Immune reconstitution inflammatory syndrome among HIV-infected South African infants initiating antiretroviral therapy
Smith, Kellya; Kuhn, Louiseb; Coovadia, Ashrafc; Meyers, Tammyd; Hu, Chih-Chib; Reitz, Cordulab; Barry, Gillianc; Strehlau, Renatec; Sherman, Gaylee; Abrams, Elaine Jf
aColumbia University College of Physicians & Surgeons, USA
bGertrude H. Sergievsky Center, and Department of Epidemiology, Mailman School of Public Health, Columbia University, New York, New York, USA
cEmpilweni Clinic, Coronation Women and Children Hospital, South Africa
dHarriet Shezi Clinic, Baragwanath Hospital, Enhancing Childhood HIV Outcomes (ECHO), South Africa
eDepartment of Molecular Medicine and Haematology, University of the Witwatersrand, Johannesburg, South Africa
fCollege of Physicians & Surgeons, Columbia University and International Center of AIDS Care and Treatment Programs, Mailman School of Public Health, Columbia University, New York, New York, USA.
Received 18 September, 2008
Revised 23 February, 2009
Accepted 27 February, 2009
Correspondence to Dr Elaine J. Abrams, International Center for AIDS Care and Treatment Programs (ICAP), Mailman School of Public Health, 722 West 168th Street, Room 717, New York, NY 10032, USA. Tel: +1 212 342 0543; fax: +1 212 342 1824; e-mail: firstname.lastname@example.org
Objectives: To determine the incidence, clinical manifestations and risk factors for immune reconstitution inflammatory syndrome (IRIS) in young children initiating highly active antiretroviral therapy (HAART).
Design: A prospective cohort of antiretroviral-naïve HIV-infected children less than 24 months of age enrolled in a treatment strategies trial in Johannesburg, South Africa.
Methods: Among 169 HIV-infected children initiating HAART, April 2005 to November 2006, the records of 83 children suspected to have IRIS within 6 months of starting treatment were reviewed to determine whether they met criteria for IRIS. Seven were excluded due to incomplete follow-up. Pretreatment and post-treatment characteristics of children with and without IRIS were compared.
Results: Overall, 34/162 (21%) children developed IRIS at a median of 16 days (range 7–115 days) post-HAART initiation. Bacille Calmette-Guérin reaction was most common occurring in 24/34 (71%) children, primarily injection site lesions and/or ipsilateral axillary lymphadenitis with abscess. Other IRIS conditions (not mutually exclusive) included Mycobacterium tuberculosis (n = 12), cytomegalovirus pneumonia (n = 1), Streptococcus pneumonia sepsis (n = 1), and severe seborrheic dermatitis (n = 1). Children with IRIS were younger (median age 7 vs. 10 months, P = 0.007) with a lower CD4 cell percentage (median 13.9 vs. 19.2, P = 0.009) at HAART initiation than controls. After 24 weeks on HAART, 62% of IRIS cases vs. 28% of controls had HIV RNA more than 400 copies/ml (P = 0.001), odds ratio = 2.88 (95% confidence interval = 1.14–7.29) after adjusting for baseline factors.
Conclusion: Infants and young children with advanced HIV disease initiating HAART are at high risk for developing IRIS, leading to additional morbidity and possibly impairing virologic response to antiretroviral treatment.
With increased availability of highly active antiretroviral treatment (HAART) in high HIV prevalence, resource-constrained settings, immune reconstitution inflammatory syndrome (IRIS) has been recognized as a significant complication of treatment initiation [1–7]. It is estimated that 10–32% of adults starting HAART will develop IRIS, an exacerbation or atypical presentation of opportunistic infections associated with immune recovery, within 6 months of starting treatment [1,2,8–11]. Although the number of children worldwide initiating HAART has increased substantially, there are limited data about IRIS in infants and children starting HAART [6,7,12–14]. This issue is of particular importance in Sub-Saharan Africa where tuberculosis is common, Bacille Calmette-Guérin (BCG) vaccination is routinely administered at birth, and more than 600 000 children are estimated to be in urgent need of HAART [13,15].
