CD4 cell count recovery among HIV-infected patients with very advanced immunodeficiency commencing antiretroviral treatment in sub-Saharan Africa
© Lawn et al; licensee BioMed Central Ltd. 2006
Received: 27 January 2006
Accepted: 21 March 2006
Published: 21 March 2006
Patients accessing antiretroviral treatment (ART) programmes in sub-Saharan Africa frequently have very advanced immunodeficiency. Previous data suggest that such patients may have diminished capacity for CD4 cell count recovery.
Rates of CD4 cell increase were determined over 48 weeks among ART-naïve individuals (n = 596) commencing ART in a South African community-based ART programme.
The CD4 cell count increased from a median of 97 cells/μl at baseline to 261 cells/μl at 48 weeks and the proportion of patients with a CD4 cell count <100 cells/μl decreased from 51% at baseline to just 4% at 48 weeks. A rapid first phase of recovery (0–16 weeks, median rate = 25.5 cells/μl/month) was followed by a slower second phase (16–48 weeks, median rate = 7.7 cells/μl/month). Compared to patients with higher baseline counts, multivariate analysis showed that those with baseline CD4 counts <50 cells/μl had similar rates of phase 1 CD4 cell recovery (P = 0.42), greater rates of phase 2 recovery (P = 0.007) and a lower risk of immunological non-response (P = 0.016). Among those that achieved a CD4 cell count >500 cells/μl at 48 weeks, 19% had baseline CD4 cell counts <50 cells/μl. However, the proportion of these patients that attained a CD4 count 200 cells/μl at 48 weeks was lower than those with higher baseline CD4 cell counts.
Patients in this cohort with baseline CD4 cell counts <50 cells/μl have equivalent or greater capacity for immunological recovery during 48 weeks of ART compared to those with higher baseline CD4 cell counts. However, their CD4 counts remain <200 cells/μl for a longer period, potentially increasing their risk of morbidity and mortality in the first year of ART.
The World Health Organisation (WHO) estimated that in June 2005 4.7 million people living in sub-Saharan Africa were in urgent need of antiretroviral treatment (ART) . Despite formidable logistical hurdles, the number of individuals able to access this treatment in the region is expanding. One of the programmatic challenges facing ART services in sub-Saharan Africa is that many HIV-infected patients only access healthcare once they have developed advanced symptomatic disease  and this delay may be further compounded by health-systems delays. The median CD4 cell count among those enrolling in ART programmes is often under 100 cells/μl even where programmes have been well established for several years [3–5].
Patients enrolling into ART programmes with very low CD4 cell counts have heightened risk of morbidity and mortality both before and during the initial months of ART [5–8]. Moreover, advanced pre-treatment immunodeficiency is also reported to be associated with diminished capacity for restoration of CD4 cell counts and CD4 cell functional responses during ART [9–14]. This raises the concern that many patients entering ART programmes in sub-Saharan Africa may have limited potential for immune recovery. Although previous studies from sub-Saharan Africa have reported overall CD4 cell count responses [3, 15, 16], there are no published data from the region regarding rates of CD4 cell recovery and rates of immunological non-response to ART among patients with CD4 cell <50 cells/μl.
In this study we have examined determinants of CD4 cell count recovery among patients accessing a community-based antiretroviral programme in South Africa. We focus on the hypothesis that advanced pre-treatment immunodeficiency diminishes the capacity for CD4 cell count recovery during ART as determined by rates of CD4 cell count increase and risk of immunological non-response.
We studied patients accessing ART at the Gugulethu Community Health Centre, Cape Town, South Africa . The vast majority of patients receiving treatment at this clinic live in conditions of low socioeconomic status and HIV transmission is predominantly heterosexual. The South African national ART programme guidelines are based on the World Health Organisation (WHO) 2002 recommendations , with criteria for ART including those with a prior AIDS diagnosis (WHO stage 4 disease) or a blood CD4 cell count <200 cells/μl.
The first-line ART regimen was comprised of stavudine, lamivudine plus a non-nucleoside reverse transcriptase inhibitor (efavirenz or nevirapine). The second-line regimen for those failing first-line treatment was comprised of lopinavir/ritonavir, zidovudine and didanosine. Treatment adherence exceeds 90% at one year . All treatment was free of charge and there were no interruptions in drug supply. All patients with CD4 counts <200 cells/μl received daily cotrimoxazole prophylaxis; dapsone was used as an alternative.
