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B cell intrinsic expression of IFNλ receptor suppresses the acute humoral immune response to experimental blood-stage malaria.
Virulence ( IF 5.5 ) Pub Date : 2020-06-07 , DOI: 10.1080/21505594.2020.1768329
William O Hahn 1 , Marion Pepper 2 , W Conrad Liles 1
Affiliation  

ABSTRACT

Antibodies play a critical protective role in the host response to blood-stage malaria infection. The role of cytokines in shaping the antibody response to blood-stage malaria is unclear. Interferon lambda (IFNλ), a type III interferon, is a cytokine produced early during blood-stage malaria infection that has an unknown physiological role during malaria infection. We demonstrate that B cell-intrinsic IFNλ signals suppress the acute antibody response, acute plasmablast response, and impede acute parasite clearance during a primary blood-stage malaria infection. Our findings demonstrate a previously unappreciated role for B cell intrinsic IFNλ-signaling in the initiation of the humoral immune response in the host response to experimental malaria.



中文翻译:

IFNλ受体的B细胞内在表达抑制了对实验性血液阶段疟疾的急性体液免疫反应。

摘要

抗体在宿主对血液阶段疟疾感染的反应中起着至关重要的保护作用。目前尚不清楚细胞因子在塑造对血液疟疾的抗体应答中的作用。λ干扰素(IFNλ)是一种III型干扰素,是血液阶段疟疾感染早期产生的一种细胞因子,在疟疾感染期间具有未知的生理作用。我们证明B细胞本征IFNλ信号抑制急性抗体反应,急性浆母细胞反应,并在主要的血液阶段疟疾感染过程中阻止急性寄生虫清除。我们的发现表明,在宿主对实验性疟疾的反应中,体液免疫反应的启动中,B细胞内在干扰素λ信号的作用此前未被认识到。

更新日期:2020-06-07
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