In a study of 153 children with advanced HIV disease initiating HAART as part of Thailand's national treatment program (median age 7.9 years), the incidence of IRIS was found to be 19% . The IRIS events included mycobacterial disease (44%), Varicella Zoster, Herpes Simplex, and Cryptococcus neoformans infections, and median time to IRIS onset was 4 weeks. Low CD4 cell percentage was a risk factor for developing IRIS . In Cape Town, South Africa, 11 new, recurrent or worsening Mycobacterium tuberculosis (TB) events were reported among children initiating HAART over a 2-year period . Similar to the Thai study, the children studied were older and generally developed IRIS symptoms within the first months of treatment.
BCG vaccination, using a live-attenuated form of Mycobacterium bovis, is routinely administered to newborns in sub-Saharan Africa to prevent severe forms of the disease. Concerns have been raised that BCG vaccination poses a risk to HIV-infected infants [16–18]. Hesseling et al.  reported 25 children in the Western Cape Province, South Africa, diagnosed with BCG disease . Seventeen of these children were HIV-infected and four were characterized as having IRIS reactions. In a recent report of 373 HIV-infected children initiating HAART as part of a clinical trial in South Africa, 33 (8.8%) developed BCG-associated IRIS at a median age of 4 months and a median of 4 weeks after treatment initiation .
In addition to increased morbidity, treatment of IRIS-related conditions can complicate HAART. In particular, cotreatment of TB is especially complex in young children because of interactions between nevirapine and rifampin. Efavirenz cannot be substituted for nevirapine, as dosing has not yet been determined for children less than 3 years of age. Although international guidelines suggest antiretroviral treatment with three nucleoside reverse transcriptase inhibitors (NRTI) when using rifampin , in practice South African clinicians either use ritonavir or higher doses of lopinavir–ritonavir with two NRTI [20,21]. Furthermore, the efficacy of HAART in infants receiving treatment for IRIS-related conditions, particularly for TB, has not been described.
This report describes the incidence, risk factors and characteristics of IRIS among a cohort of HIV-infected children less than 2 years of age initiating HAART as part of a clinical trial in Johannesburg, South Africa. We also compare virologic, immunologic and clinical outcomes after 6 months of HAART between children with and without IRIS.
HAART-naïve HIV-infected infants less than 24 months of age who were exposed to nevirapine for prevention of mother-to-child transmission were enrolled into a clinical trial of HAART strategies, between April 2005 and November 2006 at Coronation Hospital in Johannesburg, South Africa (clinicaltrials.gov NCT00117728). Children were referred from inpatient wards and pediatric HIV clinics at Coronation and Chris Hani Baragwanath hospitals as well as from nearby HIV clinics. HIV infection was documented with at least one positive test using DNA PCR or at least one HIV RNA viral load more than 5000 copies/ml. The parent or legal guardian of each child provided written informed consent and the study was approved by the Institutional Review Boards of Columbia University and the University of the Witwatersrand.
Treatment and monitoring
Children were eligible for HAART if they had WHO stage III or IV disease, or CD4 cell% less than 25% in children less than 12 months or less than 20% in children less than 35 months, or had recurrent (>2/year) or prolonged (>4 weeks) hospitalization for HIV-related infections. Children requiring acute treatment for opportunistic infections or tumors were excluded with the exception of children requiring treatment for TB. Severe liver dysfunction evidenced by elevated alanine aminotransferase precluded HAART initiation. Children were initiated on a regimen of lopinavir/ritonavir, lamivudine (3TC) and stavudine (d4T). Dosing was determined using body surface area and was recalculated at each study visit. Ritonavir was substituted for lopinavir/ritonavir in children aged less than 6 months or those who were receiving concomitant treatment with rifampin.
HIV RNA viral load (Roche Diagnostics, Branchburg, New Jersey, USA) was measured at treatment initiation, and weeks 12 and 24 post-treatment. CD4 cell counts and percents were measured at treatment initiation and at week 24. Children were examined by a study physician every 4 weeks. Physicians were available between visits to address acute problems and families were encouraged to use the study clinic for all of their children's medical needs. Caretakers were counseled regarding medication administration and adherence was reviewed through structured questionnaires and measurement of unused medications. Laboratory and clinical data were collected at each visit and maintained in an electronic database.