Plasma HIV-1 load was measured at baseline and 4 monthly during treatment using Versant™ HIV-1 RNA 3.0 branched chain DNA assay (Bayer HealthCare, Leverkusen, Germany) with a lower limit of detection of 50 RNA copies/ml. Blood CD4 cell counts were measured at the same time-points by flow cytometry using FACSCount™ (Becton Dickinson Inc., Franklin Lakes, NJ, USA). These assays were all performed in a single nationally accredited laboratory which has rigorous quality assurance procedures.
Structured clinical and laboratory records were maintained on all patients screened on entry to the ART programme and this information was transferred on a weekly basis to a computer database. Data were analysed from the start of the programme in September 2002 until data censorship in August 2005. All treatment-naive patients aged over 15 years and with at least a 16-week follow-up time point were included in the analysis. Study of these patients was in compliance with the Declaration of Helsinki and was approved by the Research Ethics Committee of the University of Cape Town; all patients enrolled gave written informed consent.
Data were analysed using Stata version 9.0 (College Station, Texas, USA). We calculated absolute responses in CD4 cell counts during three intervals (from baseline to 16 weeks of ART, 16 to 32 weeks, and 32 to 48 weeks), as well as rates of CD4 cell increase (cells/μl/month) during each interval. The first interval was used as an estimate of the initial (phase 1) response to ART. The CD4 cell count responses observed during the latter two intervals (16 to 32 and 32 to 48 weeks after treatment initiation) were very similar, and were combined into a single measure of the second phase of CD4 cell responses (phase 2).
We further evaluated CD4 cell responses in the following ways: i) whether patients failed to attain an absolute CD4 cell count increase from baseline of at least 50 cells/μl at 48 weeks (defined as immunological non-response); ii) whether patients achieved an absolute CD4 count of 200 cells/μl at the 48 week visit; iii) and whether patients had achieved an absolute CD4 cell count of 500 cells/μl at 48 weeks (super-responders).
In bivariate analyses, medians were compared using Wilcoxon rank-sum and sign-rank tests; proportions were compared using chi-square tests. All statistical tests were two-sided at alpha = 0.05. Separate multiple linear regression models were used to examine factors associated with rates of CD4 cell count increase per month during the first and second phases. Baseline CD4 cell counts were categorised as follows: <50, 50–99, 100–149 and >150 cells/μl. Multiple logistic regression was used to assess factors associated with the binary outcomes of a CD4 cell increase of ≥ 50 cells/μl and ≥ 100 cells/μl during the 48 weeks of ART, as well as achieving an absolute CD4 cell count of ≥ 200 cells/μl during follow-up. Variables were included in multivariate models if they demonstrated a persistent association with the outcome of interest, or if their removal affected appreciably associations involving other variables .
Baseline characteristics and follow-up
Of 698 individuals who commenced ART between September 2002 and April 2005, 596 (85%) had completed a 16-week follow-up visit at the time of data censorship, 34 (5%) were awaiting this appointment, 48 (7%) had died and 20 (3%) were either transferred out or were lost to follow-up. Of the 596 individuals who met the inclusion criteria for the study, 580 (97%) remained within the programme at study censorship, 11 (2%) died and 7 (1%) were lost from the programme.
At baseline the median age was 32 years (IQR, 28–38) and 75% were female. The median plasma viral load was 4.88 log10 RNA copies/ml (IQR, 4.50–5.27) and 58% of patients had a viral load >100,000 copies/ml. The median blood CD4 cell count was 97 cells/μl (IQR, 50–153) and the proportions of patients with CD4 cell counts within the ranges <50, 50–99, 100–149 and ≥ 150 cells/μl were 25%, 26%, 23% and 26%, respectively. Eighty per cent of patients had symptomatic disease, with 53% and 27% of patients having WHO stages 3 and 4 disease, respectively. During follow-up, only 7 (1%) patients switched to the second-line drug regimen.
Virological and CD4 cell responses to ART
Changes in blood CD4 cell counts and plasma viral load during ART.
