Full-length HIV-1 Tat protein necessary for a vaccine

被引:21
|
作者
Opi, S
Peloponese, JM
Esquieu, D
Watkins, J
Campbell, G
de Mareuil, J
Jeang, KT
Yirrell, DL
Kaleebu, P
Loret, EP
机构
[1] Fac Pharm Marseille, CNRS FRE 2737, F-13385 Marseille 5, France
[2] NIAID, Mol Microbiol Lab, NIH, Bethesda, MD 20892 USA
[3] Gartnavel Royal Hosp, Glasgow G12 0ZA, Lanark, Scotland
[4] MRC UK Programme AIDS Uganda, Uganda Virus Res Inst, Entebbe, Uganda
关键词
HIV vaccine; Tat; conformational epitopes;
D O I
10.1016/j.vaccine.2004.01.057
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
AIDS vaccines now use a truncated version of 86 residues of the Tat protein related to the HIV-1 HXB2 strain predominant in Europe and North America. We compared antibodies raised in rabbits using a B subtype short Tat HXB2(86) and a full-length Tat HXB2(100). Serum against HXB2(86) recognizes only B and D subtypes while serum against HXB2(100) recognizes B, D, and C subtype variants. Conformational epitopes appear to be involved in the capacity of anti-Tat HXB2 sera to recognized non-homologous Tat variants. A linear B-epitope identified in sequence 71-81 in HXB2(86) disappears in HXB2(100), which has a new linear B-epitope identified at the C-terminus. Anti-HXB2(100) serum has a higher titer in neutralizing antibody against homologous and non-homologous variants compared to anti-HXB2(86) serum. We suggest that a Tat vaccine should contain a Tat variant with regular size, up to 99-101 residues now found in the field. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3105 / 3111
页数:7
相关论文
共 50 条
  • [1] THE FULL-LENGTH TAT PROTEIN OF HIV-2 CAN TRANS-ACTIVATE HIV-1
    TONG, SE
    BAUR, A
    LU, X
    PECK, E
    PETERLIN, BM
    CLINICAL RESEARCH, 1992, 40 (02): : A197 - A197
  • [2] Molecular characterization of full-length Tat in HIV-1 subtypes B and C
    Roy, Chandra Nath
    Khandaker, Irona
    Furuse, Yuki
    Oshitani, Hitoshi
    BIOINFORMATION, 2015, 11 (03) : 151 - 160
  • [3] Structure and Dynamics of Full-Length HIV-1 Capsid Protein in Solution
    Deshmukh, Lalit
    Schwieters, Charles D.
    Grishaev, Alexander
    Ghirlando, Rodolfo
    Baber, James L.
    Clore, G. Marius
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2013, 135 (43) : 16133 - 16147
  • [4] The 5′ UTR of HIV-1 full-length mRNA and the Tat viral protein modulate the programmed-1 ribosomal frameshift that generates HIV-1 enzymes
    Charbonneau, Johanie
    Gendron, Karine
    Ferbeyre, Gerardo
    Brakier-Gingras, Lea
    RNA, 2012, 18 (03) : 519 - 529
  • [5] HIV-1 IS TRANS-ACTIVATED BY THE FULL-LENGTH GENE-PRODUCT OF TAT OF HIV-2
    TONG, SE
    BAUR, A
    LU, X
    PECK, E
    PETERLIN, BM
    FASEB JOURNAL, 1992, 6 (05): : A1978 - A1978
  • [6] The complex life of the HIV-1 full-length RNA
    Soto-Rifo, Ricardo
    NATURE REVIEWS MICROBIOLOGY, 2024, 22 (06) : 325 - 325
  • [7] HIV-1 Tat protein as a potential AIDS vaccine
    Goldstein, G
    NATURE MEDICINE, 1996, 2 (09) : 960 - 964
  • [8] Functional expression and purification of recombinant full-length human ATG7 protein with HIV-1 Tat peptide in Escherichia coli
    Dong, Guofu
    Zhao, Xi
    Guo, Junwang
    Ma, Lei
    Zhou, Hongmei
    Liu, Qi
    Zhao, Xuelong
    Wang, Changzhen
    Wu, Ke
    PROTEIN EXPRESSION AND PURIFICATION, 2021, 182
  • [9] Visualizing the translation and packaging of HIV-1 full-length RNA
    Chen, Jianbo
    Liu, Yang
    Wu, Bin
    Nikolaitchik, Olga A.
    Mohan, Preeti R.
    Chen, Jiji
    Pathak, Vinay K.
    Hu, Wei-Shau
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2020, 117 (11) : 6145 - 6155
  • [10] Epitranscriptomic regulation of HIV-1 full-length RNA packaging
    Pereira-Montecinos, Camila
    Toro-Ascuy, Daniela
    Ananias-Saez, Catarina
    Gaete-Argel, Aracelly
    Rojas-Fuentes, Cecilia
    Riquelme-Barrios, Sebastian
    Rojas-Araya, Barbara
    Garcia-de-Gracia, Francisco
    Aguilera-Cortes, Paulina
    Chnaiderman, Jonas
    Acevedo, Monica L.
    Valiente-Echeverria, Fernando
    Soto-Rifo, Ricardo
    NUCLEIC ACIDS RESEARCH, 2022, 50 (04) : 2302 - 2318