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特异性单克隆IgM在鼠疟疫苗接种中是一种有效的佐剂。

Specific monoclonal IgM is a potent adjuvant in murine malaria vaccination.

作者信息

Harte P G, Cooke A, Playfair J H

出版信息

Nature. 1983;302(5905):256-8. doi: 10.1038/302256a0.

Abstract

Recent experiments in the murine system have indicated that the passive acquisition by offspring of maternal anti-malarial IgG antibodies while conferring some degree of immunity against a primary infection, paradoxically prevents the generation of acquired immunity through vaccination. Therefore, in view of earlier findings concerning the competitive effects of specific IgM and IgG antibodies, we investigated whether specific monoclonal IgM antibodies could be used to potentiate the response to a blood-stage murine malaria vaccine. We now report that small amounts of purified monoclonal anti-parasite IgM can specifically potentiate both priming and memory cell generation in response to vaccination as evidenced by survival after infection, and that the magnitude of this effect is greater than that found with a more conventional nonspecific adjuvant (Bordetella pertussis). Additionally, in offspring of immune mothers, where vaccination is ineffective for up to 8 weeks due to the presence of maternal IgG, we have found that IgM when administered with the vaccine can completely overcome this inhibition by its adjuvant effect.

摘要

最近在小鼠系统中进行的实验表明,子代被动获得母体抗疟疾IgG抗体,虽然能赋予一定程度的针对初次感染的免疫力,但矛盾的是,这会阻碍通过疫苗接种产生获得性免疫。因此,鉴于早期有关特异性IgM和IgG抗体竞争效应的研究结果,我们研究了特异性单克隆IgM抗体是否可用于增强对血期小鼠疟疾疫苗的反应。我们现在报告,少量纯化的抗寄生虫单克隆IgM可特异性增强接种疫苗后的致敏和记忆细胞生成,感染后的存活情况证明了这一点,而且这种效应的强度大于使用更传统的非特异性佐剂(百日咳博德特氏菌)时的效应。此外,在免疫母鼠的子代中,由于母体IgG的存在,疫苗接种在长达8周内无效,我们发现,与疫苗一起给药时,IgM可通过其佐剂效应完全克服这种抑制作用。

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