Hubei Province Key Laboratory of Allergy and Immunology, Department of Parasitology, Wuhan University School of Basic Medical Sciences, Wuhan, 430071, Hubei Province, China.
Parasitol Res. 2020 May;119(5):1619-1628. doi: 10.1007/s00436-020-06647-x. Epub 2020 Mar 17.
Schistosomiasis is still prevalent and seriously endangering the health of people and livestock in many countries. There have been great efforts to develop vaccines against schistosomiasis for prolonged protection in epidemic areas. Molecules from lung-stage schistosomula have been regarded as potential vaccine candidates against schistosomiasis. Our previous work has shown that cathepsin L3 from Schistosoma japonicum (SjCL3) is expressed in lung-stage schistosomula, but its role is not well known. In the present study, we characterized SjCL3 and detected its effect as a possible vaccine in vivo and in vitro. From the results of quantitative PCR (qPCR) and western blot, SjCL3 was present throughout the lifecycle of the worm, and its relative expressed level was higher in the liver eggs and adult worms than other stages. Additionally, immunofluorescence assay showed that SjCL3 was mainly concentrated in the eggshell, alimentary canal, and musculature of worms. Compared with the adjuvant group, the immunization of SjCL3 in mice resulted in a 28.9% decrease in worm burden and a 29.2% reduction in egg number in the host liver. In antibody-dependent cell-mediated cytotoxicity (ADCC) insecticidal experiments in vitro, the existence of SjCL3 could in part suppress adherence between macrophages and worm. The above results indicated that the immunization of SjCL3 could induce limited immune protection against S. japonicum infection in mice, and this protease played a role in breaking the process of ADCC, which was beneficial to the survival of worms.
血吸虫病在许多国家仍然流行,严重威胁着人类和牲畜的健康。为了在疫区提供长期保护,人们一直在努力开发血吸虫病疫苗。来自肺期血吸虫童虫的分子被认为是抗血吸虫病的潜在疫苗候选物。我们之前的工作表明,日本血吸虫(SjCL3)组织蛋白酶 L3 在肺期血吸虫童虫中表达,但它的作用尚不清楚。在本研究中,我们对 SjCL3 进行了表征,并检测了其作为潜在疫苗在体内和体外的作用。从定量 PCR(qPCR)和 Western blot 的结果来看,SjCL3 存在于蠕虫的整个生命周期中,其相对表达水平在肝卵和成虫中高于其他阶段。此外,免疫荧光分析表明 SjCL3 主要集中在蠕虫的卵壳、消化道和肌肉中。与佐剂组相比,SjCL3 免疫接种可使小鼠体内的蠕虫负荷减少 28.9%,宿主肝脏中的卵数减少 29.2%。在体外抗体依赖性细胞介导的细胞毒性(ADCC)杀虫实验中,SjCL3 的存在部分抑制了巨噬细胞与蠕虫之间的黏附。上述结果表明,SjCL3 免疫接种可诱导小鼠对日本血吸虫感染产生有限的免疫保护,这种蛋白酶在打破 ADCC 过程中发挥作用,有利于蠕虫的存活。