共 26 条
Overcoming original (antigenic) sin
被引:16
作者:

Anderson, DE
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Calif Davis, Sch Med Med Microbiol& Immunol, Davis, CA 95616 USA Univ Calif Davis, Sch Med Med Microbiol& Immunol, Davis, CA 95616 USA

Carlos, MP
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h-index: 0
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Univ Calif Davis, Sch Med Med Microbiol& Immunol, Davis, CA 95616 USA Univ Calif Davis, Sch Med Med Microbiol& Immunol, Davis, CA 95616 USA

Nguyen, L
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h-index: 0
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Univ Calif Davis, Sch Med Med Microbiol& Immunol, Davis, CA 95616 USA Univ Calif Davis, Sch Med Med Microbiol& Immunol, Davis, CA 95616 USA

Torres, JV
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h-index: 0
机构:
Univ Calif Davis, Sch Med Med Microbiol& Immunol, Davis, CA 95616 USA Univ Calif Davis, Sch Med Med Microbiol& Immunol, Davis, CA 95616 USA
机构:
[1] Univ Calif Davis, Sch Med Med Microbiol& Immunol, Davis, CA 95616 USA
关键词:
HIV;
AIDS;
vaccine;
peptide;
T cell;
memory;
D O I:
10.1006/clim.2001.5114
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Original antigenic sin describes a phenomenon in which the antibody response elicited in an individual after a secondary viral infection reacts more strongly to the viral variant that originally infected the individual. As T helper cells play critical roles in promoting antibody responses, a similar phenomenon may hold true for T helper cell responses. This concept is particularly relevant to the development of vaccines. against viruses such as human immunodeficiency virus and hepatitis C virus, in which myriad viral variants are present throughout the human population. We have compared the effects of priming the immune system with a single peptide epitope or with a cocktail of related peptides based on the epitope. Our data demonstrate that immunization with multiple peptide variants expands a more broadly reactive and durable T helper cell response than does immunization with a single peptide. This vaccine strategy may circumvent original antigenic sin. (C) 2001 Academic Press.
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页码:152 / 157
页数:6
相关论文
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机构: NCI, Retroviral Pathogenesis Lab, AIDS Vaccine Program, SAIC Frederick,Frederick Canc Res & Dev Ctr, Frederick, MD 21702 USA

Walsh, G
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Imming, RJ
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Fisher, B
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Flynn, BM
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Bischofberger, N
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Piatak, M
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Hirsch, VM
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Nowak, MA
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Wodarz, D
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