Department of Microbiology and Immunology, Center for Molecular Parasitology, Drexel University College of Medicine, 2900 Queen Lane, Philadelphia, PA, 19129, USA.
BMC Med. 2018 Nov 9;16(1):204. doi: 10.1186/s12916-018-1197-1.
Efforts to develop an effective malaria vaccine have encountered multiple challenges, and have had limited success to date. As the need remains urgent, novel approaches must be explored. One concept that has gained attention uses whole malaria parasites. Building on preclinical studies in animal models, Stanisic et al. describe the development of a vaccine based on chemically attenuated Plasmodium falciparum blood-stage parasites, with an evaluation of safety and immunogenicity in malaria-naïve human subjects. The vaccine was shown to be safe, well tolerated, and capable of priming antigen-specific T cells. This work, and the completion of an initial clinical trial in human subjects, represents a significant advance. While the path forward for this attenuated vaccine remains challenging, these initial findings are encouraging. Importantly, the results provide the foundation and framework for testing modified immunization protocols, and designing subsequent clinical trials to further evaluate safety, test for enhanced immunogenicity, and ultimately measure protective efficacy.Please see related article: https://bmcmedicine.biomedcentral.com/articles/10.1186/s12916-018-1173-9.
开发有效疟疾疫苗的努力遇到了多种挑战,迄今为止收效有限。由于需求仍然紧迫,必须探索新方法。一种备受关注的概念是使用完整的疟原虫。基于动物模型的临床前研究,Stanisic 等人描述了一种基于化学减毒恶性疟原虫血期寄生虫的疫苗的开发,评估了疟疾-naive 人体受试者的安全性和免疫原性。该疫苗被证明是安全的,耐受性良好,并能够刺激抗原特异性 T 细胞。这项工作以及在人体受试者中完成的初步临床试验代表了重大进展。虽然这种减毒疫苗的前进道路仍然具有挑战性,但这些初步发现令人鼓舞。重要的是,这些结果为测试改良免疫方案以及设计后续临床试验以进一步评估安全性、测试增强的免疫原性以及最终衡量保护效力提供了基础和框架。请参阅相关文章:https://bmcmedicine.biomedcentral.com/articles/10.1186/s12916-018-1173-9。