Comprehensive AIDS Research Center, School of Medicine, Tsinghua University, Beijing 100084, China.
J Biol Chem. 2011 Sep 23;286(38):33511-9. doi: 10.1074/jbc.M111.270553. Epub 2011 Jul 27.
Host antibody response is a crucial defense against pathogenic infection. Here, we report a novel technique allowing quantitative measurement of polyclonal antibody response in vivo. This involves expression of a combinatorial library of target proteins from a candidate pathogen on the surface of yeast Saccharomyces cerevisiae. After mixing with serum/plasma from infected or immunized subjects, positive yeast clones were isolated via fluorescence-activated cell sorting (FACS). Using this technique, we have studied mouse immunized serum with recombinant hemagglutinin (HA) protein from a human influenza H5N1 strain (A/Anhui/1/2005) and convalescent plasma from an infected human in China. Our technique has identified novel antigenic domains targeted by serum/plasma and allowed calculation of the relative proportion of the antibody response against each domain. We believe such systematic measurement of an antibody response is unprecedented, and applying this method to different pathogens will improve understanding of protective immunity and guide development of vaccines and therapeutics.
宿主抗体反应是对抗病原感染的重要防御机制。在这里,我们报告了一种新的技术,可定量测量体内的多克隆抗体反应。该技术涉及将候选病原体的靶蛋白组合文库在酵母酿酒酵母的表面表达。与感染或免疫的受试者的血清/血浆混合后,通过荧光激活细胞分选(FACS)分离阳性酵母克隆。使用该技术,我们研究了用来自人感染流感 H5N1 株(A/Anhui/1/2005)的重组血凝素(HA)蛋白免疫的小鼠血清和来自中国感染者的恢复期血浆。我们的技术鉴定了针对血清/血浆的新抗原表位,并可计算针对每个表位的抗体反应的相对比例。我们认为这种对抗体反应的系统测量是前所未有的,并且将该方法应用于不同的病原体将有助于提高对保护性免疫的认识,并指导疫苗和疗法的开发。