Association of variations of NAb 2F5 and 4E10 epitopes and disease progression in Chinese antiretroviral treatment-naive patients infected with HIV-1 clade B'

被引:1
作者
Zhang Xiao-li [1 ,2 ]
Han Xiao-xu [1 ]
Dai Di [1 ]
Bao Ming-jia [1 ]
Xu Dong-bing [1 ]
Zhang Zi-ning [1 ]
Wang Ya-nan [1 ]
Zhao Min [1 ]
Bice, Tristan [1 ]
Jiang Yong-jun [1 ]
Shang Hong [1 ]
机构
[1] China Med Univ, Affiliated Hosp 1, Minist Hlth, Key Lab Immunol AIDS, Shenyang 110001, Liaoning, Peoples R China
[2] Jiamusi Univ, Affiliated Hosp 1, Dept Lab Med, Jiamusi 154003, Heilongjiang, Peoples R China
关键词
gp41; neutralizing epitope; 2F5; 4E10; mutation; IMMUNODEFICIENCY-VIRUS TYPE-1; BROADLY NEUTRALIZING ANTIBODIES; PROXIMAL EXTERNAL REGION; MONOCLONAL-ANTIBODIES; GP41; EPITOPE; IN-VITRO; GLYCOPROTEIN GP41; ELDKWA-EPITOPE; MEMBRANE; VACCINE;
D O I
10.3760/cma.j.issn.0366-6999.2010.23.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Studies on human immunodeficiency virus type 1 (HIV-1) vaccines have recently focused on targeting the conserved neutralizing epitopes 2F5 and 4E10, and hence it is important to understand the extent of mutations in these two viral epitopes Here we investigated the amino acid mutations in epitopes of 2F5 (ELDKWA HIV-1 HXB2 env 662-667 aa) and 4E10 (NWFDIT, HIV-1 HXB2 env 671-676 aa) in the membrane proximal-external region of gp41 from clade B' HIV 1-infected individuals living in Henan province, China We also examined the frequency of a mutation and its relation to disease progression Methods A cohort of 54 treatment naive HIV-1-infected individuals was recruited in this study, and 16 individuals were selected for a short-term longitudinal study on sequence evolution The HIV 1 env gp41 gene was amplified cloned, and sequenced, and predicted amino acid sequences were aligned for analysis Results The mutations E662A and K665E on the 2F5 epitope and N671S and T676S on the 4E10 epitope were seen Simultaneous RNA sequencing showed some discrepancies with proviral DNA sequences In our longitudinal study mutation levels of these two neutralizing epitopes were low but diverse and persistent The frequencies of mutations within the 4E10 peptide NWFDIT in slow progressors were noticeably lower than those in AIDS patients (P<0 05) Conclusions Antigenic variation of the neutralizing epitopes 2F5 and 4E10 is limited in subtype B' infection, and that 4E10 peptide mutation is correlated with disease progression Monitoring epitope mutations will offer useful data for development of the candidate 2F5 like and 4E10-like antibodies to prevent and treat AIDS
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页码:3406 / 3411
页数:6
相关论文
共 46 条
  • [1] Role of HIV membrane in neutralization by two broadly neutralizing antibodies
    Alam, S. Munir
    Morelli, Marco
    Dennison, S. Moses
    Liao, Hua-Xin
    Zhang, Ruijun
    Xia, Shi-Mao
    Rits-Volloch, Sophia
    Sun, Li
    Harrison, Stephen C.
    Haynes, Barton F.
    Chen, Bing
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (48) : 20234 - 20239
  • [2] Broad Neutralization of Human Immunodeficiency Virus Type 1 (HIV-1) Elicited from Human Rhinoviruses That Display the HIV-1 gp41 ELDKWA Epitope
    Arnold, Gail Ferstandig
    Velasco, Paola K.
    Holmes, Andrew K.
    Wrin, Terri
    Geisler, Sheila C.
    Phung, Pham
    Tian, Yu
    Resnick, Dawn A.
    Ma, Xuejun
    Mariano, Thomas M.
    Petropoulos, Christos J.
    Taylor, John W.
    Katinger, Hermann
    Arnold, Eddy
    [J]. JOURNAL OF VIROLOGY, 2009, 83 (10) : 5087 - 5100
  • [3] Structural analysis of the epitope of the Anti-HIV antibody 2F5 sheds light into its mechanism of neutralization and HIV fusion
    Barbato, G
    Bianchi, E
    Ingallinella, P
    Hurni, WH
    Miller, MD
    Cilibertol, G
    Cortese, R
    Bazzo, R
    Shiver, JW
    Pessi, A
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 2003, 330 (05) : 1101 - 1115
  • [4] Comprehensive cross-clade neutralization analysis of a panel of anti-human immunodeficiency virus type 1 monoclonal antibodies
    Binley, JA
    Wrin, T
    Korber, B
    Zwick, MB
    Wang, M
    Chappey, C
    Stiegler, G
    Kunert, R
    Zolla-Pazner, S
    Katinger, H
    Petropoulos, CJ
    Burton, DR
    [J]. JOURNAL OF VIROLOGY, 2004, 78 (23) : 13232 - 13252
  • [5] Antibodies to conserved epitopes of the HIV-1 envelope in sera from long-term non-progressors: prevalence and association with neutralizing activity
    Braibant, Martine
    Brunet, Sylvie
    Costagliola, Dominique
    Rouzioux, Christine
    Agut, Henri
    Katinger, Hermann
    Autran, Brigitte
    Barin, Francis
    [J]. AIDS, 2006, 20 (15) : 1923 - 1930
  • [6] Structure-function analysis of the epitope for 4E10, a broadly neutralizing human immunodeficiency virus type 1 antibody
    Brunel, FM
    Zwick, MB
    Cardoso, RMF
    Nelson, JD
    Wilson, IA
    Burton, DR
    Dawson, PE
    [J]. JOURNAL OF VIROLOGY, 2006, 80 (04) : 1680 - 1687
  • [7] Changing sensitivity to broadly neutralizing antibodies b12, 2G12, 2F5, and 4E10 of primary subtype B human immunodeficiency virus type 1 variants in the natural course of infection
    Bunnik, Evelien M.
    van Gils, Marit J.
    Lobbrecht, Marilie S. D.
    Pisas, Linaida
    van Nuenen, Ad C.
    Schuitemaker, Hanneke
    [J]. VIROLOGY, 2009, 390 (02) : 348 - 355
  • [8] HIV vaccine design and the neutralizing antibody problem
    Burton, DR
    Desrosiers, RC
    Doms, RW
    Koff, WC
    Kwong, PD
    Moore, JP
    Nabel, GJ
    Sodroski, J
    Wilson, IA
    Wyatt, RT
    [J]. NATURE IMMUNOLOGY, 2004, 5 (03) : 233 - 236
  • [9] Broadly neutralizing anti-HIV antibody 4E10 recognizes a helical conformation of a highly conserved fusion-associated motif in gp41
    Cardoso, RMF
    Zwick, MB
    Stanfield, RL
    Kunert, R
    Binley, JM
    Katinger, H
    Burton, DR
    Wilson, IA
    [J]. IMMUNITY, 2005, 22 (02) : 163 - 173
  • [10] Structural basis of enhanced binding of extended and helically constrained peptide epitopes of the broadly neutralizing HIV-1 antibody 4E10
    Cardoso, Rosa M. F.
    Brunel, Florence M.
    Ferguson, Sharon
    Zwick, Michael
    Burton, Dennis R.
    Dawson, Philip E.
    Wilson, Ian A.
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 2007, 365 (05) : 1533 - 1544