Immune reconstitution inflammatory syndrome case definition
At each visit, study physicians who had received clinical training in likely presentation of IRIS in children evaluated and recorded whether there were signs and symptoms consistent with IRIS. The records of all children flagged as ‘suspect IRIS’ by study physicians within the first 24 weeks of treatment were retrospectively reviewed by an independent member of the research team who was not directly involved in patient care. In addition, the records of all children who died, who initiated TB treatment, or who had been hospitalized and treated with antimicrobials during the first 24 weeks of treatment were also reviewed. All study documents, as well as all available clinic and hospital records, were reviewed.
We adapted the definition of IRIS used by Puthanakit et al. . Children meeting any of the following criteria were classified as ‘IRIS’ cases: new symptomatic presentation of infections with pathogens previously reported to be associated with IRIS in the adult or pediatric literature; new reaction to BCG; reemergence or exacerbation of TB; exacerbation of prior condition, for example, dermatitis. Given the complexity of TB diagnosis in young children, the diagnosis was based on overall clinical picture and clinician decision to initiate TB treatment . Microscopy, culture, biopsy and radiography results were recorded when available. Standard treatment for TB in South Africa is rifampin, isoniazid and pyrazinamide for 2 months followed by 4 months of rifampin and isoniazid. All newborns in South Africa routinely receive intradermal Danish strain BCG vaccination (Statens Serum Institute, Copenhagen, Denmark). Recommended treatment for BCG disease is rifampin, isoniazid and ethionamide. For children already receiving TB treatment, ethionamide is added to the regimen.
All children whose records were not reviewed, as well as those who were reviewed but did not meet IRIS case definition, were classified as controls. Surviving children who did not complete at least 12 weeks of follow-up (lost-to-follow-up, withdrawn, or transferred out) were excluded.
Pretreatment and post-treatment characteristics of IRIS cases and controls were compared using chi-squared tests for categorical variables or Fisher's exact test if expected cell sizes were less than five, t-tests for normally distributed continuous variables and Wilcoxon tests for nonnormal continuous variables. The child's weight was expressed as the sex and age-adjusted Z-score . Laboratory values were included if they were done within 6 weeks of scheduled visits. Multivariable analysis was conducted using logistic regression and SAS statistical software (Cary, North Carolina, USA) and variables were included in the final model if associated with the outcome (P < 0.05) or if their inclusion modified the association between IRIS and the outcome by more than 10%.
Incidence of immune reconstitution inflammatory syndrome
A total of 169 HIV-infected children were initiated on HAART between April 2005 and November 2006. Fifty-one percent were male and the median age was 8 months (range 2–24 months) with 31% initiating treatment less than 6 months of age.
The records of 83 (49.1%) children were reviewed as possible IRIS cases (Fig. 1). Of these, 34 met IRIS case definition. Seven children not followed to 12 weeks were excluded. Thus, of 162 HIV-infected children who initiated HAART and were retained in care for more than 12 weeks, 34 (21.0%) developed IRIS within the first 24 weeks of treatment.
Profile of immune reconstitution inflammatory syndrome cases
Table 1 describes the clinical manifestations of children who met study criteria for IRIS. The median time to first symptom presentation following HAART was 16 days [range 7–115 days, interquartile range (IQR) = 13–53 days], with 73.5% manifesting symptoms within 30 days. BCG-related complications were the most frequent IRIS manifestations occurring in 24/34 (70.6%) children with IRIS, that is, 24/162 (14.8%) of the treatment cohort. Median time to first symptom from treatment initiation was 14 days (IQR = 12–27) among children with BCG-related IRIS vs. 54 days (IQR = 18–84) for other IRIS conditions; median age at start of treatment was 6 months (IQR = 4–9) for the BCG IRIS group and 9 months (IQR = 6–11) for the other IRIS cases.
