Obiero Joshua M, Shekalaghe Seif, Hermsen Cornelus C, Mpina Maxmillian, Bijker Else M, Roestenberg Meta, Teelen Karina, Billingsley Peter F, Sim B Kim Lee, James Eric R, Daubenberger Claudia A, Hoffman Stephen L, Abdulla Salim, Sauerwein Robert W, Scholzen Anja
Radboud University Medical Center, Department of Medical Microbiology, Nijmegen, The Netherlands.
Ifakara Health Institute, Bagamoyo Research and Training Center, Bagamoyo, Tanzania.
Infect Immun. 2015 May;83(5):2185-96. doi: 10.1128/IAI.03069-14. Epub 2015 Mar 16.
To understand the effect of previous malaria exposure on antiparasite immune responses is important for developing successful immunization strategies. Controlled human malaria infections (CHMIs) using cryopreserved Plasmodium falciparum sporozoites provide a unique opportunity to study differences in acquisition or recall of antimalaria immune responses in individuals from different transmission settings and genetic backgrounds. In this study, we compared antiparasite humoral and cellular immune responses in two cohorts of malaria-naive Dutch volunteers and Tanzanians from an area of low malarial endemicity, who were subjected to the identical CHMI protocol by intradermal injection of P. falciparum sporozoites. Samples from both trials were analyzed in parallel in a single center to ensure direct comparability of immunological outcomes. Within the Tanzanian cohort, we distinguished one group with moderate levels of preexisting antibodies to asexual P. falciparum lysate and another that, based on P. falciparum serology, resembled the malaria-naive Dutch cohort. Positive P. falciparum serology at baseline was associated with a lower parasite density at first detection by quantitative PCR (qPCR) after CHMI than that for Tanzanian volunteers with negative serology. Post-CHMI, both Tanzanian groups showed a stronger increase in anti-P. falciparum antibody titers than Dutch volunteers, indicating similar levels of B-cell memory independent of serology. In contrast to the Dutch, Tanzanians failed to increase P. falciparum-specific in vitro recall gamma interferon (IFN-γ) production after CHMI, and innate IFN-γ responses were lower in P. falciparum lysate-seropositive individuals than in seronegative individuals. In conclusion, positive P. falciparum lysate serology can be used to identify individuals with better parasite control but weaker IFN-γ responses in circulating lymphocytes, which may help to stratify volunteers in future CHMI trials in areas where malaria is endemic.
了解既往疟疾暴露对抗寄生虫免疫反应的影响对于制定成功的免疫策略至关重要。使用冷冻保存的恶性疟原虫子孢子进行的受控人体疟疾感染(CHMI)为研究来自不同传播环境和遗传背景的个体在获得或回忆抗疟疾免疫反应方面的差异提供了独特的机会。在本研究中,我们比较了两组未感染疟疾的荷兰志愿者和来自低疟疾流行地区的坦桑尼亚人的抗寄生虫体液免疫和细胞免疫反应,他们通过皮内注射恶性疟原虫子孢子接受相同的CHMI方案。两个试验的样本在单一中心进行平行分析,以确保免疫结果的直接可比性。在坦桑尼亚队列中,我们区分出一组对恶性疟原虫无性体裂解物有中等水平预先存在抗体的人群,以及另一组基于恶性疟原虫血清学与未感染疟疾的荷兰队列相似的人群。基线时恶性疟原虫血清学阳性与CHMI后通过定量PCR(qPCR)首次检测时较低的寄生虫密度相关,低于血清学阴性的坦桑尼亚志愿者。CHMI后,两个坦桑尼亚组的抗恶性疟原虫抗体滴度升高幅度均大于荷兰志愿者,表明无论血清学如何,B细胞记忆水平相似。与荷兰人不同,坦桑尼亚人在CHMI后未能增加恶性疟原虫特异性的体外回忆γ干扰素(IFN-γ)产生,并且在恶性疟原虫裂解物血清阳性个体中先天IFN-γ反应低于血清阴性个体。总之,恶性疟原虫裂解物血清学阳性可用于识别寄生虫控制较好但循环淋巴细胞中IFN-γ反应较弱的个体,这可能有助于在疟疾流行地区未来的CHMI试验中对志愿者进行分层。