ALTERED REPRESENTATION OF NAIVE AND MEMORY CD8 T-CELL SUBSETS IN HIV-INFECTED CHILDREN

被引:148
作者
RABIN, RL
ROEDERER, M
MALDONADO, Y
PETRU, A
HERZENBERG, LA
HERZENBERG, LA
机构
[1] STANFORD UNIV, SCH MED, DEPT GENET, STANFORD, CA 94305 USA
[2] STANFORD UNIV, SCH MED, DEPT PEDIAT, DIV PEDIAT INFECT DIS, STANFORD, CA 94305 USA
[3] CHILDRENS HOSP, DIV PEDIAT INFECT DIS, OAKLAND, CA 94609 USA
关键词
T CELL SUBSETS; ACQUIRED IMMUNODEFICIENCY SYNDROME; T4; CELLS; T8; NAIVE T CELLS;
D O I
10.1172/JCI117891
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
CD8 T cells are divided into naive and memory subsets according to both function and phenotype, In HIV-negative children, the naive subset is present at high frequencies, whereas memory cells are virtually absent, Previous studies have shown that the overall number of CD8 T cells does not decrease in HIV-infected children, In studies here, we use multiparameter Bow cytometry to distinguish naive from memory CD8 T cells based on expression of CD11a, CD45RA, and CD62L, With this methodology, we show that within the CD8 T cell population, the naive subset decreases markedly (HIV+ vs, HIV-, 190 vs, 370 cells/mu l; P less than or equal to 0.003), and that there is a reciprocal increase in memory cells, such that the total CD8 T cell counts remained unchanged (800 vs. 860 cells/mu l; P less than or equal to 0.76), In addition, we show that for HIV-infected children, the naive CD8 T cell and total CD4 T cell counts correlate (chi(2)P less than or equal to 0.001), This correlated loss suggests that the loss of naive CDS T cells in HIV infection may contribute to the defects in cell-mediated immunity which become progressively worse as the HIV disease progresses and CD4 counts decrease.
引用
收藏
页码:2054 / 2060
页数:7
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  • [1] Mackewicz C., Levy J.A., CD8<sup>+</sup> cell anti-HIV activity: Nonlytic suppression of virus replication, AIDS Res. Hum. Retroviruses, 8, pp. 1039-1050, (1992)
  • [2] Sohen S., Rothstein D., Tallman T., Gaudette D., Schlossman S., Morimoto C., The functional heterogeneity of CD8<sup>+</sup> cells defined by anti-CD45RA (2H4) and anti-CD29 (4B4) antibodies, Cell. Immunol., 128, pp. 314-328, (1990)
  • [3] De Jong R., Brouwer M., Miedema F., Van Lier R.A., Human CD8<sup>+</sup> T lymphocytes can be divided into CD45RA<sup>+</sup> and CD45RO<sup>+</sup> cells with different requirements for activation and differentiation, J. Immunol., 146, pp. 2088-2094, (1991)
  • [4] Clement L.T., Isoforms of the CD45 common leukocyte antigen family: Markers for human T-cell differentiation, J. Clin. Immunol., 12, pp. 1-10, (1992)
  • [5] McGrath M.S., T cell abnormalities, AIDS Knowledge Base. Textbook on HIV from the University of California, pp. 322-413, (1990)
  • [6] Steihm E.R., Wara D.W., Immunology of HIV, Pediatric AIDS: The Challenge of HIV Infection in Infants, Children, and Adolescents, pp. 95-112, (1991)
  • [7] Prince H.E., Kleinman S., Czaplicki C., John J., Williams A.E., Interrelationships between serologic markers of immune activation and T lymphocyte subsets in HIV infection, J. Acquired Immune Defic. Syndr., 3, pp. 525-530, (1990)
  • [8] Giorgi J.V., Detels R., T-cell subset alterations in HIV-infected homosexual men: NIAlD multicenter AIDS cohort study, Clin. Immunol. Immunopathol., 52, pp. 10-18, (1989)
  • [9] Teitel J.M., Freedman J.J., Garvey M.B., Kardish M., Two-year evaluation of clinical and laboratory variables of immune function in 117 hemophiliacs seropositive or seronegative for HIV-1, Am. J. Hematol., 32, pp. 262-272, (1989)
  • [10] Froebel K.S., Doherty K.V., Whitelaw J.A., Hague R.A., Mok J.Y., Bird A.G., Increased expression of the CD45RO (memory) antigen on T cells in HIV-infected children, AIDS (Phila.), 5, pp. 97-99, (1991)