Phillips A N, Sabin C A, Elford J, Bofill M, Lee C A, Janossy G
Department of Public Health and Primary Care, Royal Free Hospital and School of Medicine, London, UK.
AIDS. 1993 Jul;7(7):975-80. doi: 10.1097/00002030-199307000-00011.
To assess the ability of the CD8 lymphocyte count and immunoglobulin (Ig) A level, measured at the early stage of HIV infection when the CD4 lymphocyte count remains relatively high, to predict the future rate of CD4 lymphocyte loss and hence the risk of AIDS.
Cohort of recently infected haemophiliacs with relatively high CD4 lymphocyte counts followed for up to 8.5 years from baseline measurement of CD8 lymphocyte counts and IgA levels.
A regional haemophilia centre based in a major teaching hospital.
Eighty-four of 111 patients with haemophilia who seroconverted to HIV between 1979 and 1985 in whom CD8 lymphocyte counts and IgA levels were measured soon after seroconversion (mean, 2.7 years; maximum, 5 years) while CD4 lymphocyte counts remained relatively high (median, 600 x 10(6)/l; minimum, 300 x 10(6)/l).
Development of severe immunodeficiency defined by a CD4 lymphocyte count falling below 50 x 10(6)/l, and AIDS.
Individuals with high CD8 counts (P < 0.008) and high IgA levels (P < 0.003) at baseline experienced a more rapid rate of CD4 lymphocyte loss than those with low baseline levels. A score was derived to combine the predictive ability of CD8 count and IgA level. Estimated proportions with CD4 counts below 50 x 10(6)/l after 8 years of follow-up were 100, 30 and 14% for those with high, intermediate and low baseline scores, respectively. The CD8/IgA score showed similar ability to predict the future occurrence of AIDS (P < 0.0001; log-rank test).
Immune activation seen in HIV infection, as reflected by raised CD8 counts and IgA levels, appears to be linked to the process of CD4 lymphocyte depletion. Measurement of these markers in the years following infection, when CD4 lymphocyte counts remain high, provides a first indication of a patient's long-term prognosis.
评估在HIV感染早期,当CD4淋巴细胞计数仍相对较高时所测得的CD8淋巴细胞计数和免疫球蛋白(Ig)A水平预测未来CD4淋巴细胞丢失率以及艾滋病风险的能力。
对近期感染且CD4淋巴细胞计数相对较高的血友病患者队列进行研究,从基线测量CD8淋巴细胞计数和IgA水平开始随访长达8.5年。
一家大型教学医院的地区血友病中心。
1979年至1985年间血清转化为HIV阳性的111例血友病患者中的84例,在血清转化后不久(平均2.7年;最长5年)测量了CD8淋巴细胞计数和IgA水平,此时CD4淋巴细胞计数仍相对较高(中位数为600×10⁶/l;最低为300×10⁶/l)。
以CD4淋巴细胞计数降至50×10⁶/l以下定义的严重免疫缺陷的发生情况以及艾滋病。
基线时CD8计数高(P<0.008)和IgA水平高(P<0.003)的个体比基线水平低的个体CD4淋巴细胞丢失速度更快。得出一个分数来综合CD8计数和IgA水平的预测能力。随访8年后,基线分数高、中、低的患者CD4计数低于50×10⁶/l的估计比例分别为100%、30%和14%。CD8/Iga分数在预测未来艾滋病发生方面显示出相似的能力(P<0.0001;对数秩检验)。
如CD8计数升高和IgA水平升高所反映的HIV感染中出现的免疫激活似乎与CD4淋巴细胞耗竭过程有关。在感染后的几年里,当CD4淋巴细胞计数仍较高时测量这些标志物,可为患者的长期预后提供初步指示。