The susceptibility of macrophages to human immunodeficiency virus type 1 X4 isolates depends on their activation state

被引:7
作者
Bakri, Y
Amzazi, S
Mannioui, A
Benjouad, A
机构
[1] Fac Sci, Agence Univ Francophone, Lab Biochim Immunol, JER 3012, Rabat 11400, Morocco
[2] Fac Med St Antoine, INSERM E0013, F-75571 Paris 12, France
关键词
activation status; cytokines; macrophages; X4; HIV-1;
D O I
10.1016/S0753-3322(00)00015-9
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The demonstration that macrophages express CXCR4 has led to a reexamination of their susceptibility to human immunodeficiency (HIV)-1 X4 strains. Here, we examined the susceptibility to X4 HIV-1Lai of two previously characterized macrophage populations, obtained either as 1) adherent cells of five-day cultures of blood mononuclear cells (PBMC), followed by two days without nonadherent PBMC nor added cytokines (MDM-5d); or 2) as adherent cells recovered from one-hour incubation of PBMC, which were cultured for seven days with macrophage colony-stimulating factor (MDM-MCSF), Exposing MDM-5d or MDM-MCSF to HIV-1 Lai did not lead to productive infection, as indicated by a lack of (MDM-MCSF) or low (MDM-5d) viral p24 levels in culture supernatants, However, MDM-5d vigorously transmitted HIV-1Lai to autologous T lymphocytes, which was not the case of HIV-1Lai-exposed MDM-MCSF. PCR analysis of the LTR RU5 region showed that X4 HIV-1Lai entered into both types of macrophages in the same manner as R5 HIV-1BaL. However, in contrast to MDM-5d, there was a block of HIV-1Lai retrotransciption in MDM-MCSF, Cytokine profile analysis of the two types of macrophages showed that TNF-alpha, IL-6 and RANTES levels were higher in MDM-5d than in MDM-MSCF, while the IL10 level was higher in MDM-MCSF, both producing similar IL16 levels. Altogether, these data indicate that HIV-1 X4 strains enter into macrophages but that their replication is blocked thereafter in a different manner according to the activation status of the cells. (C) 2001 Editions scientifiques et medicates Elsevier SAS.
引用
收藏
页码:32 / 38
页数:7
相关论文
共 30 条
[1]   The inhibitory effect of RANTES on the infection of primary macrophages by R5 human immunodeficiency virus type-1 depends on the macrophage activation state [J].
Amzazi, S ;
Ylisastigui, L ;
Bakri, Y ;
Rabehi, L ;
Gattegno, L ;
Parmentier, M ;
Gluckman, JC ;
Benjouad, A .
VIROLOGY, 1998, 252 (01) :96-105
[2]   AIDS research - HIV's other immune-system targets: Macrophages [J].
Balter, M .
SCIENCE, 1996, 274 (5292) :1464-1465
[3]   The susceptibility to X4 and R5 human immunodeficiency virus-1 strains of dendritic cells derived in vitro from CD34+ hematopoietic progenitor cells is primarily determined by their maturation stage [J].
Canque, B ;
Bakri, Y ;
Camus, S ;
Yagello, M ;
Benjouad, A ;
Gluckman, JC .
BLOOD, 1999, 93 (11) :3866-3875
[4]   Inactivation of HIV-1 chemokine co-receptor CXCR-4 by a novel intrakine strategy [J].
Chen, JD ;
Bai, XF ;
Yang, AG ;
Cong, YP ;
Chen, SY .
NATURE MEDICINE, 1997, 3 (10) :1110-1116
[5]   Presence of an inducible HIV-1 latent reservoir during highly active antiretroviral therapy [J].
Chun, TW ;
Stuyver, L ;
Mizell, SB ;
Ehler, LA ;
Mican, JAM ;
Baseler, M ;
Lloyd, AL ;
Nowak, MA ;
Fauci, AS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (24) :13193-13197
[6]   Host factors in the pathogenesis of HIV disease [J].
Cohen, OJ ;
Kinter, A ;
Fauci, AS .
IMMUNOLOGICAL REVIEWS, 1997, 159 :31-48
[7]   Cofactors for human immunodeficiency virus entry into primary macrophages [J].
Collman, RG ;
Yi, YJ .
JOURNAL OF INFECTIOUS DISEASES, 1999, 179 :S422-S426
[8]   Change in coreceptor use correlates with disease progression in HIV-1-infected individuals [J].
Connor, RI ;
Sheridan, KE ;
Ceradini, D ;
Choe, S ;
Landau, NR .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (04) :621-628
[9]  
Di Marzio P, 1998, AIDS RES HUM RETROV, V14, P129, DOI 10.1089/aid.1998.14.129
[10]   TUMOR NECROSIS FACTOR A ACTIVATES HUMAN IMMUNODEFICIENCY VIRUS TYPE-1 THROUGH INDUCTION OF NUCLEAR FACTOR BINDING TO THE NF-KAPPA-B SITES IN THE LONG TERMINAL REPEAT [J].
DUH, EJ ;
MAURY, WJ ;
FOLKS, TM ;
FAUCI, AS ;
RABSON, AB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (15) :5974-5978