Maladies Infectieuses et Vecteurs, Ecologie, Génétique, Evolution et Contrôle (IRD 224-CNRS 5290 UM1-UM2), Institut de Recherche pour le Développement (IRD), University of Montpellier, Montpellier, France.
Shoklo Malaria Research Unit, Mahidol Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Mae Sot, Tak, Thailand.
Am J Trop Med Hyg. 2018 Aug;99(2):350-356. doi: 10.4269/ajtmh.18-0081. Epub 2018 May 31.
Timely identification and treatment of malaria transmission "hot spots" is essential to achieve malaria elimination. Here we investigate the relevance of using an salivary biomarker to estimate malaria exposure risk along the Thailand-Myanmar border to guide malaria control. Between May 2013 and December 2014, > 9,000 blood samples collected in a cluster randomized control trial were screened with serological assays to measure the antibody responses to salivary antigen (gSG6-P1) and malaria antigens (circumsporozoite protein, merozoite surface protein 119 [MSP-1]). infections were monitored through passive and active case detection. Seroprevalence to gSG6-P1, MSP-1, and CSP were 71.8% (95% Confidence interval [CI]: 70.9, 72.7), 68.6% (95% CI: 67.7, 69.5), and 8.6% (95% CI: 8.0, 9.2), respectively. Multivariate analysis showed that individuals with the highest Ab response to gSG6-P1 had six times the odds of being positive to CSP antigens ( < 0.001) and two times the odds of infection compared with low gSG6-P1 responders ( = 0.004). Spatial scan statistics revealed the presence of clusters of gSG6-P1 that partially overlapped infections. The gSG6-P1 salivary biomarker represents a good proxy for estimating malaria risk and could serve to implement hot spot-targeted vector control interventions to achieve malaria elimination.
及时识别和治疗疟疾传播“热点”对于实现消除疟疾至关重要。在这里,我们研究了使用唾液生物标志物来评估泰国-缅甸边境地区疟疾暴露风险的相关性,以指导疟疾控制。在 2013 年 5 月至 2014 年 12 月期间,在一项集群随机对照试验中采集了超过 9000 份血样,用血清学检测方法检测了针对唾液抗原(gSG6-P1)和疟原虫抗原(环子孢子蛋白、疟原虫表面蛋白 119[MSP-1])的抗体反应。通过被动和主动病例检测监测感染情况。gSG6-P1、MSP-1 和 CSP 的血清阳性率分别为 71.8%(95%置信区间[CI]:70.9,72.7)、68.6%(95% CI:67.7,69.5)和 8.6%(95% CI:8.0,9.2)。多变量分析显示,对 gSG6-P1 具有最高 Ab 反应的个体对 CSP 抗原呈阳性的可能性是低 gSG6-P1 反应者的六倍(<0.001),感染的可能性是低 gSG6-P1 反应者的两倍(=0.004)。空间扫描统计显示 gSG6-P1 存在部分重叠的感染簇。gSG6-P1 唾液生物标志物是估计疟疾风险的良好替代指标,可以用于实施针对热点的病媒控制干预措施,以实现消除疟疾。