No. of patients
Number (%) patients wilh VL ≥ 400
Number (%) patients with VL ≥ 50
CD4 Cell Count Response
Median (IQR) CD4 cell count (cells/μl)
226 (162, 314)
261 (193, 363)
Median (IQR) CD4 cell slope in preceding interval (cells/μl/month)
25.5 (12.7, 42.9)
7.5 (-4.6, 19.8)
7.9 (-3.0, 20.0)
The rate of CD4 cell count increase in the first 16 week period greatly exceeded the rates in both the 16–32 week and 32–48 week intervals, but the rates did not differ comparing the latter two intervals. Thus, the pattern of CD4 cell count increase was divided into 2 phases: a ra–pid phase 1 (0–16 weeks; median = 25.5 cells/μl/month) and a slower phase 2 (16–48 weeks; median = 7.7 cells/μl/month).
Baseline characteristics and rates of CD4 cell count change in phase 1 and phase 2 did not differ when comparing the results of analyses of all eligible patients with those restricted to subjects who had data for every time-point (n = 292); this was also the case for all subsequent stratified analyses. Use of data from the larger cohort (n = 596) was therefore validated.
Effect of baseline CD4 cell count on rates of CD4 cell increases
Multiple linear regression models estimating the average change in CD4 cell count per month (CD4 slope). Separate models analyse the first (0 – 16 weeks) and second (16 – 48 weeks) phases of immune recovery during ART.
Phase 1 (0–16 weeks) CD4 slope (n = 596)
Phase 2 (16–48 weeks) CD4 slope (n = 311)1
(-12.11, -2. 50)
Baseline CD4 coimt (cells/μl)
WHO clinical stage
1 & 2
Baseline viral load (copies/ml)
In the multivariate model predicting rates of phase 2 CD4 cell increase, factors associated with the response to ART during the first 16 weeks were also included. A lower rate of phase 1 CD4 cell increase and full suppression of viral load at 16 weeks were both strongly associated with greater rate of phase 2 CD4 cell increase. Viral load suppression <400 copies/ml at 16 weeks was associated with a subsequent rate of CD4 cell increase of 6.8 cells/μl/month compared to 0.7 cells/μl/month among those whose viral load remained >400 copies/ml (P < 0.001).
Baseline CD4 cell count and risk of immunological non-response
Results of logistic regression models predicting overall change in blood CD4 cell count during ART. Responses are defined as either (i) the risk of immunological non-response (an increase of <50 cells/μl) or (ii) failure to attain an absolute CD4 cell count of ≥ 200 cells/μl after 48 weeks ART.
Risk of immumological non-respouse at 48 weeks
Risk of failure to attain CD4 cell count of ≥ 200 cells/μl at 48 weeks
Baseline CD4 count
WHO clinical stage
1 & 2
Baseline viral load
Follow-up viral load
<400 all visits
>400 any visit
Baseline CD4 cell count and failure to attain a CD4 cell count of ≥ 200 cells/μl
We next determined factors associated with failure to attain an absolute CD4 cell count of 200 cells/μl at 48 weeks. Although patients with a baseline CD4 cell count <50 cells/μl had similar rates of phase 1 CD4 cell recovery and greater rates of phase 2 CD4 cell recovery compared to those with higher baseline counts, such patients nevertheless had a reduced likelihood of attaining a CD4 cell count of 200 cells/μl at 48 weeks (Table 3). The proportions of patients with baseline CD4 cell counts of <50, 50–99, 100–149 and 150 cells/μl who failed to attain a CD4 cell count of 200 cells/μl at 48 weeks were 49%, 35%, 18%, and 9%, respectively. Failure to attain 200 cells/μl was also significantly associated with older age, lower baseline plasma viral load, and a viral load >400 copies/ml at any follow-up time-point (Table 3).
Of 311 patients studied out to 48 weeks, 21 (6.8%) achieved an absolute CD4 cell count of >500 cells/μl. These super-responders were principally characterised by age <40 years and by all having follow-up viral loads persistently suppressed <50 copies/ml and a CD4 cell count of 150 cells/μl after 16 weeks of ART. This group of patients had a wide distribution of baseline CD4 cell counts, and included among them were 4 (19%) who had baseline CD4 cell counts of <50 cells/μl. Thus, a low baseline CD4 cell count did not preclude patients from having an excellent immunological response.
