GB virus C coinfection and HIV-1 disease progression: The Amsterdam Cohort Study

被引:76
作者
Van der Bij, AK
Kloosterboer, N
Prins, M
Boeser-Nunnink, B
Geskus, RB
Lange, JMA
Coutinho, RA
Schuitemaker, H
机构
[1] Municipal Hlth Serv Amsterdam, Dept HIV & STD Res, Cluster Infect Dis, Amsterdam, Netherlands
[2] Univ Amsterdam, Sanquin Res Landsteiner Lab, Amsterdam, Netherlands
[3] Univ Amsterdam, Acad Med Ctr, Dept Human Retrovirol, NL-1105 AZ Amsterdam, Netherlands
[4] Univ Amsterdam, Natl AIDS Therapy Evaluat Ctr, Amsterdam, Netherlands
[5] Univ Amsterdam, Dept Internal Med, Div Infect Dis Trop Med & AIDS, Amsterdam, Netherlands
关键词
D O I
10.1086/427559
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. The effect that GB virus C (GBV-C) coinfection has on human immunodeficiency virus type 1 (HIV-1) disease progression is controversial and therefore was studied in 326 homosexual men from the prospective Amsterdam Cohort Studies who had an accurately estimated date of HIV-1 seroconversion and were followed up for a median period of 8 years. Methods. A first plasma sample, obtained shortly after HIV-1 seroconversion, and a last plasma sample, obtained before 1996, were tested for GBV-C RNA and envelope protein-2 antibodies. The effect that GBV-C has on HIV-1 disease progression was studied by use of time-dependent Cox proportional-hazards models with adjustment for baseline variables and time-updated HIV-1 RNA and CD4(+) cell count. Results. Men who lost GBV-C RNA between collection of the first sample and collection of the last sample had a nearly 3-fold-higher risk of HIV-1 disease progression than did men who had never had GBV-C RNA. This effect became much smaller after adjustment for time-updated CD4(+) cell count. Conclusion. Rather than a positive effect of GBV-C RNA presence, a negative effect of GBV-C RNA loss on HIV-1 disease progression was found, which disappeared after adjustment for time-updated CD4(+) cell count. We therefore hypothesize that GBV-C RNA persistence depends on the presence of a sufficient number of CD4(+) cells- and that the CD4(+) cell decrease associated with HIV-1 disease progression is a cause, not a consequence, of GBVC RNA loss.
引用
收藏
页码:678 / 685
页数:8
相关论文
共 33 条
[1]   No influence of GB virus C replication on the prognosis in a cohort of HIV-1-infected patients [J].
Birk, M ;
Lindbäck, S ;
Lidman, C .
AIDS, 2002, 16 (18) :2482-2485
[2]  
Björkman P, 2004, AIDS, V18, P877, DOI [10.1097/00002030-200404090-00005, 10.1097/01.aids.0000125908.52357.4c]
[3]   Prevalence of hepatitis G virus RNA in the sera of patients with HIV infection [J].
Bonacini, M ;
Qian, DJ ;
Govindarajan, S ;
Valinluck, B .
JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, 1998, 19 (01) :40-43
[4]   RAPID AND SIMPLE METHOD FOR PURIFICATION OF NUCLEIC-ACIDS [J].
BOOM, R ;
SOL, CJA ;
SALIMANS, MMM ;
JANSEN, CL ;
WERTHEIMVANDILLEN, PME ;
VANDERNOORDAA, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 1990, 28 (03) :495-503
[5]  
CDC - Centers for Disease Control and Prevention, 1992, MMWR, V41
[6]   STORAGE-CONDITIONS OF BLOOD-SAMPLES AND PRIMER SELECTION AFFECT THE YIELD OF CDNA POLYMERASE CHAIN-REACTION PRODUCTS OF HEPATITIS-C VIRUS [J].
CUYPERS, HTM ;
BRESTERS, D ;
WINKEL, IN ;
REESINK, HW ;
WEINER, AJ ;
HOUGHTON, M ;
VANDERPOEL, CL ;
LESLIE, PN .
JOURNAL OF CLINICAL MICROBIOLOGY, 1992, 30 (12) :3220-3224
[7]  
Geskus RB, 2000, STAT MED, V19, P1753, DOI 10.1002/1097-0258(20000715)19:13&lt
[8]  
1753::AID-SIM487&gt
[9]  
3.0.CO
[10]  
2-F