Three children had local injection site lesions, 15 children had BCG disease involving the regional lymph nodes and/or other local lesions primarily ipsilateral axillary lymphadenitis with abscess formation, five children had both regional and local lesions, and one child was diagnosed with probable disseminated TB/BCGosis. One child was already receiving BCG treatment but developed an enlarged, suppurative right axillary node 4 weeks after HAART initiation. Six children who developed BCG disease were also newly diagnosed with TB, including the child diagnosed with disseminated infection who died and two who were already on TB treatment when BCG symptoms developed. Overall, 11 children had abscess aspirations and two children required surgical incision and drainage. Six samples sent to the laboratory were smear positive for acid-fast bacilli and three yielded positive cultures for M. tuberculosis complex. The majority of children, 17/24 (70.8%), received treatment for BCG disease (including the child who continued on previously prescribed therapy).
It was difficult to clearly identify children with TB-related IRIS because of nonspecific presentation (cough, fevers, respiratory distress, gastrointestinal complaints and failure-to-thrive) and inconsistent implementation of diagnostic protocols (five children had abnormal chest radiograph consistent with TB and four were documented as Mantoux test positive). Overall, twelve children were newly treated for TB including six children with concomitant BCG disease.
Other IRIS manifestations included cytomegalovirus pneumonia, Streptococcus pneumonia sepsis with empyema, severe herpes labialis and acute, severe worsening of seborrheic dermatitis with bacterial superinfection requiring hospitalization. One child already receiving TB treatment at HAART initiation was hospitalized for fever, cough, respiratory distress and hypoxemia, developed concomitant BCG-related complications while hospitalized and was discharged with a diagnosis of Pneumocystis pneumonia and BCGosis.
Three of 34 (8.8%) children who developed IRIS died: two children with localized BCG disease and one child with disseminated BCG and TB. There were 14 deaths among 128 (10.9%) controls (P = 1.0).
Risk factors for immune reconstitution inflammatory syndrome
Univariable risk factors for IRIS are displayed in Table 2. Children who developed IRIS were significantly younger at treatment initiation than controls, median age 7 months (range 2–18 months) vs. 10 months (range 2–24 months), P = 0.007. WHO stage was similar between groups, but children with IRIS had significantly lower pretreatment CD4 cell percents. Children with IRIS had higher pretreatment HIV RNA levels and lower sex-adjusted and age-adjusted weight-for-age Z-scores than controls, for example, 82% of children with IRIS were less than −2 SD below the mean compared with 49% of controls, P = 0.0005. There was a trend towards less cotreatment for TB at the time of HAART initiation among children with IRIS but this association was not significant.
In multivariable analysis, young age at treatment initiation, low pretreatment CD4 cell% and low weight-for-age were each independently associated with developing IRIS. In a model including these variables: age less than 6 months [odds ratio (OR) = 4.41; 95% confidence interval (CI) = 1.73–11.24], CD4 cell% less than 10 vs. more than 10 (OR = 5.45; 95% CI = 1.87–15.93), and weight-for-age Z-score less than −2 (OR = 4.19; 95% CI = 1.56–11.24) were associated with increased risk of developing IRIS.
Immunologic, clinical and virologic responses to HAART
Immunologic, clinical and virologic responses to HAART at 24 weeks were compared between children in the IRIS and control groups (Table 3). After 24 weeks of HAART, mean CD4 cell% remained significantly lower in the IRIS group compared with controls (21.8 vs. 29.6, P = 0.0001) but the mean change in CD4 cell% was similar (mean increase from pretreatment to 24 weeks of 7.8 and 9.0 CD4 cell% point for IRIS vs. controls, respectively). Similarly, at 24 weeks, the mean Z-score for the IRIS group remained lower than the control group (−1.76 vs. −0.68, P = 0.0029) but the mean change over time in weight-for-age Z-scores was similar across groups.
At 24 weeks post-HAART initiation, there were a significantly greater proportion of children in the IRIS group who had not suppressed: of children who had developed IRIS, 62% had a viral load more than 400 copies/ml at 24 weeks compared with 28% of controls (P = 0.001) (Table 3). There remained a significantly higher rate of failure in the IRIS group compared with the controls if exclusions and deaths were counted as failures. A nonsignificant trend in the same direction was seen at 12 weeks. Because viral loads more than 750 000 copies/ml were not further quantified and the majority of children had high pretreatment viral loads, we were unable to accurately evaluate the magnitude of change from baseline.
