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恶性疟原虫子孢子免疫诱导的记忆B细胞和抗体反应。

Memory B-cell and antibody responses induced by Plasmodium falciparum sporozoite immunization.

作者信息

Nahrendorf Wiebke, Scholzen Anja, Bijker Else M, Teirlinck Anne C, Bastiaens Guido J H, Schats Remko, Hermsen Cornelus C, Visser Leo G, Langhorne Jean, Sauerwein Robert W

机构信息

Department of Medical Microbiology, Radboud university medical center, Nijmegen Division of Parasitology, MRC National Institute for Medical Research, London, United Kingdom.

Department of Medical Microbiology, Radboud university medical center, Nijmegen.

出版信息

J Infect Dis. 2014 Dec 15;210(12):1981-90. doi: 10.1093/infdis/jiu354. Epub 2014 Jun 25.

Abstract

BACKGROUND

Immunization of healthy volunteers during receipt of chemoprophylaxis with Plasmodium falciparum sporozoites (CPS-immunization) induces sterile protection from malaria. Antibody responses have long been known to contribute to naturally acquired immunity against malaria, but their association with sterile protection after whole sporozoite immunization is not well established. We therefore studied the induction and kinetics of malaria parasite antigen-specific antibodies and memory B-cells (MBCs) during CPS-immunization and their correlation with protection from challenge infection.

METHODS

We assessed humoral reactivity to 9 antigens representing different stages of the life cycle of P. falciparum by performing standardized MBC enzyme-linked immunospot and enzyme-linked immunosorbent assays on peripheral blood mononuclear cells and plasma samples from 38 Dutch volunteers enrolled in 2 randomized controlled clinical trials.

RESULTS

MBCs and antibodies recognizing pre-erythrocytic and cross-stage antigens were gradually acquired during CPS-immunization. The magnitude of these humoral responses did not correlate with protection but directly reflected parasite exposure in CPS-immunization and challenge.

CONCLUSIONS

Humoral responses to the malarial antigens circumsporozoite protein, liver-stage antigen-1, apical membrane antigen-1, and merozoite surface protein-1 do not to predict protection from challenge infection but can be used as sensitive marker of recent parasite exposure.

CLINICAL TRIALS REGISTRATION

NCT01236612 and NCT01218893.

摘要

背景

在健康志愿者接受恶性疟原虫子孢子化学预防(CPS免疫)期间进行免疫接种可诱导对疟疾的无菌保护。长期以来,人们已知抗体反应有助于自然获得抗疟疾免疫力,但它们与全子孢子免疫后的无菌保护之间的关联尚未明确确立。因此,我们研究了CPS免疫期间疟原虫抗原特异性抗体和记忆B细胞(MBC)的诱导和动力学,以及它们与预防攻击感染的相关性。

方法

我们通过对参与两项随机对照临床试验的38名荷兰志愿者的外周血单核细胞和血浆样本进行标准化的MBC酶联免疫斑点试验和酶联免疫吸附试验,评估了对代表恶性疟原虫生命周期不同阶段的9种抗原的体液反应性。

结果

在CPS免疫期间逐渐获得了识别前红细胞期和跨阶段抗原的MBC和抗体。这些体液反应的强度与保护无关,但直接反映了CPS免疫和攻击中的寄生虫暴露情况。

结论

对疟原虫抗原环子孢子蛋白、肝期抗原-1、顶膜抗原-1和裂殖子表面蛋白-1的体液反应不能预测预防攻击感染的效果,但可作为近期寄生虫暴露的敏感标志物。

临床试验注册

NCT01236612和NCT01218893。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1032/4241945/b22881a92cb5/jiu35401.jpg

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