To our knowledge this is the first analysis to examine the determinants of CD4 cell count recovery among patients receiving ART in resource limited settings. These data indicate that those with baseline CD4 cell counts <50 cells/μl had similar rates of phase 1 CD4 recovery (0–16 weeks) and greater rates of phase 2 recovery (16–48 weeks) compared to rates among those with higher baseline CD4 cell counts. Moreover, those with the lowest baseline counts were least likely to be immunological non-responders to ART. Despite these observations, those with baseline CD4 cell counts <50 cells/μl were nevertheless least likely to attain a CD4 cell count 200 cells/μl at 48 weeks. Taken together, these results suggest that although patients with very low baseline CD4 cell counts retain capacity for similar or slightly greater rates of CD4 cell count recovery compared to those with higher counts, they are nevertheless likely to require a longer period of time to attain a CD4 cell count threshold of 200 cells/μl. Thus, a prolonged period below a 'safe' CD4 cell count threshold rather than a diminished rate of immunological recovery is likely to underlie the high rates of morbidity and mortality observed among those with advanced disease during the early months of ART [4, 5, 8].
The findings of this analysis are strengthened by the relatively homogeneous study population receiving treatment at a single facility using standardised clinical protocols. Patients were all ART-naïve and received a standard triple-drug regimen with uniform follow-up time points. Quality-assured laboratory assays were all performed in a single nationally accredited laboratory. In contrast, previous studies of the determinants of CD4 cell count recovery have examined heterogeneous study populations in multiple centres and used diverse treatment regimens. Moreover, these studies included many patients with prior ART exposure [20–22] and some included only those who maintained suppression of plasma HIV load [9, 23, 24]. Our patient population was treated under the government ART roll-out programme and data are therefore likely to be generalisable to other ART programmes in sub-Saharan Africa. Our study is limited to analysis of CD4 cell recovery during the first year of ART and long-term outcomes and their sustainability remain to be determined. Moreover, in the present analysis we have examined recovery of CD4 cell counts but not CD4 cell functional responses.
The immunological response to ART among those with low CD4 cell counts was excellent with the proportion of patients with a CD4 cell count <100 cells/μl decreasing from 51% at baseline to just 4% at 48 weeks. However, our most important finding was that in multivariate analysis baseline CD4 cell counts <50 cells/μl were independently associated with similar rates of phase 1 CD4 cell recovery and greater rates of phase 2 CD4 cell recovery compared to individuals with higher baseline CD4 cell counts. This has not been clearly highlighted in previous publications from Europe and North America although comparison of our data with previous studies is difficult in view of differing cohort compositions. However, this overall observation is consistent with the findings of Bennett et al., and Le Moing et al. showed a similar but non-significant trend when comparing patients with baseline CD4 cell counts <200 cells/μl with those with higher counts . Kaufmann et al. found that CD4 cell increases in the first year of ART were similar comparing those with baseline counts <100 cells/μl with those with counts 100–199 cells/μl .
Survival bias could potentially have affected our findings. We have previously shown in this cohort that patients with the lowest baseline CD4 cell counts had a higher risk of death  and immunological non-responders or poor responders may have a greater mortality risk, leading to a survivor effect. However, we were careful to ensure that rates of CD4 cell recovery in the CD4 cell strata did not differ when comparing analyses of the whole cohort with those for whom data points were available at every time-point. Secondly, WHO clinical stage of disease is the strongest predictor of death in this cohort  and yet this variable was not associated with CD4 cell responses. Thirdly, the majority of deaths occurred in the first few weeks of ART among those whose disease was simply too far advanced; such deaths probably do not reflect a lack of immunological response to ART. Finally, we have previously reported that over 20% of early deaths in this cohort are due to immune reconstitution disease [5, 25]; such deaths typically occur among those with low baseline CD4 cell counts and good CD4 cell recovery. These deaths would tend to cause exactly the opposite bias. Thus, although an important consideration, we do not think that survival bias had an overall dominant effect.
We have previously shown that low baseline CD4 count at entry to an ART programme was associated with increased risks of tuberculosis and of mortality during the first year of ART [5, 8]. Results from the present study suggest that these increased risks are likely to reflect an increased period of time required for such patients to achieve a 'safe' level of immune function rather than reflecting impaired rates of immune recovery and this is consistent with the findings of a study from Spain with longer term follow-up . More recently we have found that risk of mortality and risk of incident tuberculosis is strongly associated with the current CD4 cell count during ART rather than the baseline count (unpublished data). Thus, if patients with profound baseline CD4 lymphocytopenia survive the initial few months of treatment and achieve full viral load suppression, then high rates of immune recovery are likely to result in a better prognosis that might have been anticipated.
