Ullum H, Lepri A C, Victor J, Skinhøj P, Phillips A N, Pedersen B K
Department of Infectious Diseases, Rhima Centre, Rigshospitalet, Copenhagen, Denmark.
AIDS. 1997 Oct;11(12):1479-85. doi: 10.1097/00002030-199712000-00012.
To examine changes in the distribution of CD4+CD45RA+ (naive) and CD4+CD45RO+ (memory) lymphocytes in various stages of HIV infection and the effect of these changes on disease progression.
Expression of CD45RA+ and CD45RO+ on CD4+ lymphocytes was analysed by flow cytometry in a prospectively followed cohort of 300 HIV-infected individuals (median follow-up time, 2.90 years; range, 0.02-4.54 years) and in a group of 102 age- and sex-matched uninfected controls. Survival analysis was performed considering AIDS development and death as endpoints.
The median CD4+CD45RA+/CD45RO+ ratio was 1.3 (25-75% quartiles, 0.9-2.4) in controls; it was increased to 1.8 (1.1-2.5) in 40 HIV-infected individuals with CD4+ cell counts > 500 x 10(6)/l (P < 0.05); it was similar at 1.4 (0.8-2.0) in 106 HIV-infected individuals with CD4+ cell counts of 200-500 x 10(6)/l; and it was decreased to 0.9 (0.5-1.4) in 154 HIV-infected individuals with CD4+ cell counts < 200 x 10(6)/l (P < 10[-6]). When fitted in a Cox model adjusting for the total number of CD4+ cells and age a lower concentration of CD4+CD45RA+ cells was associated with an increased risk of dying. The concentration of CD4+CD45RO+ cells was not significantly associated with AIDS or death in age- and CD4+ cell count-adjusted Cox models.
This study confirms a selective loss of memory CD4+ cells early in HIV infection followed by increased loss of naive CD4+ cells in later stages of the infection. The loss of naive CD4+ cells seems to be important in the pathogenesis of terminal HIV infection.
研究HIV感染各阶段CD4+CD45RA+(初始)和CD4+CD45RO+(记忆)淋巴细胞分布的变化及其对疾病进展的影响。
采用流式细胞术分析300例HIV感染患者(中位随访时间2.90年;范围0.02 - 4.54年)前瞻性队列以及102例年龄和性别匹配的未感染对照人群中CD4+淋巴细胞上CD45RA+和CD45RO+的表达。以艾滋病发病和死亡为终点进行生存分析。
对照组CD4+CD45RA+/CD45RO+比值中位数为1.3(四分位数间距25 - 75%,0.9 - 2.4);40例CD4+细胞计数>500×10⁶/l的HIV感染患者该比值增至1.8(1.1 - 2.5)(P<0.05);106例CD4+细胞计数为200 - 500×10⁶/l的HIV感染患者该比值为1.4(0.8 - 2.0),无明显差异;154例CD4+细胞计数<200×10⁶/l的HIV感染患者该比值降至0.9(0.5 - 1.4)(P<10⁻⁶)。在调整CD4+细胞总数和年龄的Cox模型中,较低浓度的CD4+CD45RA+细胞与死亡风险增加相关。在调整年龄和CD4+细胞计数的Cox模型中,CD4+CD45RO+细胞浓度与艾滋病或死亡无显著关联。
本研究证实HIV感染早期记忆性CD4+细胞选择性丢失,随后感染后期初始CD4+细胞丢失增加。初始CD4+细胞的丢失似乎在晚期HIV感染发病机制中起重要作用。