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Postinflammation stage of autoimmune orchitis induced by immunization with syngeneic testicular germ cells alone in mice.

Abstract
We previously established an immunological infertility model, experimental autoimmune orchitis (EAO), which can be induced by two subcutaneous injections of viable syngeneic testicular germ cells on days 0 and 14 in mice without using any adjuvant. In this EAO model, CD4+ T-cell-dependent lymphocytic infiltration and immune deposits were found with spermatogenic disturbance on day 120. However, the late stage of EAO (= postactive inflammation stage on day 365) has not yet been investigated. Therefore, we investigated the histopathological characteristics of the late stage. The results revealed that the lymphocytic infiltration finally resolved; however, the seminiferous epithelium persistently showed maturation arrest and the Sertoli cell-only feature. In the seminiferous tubules showing maturation arrest, both proliferation and apoptosis of germ cells had occurred simultaneously. It was also noted that there were deposits of immunoglobulin G and the third component of complement on the thickened basement membrane of seminiferous tubules in the late stage of EAO. These results indicate that histopathology after active inflammation in EAO comprises persistent damage to the seminiferous epithelium and may resemble the histopathology of "idiopathic disturbance of spermatogenesis" in man.
AuthorsMunekazu Naito, Shuichi Hirai, Hayato Terayama, Ning Qu, Maimaiti Kuerban, Muhetaerjiang Musha, Miyuki Kitaoka, Yuki Ogawa, Masahiro Itoh
JournalMedical molecular morphology (Med Mol Morphol) Vol. 45 Issue 1 Pg. 35-44 (Dec 2012) ISSN: 1860-1499 [Electronic] Japan
PMID22431182 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Topics
  • Animals
  • Autoimmune Diseases (immunology, physiopathology)
  • CD4-Positive T-Lymphocytes (immunology)
  • Disease Models, Animal
  • Humans
  • Immunization
  • Infertility, Male (immunology, physiopathology)
  • Inflammation
  • Injections, Subcutaneous
  • Male
  • Mice
  • Orchitis (immunology, physiopathology)
  • Seminiferous Epithelium (immunology, pathology)
  • Spermatozoa (immunology, transplantation)
  • Testis (immunology, pathology)
  • Transplantation, Isogeneic

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