Paucity of CD4+CCR5+ T cells is a typical feature of natural SIV hosts

被引:149
作者
Pandrea, Ivona
Apetrei, Cristian
Gordon, Shari
Barbercheck, Joseph
Dufour, Jason
Bohm, Rudolf
Sumpter, Beth
Roques, Pierre
Marx, Preston A.
Hirsch, Vanessa M.
Kaur, Amitinder
Lackner, Andrew A.
Veazey, Ronald S.
Silvestri, Guido
机构
[1] Tulane Natl Primate Res Ctr, Dept Comparat Pathol, Covington, LA 70433 USA
[2] Univ Penn, Dept Pathol, Philadelphia, PA 19104 USA
[3] Yerkes Natl Primate Res Ctr, Atlanta, GA USA
[4] Ctr Int Rech Med, Franceville, Gabon
[5] NIAID, Mol Microbiol Lab, NIH, Bethesda, MD 20892 USA
[6] New England Reg Primate Res Ctr, Southborough, MA 01772 USA
关键词
D O I
10.1182/blood-2006-05-024364
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In contrast to lentiviral infections of humans and macaques, simian immunodeficiency virus (SIV) infection of natural hosts is nonpathogenic despite high levels of viral replication. However, the mechanisms underlying this absence of disease are unknown. Here we report that natural hosts for SIV infection express remarkably low levels of CCR5 on CD4(+) T cells isolated from blood, lymph nodes, and mucosal tissues. Given that this immunologic feature is found in 5 different species of natural SIV hosts (sooty mangabeys, African green monkeys, mandrills, sun-tailed monkeys, and chimpanzees) but is absent in 5 normatural/recent hosts (humans, rhesus, pigtail, cynomolgus macaques, and baboons), it may represent a key feature of the coevolution between the virus and its natural hosts that led to a nonpathogenic infection. Beneficial effects of low CCR5 expression on CD4(+) T cells may include the reduction of target cells for viral replication and a decreased homing of activated CD4(+) T cells to inflamed tissue.
引用
收藏
页码:1069 / 1076
页数:8
相关论文
共 56 条
[1]   AN AIDS-LIKE CONDITION INDUCED IN BABOONS BY HIV-2 [J].
BARNETT, SW ;
MURTHY, KK ;
HERNDIER, BG ;
LEVY, JA .
SCIENCE, 1994, 266 (5185) :642-646
[2]   Immunodeficiency in the absence of high viral load in pig-tailed macaques infected with simian immunodeficiency virus SIVsun or SIVlhoest [J].
Beer, BE ;
Brown, CR ;
Whitted, S ;
Goldstein, S ;
Goeken, R ;
Plishka, R ;
Buckler-White, A ;
Hirsch, VM .
JOURNAL OF VIROLOGY, 2005, 79 (22) :14044-14056
[3]   CD4+ T cell depletion during all stages of HIV disease occurs predominantly in the gastrointestinal tract [J].
Brenchley, JM ;
Schacker, TW ;
Ruff, LE ;
Price, DA ;
Taylor, JH ;
Beilman, GJ ;
Nguyen, PL ;
Khoruts, A ;
Larson, M ;
Haase, AT ;
Douek, DC .
JOURNAL OF EXPERIMENTAL MEDICINE, 2004, 200 (06) :749-759
[4]   Simian immunodeficiency virus replicates to high levels in naturally infected African green monkeys without inducing immunologic or neurologic disease [J].
Broussard, SR ;
Staprans, SI ;
White, R ;
Whitehead, EM ;
Feinberg, MB ;
Allan, JS .
JOURNAL OF VIROLOGY, 2001, 75 (05) :2262-2275
[5]   Normal T-cell turnover in sooty mangabeys harboring active simian immunodeficiency virus infection [J].
Chakrabarti, LA ;
Lewin, SR ;
Zhang, LQ ;
Gettie, A ;
Luckay, A ;
Martin, LN ;
Skulsky, E ;
Ho, DD ;
Cheng-Mayer, C ;
Marx, PA .
JOURNAL OF VIROLOGY, 2000, 74 (03) :1209-1223
[6]   Human immunodeficiency virus type 2 (HIV-2) seroprevalence and characterization of a distinct HIV-2 genetic subtype from the natural range of simian immunodeficiency virus-infected sooty mangabeys [J].
Chen, ZW ;
Luckay, A ;
Sodora, DL ;
Telfer, P ;
Reed, P ;
Gettie, A ;
Kanu, JM ;
Zhang, LQ ;
Sadek, RF ;
Yee, J ;
Ho, DD ;
Marx, PA .
JOURNAL OF VIROLOGY, 1997, 71 (05) :3953-3960
[7]   Primary SIVsm isolates use the CCR5 coreceptor from sooty mangabeys naturally infected in west Africa: A comparison of coreceptor usage of primary SIVsm, HIV-2, and SIVmac [J].
Chen, ZW ;
Gettie, A ;
Ho, DD ;
Marx, PA .
VIROLOGY, 1998, 246 (01) :113-124
[8]   Natural infection of a homozygous Δ24 CCR5 red-capped mangabey with an R2b-tropic simian immunodeficiency virus [J].
Chen, ZW ;
Kwon, D ;
Jin, ZQ ;
Monard, S ;
Telfer, P ;
Jones, MS ;
Lu, CY ;
Aguilar, RF ;
Ho, DD ;
Marx, PA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (11) :2057-2065
[9]   High levels of viral replication during primary simian immunodeficiency virus SIVagm infection are rapidly and strongly controlled in African green monkeys [J].
Diop, OM ;
Gueye, P ;
Dias-Tavares, M ;
Kornfeld, C ;
Faye, A ;
Ave, P ;
Huerre, M ;
Corbet, S ;
Barre-Sinoussi, F ;
Müller-Trutwin, MC .
JOURNAL OF VIROLOGY, 2000, 74 (16) :7538-7547
[10]   Receptor function of CD4 structures from African green monkey and pig-tail macaque for simian immunodeficiency virus, SIVsm, SIVagm, and human immunodeficiency virus type-1 [J].
Fomsgaard, A ;
Johnson, PR ;
Nielsen, C ;
Novembre, FJ ;
Hansen, J ;
Goldstein, S ;
Hirsch, VM .
VIRAL IMMUNOLOGY, 1995, 8 (03) :121-133