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首页> 外文期刊>Parasite Immunology >Schistosoma haematobium infection affects Plasmodium falciparum-specific IgG responses associated with protection against malaria.
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Schistosoma haematobium infection affects Plasmodium falciparum-specific IgG responses associated with protection against malaria.

机译:血吸虫血吸虫感染会影响与疟疾保护相关的恶性疟原虫特异性IgG反应。

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摘要

We have previously shown that antibody responses directed to Plasmodium falciparum merozoite surface protein (MSP)-1, MSP-2 and glutamate-rich protein (GLURP) are associated with anti-malarial protection in residents of the Niakhar area of Senegal. In the same area, urinary schistosomiasis is frequent and we therefore assessed the possible influence of Schistosoma haematobium infection on these protective anti-malarial IgG responses. After adjustment for confounders, we found that the levels of IgG1 directed to MSP1 and GLURP were significantly lower in helminth carriers. The higher circulating levels of interleukin (IL)-10 present in the plasma of co-infected individuals were associated with decreased anti-plasmodial IgG responses, particularly of those directed to MSP-2. Our data thus reveal a modulation of P. falciparum-specific immune responses in the presence of a trematode helminth infection, potentially increasing infected individuals' risk of plasmodial infection or disease.
机译:先前我们已经证明,针对恶性疟原虫裂殖子表面蛋白(MSP)-1,MSP-2和富含谷氨酸的蛋白(GLURP)的抗体反应与Niakhar居民的抗疟疾保护相关塞内加尔地区。在同一地区,尿血吸虫病很常见,因此我们评估了血吸虫血吸虫感染对这些保护性抗疟疾IgG应答的可能影响。调整混杂因素后,我们发现在蠕虫携带者中针对MSP1和GLURP的IgG1水平显着降低。共感染个体血浆中存在的较高白细胞介素(IL)-10循环水平与抗血浆IgG应答降低有关,尤其是针对MSP-2的应答。因此,我们的数据揭示了 P的调制。在存在吸虫性蠕虫感染的情况下,对恶性疟原虫的特异性免疫反应可能会增加被感染者患疟原虫感染或疾病的风险。

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