Knecht M
Contraception. 1980 Apr;21(4):425-32. doi: 10.1016/s0010-7824(80)80019-9.
Histological analysis of ovaries from hamsters immunized with hCGbeta-tt and implanted with human choriocarcinoma has shown that the gonadotropic activity of hCG was neutralized for 5 days of tumor growth. In control immunized hamsters, hCG secreted from the tumor induced the formation of large, cystic follicles, thecal luteinization and an increase in ovarian mass from Days 1-10 of tumor growth. In contrast, ovarian morphology in hCGbeta-tt immunized hamsters on Days 1-5 of tumor growth resembled that of non-tumor bearing hamsters. Normal follicular growth and corpora lutea formation were observed despite the secretion of hCG by the tumor. Gonadotropic stimulation, as indicated by the presence of cystic follicles, was not evident until Day 10 of tumor growth in hamsters immunized with hCGbeta-tt. hCGbeta-tt immunization did not affect ovarian structure or the normal estrus cycle in hamsters without tumors. These results indicate that the biological activity of hCG in vivo can be inhibited by active immunization with hCGbeta-tt.
对用hCGβ-tt免疫并植入人绒毛膜癌的仓鼠卵巢进行组织学分析表明,在肿瘤生长的5天内,hCG的促性腺活性被中和。在对照免疫的仓鼠中,肿瘤分泌的hCG在肿瘤生长的第1 - 10天诱导形成大的囊性卵泡、卵泡膜黄素化并使卵巢质量增加。相比之下,在肿瘤生长第1 - 5天,用hCGβ-tt免疫的仓鼠的卵巢形态与未荷瘤仓鼠相似。尽管肿瘤分泌hCG,但仍观察到正常的卵泡生长和黄体形成。在用hCGβ-tt免疫的仓鼠中,直到肿瘤生长第10天,由囊性卵泡的存在所表明的促性腺刺激才明显。hCGβ-tt免疫不影响无肿瘤仓鼠的卵巢结构或正常发情周期。这些结果表明,用hCGβ-tt主动免疫可抑制体内hCG的生物活性。