Department of Epidemiology, Colorado School of Public Health, Denver, Colorado, USA.
Department of Immunology and Microbiology, University of Colorado, Denver, Colorado, USA.
J Infect Dis. 2021 Jul 15;224(2):303-311. doi: 10.1093/infdis/jiaa740.
We aimed to determine whether Plasmodium falciparum infection affects age of Kaposi sarcoma-associated herpesvirus (KSHV) seroconversion in Kenyan children.
Kenyan children (n = 144) enrolled at age 1 month, from 2 sites with different levels of malaria transmission (stable/high vs unstable/low) were followed to age 24 months. Plasma was tested for KSHV antibodies using enzyme-linked immunosorbent assay (ELISA; K8.1 and LANA) and a multiplex bead-based assay (K8.1, K10.5, ORF38, ORF50, and LANA) and whole blood tested for P. falciparum DNA using quantitative PCR. Cox proportional hazards models were used to assess associations between P. falciparum DNA detection, malaria annualized rate (P. falciparum detections/person-years), and enrollment site (malaria-high vs malaria-low) with time to KSHV seroconversion.
KSHV seroprevalence was 63% by age 2 years when assessed by multiplex assay. Children with P. falciparum were at increased hazards of earlier KSHV seroconversion and, among children with malaria, the hazard of becoming KSHV seropositive increased significantly with increasing malaria annualized rate. Children from the malaria-high transmission region had no significant difference in hazards of KSHV seroconversion at 12 months but were more likely to become KSHV seropositive by age 24 months.
Malaria exposure increases the risk for KSHV seroconversion early in life.
我们旨在确定疟原虫感染是否会影响肯尼亚儿童卡波西肉瘤相关疱疹病毒(KSHV)血清转化的年龄。
在肯尼亚,144 名儿童在 1 个月大时入组,来自疟疾传播水平不同的 2 个地点(稳定/高 vs 不稳定/低),随访至 24 个月大。使用酶联免疫吸附试验(ELISA;K8.1 和 LANA)和基于多重微珠的检测方法(K8.1、K10.5、ORF38、ORF50 和 LANA)检测血浆 KSHV 抗体,并使用定量 PCR 检测全血中的疟原虫 DNA。Cox 比例风险模型用于评估疟原虫 DNA 检测、疟疾年化率(疟原虫检测/人年)和入组地点(疟疾高发 vs 疟疾低发)与 KSHV 血清转化时间之间的关联。
通过多重检测方法,2 岁时 KSHV 血清阳性率为 63%。疟原虫阳性儿童的 KSHV 血清转化时间更早,具有更高的风险,且在患有疟疾的儿童中,疟疾年化率越高,成为 KSHV 血清阳性的风险显著增加。来自疟疾高传播地区的儿童在 12 个月时 KSHV 血清转化的风险无显著差异,但在 24 个月时更有可能成为 KSHV 血清阳性。
疟原虫暴露增加了儿童早期 KSHV 血清转化的风险。