Cai Jingjing, Chen Suilin, Zhu Feng, Lu Xiao, Liu Taiping, Xu Wenyue
College of Basic Medicine, Army Medical University (Third Military Medical University), Chongqing, China.
Department of Pathogenic Biology, Army Medical University (Third Military Medical University), Chongqing, China.
Front Microbiol. 2021 Apr 30;12:670775. doi: 10.3389/fmicb.2021.670775. eCollection 2021.
Major challenges have been encountered regarding the development of highly efficient subunit malaria vaccines, and so whole-parasite vaccines have regained attention in recent years. The whole-killed blood-stage vaccine (WKV) is advantageous as it can be easily manufactured and efficiently induced protective immunity against a blood-stage challenge, as well as inducing cross-stage protection against both the liver and sexual-stages. However, it necessitates a high dose of parasitized red blood cell (pRBC) lysate for immunization, and this raises concerns regarding its safety and low immunogenicity. Knowledge of the major components of WKV that can induce or evade the host immune response, and the development of appropriate human-compatible adjuvants will greatly help to optimize the WKV. Therefore, we argue that the further development of the WKV is worthwhile to control and potentially eradicate malaria worldwide.
在高效亚单位疟疾疫苗的研发方面遇到了重大挑战,因此全寄生虫疫苗近年来重新受到关注。全灭活血液阶段疫苗(WKV)具有优势,因为它易于生产,能有效诱导针对血液阶段攻击的保护性免疫,还能诱导针对肝脏和性阶段的跨阶段保护。然而,它需要高剂量的寄生红细胞(pRBC)裂解物进行免疫,这引发了对其安全性和低免疫原性的担忧。了解能诱导或逃避宿主免疫反应的WKV主要成分,以及开发合适的与人类兼容的佐剂,将极大地有助于优化WKV。因此,我们认为进一步研发WKV对于在全球范围内控制并可能根除疟疾是值得的。