Subsets of CD8+ T cells in longterm asymptomatic vertically HIV-1 infected children

被引:2
作者
Resino, S
Bellón, JM
Pérez, A
Gutiérrez, MDG
Muñoz-Fernández, MA
机构
[1] Hosp Gen Gregorio Maranon, Dept Inmunol, Lab Inmunobiol Mol, Madrid 28007, Spain
[2] Hosp Gen Gregorio Maranon, Unidad Invest, Madrid 28007, Spain
[3] Hosp Gen Gregorio Maranon, Secc Inmunopediat, Madrid 28007, Spain
来源
MEDICINA CLINICA | 2004年 / 122卷 / 01期
关键词
HIV-1; children; CD8+T cell subsets; non-progression;
D O I
10.1016/S0025-7753(04)74125-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND AND OBJECTIVE: HIV-infection has distinct patterns of disease progression with heterogeneous manifestations. We analyzed the subsets of CD8+ T cells in a group of long term asymptomatic (LTA) HIV-1-infected children who had stable CD4+ T cell counts (> 600/mul). PATIENTS AND METHODS: Cross-sectional study in HIV-1-vertically infected children older than 7 years who were rated into two groups according to the clinical and immunological classification: a) LTA: 7 asymptornatic HIV-1-infected children in A1, and b) rapid progressor (PR): 14 age-matched C3 HIV-1-infected children. Controls included 17 age-matched uninfected children. Characterization of CD8+ T-cell subsets was done by three-color flow cytometry. RESULTS: LTA children displayed similar values of memory CD8+ T cells (CD8+CD45RO+, CD8+CD45RA-CD28+, CD8+ CD45RA-CD62L+) as controls but lower than PR children. LTA patients also showed similar values of naive CD8+ T cells (CD8+CD45RA+CD62L+, CD8+CD45RA+CD28+, CD8+CD45RA+, CD8+CD28+ and CD8+CD62L+) as controls but higher values than PR children. The values of CD8+CD38+ T cells were similar in LTA and controls but lower in PR. However, LTA children had higher values of CD8+HLA-DR+CD38+ and CD8+HLA-DR+ T cells than controls. Additionally, LTA patients had higher values of pre-effector CD8+ T cells than controls yet the values of effector CD8+ T-cells were similar in both LTA and controls. Moreover, the LTA group had lower values of CD8+CD11b+ T cells than controls. CONCLUSIONS: Asymptomatic HIV-1 infected children have an almost normal CD8+ subset distribution, with the exception of activated and pre-effector CD8+ T cells which were higher.
引用
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页码:6 / 11
页数:6
相关论文
共 54 条
[1]  
AKBAR A, 1988, J IMMUNOL, V140, P217
[2]   Memory CD8+ T cells vary in differentiation phenotype in different persistent virus infections [J].
Appay, V ;
Dunbar, PR ;
Callan, M ;
Klenerman, P ;
Gillespie, GMA ;
Papagno, L ;
Ogg, GS ;
King, A ;
Lechner, F ;
Spina, CA ;
Little, S ;
Havlir, DV ;
Richman, DD ;
Gruener, N ;
Pape, G ;
Waters, A ;
Easterbrook, P ;
Salio, M ;
Cerundolo, V ;
McMichael, AJ ;
Rowland-Jones, SL .
NATURE MEDICINE, 2002, 8 (04) :379-385
[3]  
AZUMA M, 1993, J IMMUNOL, V150, P2091
[4]   Quantitative alterations of the functionally distinct subsets of CD4 and CD8 T lymphocytes in asymptomatic HIV infection: Changes in the expression of CD45RO, CD45RA, CD11b, CD38, HLA-DR, and CD25 antigens [J].
Benito, JM ;
Zabay, JM ;
Gil, J ;
Bermejo, M ;
Escudero, A ;
Sanchez, E ;
FernandezCruz, E .
JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES AND HUMAN RETROVIROLOGY, 1997, 14 (02) :128-135
[5]  
BORTHWICK NJ, 1994, CLIN IMMUNOL IMMUNOP, V71, P2
[6]   Correlation of CD8 lymphocyte activation with cellular viremia and plasma HIV RNA levels in asymptomatic patients infected by human immunodeficiency virus type 1 [J].
Bouscarat, F ;
LevacherClergeot, M ;
Dazza, MC ;
Strauss, KW ;
Girard, PM ;
Ruggeri, C ;
Sinet, M .
AIDS RESEARCH AND HUMAN RETROVIRUSES, 1996, 12 (01) :17-24
[7]   EXPRESSION OF COSTIMULATORY MOLECULE CD28 ON T-CELLS IN HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 INFECTION - FUNCTIONAL AND CLINICAL CORRELATIONS [J].
BRINCHMANN, JE ;
DOBLOUG, JH ;
HEGER, BH ;
HAAHEIM, LL ;
SANNES, M ;
EGELAND, T .
JOURNAL OF INFECTIOUS DISEASES, 1994, 169 (04) :730-738
[8]  
Bürgisser P, 1999, CLIN EXP IMMUNOL, V115, P458
[9]  
BURKE AP, 1995, ARCH PATHOL LAB MED, V119, P36
[10]   VIROLOGICAL AND IMMUNOLOGICAL CHARACTERIZATION OF LONG-TERM SURVIVORS OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 INFECTION [J].
CAO, YZ ;
QIN, LM ;
ZHANG, LQ ;
SAFRIT, J ;
HO, DD .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 332 (04) :201-208