Wang Zhaoyang, Liang Yan, Zeng Fen, Li Tingting, Cheng Gong
New Cornerstone Science Laboratory, Tsinghua University-Peking University Joint Center for Life Sciences, School of Basic Medical Sciences, Tsinghua University, Beijing Key Laboratory of Viral Infectious Diseases, Beijing, China.
Institute of Infectious Diseases, Shenzhen Bay Laboratory, Shenzhen, China.
PLoS Negl Trop Dis. 2025 Aug 28;19(8):e0013468. doi: 10.1371/journal.pntd.0013468. eCollection 2025 Aug.
Mosquito saliva contains numerous distinct mosquito salivary proteins (MSPs) that mediate mosquito-host interactions. Repeated mosquito exposure can trigger allergic reactions, with MSP-specific IgE playing a central role. Current enzyme-linked immunosorbent assay (ELISA) and immunoblotting methods for detecting MSP-specific IgE suffer from interference by much more abundant MSP-specific IgG, leading to low sensitivity. Here, we developed a capture ELISA to overcome these limitations. We compared the performance of this capture ELISA with the conventional indirect ELISA in detecting MSP-specific IgE titers in sera from both repeatedly exposed mice and human volunteers. The results demonstrated that, compared to the indirect ELISA, the novel capture ELISA exhibited significantly superior sensitivity and specificity. Using serum samples from 20 volunteers with confirmed exposure to Aedes aegypti bites and 20 volunteers without such exposure, we found that the capture ELISA achieved 100% diagnostic sensitivity and specificity (20/20), with both false-positive and false-negative rates at 0% (0/20). The limit of detection was determined to be 87.42 ng/mL total IgE equivalent in human serum. Furthermore, we dynamically monitored Aedes aegypti salivary protein AAEL000749-specific IgE titers in healthy individuals from areas with widespread mosquito distribution using the capture ELISA. The results showed that both the positive rate and titer of AAEL000749-specific IgE in the sera were significantly higher during months with elevated mosquito population densities, compared to months with lower densities. This indicates that, under natural exposure conditions, the levels of MSP-specific IgE in human sera are closely correlated with local mosquito densities. In summary, our novel capture ELISA demonstrates excellent diagnostic performance and can be used for the quantitative analysis of MSP-specific IgE in mammalian sera. This provides a powerful tool for the diagnosis and prognosis of mosquito allergy, as well as for monitoring mosquito exposure levels in endemic areas.
蚊子唾液中含有许多独特的蚊子唾液蛋白(MSP),这些蛋白介导蚊子与宿主的相互作用。反复接触蚊子会引发过敏反应,其中MSP特异性IgE起着核心作用。目前用于检测MSP特异性IgE的酶联免疫吸附测定(ELISA)和免疫印迹方法受到更为丰富的MSP特异性IgG的干扰,导致灵敏度较低。在此,我们开发了一种捕获ELISA以克服这些局限性。我们将这种捕获ELISA与传统间接ELISA在检测反复接触蚊子的小鼠和人类志愿者血清中MSP特异性IgE滴度方面的性能进行了比较。结果表明,与间接ELISA相比,新型捕获ELISA具有显著更高的灵敏度和特异性。使用来自20名确认接触过埃及伊蚊叮咬的志愿者和20名未接触过的志愿者的血清样本,我们发现捕获ELISA的诊断灵敏度和特异性均达到100%(20/20),假阳性率和假阴性率均为0%(0/20)。确定人血清中总IgE等效物的检测限为87.42 ng/mL。此外,我们使用捕获ELISA动态监测了来自蚊子广泛分布地区的健康个体中埃及伊蚊唾液蛋白AAEL000749特异性IgE滴度。结果显示,与蚊子种群密度较低的月份相比,在蚊子种群密度升高的月份,血清中AAEL000749特异性IgE的阳性率和滴度均显著更高。这表明,在自然接触条件下,人血清中MSP特异性IgE的水平与当地蚊子密度密切相关。总之,我们的新型捕获ELISA表现出出色的诊断性能,可用于定量分析哺乳动物血清中的MSP特异性IgE。这为蚊子过敏的诊断和预后以及监测流行地区的蚊子接触水平提供了一个强大的工具。