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小鼠对约氏疟原虫裂殖子表面蛋白1的19千道尔顿羧基末端片段产生持久的保护性免疫反应。

Long-lasting protective immune response to the 19-kilodalton carboxy-terminal fragment of Plasmodium yoelii merozoite surface protein 1 in mice.

作者信息

Jeamwattanalert Pimmada, Mahakunkijcharoen Yuvadee, Kittigul Leera, Mahannop Pakpimol, Pichyangkul Sathit, Hirunpetcharat Chakrit

机构信息

Department of Microbiology, Mahidol University, Bangkok, Thailand.

出版信息

Clin Vaccine Immunol. 2007 Apr;14(4):342-7. doi: 10.1128/CVI.00397-06. Epub 2007 Feb 21.

Abstract

Merozoite surface protein 1 (MSP1) is the major protein on the surface of the plasmodial merozoite, and its carboxy terminus, the 19-kDa fragment (MSP1(19)), is highly conserved and effective in induction of a protective immune response against malaria parasite infection in mice and monkeys. However, the duration of the immune response has not been elucidated. As such, we immunized BALB/c mice with a standard four-dose injection of recombinant Plasmodium yoelii MSP1(19) formulated with Montanide ISA51 and CpG oligodeoxynucleotide (ODN) and monitored the MSP1(19)-specific antibody levels for up to 12 months. The antibody titers persisted constantly over the period of time without significant waning, in contrast to the antibody levels induced by immunization with Freund's adjuvant, where the antibody levels gradually declined to significantly lower levels 12 months after immunization. Investigation of immunoglobulin G (IgG) subclass longevity revealed that only the IgG1 antibody level (Th2 type-driven response) decreased significantly by 6 months, while the IgG2a antibody level (Th1 type-driven response) did not change over the 12 months after immunization, but the boosting effect was seen in the IgG1 antibody responses but not in the IgG2a antibody responses. After challenge infection, all immunized mice survived with negligibly patent parasitemia. These findings suggest that protective immune responses to MSP1(19) following immunization using oil-based Montanide ISA51 and CpG ODN as an adjuvant are very long-lasting and encourage clinical trials for malaria vaccine development.

摘要

裂殖子表面蛋白1(MSP1)是疟原虫裂殖子表面的主要蛋白,其羧基末端,即19-kDa片段(MSP1(19))高度保守,能有效诱导小鼠和猴子产生针对疟原虫感染的保护性免疫反应。然而,免疫反应的持续时间尚未阐明。因此,我们用含有Montanide ISA51和CpG寡脱氧核苷酸(ODN)配制的重组约氏疟原虫MSP1(19)对BALB/c小鼠进行标准的四剂注射免疫,并监测MSP1(19)特异性抗体水平长达12个月。与用弗氏佐剂免疫诱导的抗体水平不同,抗体滴度在这段时间内持续稳定,没有明显下降,后者在免疫12个月后抗体水平逐渐下降到显著更低的水平。对免疫球蛋白G(IgG)亚类持久性的研究表明,只有IgG1抗体水平(由Th2型驱动的反应)在6个月时显著下降,而IgG2a抗体水平(由Th1型驱动的反应)在免疫后的12个月内没有变化,但在IgG1抗体反应中观察到增强效应,而在IgG2a抗体反应中未观察到。攻击感染后,所有免疫小鼠存活,疟原虫血症可忽略不计。这些发现表明,使用油包水型Montanide ISA51和CpG ODN作为佐剂免疫后对MSP1(19)的保护性免疫反应非常持久,并鼓励开展疟疾疫苗开发的临床试验。

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