Keitany Gladys J, Kim Karen S, Krishnamurty Akshay T, Hondowicz Brian D, Hahn William O, Dambrauskas Nicholas, Sather D Noah, Vaughan Ashley M, Kappe Stefan H I, Pepper Marion
Department of Immunology, University of Washington School of Medicine, 750 Republican Street, Seattle, WA 98109, USA.
Center for Infectious Disease Research, 307 Westlake Avenue North, No. 500, Seattle, WA 98109, USA.
Cell Rep. 2016 Dec 20;17(12):3193-3205. doi: 10.1016/j.celrep.2016.11.060.
Many current malaria vaccines target the pre-erythrocytic stage of infection in the liver. However, in malaria-endemic regions, increased blood stage exposure is associated with decreased vaccine efficacy, thereby challenging current vaccine efforts. We hypothesized that pre-erythrocytic humoral immunity is directly disrupted by blood stage infection. To investigate this possibility, we used Plasmodium-antigen tetramers to analyze B cells after infection with either late liver stage arresting parasites or wild-type parasites that progress to the blood stage. Our data demonstrate that immunoglobulin G (IgG) antibodies against the pre-erythrocytic antigen, circumsporozoite protein (CSP), are generated only in response to the attenuated, but not the wild-type, infection. Further analyses revealed that blood stage malaria inhibits CSP-specific germinal center B cell differentiation and modulates chemokine expression. This results in aberrant memory formation and the loss of a rapid secondary B cell response. These data highlight how immunization with attenuated parasites may drive optimal immunity to malaria.
许多当前的疟疾疫苗针对的是肝脏中感染的红细胞前期阶段。然而,在疟疾流行地区,血液阶段暴露增加与疫苗效力降低相关,从而对当前的疫苗研发工作构成挑战。我们推测红细胞前期体液免疫会被血液阶段感染直接破坏。为了研究这种可能性,我们使用疟原虫抗原四聚体来分析感染晚期肝脏阶段停滞寄生虫或进展到血液阶段的野生型寄生虫后的B细胞。我们的数据表明,针对红细胞前期抗原环子孢子蛋白(CSP)的免疫球蛋白G(IgG)抗体仅在对减毒感染而非野生型感染的反应中产生。进一步分析表明,血液阶段疟疾会抑制CSP特异性生发中心B细胞分化并调节趋化因子表达。这导致异常记忆形成以及快速二次B细胞反应丧失。这些数据突出了减毒寄生虫免疫如何可能驱动对疟疾的最佳免疫。