首页> 美国卫生研究院文献>PLoS Clinical Trials >CD8+ T Cells Mediate Robust Stage-Specific Immunity to P. berghei under Chemoprophylaxis and This Protective Environment Is Not Downregulated by the Presence of Blood-Stage Infection
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CD8+ T Cells Mediate Robust Stage-Specific Immunity to P. berghei under Chemoprophylaxis and This Protective Environment Is Not Downregulated by the Presence of Blood-Stage Infection

机译:CD8 + T细胞在化学预防作用下介导针对伯氏疟原虫的稳健阶段特异性免疫,并且该保护性环境不会因存在血期感染而被下调

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摘要

Sterile protection against malaria infection can be achieved by the inoculation of intact sporozoites while treating concomitantly with the 4-aminoquinoline chloroquine. We present an analysis of protective immunity elicited by successive immunization with Plasmodium berghei sporozoites under chemoprophylaxis. Immunization resulted in a protective, stage-specific immune response. Protection appeared to be mediated by CD8+ T cells and was abrogated upon their specific depletion. Adoptive transfer of splenocytes rendered recipient animals resistant to sporozoite infection, but not to blood-stage challenge. Immunization with sporozoites under chemoprophylaxis results in robust immunity, and the presence of blood-stage infection at sporozoite immunization had no downregulating effect on the protective immune response.
机译:通过接种完整的子孢子,同时用4-氨基喹啉氯喹进行治疗,可以实现针对疟疾感染的无菌保护。我们提出了化学预防下连续感染伯氏疟原虫子孢子引起的保护性免疫的分析。免疫导致了保护性的,阶段特异性的免疫反应。保护似乎是由CD8 + T细胞介导的,并且由于其特定的消耗而被废除。脾细胞的过继转移使受体动物对子孢子感染具有抵抗力,但对血液阶段的挑战没有抵抗力。在化学预防下用子孢子免疫可产生强大的免疫力,在子孢子免疫时血液阶段感染的存在对保护性免疫应答没有下调作用。

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