Marcus Z H, Nebel L, Stahl Y, Domingue G
Fertil Steril. 1976 Jun;27(6):713-22. doi: 10.1016/s0015-0282(16)41904-7.
In vitro delayed type hypersensitivity was demonstrated with peritoneal exudate cells from guinea pigs immunized with different preparations of human and guinea pig seminal components emulsified with complete Freund's adjuvant-H37Ra. The seminal components were intact human spermatozoa (HuSp); intact guinea pig spermatozoa (GPSp); human seminal plasma (HuSePlFr); and fractions of human spermatozoa obtained by centrifugation of the homogenate at 5,000 X g (5S30 and 5p30), at 20,000 X g (20S30 and 20p30), and at 144,000 X g (144p120). Cellular sensitivity was demonstrated in vivo by skin testing and in vitro by the macrophage inhibition technique. Peritoneal exudate cells from guinea pigs sensitized with fractions 5p30 and 20p30 elicited a delayed hypersensitivity reaction which could be detected only with intact human spermatozoa. Other human spermatozoal fractions (5S30, 20S30, and 144p120) were weak immunogens. Sensitization of guinea pigs with fractions of human spermatozoa, in addition to causing delayed hypersensitivity reactions, elicited low titers of spermatoxic antibodies. Antibodies to human spermatozoal fractions 5S30, 5p30, 20S30, and 20p30 cross-reacted with intact human spermatozoa and intact guinea pig spermatozoa. It is postulated that the existence of "spermatozoa-specific" coating antigen(s) derived from other components of the reproductive tract might be responsible for human spermatozoal antigenicity.
用不同的人及豚鼠精液成分制剂与完全弗氏佐剂 - H37Ra乳化后免疫豚鼠,其腹腔渗出细胞可证明体外迟发型超敏反应。精液成分包括完整的人精子(HuSp);完整的豚鼠精子(GPSp);人精浆(HuSePlFr);以及通过将匀浆在5000×g(5S30和5p30)、20000×g(20S30和20p30)和144000×g(144p120)离心获得的人精子部分。细胞敏感性通过体内皮肤试验和体外巨噬细胞抑制技术得以证明。用5p30和20p30部分致敏的豚鼠腹腔渗出细胞引发了迟发型超敏反应,该反应仅能与完整的人精子检测到。其他人精子部分(5S30、20S30和144p120)是弱免疫原。用人精子部分致敏豚鼠,除了引起迟发型超敏反应外,还引发了低滴度的精子毒性抗体。针对人精子部分5S30、5p30、20S30和20p30的抗体与完整的人精子和完整的豚鼠精子发生交叉反应。据推测来自生殖道其他成分的“精子特异性”包被抗原的存在可能是人精子抗原性的原因。