Talwar G P
International Centre for Genetic Engineering and Biotechnology, Aruna Asaf Ali Marg, New Delhi, India.
Hum Reprod Update. 1997 Jul-Aug;3(4):301-10. doi: 10.1093/humupd/3.4.301.
The progress and current status of vaccines which induce antibodies against human chorionic gonadotrophin (HCG) and luteinizing hormone-releasing hormone (LHRH) are reviewed. Three vaccines devised against HCG have undergone phase I clinical trials documenting their safety, and reversibility. One of these, the heterospecies dimer (HSD)-HCG vaccine has also completed phase II efficacy trials in sexually active women of proven fertility. Immunization with the vaccine prevents pregnancy, as long as the antibody titres remain > or =50 ng/ml HCG bioneutralization capacity. There is no disturbance of menstrual regularity and women continue to ovulate normally. The antibody response is predominantly against an epitope in the core part of beta-HCG. Fertility is regained at titres <35 ng. These observations have laid the scientific foundations of a birth control vaccine. Research suggests the feasibility of making a cost-effective recombinant vaccine. The carriers tetanus toxoid (TT) and diptheria toxoid (DT) can be advantageously replaced by peptide determinants recognizing T, not B cells. In addition to optional fertility control, HCG vaccines may have tumour growth inhibition potential in lung cancers which produce HCG. The vaccine against LHRH can be used in both males and females. As it is a structurally conserved molecule, the same vaccine is applicable to both animals and humans. Antibodies against LHRH block the generation of gametes and sex steroids, with the result that the vaccine can be used for fertility control (domestic pets, prolongation of lactation amenorrhoea); as well as for sex hormone-dependent cancers. Phase I/phase II clinical trials have been conducted with the LHRH vaccine in advanced metastazing carcinoma of prostate patients with encouraging results. Bioeffective monoclonal antibodies have been developed against both LHRH and HCG. These can be 'humanized' and produced cost-effectively in bacteria and plants, thus paving the way for passive use of such antibodies for immunotherapy of cancers and fertility control.
本文综述了诱导抗人绒毛膜促性腺激素(HCG)和促黄体生成素释放激素(LHRH)抗体的疫苗的研究进展及现状。三种针对HCG设计的疫苗已完成I期临床试验,证明了其安全性和可逆性。其中一种,异种二聚体(HSD)-HCG疫苗也已在具有生育能力的性活跃女性中完成了II期疗效试验。接种该疫苗可预防妊娠,只要抗体效价保持在≥50 ng/ml HCG生物中和能力。月经周期无紊乱,女性继续正常排卵。抗体反应主要针对β-HCG核心部分的一个表位。当抗体效价<35 ng时生育能力恢复。这些观察结果为避孕疫苗奠定了科学基础。研究表明制备具有成本效益的重组疫苗是可行的。载体破伤风类毒素(TT)和白喉类毒素(DT)可有利地被识别T细胞而非B细胞的肽决定簇所取代。除了选择性生育控制外,HCG疫苗可能对产生HCG的肺癌具有抑制肿瘤生长的潜力。抗LHRH疫苗可用于男性和女性。由于它是一种结构保守的分子,同一疫苗适用于动物和人类。抗LHRH抗体可阻断配子和性类固醇的产生,因此该疫苗可用于生育控制(家养宠物、延长哺乳期闭经);也可用于性激素依赖性癌症。LHRH疫苗已在晚期转移性前列腺癌患者中进行了I期/II期临床试验,结果令人鼓舞。已开发出针对LHRH和HCG的生物有效单克隆抗体。这些抗体可以被“人源化”,并在细菌和植物中低成本生产,从而为被动使用此类抗体进行癌症免疫治疗和生育控制铺平了道路。