CD8(+),CD38(+) lymphocyte percent: A useful immunological marker for monitoring HIV-1-infected patients

被引:103
作者
Mocroft, A
Bofill, M
Lipman, M
Medina, E
Borthwick, N
Timms, A
Batista, L
Winter, M
Sabin, CA
Johnson, M
Lee, CA
Phillips, A
Janossy, G
机构
[1] ROYAL FREE HOSP,SCH MED,DEPT IMMUNOL,LONDON NW3 2PF,ENGLAND
[2] ROYAL FREE HOSP,SCH MED,DEPT THORAC MED,LONDON NW3 2PF,ENGLAND
[3] ROYAL FREE HOSP,SCH MED,DEPT HAEMATOL,HAEMOPHILIA CTR,LONDON NW3 2PF,ENGLAND
来源
JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES AND HUMAN RETROVIROLOGY | 1997年 / 14卷 / 02期
关键词
CD4 lymphocyte count; beta; 2-microglobulin; CD8(+); CD38(+) lymphocyte subset; patient monitoring;
D O I
10.1097/00042560-199702010-00009
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We investigated the relationship between three prognostic markers, CD4 lymphocyte count, serum beta(2)-microglobulin (beta 2(M)) levels, and CD8(+),CD38(+) lymphocyte percent, and the association with the rate of development of AIDS. The markers were measured regularly throughout follow-up in 224 patients. The risk of developing AIDS during follow-up was investigated using Cox proportional hazards models. Time-updated values of the prognostic markers were used, which modelled the risk of AIDS according to the latest measurement of the marker rather than using a single value of the marker at baseline. During a median follow-up period of 13.6 months (range 0.5-31.9 months), 34 cases of AIDS occurred. In a univariate analysis, all three markers predicted the development of AIDS; a 10% increase in the percentage of CD8(+) T cells expressing CD38(+) resulted in an 88% increase in the risk of AIDS (95% confidence interval: 53-130%; p < 0.0001). After adjustment for the current CD4 count and beta(2)M, a 10% increase in the CD8(+),CD38(+) population was associated with a 37% increase in the risk of AIDS (95% confidence interval: 4-81%; p = 0.02). Thus, the percentage CD8(+),CD38(+) level predicts the development of AIDS independently of the latest CD4 count and beta(2)M. This assay is therefore potentially useful in conjunction with blood CD4 counts and serum beta(2)M levels in patient management and clinical trial design.
引用
收藏
页码:158 / 162
页数:5
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