Heat shock protein A4L is a potent autoantigen for testicular autoimmunity in mice

•Immunization with testicular germ cells (TGC) induces experimental autoimmune orchitis (EAO).•HSPA4L, a purified TGC protein, was found to be a strong EAO inducer.•HSPA4L could be a target and a useful biomarker of EAO. Experimental autoimmune orchitis (EAO) may be used as a model to investigate im...

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Veröffentlicht in:Journal of reproductive immunology 2021-06, Vol.145, p.103318-103318, Article 103318
Hauptverfasser: Nagahori, Kenta, Hirai, Shuichi, Hatayama, Naoyuki, Kuramasu, Miyuki, Omotehara, Takuya, Kawata, Shinichi, Li, Zhonglian, Miyaso, Hidenobu, Ogawa, Yuki, Qu, Ning, Terayama, Hayato, Hayashi, Shogo, Yi, Shuang-Qin, Naito, Munekazu, Itoh, Masahiro
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Sprache:eng
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Zusammenfassung:•Immunization with testicular germ cells (TGC) induces experimental autoimmune orchitis (EAO).•HSPA4L, a purified TGC protein, was found to be a strong EAO inducer.•HSPA4L could be a target and a useful biomarker of EAO. Experimental autoimmune orchitis (EAO) may be used as a model to investigate immunological infertility in men. Murine EAO is induced via immunization with auto-immunogenic antigens (AIAgs) from testicular germ cells (TGCs). CD4 + T cells play a crucial role in EAO induction. However, whether AIAgs induce an immune response remains unclear. We aimed to identify self-antigens that induce EAO by screening a phage display library of random TGC peptides using IgG from EAO-induced A/J mice. Twenty TGC-specific AIAgs were detected, and G protein-coupled receptor kinase 2 interacting protein-1 (GIT1) and heat shock protein A4L (HSPA4L) were identified as candidate AIAgs that induce EAO. Immunization with GIT1 or HSPA4L, emulsified in complete Freund’s adjuvant, resulted in 66 % or 100 % incidence of EAO, respectively, indicating that HSPA4L is a most potent AIAg that induces EAO in mice. These findings may expectedly help improve the diagnostic procedures and treatment of immunological infertility in men.
ISSN:0165-0378
1872-7603
DOI:10.1016/j.jri.2021.103318