The lower rates of viral suppression at 24 weeks among children who had developed IRIS were not explained by age or by their severity of disease pretreatment as measured by pretreatment viral load, CD4 cell%, weight-for-age Z-score and clinical stage. In a multivariable model, only IRIS status was significantly associated with lack of viral suppression. If weight-for-age Z-score and pretreatment viral load were included in the model, IRIS remained significantly associated with a reduced likelihood of achieving viral suppression less than 400 copies/ml at 24 weeks (OR = 2.88 95% CI = 1.14–7.29) (Table 4). We included these two factors as they slightly attenuated the association between IRIS and lack of viral suppression. Inclusion of any of the other pretreatment characteristics had no effect.
Despite its clinical importance, IRIS has not been well studied in children. This is the first report to describe the incidence of and risk factors for IRIS in a cohort of infants and young children less than 24 months of age initiating HAART. Approximately 21% of these children met criteria for IRIS and, similar to findings in cohorts of older children and adults, children with advanced immune suppression were at higher risk for developing the syndrome than those with a less severe disease profile [1,3–6,9,11,14]. We also determined that younger age at HAART initiation was associated with increased risk for IRIS. Intriguingly, our results suggest that children with IRIS may be less likely to suppress HIV after 6 months of HAART than those without the syndrome.
Diagnosis of IRIS in children is complex due to a lack of standard definitions and diagnostic dilemmas associated with several other infectious and pulmonary conditions in young children, particularly TB . BCG-related IRIS was the most common diagnosis in our cohort perhaps due in part to the ease of diagnosis: 14.8% of all children starting HAART were diagnosed with a BCG-related complication. This is far higher than the incidence rate of 2% for vaccine site abscesses and 0.7% for lymphadenitis reported in a Thai study of older children  and higher than that reported in another cohort of infants 6–12 weeks of age enrolled in a HAART strategies trial in South Africa in which 8.8% were reported to have developed BCG regional IRIS [14,24]. It has been pointed out that BCG vaccination poses a significant risk to HIV-infected infants [17,18]. In our cohort, morbidity associated with BCG IRIS was substantial. Three deaths occurred: one in a child with presumed disseminated BCG and TB, and two in children with localized disease (not thought to be related to the children's deaths). Furthermore, the majority of children required single or repeated abscess aspirations or surgical incision and drainage as well as new medication in addition to their already complex regimens. Recent WHO guidelines discourage BCG for HIV-infected children . However, as the vaccine is routinely given prior to knowledge of the child's HIV status, this recommendation has little practical utility. The high rate of BCG-related complications experienced by young HIV-infected children initiating HAART in our study supports recent recommendations for careful monitoring of HIV-infected BCG vaccinated infants particularly during the immediate period following HAART initiation .
Twelve of the 34 IRIS cases were attributed to TB, including six with BCG comorbidity. TB is notoriously difficult to diagnose in infants and we relied on TB treatment as confirmation of the diagnosis . For some children, medical records provided further evidence supporting the diagnosis, including tuberculin skin tests, radiographs and bacteriologic cultures. The overwhelming predominance of BCG-related and TB-related causes of IRIS in young children suggests that further investigation of prophylaxis with anti-TB drugs and other approaches to decrease the risk of TB exposure and acquisition are warranted.
The median time to IRIS symptoms was 16 days. This is somewhat shorter than reported from Thailand, but may be explained by our focus on the first 6 months of treatment compared with 48 weeks of observation in the Thai study  or to the younger age of our cohort. We also found that lower CD4 cell%; younger age and lower weight-for-age Z-score pretreatment were each associated with a significantly higher risk for developing IRIS. Children less than 6 months of age were four-times more likely to be diagnosed with IRIS than older children, whereas CD4 cell% less than 10 was associated with a more than five-fold increase over higher CD4 cell%. Advanced disease has been associated with IRIS in adult and pediatric populations but age has not been previously identified as a risk factor [1,3,4,6,9,11,14].
