Recognition of prominent viral epitopes induced by immunization with human immunodeficiency virus type 1 regulatory genes

被引:88
作者
Hinkula, J
Svanholm, C
Schwartz, S
Lundholm, P
Brytting, M
Engstrom, G
Benthin, R
Glaser, H
Sutter, G
Kohleisen, B
Erfle, V
Okuda, K
Wigzell, H
Wahren, B
机构
[1] KAROLINSKA INST,CTR MICROBIOL & TUMOR BIOL,S-10521 STOCKHOLM,SWEDEN
[2] FORSCHUNGSZENTRUM NEUBERG,INST MOL VIROL,D-85764 OBERSCHLEISSHEIM,GERMANY
[3] YOKOHAMA CITY UNIV,SCH MED,KANAZAWA KU,YOKOHAMA,KANAGAWA 232,JAPAN
关键词
D O I
10.1128/JVI.71.7.5528-5539.1997
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Mice immunized with the regulatory genes nef, rev, and tat from human immunodeficiency virus type 1 developed both humoral and cellular immune responses to the gene products Nef, Rev, and Tat. This study demonstrates that it is feasible to induce immune reactions to all of these regulatory gene products. Humoral responses were seen after DNA boosts, while potent T-cell proliferative responses were noted already after a single immunization. A Th1-directed immune response was demonstrated early after immunization. A 3- to 75-fold-stronger T-cell response mas seen in animals receiving DNA epidermally compared to that in animals receiving intramuscular injections. Nef, Rev, and Tat putative B- and T-cell epitopes were clearly mapped by using peptides derived from the regulatory proteins and were similar to those which are detected in human immunodeficiency virus infection. Although immunization by the Nef, Rev, and Tat proteins raised high immunoglobulin G titers in serum, the epitope spreading appeared broader after DNA immunization, The combination of all of these regulatory genes together with two genes for structural proteins, the envelope and gag genes, demonstrated that a combined approach is feasible in that reactivities to all antigens persisted or were even augmented. No interference between plasmids was noted.
引用
收藏
页码:5528 / 5539
页数:12
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