Viral Pathogenesis Section, Laboratory of Viral Diseases, National Institute of Allergy & Infectious Diseases, NIH, Bethesda, MD 20852, USA.
Virology. 2013 Mar 1;437(1):20-7. doi: 10.1016/j.virol.2012.11.016. Epub 2013 Jan 10.
Neutralization of flaviviruses requires engagement of the virion by antibodies with a stoichiometry that exceeds a required threshold. Factors that modulate the number of antibodies bound to an individual virion when it contacts target cells impact neutralization potency. However, the contribution of cellular factors to the potency of neutralizing antibodies has not been explored systematically. Here we investigate the relationship between expression level of a viral attachment factor on cells and the neutralizing potency of antibodies. Analysis of the attachment factor DC-SIGNR on cells in neutralization studies failed to identify a correlation between DC-SIGNR expression and antibody-mediated protection. Furthermore, neutralization potency was equivalent on a novel Jurkat cell line induced to express DC-SIGNR at varying levels. Finally, blocking virus-attachment factor interactions had no impact on neutralization activity. Altogether, our studies suggest that cellular attachment factor expression is not a significant contributor to the potency of neutralizing antibodies to flaviviruses.
中和黄病毒需要抗体以超过所需阈值的化学计量与病毒粒子结合。当病毒粒子接触靶细胞时,调节与单个病毒粒子结合的抗体数量的因素会影响中和效力。然而,细胞因子对中和抗体效力的贡献尚未被系统地探索。在这里,我们研究了细胞上病毒附着因子的表达水平与抗体中和效力之间的关系。在中和研究中对细胞上的附着因子 DC-SIGNR 的分析未能确定 DC-SIGNR 表达与抗体介导的保护之间的相关性。此外,在诱导表达不同水平 DC-SIGNR 的新型 Jurkat 细胞系上,中和效力相当。最后,阻断病毒附着因子相互作用对中和活性没有影响。总的来说,我们的研究表明,细胞附着因子的表达不是中和抗体对黄病毒效力的重要贡献者。