Recovery of replication-competent virus from CD4 T cell reservoirs and change in coreceptor use in human immunodeficiency virus type 1-infected children responding to highly active antiretroviral therapy

被引:32
作者
Equils, O
Garratty, E
Wei, LS
Plaeger, S
Tapia, M
Deville, J
Krogstad, P
Sim, MS
Nielsen, K
Bryson, YJ
机构
[1] Univ Calif Los Angeles, Childrens Hosp, Dept Pediat, UCLA AIDS Inst, Los Angeles, CA 90095 USA
[2] Cedars Sinai Med Ctr, Div Pediat Infect Dis, Los Angeles, CA 90048 USA
[3] Cornell Univ, Sch Med, New York, NY 10021 USA
关键词
D O I
10.1086/315758
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Highly active antiretroviral therapy (HAART) suppresses plasma viremia in most patients with human immunodeficiency virus (HIV) infection. Prospective study of HIV-infected children (n = 27) shows that, in 8 of 12 who responded to HAART (greater than or equal to 0.5 log reduction in plasma HIV RNA), HAART restricted the number of coreceptors used by the predominant HIV isolate (mean number of coreceptors used at baseline was 4, vs. 1 coreceptor used at 6 months after treatment). This decrease was most striking in 6 of 8 children whose HIV coreceptor tropism changed from X4-tropic at baseline to R5-tropic. In 6 of 10 children tested, with plasma HIV RNA levels of <50 copies/mL, R5-tropic virus was isolated from CD4 T cell reservoirs. All the responding children had a significant increase in naive CD4 T cells (P < .05). These results show that persistent HIV T cell reservoirs are present in children and that HAART may influence the number and type of coreceptors used by the predominant virus isolate.
引用
收藏
页码:751 / 757
页数:7
相关论文
共 40 条
[1]  
*ACTG NAT I ALL IN, 1997, ACTG VIR MAN HIV LAB
[2]  
Bjorndal A, 1997, J VIROL, V71, P7478
[3]   Combination therapy with zidovudine, didanosine and saquinavir [J].
Collier, AC ;
Coombs, RW ;
Schoenfeld, DA ;
Bassett, R ;
Baruch, A ;
Corey, L .
ANTIVIRAL RESEARCH, 1996, 29 (01) :99-99
[4]   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
[5]  
DEEKS S, 1999, 6 C RETR OPP INF CHI, P160
[6]   REPLICATION AND TROPISM OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 AS PREDICTORS OF DISEASE OUTCOME IN INFANTS WITH VERTICALLY ACQUIRED INFECTION [J].
DEROSSI, A ;
GIAQUINTO, C ;
OMETTO, L ;
MAMMANO, F ;
ZANOTTO, C ;
DUNN, D ;
CHIECOBIANCHI, L .
JOURNAL OF PEDIATRICS, 1993, 123 (06) :929-936
[7]   RAPID INCREASES IN LOAD OF HUMAN-IMMUNODEFICIENCY-VIRUS CORRELATE WITH EARLY DISEASE PROGRESSION AND LOSS OF CD4 CELLS IN VERTICALLY INFECTED INFANTS [J].
DICKOVER, RE ;
DILLON, M ;
GILLETTE, SG ;
DEVEIKIS, A ;
KELLER, M ;
PLAEGERMARSHALL, S ;
CHEN, I ;
DIAGNE, A ;
STIEHM, ER ;
BRYSON, Y .
JOURNAL OF INFECTIOUS DISEASES, 1994, 170 (05) :1279-1284
[8]  
DOMS RW, 1998, COR US PRIM LENT
[9]   A dual-tropic primary HIV-1 isolate that uses fusin and the beta-chemokine receptors CKR-5, CKR-3, and CKR-2b as fusion cofactors [J].
Doranz, BJ ;
Rucker, J ;
Yi, YJ ;
Smyth, RJ ;
Samson, M ;
Peiper, SC ;
Parmentier, M ;
Collman, RG ;
Doms, RW .
CELL, 1996, 85 (07) :1149-1158
[10]   Changes in thymic function with age and during the treatment of HIV infection [J].
Douek, DC ;
McFarland, RD ;
Keiser, PH ;
Gage, EA ;
Massey, JM ;
Haynes, BF ;
Polis, MA ;
Haase, AT ;
Feinberg, MB ;
Sullivan, JL ;
Jamieson, BD ;
Zack, JA ;
Picker, LJ ;
Koup, RA .
NATURE, 1998, 396 (6712) :690-695