LaVerriere Emily, Johnson Zachary M, Shieh Meg, Nziza Nadege, Alter Galit, Buckee Caroline O, Crompton Peter D, Traore Boubacar, Tran Tuan M, Neafsey Daniel E
Department of Immunology and Infectious Diseases, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Infectious Disease and Microbiome Program, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Nat Commun. 2025 Jul 15;16(1):6512. doi: 10.1038/s41467-025-61462-1.
Variation in malaria infection risk, a product of disease exposure and immunity, is poorly understood. We genotypically profiled over 13,000 blood samples from a six-year longitudinal cohort in Mali to characterize malaria infection dynamics with detail. We generated Plasmodium falciparum amplicon sequencing data from 464 participants (aged 3 months - 25 years) across the six-month 2011 transmission season and profiled a subset of 120 participants across the subsequent five annual transmission seasons. We measured infection rate as the molecular force of infection (molFOI, number of genetically distinct parasites acquired over time). We found that molFOI varied extensively among individuals (0-55 in 2011) but was independent of age and consistent within individuals over multiple seasons. Reported bednet usage was nearly universal. The HbS allele was associated with lower molFOI, and functional antibody signatures for the CSP C-term and RH5 antigens were correlated with low molFOI participants, identifying candidate immune correlates of protection. The large inter-individual variability in molFOI and consistency of intra-individual infection rate over time exhibits much greater dynamic range than malaria case incidence, and is most likely due to heterogeneous exposure to infectious mosquito bites. This and other factors contributing to variable infection risk should be considered in future clinical trials and implementation of malaria interventions.
疟疾感染风险的变化,这是疾病暴露和免疫力的产物,目前了解甚少。我们对来自马里一个为期六年的纵向队列的13000多个血样进行了基因分型分析,以详细描述疟疾感染动态。我们在2011年为期六个月的传播季节中,从464名参与者(年龄在3个月至25岁之间)中生成了恶性疟原虫扩增子测序数据,并在随后的五个年度传播季节中对120名参与者的一个子集进行了分析。我们将感染率测量为感染的分子力(molFOI,随时间获得的基因上不同的寄生虫数量)。我们发现molFOI在个体之间差异很大(2011年为0至55),但与年龄无关,并且在多个季节中个体内部保持一致。报告的蚊帐使用率几乎普及。HbS等位基因与较低的molFOI相关,针对CSP C端和RH5抗原的功能性抗体特征与低molFOI参与者相关,确定了保护的候选免疫相关因素。molFOI在个体间的巨大变异性以及个体内部感染率随时间的一致性,其动态范围比疟疾病例发病率大得多,很可能是由于接触感染性蚊虫叮咬的异质性所致。在未来的临床试验和疟疾干预措施的实施中,应考虑这一因素以及其他导致感染风险变化的因素。