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. 2022 Apr 20;13:822272. doi: 10.3389/fimmu.2022.822272

Table 1.

Baseline characteristics of the study participants.

Clinical characteristics No-LTEC (n = 9) LTEC-losing (n = 20) LTEC-extreme (n = 13) p-Value*
Age (years) 37 [34–45] 46 [43–50] 48 [42–51] 0.075
Time of control (years) 2.5 [1.3–3.3] 13.7 [8.6–17.1] 14.3 [13.2–15.6] <0.001
Male 5 (55.6) 8 (40) 9 (69.2) 0.262
HIV risk factor 0.141
Heterosexual 6 (66.7) 6 (30) 2 (15.4)
Homo/bisexual 1 (11.1) 2 (10)
Intravenous drug abuse 2 (22.2) 10 (50) 10 (76.9)
Other/unknown 2 (10) 1 (7.7)
CD4+ T-cell count (cells/µl) 724 [430–1029] 756 [646–1041] 830 [522–1028] 0.772
CD4 count slope (cells/month) −0.35 [−1.23 to 0.99] −1.98 [−2.80 to −1.31] 0.012
HIV viral load (log) 1.6 [1.45–1.7] 1.7 [1.6–1.7] 1.6 [1.3–1.7] 0.337
HCV coinfection (positive) 3 (33.3) 13 (65) 13 (100) 0.003
Active HCV coinfection (positive) 1 (11.1) 10 (50) 10 (77) 0.010

All plasma samples analyzed were obtained before the loss of HIV control (in the case of no-LTEC and LTEC-losing groups) compared to LTEC-extreme. Data are presented as n (%) or median (interquartile range). Categorical data were compared through a χ2 test, whereas continuous data were compared using the non-parametric Kruskal–Wallis test*. (P values < 0.05 in bold).

no-LTEC, no long-term elite controllers; LTEC-losing, long-term elite controllers patients who lost HIV control during follow-up; LTEC-extreme, long-term elite controllers patients maintaining HIV control during the whole follow-up and for more than 10 years.