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. Author manuscript; available in PMC: 2018 Jul 1.
Published in final edited form as: Clin Immunol. 2017 Apr 18;180:69–79. doi: 10.1016/j.clim.2017.04.006

Table 1.

Characteristics of HIV-1-infected black South African study participants classified according different clinical phenotypes of HIV-1 disease control

Clinical Phenotype Group n Age (years) Gender (%females) CD4+ T cell counts(cells/μl)1 (Median and IQR) Viral load(HIV RNA copies/ml)1 (Median and IQR) logVL (Median and IQR) Time since HIV-1 diagnosis (years) (Median and IQR)
Elite controllers (ECs) 11 44 (19–54) 81.8 853 (718 – 1022) <40 (<40 (n=2), <20 (n=9)) - 11 9–12)
Viraemic controllers (VCs) 30 36 (19–46) 90.0 651 (555–832)2 495 (327 - 965)3 2.69 (2.51–2.98) 3 (0–10.35)
High viral load long term nonprogressors (HVL LTNPs) 11 41 (31–51) 81.8 663 (635–749) 54 375 (13 415–77 820) 4.74 (4.12–4.89) 8 (8–11)
Progressors 72 38 (24–66) 83.3 177 (146–210) 38 444 (19–853–103 042) 4.58 (4.30–5.01) 6 (1–7)
1

CD4+ T cell counts and viral loads of controllers used were from time of enrolment whereas for the progressors the last CD4+ T cell count and viral load prior to ART initiation was used.

2

Three individuals had CD4+ T cell counts <500 cells/μl at time of enrolment; however were included based on length of time of infection since diagnosis to time of enrolment, in the absence of ART (≥9 years).

3

One individual had a VL>2 000 (VL=6070), but was classified as a VC also due to length of infection since diagnosis with viral control in the absence of ART (9 years).