CD4/CD8 ratio normalisation and non-AIDS-related events in individuals with HIV who achieve viral load suppression with antiretroviral therapy: an observational cohort study

被引:252
|
作者
Mussini, Cristina [1 ]
Lorenzini, Patrizia [2 ]
Cozzi-Lepri, Alessandro [3 ]
Lapadula, Giuseppe [4 ]
Marchetti, Giulia [5 ]
Nicastri, Emanuele [2 ]
Cingolani, Antonella [6 ]
Lichtner, Miriam [7 ]
Antinori, Andrea [2 ]
Gori, Andrea [4 ]
Monforte, Antonella d'Arminio [5 ]
机构
[1] Univ Modena & Reggio Emilia, Clin Infect Dis, Modena, Italy
[2] Natl Inst Infect Dis, Rome, Italy
[3] UCL, Hlth Div Populat Hlth, Dept Infect & Populat, London, England
[4] Univ Milano Bicocca, San Gerardo Hosp, Dept Infect Dis, Monza, Italy
[5] Univ Milan, San Paolo Hosp, Dept Hlth Sci, Clin Infect Dis, Milan, Italy
[6] Univ Cattolica Sacro Cuore, Clin Infect Dis, Rome, Italy
[7] Univ Roma La Sapienza, Dept Publ Hlth & Infect Dis, Polo Pontino, Italy
来源
LANCET HIV | 2015年 / 2卷 / 03期
关键词
T-CELL-ACTIVATION; CLINICAL PROGRESSION; IMMUNE PARAMETERS; INFECTED PATIENTS; OLD POPULATION; SWEDISH PEOPLE; MORTALITY; INFLAMMATION; RISK; COAGULATION;
D O I
10.1016/S2352-3018(15)00006-5
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background In patients with HIV, immune reconstitution after antiretroviral therapy (ART) is often incomplete. We assessed the probability of patients reaching a CD4/CD8 ratio of 1 or more after the start of ART and its association with the onset of non-AIDS-defi ning events and death. Methods We did an analysis of the ICONA cohort, which recruited treatment-naive patients with HIV in Italy. We included participants in the cohort who started ART, reached an undetectable viral load (<= 80 copies per mL), and had a CD4/CD8 ratio of less than 0.8 at the time of an undetectable viral load. We defined ratio normalisation in patients as two consecutive values of 1 or more. We used Kaplan-Meier curves to estimate the cumulative probability of ratio normalisation. We then used Poisson regression models to identify factors independently associated with normalisation and with progression to non-AIDS-defi ning events or death. Findings We included 3236 participants, enrolled between Jan 22, 1997, and Feb 25, 2013. At the start of ART, median CD4/CD8 ratio in our population was 0.39 (IQR 0.26-0.55). 458 (14%) patients reached a CD4/CD8 ratio of 1 or more; the estimated probability of normalisation was 4.4% (95% CI 3.7-5.2) by 1 year from baseline, 11.5% (10.2-13.0) by 2 years, and 29.4% (26.7-32.4) by 5 years. Factors associated with normalisation were high pre-ART CD4 cell counts, a high CD4/CD8 ratio at baseline, and negative cytomegalovirus serological findings. The incidence rate of non-AIDS-defi ning events for patients with a CD4/CD8 ratio of less than 0.30 (4.2 per 100 patient-years, 95% CI 3.4-5.3) was double that for those with a ratio of 0.30-0.45 (2.3, 2.1-2.5) or more than 0.45 (2.2, 1.7-2.9). A ratio of less than 0.30 was independently associated with an increased risk of non-AIDS-defi ning events or death compared with one of more than 0.45. Interpretation Few patients had normalised CD4/CD8 ratios, even though they had viral suppression. Low ratios were associated with increased risk of serious events and deaths. The CD4/CD8 ratio could be used by clinicians to identity patients at risk of non-AIDS-related events.
引用
收藏
页码:E98 / E106
页数:9
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