Effect af peptide-carrier coupling an peptide-specific immune responses

被引:13
作者
Kirkley, JE
Goldstein, AL
Naylor, PH
机构
[1] Knox Coll, Dept Biol, Galesburg, IL 61401 USA
[2] Knox Coll, Dept Chem, Galesburg, IL 61401 USA
[3] George Washington Univ, Dept Biochem & Mol Biol, Washington, DC 20037 USA
[4] Wayne State Univ, Sch Med, Dept Med Internal Med, Detroit, MI USA
关键词
D O I
10.1016/S0171-2985(01)80010-3
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Synthetic peptides are covalently linked to immunogenic carrier proteins to enhance the anti-peptide immune response. To investigate whether the method of conjugation influences the immune response, we evaluated two distinctly different choices of linker for a peptide-carrier construct. HPG-30, a synthetic peptide derived from the p17 gag protein of human immunodeficiency virus 1, was covalently linked to keyhole limper hemocyanin by either glutaraldehyde or a maleimide ester. Glutaraldehyde linkage enhanced the anti-peptide antibody and native protein response compared to maleimide. The maleimide-linked conjugate was more effective at inducing a peptide-specific cellular response. Thus, manipulation of the conjugation method can modify the magnitude and character of the immune response to a synthetic peptide vaccine.
引用
收藏
页码:601 / 615
页数:15
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