The association between young age and increased risk for IRIS could pose significant challenges in light of new recommendations to initiate HAART in all HIV-infected children less than 1 year of age, regardless of clinical or immunologic status . It is possible that early initiation of HAART prior to disease progression may decrease the risk for IRIS. This might explain the lower rates of BCG IRIS observed in the treatment strategy trial mentioned earlier . As all children in our study had evidence of advanced HIV disease to meet enrollment criteria, we could not tease out the relationships between age, disease stage, and the development of IRIS. It will be critically important, therefore, to monitor rates and manifestations of IRIS as more infants initiate HAART early in TB endemic areas with routine newborn BCG vaccination.
After 24 weeks of treatment, mean CD4 cell% and weight-for-age Z-scores in the IRIS group remained lower than the control group, but mean increases over time for both CD4 cell% and weight were similar between groups [27,28]. In contrast, children with IRIS were significantly less likely to achieve viral suppression to less than 400 copies/ml by 24 weeks than controls. We adjusted for markers of disease severity at HAART initiation (CD4 cell%, viral load categories, weight-for-age, WHO stage, age, etc.) but these markers did not account for the difference in response rate. However, these parameters only partially capture the full spectrum of the severity of disease and residual confounding may account for the reduced viral suppression. In particular, we were unable to determine the actual viral load value pretreatment when the reported value was more than 750 000 copies/ml and therefore could not adequately adjust for pretreatment viral load. Our finding may represent the longer time needed to achieve complete viral suppression when pretreatment viral load is very high [29,30]. Also, as the IRIS-defining conditions that we identified almost all required TB treatment, we are concerned about possible drug-drug interactions. Several studies have identified pharmacokinetic interactions between rifampin and ritonavir as well as ritonavir boosted protease inhibitors that may result in sub-therapeutic antiretroviral drug levels [21,31–35]. In addition, the burdens of acute illness and concomitant medications for treatment of IRIS conditions are likely to result in adherence challenges that may impact HAART efficacy. One study of adherence in young South African children identified ritonavir treatment as a risk factor for incomplete adherence and lower rates of complete viral suppression .
There are several limitations to this study. IRIS is difficult to diagnose in children secondary to the lack of a standard definition and the well known dilemmas of diagnosing TB and other infectious diseases . We chose to use the IRIS definition used in a previous study of children and to rely, to a large extent, on study physician diagnosis . Although the suspected IRIS cases were determined prospectively during the study, a review of these cases occurred retrospectively by only one independent reviewer. We recognize that classification of some of the cases may not be entirely accurate. Given the difficulties of distinguishing disseminated BCG disease from TB, it is possible that some of the children listed as experiencing both complications were experiencing only disseminated BCG disease. This study was also limited by losses in both groups due to death and withdrawal. Given the lack of clinical detail surrounding deaths (several children died at home) as well as the severity of symptomatic disease pretreatment, it is possible that IRIS may have gone undetected and that the rate and severity of IRIS manifestations may have been underestimated.
In summary, in this cohort of infants and young children initiating HAART, IRIS was a common complication associated with significant morbidity, particularly in the youngest children with advanced HIV disease. Given the continuing large-scale rollout of HAART to infants and children in the developing world, careful monitoring is warranted following the initiation of therapy. Further research is needed to better predict and diagnose IRIS and the underlying infections associated with the syndrome and to determine best practices for prevention and treatment. In areas where BCG vaccination is routine, it will be critically important to continue to examine the consequences of vaccine policy for HIV-infected children.
Sources of funding: The study was supported in part by grants from the National Institutes of Child Health and Human Development (NICHD) HD 47177 and Secure the Future Foundation. Kelly Smith was supported by Doris Duke Charitable Foundation International Clinical Research Fellowship for Medical Students at the College of Physicians & Surgeons, Columbia University. The authors would like to thank the participating families and acknowledge the study team: E. Malan, B. Marais, D. Zisis, K. Naidoo, J. Rothberg, S. Madumo, S. Potgieter, L. Nakan, A. Smith, D. S. Maclear, K. Ncube, V. Kok, L. Thomas, L. Plaatjies, G. Ngwenya, M. Moshoeshoe and A. Mosima.
