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在一个出生队列中获得针对疟原虫血期抗原的抗体同种型。

Acquisition of antibody isotypes against Plasmodium falciparum blood stage antigens in a birth cohort.

机构信息

Department of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, UK.

出版信息

Parasite Immunol. 2010 Feb;32(2):125-34. doi: 10.1111/j.1365-3024.2009.01165.x.

Abstract

Information on the period during which infants lose their maternally derived antibodies to malaria and begin to acquire naturally their own immune responses against parasite antigens is crucial for understanding when malaria vaccines may be best administered. This study investigated the rates of decline and acquisition of serum antibody isotypes IgG1, IgG2, IgG3, IgG4, IgM and IgA to Plasmodium falciparum antigens apical membrane antigen (AMA1), merozoite surface proteins (MSP1-19, MSP2 and MSP3) in a birth cohort of 53 children living in an urban area in the Gambia, followed over the first 3 years of life (sampled at birth, 4, 9, 18 and 36 months). Antigen-specific maternally transferred antibody isotypes of all IgG subclasses were detected at birth and were almost totally depleted by 4 months of age. Acquisition of specific antibody isotypes to the antigens began with IgM, followed by IgG1 and IgA. Against the MSP2 antigen, IgG1 but not IgG3 responses were observed in the children, in contrast with the maternally derived antibodies to this antigen that were mostly IgG3. This confirms that IgG subclass responses to MSP2 are strongly dependent on age or previous malaria experience, polarized towards IgG1 early in life and to IgG3 in older exposed individuals.

摘要

有关婴儿失去母体来源的疟疾抗体并开始自然获得针对寄生虫抗原的自身免疫反应的时期的信息,对于了解疟疾疫苗何时最佳接种至关重要。本研究调查了生活在冈比亚城市地区的 53 名儿童出生队列中针对疟原虫抗原顶膜抗原(AMA1)、裂殖体表面蛋白(MSP1-19、MSP2 和 MSP3)的血清抗体同种型 IgG1、IgG2、IgG3、IgG4、IgM 和 IgA 的下降和获得率,在生命的头 3 年中进行了随访(在出生时、4 个月、9 个月、18 个月和 36 个月时采样)。出生时检测到所有 IgG 亚类的抗原特异性母体转移抗体同种型,到 4 个月大时几乎完全耗尽。针对抗原的特异性抗体同种型的获得始于 IgM,其次是 IgG1 和 IgA。与针对该抗原的母体来源抗体主要是 IgG3 不同,在儿童中观察到针对 MSP2 抗原的 IgG1 而不是 IgG3 反应。这证实了 MSP2 的 IgG 亚类反应强烈依赖于年龄或先前的疟疾经历,在生命早期偏向 IgG1,而在年龄较大的暴露个体中偏向 IgG3。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8be0/2814092/3da3c86a0700/pim0032-0125-f1.jpg

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