{"title":"Article of Significant Interest Selected from This Issue by the Editors","authors":"","doi":"10.1128/CVI.00065-17","DOIUrl":null,"url":null,"abstract":"Plasmodium vivax CelTOS Vaccine and Challenge There is no licensed vaccine against the most widely distributed human malaria parasite, Plasmodium vivax. The preerythrocytic stage is a highly attractive target for vaccination, but there is a need to assess novel vaccine candidates, platforms, and adjuvants to improve efficacy. Alves et al. (e00501-16) evaluated the protective efficacy of the Plasmodium vivax cell-traversal protein for ookinetes and sporozoites (PvCelTOS) using four different vaccine platforms and a transgenic parasite expressing the P. vivax CelTOS. Efficacy, albeit modest, was induced by an adenovirus-protein prime/boost regimen, and there was evidence of cross protection against the P. falciparum CelTOS.","PeriodicalId":10271,"journal":{"name":"Clinical and Vaccine Immunology","volume":"13 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2017-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical and Vaccine Immunology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1128/CVI.00065-17","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 0
Abstract
Plasmodium vivax CelTOS Vaccine and Challenge There is no licensed vaccine against the most widely distributed human malaria parasite, Plasmodium vivax. The preerythrocytic stage is a highly attractive target for vaccination, but there is a need to assess novel vaccine candidates, platforms, and adjuvants to improve efficacy. Alves et al. (e00501-16) evaluated the protective efficacy of the Plasmodium vivax cell-traversal protein for ookinetes and sporozoites (PvCelTOS) using four different vaccine platforms and a transgenic parasite expressing the P. vivax CelTOS. Efficacy, albeit modest, was induced by an adenovirus-protein prime/boost regimen, and there was evidence of cross protection against the P. falciparum CelTOS.
期刊介绍:
Cessation. First launched as Clinical and Diagnostic Laboratory Immunology (CDLI) in 1994, CVI published articles that enhanced the understanding of the immune response in health and disease and after vaccination by showcasing discoveries in clinical, laboratory, and vaccine immunology. CVI was committed to advancing all aspects of vaccine research and immunization, including discovery of new vaccine antigens and vaccine design, development and evaluation of vaccines in animal models and in humans, characterization of immune responses and mechanisms of vaccine action, controlled challenge studies to assess vaccine efficacy, study of vaccine vectors, adjuvants, and immunomodulators, immune correlates of protection, and clinical trials.