CMV plus Serostatus Associates Negatively with CD4:CD8 Ratio Normalization in Controlled HIV-Infected Patients on cART

被引:21
|
作者
Poizot-Martin, Isabelle [1 ,2 ]
Allavena, Clotilde [3 ]
Duvivier, Claudine [4 ,5 ,6 ]
Cano, Carla Eliana [1 ]
de Salvador, Francine Guillouet [7 ]
Rey, David [8 ]
Dellamonica, Pierre [9 ]
Cuzin, Lise [10 ]
Cheret, Antoine [11 ,12 ]
Hoen, Bruno [13 ,14 ]
机构
[1] Aix Marseille Univ, APHM Hop St Marguerite, Immunohematol Clin, Marseille, France
[2] INSERM, U912, SESSTIM, Marseille, France
[3] CHU Hotel Dieu, Serv Malad Infect, Nantes, France
[4] Univ Paris 05, IHU Imagine Paris, AP HP, Hop Necker,Serv Malad Infect & Trop,Ctr Infectiol, Paris, France
[5] Inst Pasteur, Ctr Med, Ctr Infectiol Necker Pasteur, Paris, France
[6] Univ Paris 05, Sorbonne Paris Cite, EA7327, Paris, France
[7] CHU Archet 1, Serv Malad Infect & Trop, Nice, France
[8] Hop Univ Strasbourg, Ctr HIV Care, Strasbourg, France
[9] Univ Nice Sophia Antipolis, CHU Nice, Dept Infect Dis, Nice, France
[10] Toulouse III Univ, INSERM, CHU Toulouse, COREVIH Toulouse,UMR 1027, F-31000 Toulouse, France
[11] Paris Descartes Univ, Sorbonne Paris Cite, EA 3620, Paris, France
[12] Necker Enfants Malades Hosp, Virol Lab, Paris, France
[13] Univ Antilles, Fac Med Hyacinthe Bastaraud, EA 4537, Pointe A Pitre, Guadeloupe, France
[14] CHU Pointe a Pitre, INSERM, Serv Malad Infect & Trop, CIC1424,Dermatol,Med Interne, Pointe A Pitre, Guadeloupe, France
来源
PLOS ONE | 2016年 / 11卷 / 11期
关键词
T-CELL-ACTIVATION; ANTIRETROVIRAL THERAPY; CD4/CD8; RATIO; LARGE COHORT; INFLAMMATION; INDIVIDUALS; MORTALITY; RECOVERY; CD4(+);
D O I
10.1371/journal.pone.0165774
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cytomegalovirus (CMV) infection is common among HIV-infected patients but its repercussion on the course of CD4+ and CD8+ T cells after cART initiation remains elusive. The French Dat'AIDS cohort enrolled 5,688 patients on first-line cART, from which we selected patients who achieved HIV suppression for at least 12 months without modification of cART, and for whom CMV serostatus was available. Five hundred and three patients fulfilled the selection criteria (74% male, median age 43 yrs, 15.5% CDC stage C), of whom 444 (88.3%) were seropositive for CMV (CMV+). Multivariate analyses using mixed-linear models adjusted for the time from HIV suppression, sex, age, transmission risk group, duration of HIV follow-up, the interaction between time from HIV suppression and CMV+ serology, and the nadir CD4 count revealed a negative correlation between CMV+ and CD4: CD8 ratio (coeff. = -0.16; p = 0.001). This correlation was also observed among patients displaying optimal CD4 recovery (>= 500 cells/mm3 at M12; coeff. = -0.24; p = 0.002). Hence, CMV+ serostatus antagonizes normalization of the CD4: CD8 ratio, although further analyses of the impact of co-morbidities that associate with CMV serostatus, like HCV infection, are needed to elucidate this antagonism formally. However, this might reflect a premature T cell senescence, thus advocating for a close monitoring of T cells in CMV co-infected patients. In addition, our results raise the question of the benefit of treatment for asymptomatic CMV co-infection in HIV-infected patients.
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页数:12
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