Good Michael F, Stanisic Danielle, Xu Huji, Elliott Salenna, Wykes Michelle
Queensland Institute of Medical Research, Brisbane, Australia.
Immunol Rev. 2004 Oct;201:254-67. doi: 10.1111/j.0105-2896.2004.00178.x.
Twenty-one years after malaria antigens were first cloned, a vaccine still appears to be a long way off. There have been periods of great excitement, and in model systems, subunit vaccine homologs can induce robust protection. However, significant challenges exist concerning antigenic variation and polymorphism, immunological non-responsiveness to individual vaccine antigens, parasite-induced apoptosis of immune effector and memory cells, and immune deviation as a result of maternal immunity and alterations of dendritic cell function. Novel approaches will be required. This review addresses some of the approaches that might present malaria antigens in a way designed to induce superior immune responses or that target novel conserved epitopes. Cell-mediated immunity, acting independently of antibody, may exert potent anti-parasite effects, and identification of multiple target antigens/epitopes could lead to the development of vaccines with profound efficacy.
在疟疾抗原首次被克隆21年后,疫苗似乎仍遥遥无期。曾有过令人兴奋的时期,在模型系统中,亚单位疫苗同源物可诱导强大的保护作用。然而,在抗原变异和多态性、对单个疫苗抗原的免疫无反应性、寄生虫诱导的免疫效应细胞和记忆细胞凋亡以及由于母体免疫和树突状细胞功能改变导致的免疫偏离方面,存在重大挑战。将需要新的方法。本综述探讨了一些可能以旨在诱导卓越免疫反应的方式呈现疟疾抗原或靶向新型保守表位的方法。独立于抗体发挥作用的细胞介导免疫可能发挥强大的抗寄生虫作用,识别多个靶抗原/表位可能导致开发出具有深远疗效的疫苗。