首页> 外文期刊>The Journal of Immunology: Official Journal of the American Association of Immunologists >Inhibition of 19-kDa C-Terminal Region of Merozoite Surface Protein-1-Specific Antibody Responses in Neonatal Pups by Maternally Derived 19-kDa C-Terminal Region of Merozoite Surface Protein-1-Specific Antibodies but Not Whole Parasite-Specific Antib
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Inhibition of 19-kDa C-Terminal Region of Merozoite Surface Protein-1-Specific Antibody Responses in Neonatal Pups by Maternally Derived 19-kDa C-Terminal Region of Merozoite Surface Protein-1-Specific Antibodies but Not Whole Parasite-Specific Antib

机译:母体衍生的裂殖子表面蛋白-1特异性抗体的19-kDa C末端区域对新生幼仔中新生胎的19 kDa C末端区域的抑制作用,但不是对整个寄生虫特异性的抗体的抑制作用。

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摘要

Immunizing pregnant women with a malaria vaccine is one approach to protecting the mother and her offspring from malaria infection. However, specific maternal Abs generated in response to vaccination and transferred to the fetus may interfere with the infant's ability to respond to the same vaccine. Using a murine model of malaria, we examined the effect of maternal 19-kDa C-terminal region of merozoite surface protein-1 (MSP1_(19)) and Plasmodium yoelii Abs on the pups' ability to respond to immunization with MSP1_(19). Maternal MSPl_(19)-specific Abs but not P. yoelii-specific Abs inhibited Ab production following MSP1_(19) immunization in 2-wk-old pups. This inhibition was correlated with the amount of maternal MSP1_(19) Ab present in the pup at the time of immunization and was due to fewer specific B cells. Passively acquired Ab most likely inhibited the development of an Ab response by blocking access to critical B cell epitopes. If a neonate's ability to respond to MSP1_(19) vaccination depends on the level of maternal Abs present at the time of vaccination, it may be necessary to delay immunization until Abs specific for the vaccinating Ag have decreased.
机译:用疟疾疫苗为孕妇免疫是保护母亲及其后代免受疟疾感染的一种方法。但是,由于疫苗接种而产生并转移到胎儿的特定母体抗体可能会干扰婴儿对同一疫苗的反应能力。使用疟疾的小鼠模型,我们检查了裂殖子表面蛋白1(MSP1_(19))和约氏疟原虫Abs的母体19 kDa C末端区域对幼犬对MSP1_(19)免疫反应能力的影响。在两周大的幼仔中,MSP1_(19)免疫后,母体MSP1_(19)特异的Abs而非约氏疟原虫特异性Abs抑制了Ab的产生。这种抑制作用与免疫时幼犬中母体MSP1_(19)Ab的含量有关,这是由于特异性B细胞减少所致。被动获得的Ab最有可能通过阻止进入关键B细胞表位来抑制Ab反应的发展。如果新生儿对MSP1_(19)疫苗的反应能力取决于疫苗接种时母体Abs的水平,则可能有必要延迟免疫,直到针对Ag疫苗的Abs降低。

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