1. Murdoch DM, Venter DF, Feldman C, Van Rie A. Incidence and risk factors for the immune reconstitution inflammatory syndrome in HIV patients in South Africa: a prospective study. AIDS 2008; 22:601–610.
2. Kumarasamy N, Chaguturu S, Mayer KH, Solomon S, Yepthomi T, Balakrishnan P, Flanigan TP. Incidence of immune reconstitution syndrome in HIV/tuberculosis-coinfected patients after initiation of generic antiretroviral therapy in India. J Acquir Immune Defic Sydr 2004; 37:1574–1576.
3. 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.
4. Lawn SD, Myer L, Bekker LG, Wood R. Tuberculosis-associated immune reconstitution disease: incidence, risk factors and impact in an antiretroviral treatment service in South Africa. AIDS 2007; 21:335–341.
5. Shelburne SA, Montes M, Hammill RJ. Immune reconstitution inflammatory syndrome: more answers, more questions. J Antimicrob Chemother 2006; 57:167–170.
6. Puthanakit T, Oberdorger P, Akarathum N, Wannarit P, Sirisanthana T, Sirisanthana V. Immune reconstitution syndrome after highly active antiretroviral therapy in human immunodeficiency virus-infected Thai children. Pediatr Infect Dis J 2006; 25:53–58.
7. Zampoli M, Kilborn T, Eley B. Tuberculosis during early antiretroviral-induced immune reconstitution in HIV-infected children. Int J Tuberc Lung Dis 2007; 11:417–423.
8. Shelburne SA, Visnegarwala F, Darcourt J, Graviss EA, Giordano TP, White AC, Hamill RJ. Incidence and risk factors for immune reconstitution inflammatory syndrome during highly active antiretroviral therapy. AIDS 2005; 19:399–406.
9. French MA, Price P, Stone SF. Immune restoration disease after antiretroviral therapy. AIDS 2004; 18:1615–1627.
10. Battegay M, Nuesch R, Hirschel B, Kaufmann GR. Immunological recovery and antiretroviral therapy in HIV-1 infection. Lancet Infect Dis 2006; 6:280–287.
11. Jevtovic DJ, Salemovic D, Ranin J, Pesic I, Zerjav S, Djurkovic-Djakovi O. The prevalence and risk of immune restoration disease in HIV-infected patients treated with highly active antiretroviral therapy. HIV Med 2005; 6:140–143.
14. Rabie H, Violari A, Madhi S, Gibb DM, Stayn J, Van Niekerk R, et al
. Complications of BCG vaccination in HIV infected and uninfected children: evidence from the Children with HIV Early Antiretroviral Therapy (CHER) study
. 14th Conference on Retroviruses and Opportunistic Infections
. Boston, Mass 2008. Abstract 600. http://www.retroconference.org/2008/Abstracts/33235.htm
. [Accessed March 16, 2009]
15. Boerma JT, Stanecki KA, Newell ML, Luo C, Beusenberg M, Garnett GP, et al
. Monitoring the scale-up of antiretroviral therapy programmes: methods to estimate coverage. Bull World Health Organ 2006; 84:145–160.
16. Puthanakit T, Oberdorfer P, Punjaisee S, Wannarit P, Sirisanthana T, Sirisanthana V. Immune reconstitution syndrome due to Bacillus Calmette-Guérin after initiation of antiretroviral therapy in children with HIV infection. Clin Infect Dis 2005; 41:1049–1052.
17. Hesseling AC, Rabie H, Marais BJ, Manders M, Lips M, Schaaf HS, et al
. Bacille Calmette-Guérin (BCG) vaccine induced disease in HIV-infected and uninfected children. Clin Infect Dis 2006; 42:548–558.
18. Hesseling AC, Marais BJ, Gie RP, Schaaf HS, Fine PE, Godfrey-Faussett P, et al
. The risk of disseminated Bacille Calmette-Guérin (BCG) disease in HIV-infected children. Vaccine 2007; 25:14–18.
