Corradin Giampietro, Levitskaya Jelena
Biochemistry Department, University of Lausanne , Epalinges , Switzerland.
W. Harry Feinstone Department of Molecular Microbiology and Immunology, Bloomberg School of Public Health, Johns Hopkins University , Baltimore, MD , USA.
Front Immunol. 2014 Nov 5;5:527. doi: 10.3389/fimmu.2014.00527. eCollection 2014.
While the role of malaria parasite-specific memory CD8(+) T cells in the control of exo-erythrocytic stages of malaria infection is well documented and generally accepted, a debate is still ongoing regarding both the identity of the anatomic site where the activation of naive pathogen-specific T cells is taking place and contribution of different antigen-presenting cells (APCs) into this process. Whereas some studies infer a role of professional APCs present in the lymph nodes draining the site of parasite injection by the mosquito, others argue in favor of the liver as a primary organ and hepatocytes as stimulators of naïve parasite-specific T cell responses. This review aims to critically analyze the current knowledge and outline new lines of research necessary to understand the induction of protective cellular immunity against the malaria parasite.
虽然疟原虫特异性记忆CD8(+) T细胞在控制疟疾感染的红细胞外期的作用已得到充分证明并被普遍接受,但关于初始病原体特异性T细胞激活发生的解剖部位的身份以及不同抗原呈递细胞(APC)在这一过程中的作用仍在进行辩论。一些研究推断,在蚊子注射寄生虫部位引流的淋巴结中存在的专职APC发挥了作用,而另一些研究则支持肝脏作为主要器官以及肝细胞作为初始寄生虫特异性T细胞反应的刺激物。本综述旨在批判性地分析当前的知识,并概述理解针对疟原虫的保护性细胞免疫诱导所需的新研究方向。