Dups Johanna N, Pepper Marion, Cockburn Ian A
Department of Pathogens and Immunity, John Curtin School of Medical Research, Australian National University Canberra, ACT, Australia.
Department of Immunology, School of Medicine, University of Washington Seattle, WA, USA.
Front Microbiol. 2014 Nov 18;5:625. doi: 10.3389/fmicb.2014.00625. eCollection 2014.
Antibodies are capable of blocking infection of the liver by Plasmodium sporozoites. Accordingly the induction of anti-sporozoite antibodies is a major aim of various vaccine approaches to malaria. In recent years our knowledge of the specificity and quantities of antibodies required for protection has been greatly expanded by clinical trials of various whole sporozoite and subunit vaccines. Moreover, the development of humanized mouse models and transgenic parasites have also aided our ability to assess the specificity of antibodies and their ability to block infection. Nonetheless, considerable gaps remain in our knowledge - in particular in understanding what antigens are recognized by infection blocking antibodies and in knowing how we can induce robust, long-lived antibody responses. Maintaining high levels of circulating antibodies is likely to be of primary importance, as antibodies must block infection in the short time it takes for sporozoites to reach the liver from the skin. It is clear that a better understanding of the development of protective B cell-mediated immunity will aid the development and refinement of malaria vaccines.
抗体能够阻断疟原虫子孢子对肝脏的感染。因此,诱导抗子孢子抗体是各种疟疾疫苗方法的主要目标。近年来,各种全子孢子疫苗和亚单位疫苗的临床试验极大地扩展了我们对保护所需抗体的特异性和数量的认识。此外,人源化小鼠模型和转基因寄生虫的开发也有助于我们评估抗体的特异性及其阻断感染的能力。尽管如此,我们的知识仍存在相当大的差距——特别是在了解感染阻断抗体识别哪些抗原以及如何诱导强大、持久的抗体反应方面。维持高水平的循环抗体可能至关重要,因为抗体必须在子孢子从皮肤到达肝脏的短时间内阻断感染。显然,更好地了解保护性B细胞介导的免疫的发展将有助于疟疾疫苗的开发和完善。