人绒毛膜促性腺激素β亚基与佐剂活性muramyl肽结合构建的潜在抗妊娠疫苗。

M P Schutze, C LeClerc, M Jolivet, E Deriaud, F Audibert, C C Chang, L Chedid
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引用次数: 3

摘要

人绒毛膜促性腺激素(hCG) β亚基结合破伤风类毒素正在研究作为人类生育控制疫苗。最初的临床试验表明,这种免疫原诱导的抗体反应水平并不总是足以防止怀孕。因此,人们正在努力评估β -亚基的新载体,并选择佐剂以生产更有效的疫苗。在本报告中,我们证明了hCG β -亚基与muramyl二肽(MDP)或其非热原衍生物murabutide的偶联物可能有潜力作为有效的抗妊娠疫苗。β - hCG - MDP共聚物与Al(OH)3共给药后,小鼠抗β - hCG反应明显优于β - hCG与Al(OH)3共给药后的破伤风类毒素反应。此外,这种免疫原诱导的抗体能够在体内中和hCG的生物活性。更有趣的是,hCG和murabutide的共聚物诱导了高水平的生物活性抗体。这种免疫原可能是开发有效的人类生育控制疫苗的一个有希望的候选者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A potential anti-pregnancy vaccine built by conjugation of the beta-subunit of human chorionic gonadotropin to adjuvant-active muramyl peptide.

The beta-subunit of human chorionic gonadotropin (hCG) conjugated to tetanus toxoid is being investigated as a vaccine for human fertility control. Initial clinical trials indicated that the level of antibody response induced by such an immunogen was not always sufficient to prevent pregnancy. Therefore, efforts are being made to evaluate new carriers for the beta-subunit and to select adjuvants to yield a more efficient vaccine. In the present report, we demonstrate that conjugates of the beta-subunit of hCG with muramyl dipeptide (MDP), or its nonpyrogenic derivative murabutide, may have potential as an effective antipregnancy vaccine. The copolymer of beta hCG and MDP administered with Al(OH)3 to mice induced a high anti-beta hCG response, better than that induced by the conjugate of beta hCG to tetanus toxoid given with Al(OH)3. Moreover, the antibodies induced by such an immunogen were competent for neutralizing the biological activity of hCG in vivo. Even more interesting, a copolymer of beta hCG and of murabutide induced high levels of biologically active antibodies. This immunogen may represent a promising candidate for the development of an efficient vaccine for human fertility control.

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