Rates of phase 1 and phase 2 CD4 cell increase were similar in magnitude to those previously reported from high-income countries [9, 20]. The rapid phase 1 CD4 cell recovery was strongly associated with baseline viral load as described previously [20, 21]; patients with viral loads >105 log10 copies/ml had 11-fold greater CD4 count increases than those with lower viral loads. Immune dysregulation and immune cell activation promote sequestration of CD4+CD45Ro+ memory T cells in lymphoid tissue; suppression of viral replication then triggers rapid redistribution of this cell pool and a reduction in apoptotic cell death during the initial weeks of ART [26, 27]. A positive correlation between the plasma viral load and the degree of cell sequestration may provide a possible mechanism underlying the observation that those with the highest viral loads have the greatest initial CD4 cell increment. The fact that patients with profound CD4 lymphocytopenia have good immunological recovery during ART is likely to be important in the pathogenesis of immune reconstitution disease associated with Mycobacterium tuberculosis, Cryptococcus neoformans that is frequently observed in this patient population.
Greater phase 2 CD4 cell recovery was strongly associated with age as reported elsewhere [9, 24]. Sustained suppression of viral replication is also critical to second phase recovery [20, 21] and we confirmed that viral load at 16 weeks was a strong independent predictor of subsequent immunological recovery. Ten per cent of patients were immunological non-responders (CD4 cell increment <50 cells/μl at 48 weeks) and 7% of patients had discordant responses, having immunological non-response despite a fully suppressed viral load. These rates are much lower than those reported in previous series from industrialised countries [14, 29], possibly because our study only included antiretroviral-naïve patients, rates of HIV primary drug resistance in this setting are likely to be low, and because rates of treatment adherence in our cohort are very high. However, those with CD4 cell counts <50 cells/μl were least likely to be immunological non-responders. Moreover, 19% of 'super-responders' had baseline CD4 cell counts <50 cells/μl, indicating that a very low baseline CD4 cell count does not preclude an excellent CD4 cell count response to ART.
Patients with the lowest CD4 counts in this setting do not have diminished capacity for immune recovery. Although patients with low baseline CD4 counts have increased risk of acute morbidity and mortality, if such patients survive the initial months of ART and fully suppress the viral load, their chances of immunological recovery are good during the first year. Future studies are required to determine the long-term prospects for immune recovery among patients treated in ART programmes in sub-Saharan Africa.
SDL is funded by the Wellcome Trust, London, UK with grant 074641/Z/04/Z. LM, LGB and RW are supported in part by National Institutes of Health CIPRA grant 1U19AI53217-01. The authors are grateful to staff at the Hannan Crusaid antiretroviral clinic in Gugulethu and to the staff of the Desmond Tutu HIV Centre at the University of Cape Town. Provision of ART at the programme was initially by Crusaid, London, UK and latterly by the Global Fund for Malaria, Tuberculosis and HIV/AIDS administered through a provincial grant.
- UNAIDS WHO: Progress of global access to HIV antiretroviral therapy. An update on '3 by 5'. June 2005. 2005, http://www.who.int/hiv/pub/progressreports/3by5%20Progress%20Report_E_light.pdf-Accessed 19.10.05.
