Journal of Reproductive Immunology
Volume 83, Issue 1 , Pages 56-59, December 2009

Functional aspects of CD52 in reproduction

  • Koji Koyama

      Affiliations

    • Obstetrics and Gynecology, Hyogo College of Medicine, Nishinomiya, Japan
    • Laboratory of Developmental Biology and Reproduction, Advanced Medical Sciences, Hyogo College of Medicine, Nishinomiya, Japan
    • Corresponding Author InformationCorresponding author at: Laboratory of Developmental Biology and Reproduction, Advanced Medical Sciences, Hyogo College of Medicine, Nishinomiya, Japan.
  • ,
  • Akiko Hasegawa

      Affiliations

    • Laboratory of Developmental Biology and Reproduction, Advanced Medical Sciences, Hyogo College of Medicine, Nishinomiya, Japan
  • ,
  • Shinji Komori

      Affiliations

    • Obstetrics and Gynecology, Hyogo College of Medicine, Nishinomiya, Japan
    • Laboratory of Developmental Biology and Reproduction, Advanced Medical Sciences, Hyogo College of Medicine, Nishinomiya, Japan

Received 25 December 2008; received in revised form 21 April 2009; accepted 19 June 2009. published online 19 October 2009.

Abstract 

CD52 is a GPI-anchored protein present in lymphocytes and male reproductive tissues (mrt) including mature sperm and seminal plasma. It has been shown that mrt-CD52 is synthesized in epithelial cells of the epididymis and vas deferens, but not in the testis. The mrt-CD52 is transported to mature sperm during sperm transition in the male reproductive tract. Lymphocyte CD52 functions to stimulate suppressor T cell induction, while mrt-CD52 is associated with seminogelin and involved in clot formation and liquefaction of semen. In a landmark study, a monoclonal antibody (Mab H6-3C4) from peripheral B lymphocytes of a patient with complement-dependent sperm-immobilizing antibody in the serum has been generated. Using Mab H6-3C4, the carbohydrate moiety of CD52 as an epitope for infertility-related antigen was identified. Mab H6-3C4 also shows strong complement-dependent sperm-immobilizing activity. This suggests CD52 may have a function in protecting sperm from complement activation. Indeed, purified mrt-CD52 from human sperm interferes with the classical pathway, but not lectin-binding or alternative pathways, of the complement systems. Recently, we found CD52 in ovulated cumulus cells from the female reproductive tissues (frt). The frt-CD52 is not recognized by Mab H6-3C4, suggesting that it harbors distinct carbohydrate antigenicity. Further studies are necessary to determine the molecular features and biological functions of CD52 in male and female reproductive tissues.

Keywords: Antisperm antibody, Infertility, Sperm-immobilizing antibody, Complement, Epididymis

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PII: S0165-0378(09)00470-7

doi:10.1016/j.jri.2009.06.263

Journal of Reproductive Immunology
Volume 83, Issue 1 , Pages 56-59, December 2009