EIAV Envelope Diversity: Shaping Viral Persistence and Encumbering Vaccine Efficacy

被引:19
作者
Craigo, Jodi K. [1 ]
Montelaro, Ronald C. [1 ]
机构
[1] Univ Pittsburgh, Dept Microbiol & Mol Genet, Sch Med, Ctr Vaccine Res, Pittsburgh, PA 15261 USA
关键词
EIAV; lentivirus; envelope; vaccine efficacy; viral diversity; EQUINE INFECTIOUS-ANEMIA; HUMAN-IMMUNODEFICIENCY-VIRUS; CD4(+) T-CELLS; PRINCIPAL NEUTRALIZING DOMAIN; TRANSIENT IMMUNE SUPPRESSION; TERM INAPPARENT CARRIER; LENTIVIRUS INFECTION; IN-VIVO; REVERSE-TRANSCRIPTASE; ANTIGENIC VARIATION;
D O I
10.2174/157016210790416398
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Equine infectious anemia virus (EIAV) and its associated disease have presented a considerable challenge to veterinary medicine worldwide ever since its identification in the 19(th) century. Furthermore EIAV, along with its fellow animal lentiviruses, has been utilized as an animal model of HIV-1/AIDS research since the latters identification in the late 20(th) century. Like all lentiviruses, EIAV has been shown to have a high propensity for genomic sequence and antigenic variation, principally in its envelope (Env) proteins. However, unlike other lentiviruses, EIAV possesses a unique and dynamic disease presentation that enables consummate analyses of the interactions between a virus, host immune system, and the effects of viral evolution on vaccine efficacy. Hence, EIAV provides a novel animal lentivirus system with which to dissect the viral and immune correlates of vaccine efficacy and a system with which to examine vaccine candidates for the ability to elicit broadly protective vaccine immunity. The current review summarizes the key findings that have thus far provided a fundamental understanding of the role of the viral Env in immune control of infection, disease, and vaccine efficacy.
引用
收藏
页码:81 / 86
页数:6
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