Naive and memory CD4+ T cells and T cell activation markers in HIV-1 infected children on HAART

被引:36
作者
Resino, S
Navarro, J
Bellón, JM
Gurbindo, D
León, JA
Muñoz-Fernández, MA
机构
[1] Hosp Gen Univ Gregorio Maranon, Dept Immunol, Madrid 28007, Spain
[2] Hosp Gen Univ Gregorio Maranon, Dept Paediat, Madrid 28007, Spain
[3] Hosp Virgen Rocio, Dept Paediat, Seville, Spain
关键词
CD4; subsets; children; highly active antiretroviral therapy; HIV immune reconstitution; surrogate markers;
D O I
10.1046/j.1365-2249.2001.01612.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The objective of this study was to investigate the relationship between peripheral blood CD4(+) T cell subsets and routine viro-immunological markers in vertically HIV-1-infected children undergoing highly active antiretroviral therapy (HAART). CD4(+) and CD8(+) T cell subsets were examined by three-colour flow cytometry. Plasma viraemia was quantified by a standardized molecular assay. A negative correlation between the %CD4(+) T cells and both viral load and the %CD8(+) T cells was observed. A strong positive correlation between the %CD4 T cells and naive, CD38(+) and non-activated CD4(+) T cell subsets was found, whereas the %CD4 T cells correlated negatively with the numbers of memory, activated and memory-activated CD4(+) T cell subsets. Elevated percentages of CD8 T cells were associated with increased memory and CD4(+) CD62L-T cell subsets, whereas the naive and CD4(+) HLA-DRCD38(+) subsets negatively correlated with the CD8%. Co-expression of CD62L on memory CD4(+) cells and high expression of HLA-DR (but not of CD38) were associated with high viral load. No association between viral load and naive CD4(+) T cells was observed. Specific CD4(+) T cell subsets may be more informative than routine surrogate markers in defining the evolution of HIV infection and immune reconstitution in children.
引用
收藏
页码:266 / 273
页数:8
相关论文
共 41 条
[1]  
[Anonymous], 1994, MMWR Recomm Rep, V43, P1
[2]  
AUTRAN B, 1997, J MED CHEM, V40, P2164
[3]  
BOHLER T, 1999, AM J PUBLIC HEALTH, V89, P947
[4]   HIV INDUCES THYMUS DEPLETION INVIVO [J].
BONYHADI, ML ;
RABIN, L ;
SALIMI, S ;
BROWN, DA ;
KOSEK, J ;
MCCUNE, JM ;
KANESHIMA, H .
NATURE, 1993, 363 (6431) :728-732
[5]   PREDOMINANCE OF T-CELLS THAT EXPRESS CD45R IN THE CD4+ HELPER INDUCER LYMPHOCYTE SUBSET OF NEONATES [J].
BRADLEY, LM ;
BRADLEY, JS ;
CHING, DL ;
SHIIGI, SM .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1989, 51 (03) :426-435
[6]   Antiretroviral therapy for HIV infection in 1997 - Updated recommendations of the International AIDS Society USA panel [J].
Carpenter, CCJ ;
Fischl, MA ;
Hammer, SM ;
Hirsch, MS ;
Jacobsen, DM ;
Katzenstein, DA ;
Montaner, JSG ;
Richman, DD ;
Saag, MS ;
Schooley, RT ;
Thompson, MA ;
Vella, S ;
Yeni, PG ;
Volberding, PA .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1997, 277 (24) :1962-1969
[7]  
*CDCP, 1998, MMWR-MORBID MORTAL W, V47, pRR4
[8]  
CLEMENT LT, 1988, J IMMUNOL, V141, P1464
[9]   Different meaning of CD38 molecule expression on CD4+ and CD8+ cells of children perinatally infected with human immunodeficiency virus type 1 infection surviving longer than five years [J].
De Martino, M ;
Rossi, ME ;
Azzari, C ;
Gelli, MG ;
Galli, L ;
Vierucci, A .
PEDIATRIC RESEARCH, 1998, 43 (06) :752-758
[10]   AGE-RELATED-CHANGES IN HUMAN-LYMPHOCYTE SUBSETS - PROGRESSIVE REDUCTION OF THE CD4 CD45R (SUPPRESSOR INDUCER) POPULATION [J].
DEPAOLI, P ;
BATTISTIN, S ;
SANTINI, GF .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1988, 48 (03) :290-296