Influenza and Antibody-Dependent Cellular Cytotoxicity

被引:58
|
作者
Von Holle, Tarra A. [1 ]
Moody, M. Anthony [1 ,2 ,3 ]
机构
[1] Duke Univ, Sch Med, Human Vaccine Inst, Durham, NC 27708 USA
[2] Duke Univ, Sch Med, Dept Immunol, Durham, NC 27708 USA
[3] Duke Univ, Sch Med, Dept Pediat, Durham, NC 27708 USA
来源
FRONTIERS IN IMMUNOLOGY | 2019年 / 10卷
关键词
ADCC-antibody dependent cellular cytotoxicity; influenza; antibodies; animal models; vaccine targets; mAb; HUMAN MONOCLONAL-ANTIBODY; VIRUS-INFECTED CELLS; A VIRUS; MEDIATED CYTOTOXICITY; UNITED-STATES; FC-RECEPTORS; LYMPHOCYTE CYTOTOXICITY; IMMUNIZATION PRACTICES; PANDEMIC INFLUENZA; ADVISORY-COMMITTEE;
D O I
10.3389/fimmu.2019.01457
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Despite the availability of yearly vaccinations, influenza continues to cause seasonal, and pandemic rises in illness and death. An error prone replication mechanism results in antigenic drift and viral escape from immune pressure, and recombination results in antigenic shift that can rapidly move through populations that lack immunity to newly emergent strains. The development of a "universal" vaccine is a high priority and many strategies have been proposed, but our current understanding of influenza immunity is incomplete making the development of better influenza vaccines challenging. Influenza immunity has traditionally been measured by neutralization of virions and hemagglutination inhibition, but in recent years there has been a growing appreciation of other responses that can contribute to protection such as antibody-dependent cellular cytotoxicity (ADCC) that can kill influenza-infected cells. ADCC has been shown to provide cross-strain protection and to assist in viral clearance, making it an attractive target for "universal" vaccine designs. Here we provide a brief overview of the current state of influenza research that leverages "the other end of the antibody."
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页数:8
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