [R21 HD062879, R01 HD100832]
  2. Michigan State University, Michigan State University AgBioResearch
  3. Kansas IDeA Network for Biomedical Research Excellence [P20RR016475]
  4. University of Kansas Medical Center Biomedical Research Training Grant Program

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The deficiency in autoimmune regulator (AIRE) can lead to male infertility due to impaired central immune tolerance, resulting in reduced mating frequency, hypogonadism, and increased autoantibodies against reproductive targets. This highlights the critical role of AIRE-dependent central tolerance in maintaining male fertility and preventing autoimmunity against reproductive organs.
Male factors, including those of autoimmune origin, contribute to approximately 50% of infertility cases in humans. However, the mechanisms underlying autoimmune male infertility are poorly understood. Deficiency in autoimmune regulator (AIRE) impairs central immune tolerance because of diminished expression of self-antigens in the thymus. Humans with AIRE mutations and mice with engineered ablation of Aire develop multiorgan autoimmunity and infertility. To determine the immune targets contributing to infertility in male Aire-deficient ((-/-)) mice, Aire(-/-) or wild-type (WT) males were paired with WT females. Aire(-/-) males exhibited dramatically reduced mating frequency and fertility, hypogonadism, and reduced serum testosterone. Approximately 15% of mice exhibited lymphocytic infiltration into the testis, accompanied by atrophy, azoospermia, and reduced numbers of mitotically active germ cells; the remaining mice showed normal testicular morphology, sperm counts, and motility. However, spermatozoa from all Aire(-/-) mice were defective in their ability to fertilize WT oocytes in vitro. Lymphocytic infiltration into the epididymis, seminal vesicle, and prostate gland was evident. Aire(-/-) male mice generated autoreactive antibodies in an age-dependent manner against sperm, testis, epididymis, prostate gland, and seminal vesicle. Finally, expression of Aire was evident in the seminiferous epithelium in an age-dependent manner, as well as in the prostate gland. These findings suggest that Aire-dependent central tolerance plays a critical role in maintaining male fertility by stemming autoimmunity against multiple reproductive targets.

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