Spring Michele D, Pichyangkul Sathit, Lon Chanthap, Gosi Panita, Yongvanichit Kosol, Srichairatanakul Utaiwan, Limsalakpeth Amporn, Chaisatit Chaiyaporn, Chann Soklyda, Sriwichai Sabaithip, Auayapon Montida, Chaorattanakawee Suwanna, Dutta Sheetij, Prom Satharath, Meng Chour Char, Walsh Douglas S, Angov Evelina, Saunders David L
Armed Forces Research Institute of Medical Sciences (AFRIMS), Bangkok, Thailand.
Center of Excellence for Biomedical and Public Health Informatics (BIOPHICS), Bangkok, Thailand.
Malar J. 2016 Jan 8;15:17. doi: 10.1186/s12936-015-1058-8.
In addition to evidence for a protective role of antibodies to the malaria blood stage antigen merozoite surface protein 1 (MSP1), MSP1 antibodies are also considered as a marker of past malaria exposure in sero-epidemiological studies.
In order to better assess the potential use of MSP1 serology in malaria chemoprophylaxis trials in endemic areas, an analysis for the prevalence of antibodies to both Plasmodium falciparum and Plasmodium vivax MSP142 in healthy Cambodian adults was conducted at two sites as part of an active, observational cohort evaluating the efficacy of dihydroartemisinin-piperaquine (DP) for uncomplicated malaria (ClinicalTrials.gov identifier NCT01280162).
Rates of baseline sero-positivity were high (59 and 73% for PfMSP142 and PvMSP142, respectively), and titers higher in those who lived in a higher transmission area, although there was little correlation in titers between the two species. Those volunteers who subsequently went on to develop malaria had higher baseline MSP142 titers than those who did not for both species. Titers to both antigens remained largely stable over the course of the 4-6 month study, except in those infected with P. falciparum who had multiple recurrences.
These findings illuminate the difficulties in using MSP142 serology as either a screening criterion and/or biomarker of exposure in chemoprophylaxis studies. Further work remains to identify useful markers of malarial infection and/or immunity.
除了有证据表明针对疟疾血液期抗原裂殖子表面蛋白1(MSP1)的抗体具有保护作用外,在血清流行病学研究中,MSP1抗体也被视为过去疟疾暴露的标志物。
为了更好地评估MSP1血清学在流行地区疟疾化学预防试验中的潜在用途,在两个地点对柬埔寨健康成年人中针对恶性疟原虫和间日疟原虫MSP142的抗体流行率进行了分析,这是一项评估双氢青蒿素-哌喹(DP)治疗非复杂性疟疾疗效的主动观察队列研究的一部分(ClinicalTrials.gov标识符NCT01280162)。
基线血清阳性率很高(PfMSP142和PvMSP142分别为59%和73%),生活在高传播地区的人抗体滴度更高,尽管两种疟原虫的抗体滴度之间相关性很小。随后患疟疾的志愿者,两种疟原虫的基线MSP142滴度均高于未患疟疾的志愿者。在4至6个月的研究过程中,两种抗原的滴度基本保持稳定,除了那些感染恶性疟原虫且多次复发的人。
这些发现揭示了在化学预防研究中使用MSP142血清学作为筛查标准和/或暴露生物标志物的困难。仍需进一步开展工作以确定疟疾感染和/或免疫的有用标志物。