Hashem Anwar M
Department of Medical Microbiology and Parasitology, Faculty of Medicine, King Abdulaziz University, P.O. Box 80205, Jeddah 21589, Saudi Arabia ; Special Infectious Agents Unit, King Fahd Medical Research Center, King Abdulaziz University, P.O. Box 21589, Jeddah 21589, Saudi Arabia.
Biomed Res Int. 2015;2015:414637. doi: 10.1155/2015/414637. Epub 2015 Feb 15.
Current influenza vaccines afford substantial protection in humans by inducing strain-specific neutralizing antibodies (Abs). Most of these Abs target highly variable immunodominant epitopes in the globular domain of the viral hemagglutinin (HA). Therefore, current vaccines may not be able to induce heterosubtypic immunity against the divergent influenza subtypes. The identification of broadly neutralizing Abs (BnAbs) against influenza HA using recent technological advancements in antibody libraries, hybridoma, and isolation of single Ab-secreting plasma cells has increased the interest in developing a universal influenza vaccine as it could provide life-long protection. While these BnAbs can serve as a source for passive immunotherapy, their identification represents an important step towards the design of such a universal vaccine. This review describes the recent advances and approaches used in the development of universal influenza vaccine based on highly conserved HA regions identified by BnAbs.
目前的流感疫苗通过诱导毒株特异性中和抗体(Abs)为人类提供了实质性的保护。这些抗体大多靶向病毒血凝素(HA)球状结构域中高度可变的免疫显性表位。因此,目前的疫苗可能无法诱导针对不同流感亚型的异源亚型免疫。利用抗体文库、杂交瘤以及单个分泌抗体的浆细胞分离等方面的最新技术进展,鉴定出针对流感HA的广泛中和抗体(BnAbs),这增加了人们对开发通用流感疫苗的兴趣,因为它可以提供终身保护。虽然这些BnAbs可作为被动免疫疗法的来源,但其鉴定是朝着设计此类通用疫苗迈出的重要一步。本综述描述了基于BnAbs鉴定出的高度保守HA区域开发通用流感疫苗的最新进展和方法。