- Lawn SD, Wood R: How can earlier entry of patients into antiretroviral programs in low-income countries be promoted?. Clin Infect Dis. 2006, 42: 431-432. 10.1086/499527.View ArticlePubMed
- Coetzee D, Hildebrand K, Boulle A, Maartens G, Louis F, Labatala V, Reuter H, Ntwana N, Goemaere E: Outcomes after two years of providing antiretroviral treatment in Khayelitsha, South Africa. AIDS. 2004, 18: 887-895. 10.1097/00002030-200404090-00006.View ArticlePubMed
- Colebunders R, Ronald A, Katabira E, Sande M: Rolling out antiretrovirals in Africa: there are still challenges ahead. Clin Infect Dis. 2005, 41: 386-389. 10.1086/431490.View ArticlePubMed
- Lawn SD, Myer L, Orrell C, Bekker LG, Wood R: Early mortality among adults accessing a community-based antiretroviral service in South Africa: implications for programme design. AIDS. 2005, 19: 2141-2148.View ArticlePubMed
- Bottieau E, Noe A, Florence E, Ostyn B, Colebunders R: Development of multiple abscesses in an HIV/TB co-infected patient after initiation of antituberculous and highly active antiretroviral therapy. Acta Clin Belg. 2002, 57: 219-222.View ArticlePubMed
- Wood R, Maartens G, Lombard CJ: Risk factors for developing tuberculosis in HIV-1-infected adults from communities with a low or very high incidence of tuberculosis. J Acquir Immune Defic Syndr. 2000, 23: 75-80.View ArticlePubMed
- Lawn SD, Badri M, Wood R: Tuberculosis among HIV-infected patients receiving HAART: long term incidence and risk factors in a South African cohort. AIDS. 2005, 19: 2109-2116.View ArticlePubMed
- Kaufmann GR, Bloch M, Finlayson R, Zaunders J, Smith D, Cooper DA: The extent of HIV-1-related immunodeficiency and age predict the long-term CD4 T lymphocyte response to potent antiretroviral therapy. AIDS. 2002, 16: 359-367. 10.1097/00002030-200202150-00007.View ArticlePubMed
- Lange CG, Valdez H, Medvik K, Asaad R, Lederman MM: CD4+ T-lymphocyte nadir and the effect of highly active antiretroviral therapy on phenotypic and functional immune restoration in HIV-1 infection. Clin Immunol. 2002, 102: 154-161. 10.1006/clim.2001.5164.View ArticlePubMed
- Garcia F, de Lazzari E, Plana M, Castro P, Mestre G, Nomdedeu M, Fumero E, Martinez E, Mallolas J, Blanco JL, Miro JM, Pumarola T, Gallart T, Gatell JM: Long-term CD4+ T-cell response to highly active antiretroviral therapy according to baseline CD4+ T-cell count. J Acquir Immune Defic Syndr. 2004, 36: 702-713.View ArticlePubMed
- Lederman HM, Williams PL, Wu JW, Evans TG, Cohn SE, McCutchan JA, Koletar SL, Hafner R, Connick E, Valentine FT, McElrath MJ, Roberts NJJ, Currier JS: Incomplete immune reconstitution after initiation of highly active antiretroviral therapy in human immunodeficiency virus-infected patients with severe CD4+ cell depletion. J Infect Dis. 2003, 188: 1794-1803. 10.1086/379900.View ArticlePubMed
- Lange CG, Lederman MM, Medvik K, Asaad R, Wild M, Kalayjian R, Valdez H: Nadir CD4+ T-cell count and numbers of CD28+ CD4+ T-cells predict functional responses to immunizations in chronic HIV-1 infection. AIDS. 2003, 17: 2015-2023. 10.1097/00002030-200309260-00002.View ArticlePubMed
- Moore DM, Hogg RS, Yip B, Wood E, Tyndall M, Braitstein P, Montaner JS: Discordant Immunologic and Virologic Responses to Highly Active Antiretroviral Therapy Are Associated With Increased Mortality and Poor Adherence to Therapy. J Acquir Immune Defic Syndr. 2005, 40: 288-293. 10.1097/01.qai.0000182847.38098.d1.View ArticlePubMed
- Laurent C, Diakhate N, Gueye NF, Toure MA, Sow PS, Faye MA, Gueye M, Laniece I, Toure KC, Liegeois F, Vergne L, Mboup S, Badiane S, Ndoye I, Delaporte E: The Senegalese government's highly active antiretroviral therapy initiative: an 18-month follow-up study. AIDS. 2002, 16: 1363-1370. 10.1097/00002030-200207050-00008.View ArticlePubMed
- Djomand G, Roels T, Ellerbrock T, Hanson D, Diomande F, Monga B, Maurice C, Nkengasong J, Konan-Koko R, Kadio A, Wiktor S, Lackritz E, Saba J, Chorba T: Virologic and immunologic outcomes and programmatic challenges of an antiretroviral treatment pilot project in Abidjan, Cote d'Ivoire. AIDS. 2003, 17 Suppl 3:S5-15.: S5-15.View Article
- Organisation. WH: Scaling up Antiretroviral Therapy in Resource-limited Settings: Guidelines for a Public Health Approach; Executive Summary. Geneva: World Health Organisation 2002. Accessed 15.04.05: http//www.who.int/hiv/pub/prev-care/en/WHO_ARV_Guidelines.pdf.
