EXPERIMENTAL VACCINE PROTECTION AGAINST FELINE IMMUNODEFICIENCY VIRUS

被引:108
作者
YAMAMOTO, JK
OKUDA, T
ACKLEY, CD
LOUIE, H
PEMBROKE, E
ZOCHLINSKI, H
MUNN, RJ
GARDNER, MB
机构
[1] UNIV ALABAMA,DEPT MED,DIV DEV & CLIN IMMUNOL,BIRMINGHAM,AL 35294
[2] UNIV ALABAMA,CTR COMPREHENS CANC,BIRMINGHAM,AL 35294
[3] UNIV ALABAMA,DEPT PEDIAT,BIRMINGHAM,AL 35294
[4] UNIV ALABAMA,DEPT MICROBIOL,BIRMINGHAM,AL 35294
[5] UNIV CALIF DAVIS,SCH MED,DEPT MED PATHOL,DAVIS,CA 95616
关键词
D O I
10.1089/aid.1991.7.911
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Infection of domestic cats with the feline immunodeficiency virus (FIV) represents an important veterinary health problem and a useful animal model for the development of vaccines against acquired immunodeficiency syndrome (AIDS). Two experimental FIV vaccines have been developed; one consisting of fixed infected cells (Vaccine 1), the other of inactivated whole virus (Vaccine 2). After 4-6 immunizations over 2-5 months, both vaccines induced a strong FIV-specific immune response including neutralizing antibody and T-cell proliferation. Vaccine 1 protected 6 of 9 and Vaccine 2 protected 5 of 6 recipient cats against any detectable infection with a low dose (10 animal ID50) of FIV given intraperitoneally 2 weeks after the final boost. One additional cat in each vaccine group had a transient infection at 5-7 weeks postchallenge following which virus could no longer be detected. Thus, a total of 13 of 15 vaccinated cats were protected against persistent infection. By contrast, 13 of 13 controls were persistently infected by this challenge. The infected cell vaccine failed to protect against a higher dose (5 x 10(4) ID50) of FIV. These results indicate that vaccine prophylaxis against natural FIV infection should be achievable and enhance optimism of the prospect of developing an effective AIDS vaccine for humans.
引用
收藏
页码:911 / 922
页数:12
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