Potent Intratype Neutralizing Activity Distinguishes Human Immunodeficiency Virus Type 2 (HIV-2) from HIV-1

被引:37
作者
Sahin, Gulsen Ozkaya [1 ]
Holmgren, Birgitta [1 ]
da Silva, Zacarias [2 ]
Nielsen, Jens [3 ]
Nowroozalizadeh, Salma [4 ,5 ]
Esbjornsson, Joakim [6 ]
Mansson, Fredrik [7 ]
Andersson, Soren [4 ]
Norrgren, Hans [8 ]
Aaby, Peter [2 ,3 ]
Jansson, Marianne [1 ,5 ]
Fenyo, Eva Maria [1 ]
机构
[1] Lund Univ, Dept Lab Med Lund, Lund, Sweden
[2] INDEPTH Network, Bandim Hlth Project, Bissau, Guinea Bissau
[3] Statens Serum Inst, DK-2300 Copenhagen, Denmark
[4] Swedish Inst Infect Dis Control, Dept Virol, Stockholm, Sweden
[5] Karolinska Inst, Dept Microbiol Tumor & Cell Biol, Stockholm, Sweden
[6] Lund Univ, Dept Expt Med Sci, Lund, Sweden
[7] Lund Univ, Dept Clin Sci, Infect Dis Res Unit, Malmo, Sweden
[8] Lund Univ, Dept Clin Sci, Div Infect Med, Lund, Sweden
基金
瑞典研究理事会;
关键词
WEST-AFRICA; GUINEA-BISSAU; CORECEPTOR USAGE; ANTIBODY NEUTRALIZATION; BIOLOGICAL VARIABILITY; DUAL INFECTIONS; VIRAL LOAD; V3; LOOP; INDIVIDUALS; PREVALENCE;
D O I
10.1128/JVI.06315-11
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
HIV-2 has a lower pathogenicity and transmission rate than HIV-1. Neutralizing antibodies could be contributing to these observations. Here we explored side by side the potency and breadth of intratype and intertype neutralizing activity (NAc) in plasma of 20 HIV-1-, 20 HIV-2-, and 11 dually HIV-1/2 (HIV-D)-seropositive individuals from Guinea-Bissau, West Africa. Panels of primary isolates, five HIV-1 and five HIV-2 isolates, were tested in a plaque reduction assay using U87.CD4-CCR5 cells as targets. Intratype NAc in HIV-2 plasma was found to be considerably more potent and also broader than intratype NAc in HIV-1 plasma. This indicates that HIV-2-infected individuals display potent type-specific neutralizing antibodies, whereas such strong type-specific antibodies are absent in HIV-1 infection. Furthermore, the potency of intratype NAc was positively associated with the viral load of HIV-1 but not HIV-2, suggesting that NAc in HIV-1 infection is more antigen stimulation dependent than in HIV-2 infection, where plasma viral loads typically are at least 10-fold lower than in HIV-1 infection. Intertype NAc of both HIV-1 and HIV-2 infections was, instead, of low potency. HIV-D subjects had NAc to HIV-2 with similar high potency as singly HIV-2-infected individuals, whereas neutralization of HIV-1 remained poor, indicating that the difference in NAc between HIV-1 and HIV-2 infections depends on the virus itself. We suggest that immunogenicity and/or antigenicity, meaning the neutralization phenotype, of HIV-2 is distinct from that of HIV-1 and that HIV-2 may display structures that favor triggering of potent neutralizing antibody responses.
引用
收藏
页码:961 / 971
页数:11
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