- Orrell C, Badri M, Wood R: Measuring adherence in a community setting: which measure is most valuable?. XVI International AIDS Conference, Bangkok, Thailand. 2004, July Abstract #WePEB5787
- J N, MH K, CJ N, W. W: Applied Linear Statistical Models, Fourth Edition. New York: McGraw Hill 1996.
- Le Moing V, Thiebaut R, Chene G, Leport C, Cailleton V, Michelet C, Fleury H, Herson S, Raffi F: Predictors of long-term increase in CD4(+) cell counts in human immunodeficiency virus-infected patients receiving a protease inhibitor-containing antiretroviral regimen. J Infect Dis. 2002, 185: 471-480. 10.1086/338929.View ArticlePubMed
- Bennett KK, DeGruttola VG, Marschner IC, Havlir DV, Richman DD: Baseline predictors of CD4 T-lymphocyte recovery with combination antiretroviral therapy. J Acquir Immune Defic Syndr. 2002, 31: 20-26.View ArticlePubMed
- Kaufmann GR, Perrin L, Pantaleo G, Opravil M, Furrer H, Telenti A, Hirschel B, Ledergerber B, Vernazza P, Bernasconi E, Rickenbach M, Egger M, Battegay M: CD4 T-lymphocyte recovery in individuals with advanced HIV-1 infection receiving potent antiretroviral therapy for 4 years: the Swiss HIV Cohort Study. Arch Intern Med. 2003, 163: 2187-2195. 10.1001/archinte.163.18.2187.View ArticlePubMed
- Smith K, Aga E, Bosch RJ, Valdez H, Connick E, Landay A, Kuritzkes D, Gross BH, Francis IR, McCune JM, Kessler H, Lederman M: Long-term changes in circulating CD4 T lymphocytes in virologically suppressed patients after 6 years of highly active antiretroviral therapy. AIDS. 2004, 18: 1953-1956. 10.1097/00002030-200409240-00012.View ArticlePubMed
- Kaufmann GR, Furrer H, Ledergerber B, Perrin L, Opravil M, Vernazza P, Cavassini M, Bernasconi E, Rickenbach M, Hirschel B, Battegay M: Characteristics, determinants, and clinical relevance of CD4 T cell recovery to <500 cells/microL in HIV type 1-infected individuals receiving potent antiretroviral therapy. Clin Infect Dis. 2005, 41: 361-372. 10.1086/431484.View ArticlePubMed
- Lawn SD, Bekker LG, Myer L, Orrell C, Wood R: Cryptococcocal immune reconstitution disease: a major cause of early mortality in a South African antiretroviral programme. AIDS. 2005, 19: 2050-2052.View ArticlePubMed
- Autran B, Carcelain G, Li TS, Blanc C, Mathez D, Tubiana R, Katlama C, Debre P, Leibowitch J: Positive effects of combined antiretroviral therapy on CD4+ T cell homeostasis and function in advanced HIV disease. Science. 1997, 277: 112-116. 10.1126/science.277.5322.112.View ArticlePubMed
- Carcelain G, Debre P, Autran B: Reconstitution of CD4+ T lymphocytes in HIV-infected individuals following antiretroviral therapy. Curr Opin Immunol. 2001, 13: 483-488. 10.1016/S0952-7915(00)00245-4.View ArticlePubMed
- Lawn SD, Bekker LG, Miller RF: Immune reconstitution disease associated with mycobacterial infections in HIV-infected individuals receiving antiretrovirals. Lancet Infect Dis. 2005, 5: 361-373. 10.1016/S1473-3099(05)70140-7.View ArticlePubMed
- Piketty C, Castiel P, Belec L, Batisse D, Si MA, Gilquin J, Gonzalez-Canali G, Jayle D, Karmochkine M, Weiss L, Aboulker JP, Kazatchkine MD: Discrepant responses to triple combination antiretroviral therapy in advanced HIV disease. AIDS. 1998, 12: 745-750. 10.1097/00002030-199807000-00011.View ArticlePubMed
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2334/6/59/prepub
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