Skountzou Ioanna, Satyabhama Lakshmipriyadarshini, Stavropoulou Anastasia, Ashraf Zuhha, Esser E Stein, Vassilieva Elena, Koutsonanos Dimitrios, Compans Richard, Jacob Joshy
Department of Microbiology and Immunology, Emory University Medical School and Emory Vaccine Center, Atlanta, Georgia, USA.
Department of Microbiology and Immunology, Emory Vaccine Center, Yerkes National Primate Center, Emory University, Atlanta, Georgia, USA.
Clin Vaccine Immunol. 2014 Nov;21(11):1481-9. doi: 10.1128/CVI.00374-14. Epub 2014 Aug 27.
Detection of immunoglobulin M (IgM) antibodies has long been used as an important diagnostic tool for identifying active viral infections, but their relevance in later stages has not been clearly defined in vivo. In this study, we followed the kinetics, longevity, and function of influenza virus-specific IgM antibodies for 2 years following sublethal infection of mice with live mouse-adapted A/PR/8/34 virus or immunization with formalin-inactivated virus. These groups mounted robust protective immune responses and survived lethal challenges with 50 × 50% lethal dose (LD50) mouse-adapted A/PR/8/34 virus 600 days after the primary exposure. Surprisingly, the virus-specific IgM antibodies persisted along with IgG antibodies, and we found a significantly higher number of IgM-positive (IgM(+)) virus-specific plasma cells than IgG(+) plasma cells that persisted for at least 9 months postexposure. The IgM antibodies were functional as they neutralized influenza virus in the presence of complement just as well as IgG antibodies did.
免疫球蛋白M(IgM)抗体的检测长期以来一直被用作识别活动性病毒感染的重要诊断工具,但在体内后期阶段其相关性尚未明确界定。在本研究中,我们在小鼠经致死剂量以下的活鼠适应A/PR/8/34病毒感染或用福尔马林灭活病毒免疫后,对流感病毒特异性IgM抗体的动力学、持久性和功能进行了长达2年的跟踪研究。这些组在初次暴露600天后对50×50%致死剂量(LD50)的鼠适应A/PR/8/34病毒的致死性攻击产生了强大的保护性免疫反应并存活下来。令人惊讶的是,病毒特异性IgM抗体与IgG抗体一起持续存在,并且我们发现,在暴露后至少9个月持续存在的IgM阳性(IgM(+))病毒特异性浆细胞数量明显多于IgG(+)浆细胞。IgM抗体具有功能,因为它们在补体存在的情况下中和流感病毒的能力与IgG抗体一样强。