Kong Leopold, Sattentau Quentin J
Sir William Dunn School of Pathology, University of Oxford, Oxford OX1 3RE, UK ; The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
J AIDS Clin Res. 2012;S8:3. doi: 10.4172/2155-6113. Epub 2012 Mar 22.
Neutralizing antibodies can protect from infection by immunodeficiency viruses. However, the induction by active vaccination of antibodies that can potently neutralize a broad range of circulating virus strains is a goal not yet achieved, despite more than 2 decades of research. Here we review progress made in the field, from early empirical studies to today's rational structure-based vaccine antigen design. We discuss the existence of broadly neutralizing antibodies, their implications for epitope discovery and recent progress made in antigen design. Finally, we consider the relationship between antigenicity and immunogenicity for B cell recognition and antibody production, a major hurdle for rational vaccine design to overcome.
中和抗体可以保护机体免受免疫缺陷病毒的感染。然而,尽管经过了20多年的研究,但通过主动免疫接种诱导出能够有效中和多种循环病毒株的抗体这一目标尚未实现。在此,我们回顾该领域所取得的进展,从早期的经验性研究到如今基于结构的合理疫苗抗原设计。我们讨论了广泛中和抗体的存在、它们在表位发现中的意义以及抗原设计方面取得的最新进展。最后,我们考虑了抗原性与免疫原性之间对于B细胞识别和抗体产生的关系,这是合理疫苗设计需要克服的一个主要障碍。