19. World Health Organization. Antiretroviral therapy of HIV infection in infants and children in resource-limited settings: towards universal access: recommendations for a public health approach
. Geneva, September 2006. http://www.who.int/hiv/pub/guidelines/paediatric020907.pdf
. [Accessed 16 March 2009]
21. Ren Y, Nuttall JJ, Egbers C, Eley BS, Meyers TM, Smith JP, et al
. Effect of rifampicin on lopinavir pharmacokinetics in HIV-infected children with tuberculosis. J Acquir Immune Defic Syndr 2008; 15:566–569.
22. Marais BJ, Graham SM, Cotton MF, Beyers M. Diagnostic and management challenges for childhood tuberculosis in the era of HIV. J Infect Dis 2007; 196(Suppl 1):S76–95.
24. Violari A, Cotton MF, Gibb DM, Babiker AG, Steyn J, Madhi SA, et al
. Early antiretroviral therapy and mortality among HIV-infected infants. N Engl J Med 2008; 359:2233–2244.
25. World Health Organization. Safety of BCG vaccine in HIV-infected children
. Wkly Epidemiol Rec
. [Accessed 16 March 2009]
27. Patel K, Hernan MA, Williams PL, Seeger JD, McIntosh K, Van Dyke R, et al
. Long-term effects of long term antiretroviral therapy on CD4+ cell evolution among children and adolescents infected with HIV: 5 years and counting. Clin Infect Dis 2008; 46:1751–1760.
28. Kovacs A, Montepiedra G, Carey V, Pahwa S, Weinberg A, Frenkel L, et al
. Immune reconstitution after receipt of highly active antiretroviral therapy in children with advanced or progressive HIV disease and complete or partial viral load response. J Infec Dis 2005; 192:296–302.
29. Chadwick EG, Capparelli EV, Yogev R, Pinto JA, Robbins B, Rodman JH, et al
. Pharmacokinetics, safety and efficacy of lopinavir/ritonavir in infants less than 6 months of age: 24 week results. AIDS 2008; 22:249–255.
30. Prendergast A, Mphatswe W, Tudor-Williams G, Rakgotho M, Pillay V, Thobakgale C, et al
. Early virologic suppression with three-class antiretroviral therapy in HIV-infected African infants. AIDS 2008; 22:1333–1343.
31. La Porte CJ CE, Bertz R. Pharmacokinetics of adjusted-dose lopinavir-ritonavir combined with rifampin in healthy volunteers
. Antimicrob Agents Chemother
32. Ren Y, Nuttall J, Egbers C, Eley B, Meyers T, Maartens G, et al. Plasma concentrations of efavirenz and lopinavir in children with and without rifampicin-based anti-TB treatment
. 14th Conference on Retroviruses and Opportunistic Infections
, Los Angeles, California Abstract #77, 2007.
33. Chadwick EG, Rodman JH, Britto P, Powell C, Palumbo P, Luzuriaga K, et al
. Ritonavir-based highly active antiretroviral therapy in human immunodeficiency virus type 1-infected infants younger than 24 months of age. Pediatr Infect Dis J 2005; 24:793–800.
34. Newton SM, Brent AJ, Anderson S, Whittaker E, Kampmann B. Paediatric tuberculosis. Lancet 2008; 8:498–510.
35. Ribera E, Azuaja C, Lopez RM, Domingo P, Curran A, Feijoo M, et al
. Pharmacokinetic interaction between rifampicin and the once-daily combination of saquinavir and low-dose ritonavir in HIV-infected patients with tuberculosis. J Antimicrob Chemother 2007; 59:690–697.
36. Davies MA, Boulle A, Fakir T, Nuttall J, Eley B. Adherence to antiretroviral therapy in young children in Cape Town, South Africa, measured by medication return and caregiver self-report: a prospective cohort study. BMC Pediatr 2008; 8:34.
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Case 18-2010: A 7-Year-Old Boy with Elevated HIV RNA Levels despite Antiretroviral Medications HIV infection with drug-resistance mutations
New England Journal of Medicine, 362():
Brazilian Journal of Infectious DiseasesIdentifying risk factors of immune reconstitution inflammatory syndrome in AIDS patients receiving highly active anti-retroviral therapyBrazilian Journal of Infectious Diseases
Diagnostic Microbiology and Infectious DiseaseMycobacterium simiae pulmonary infection unmasked during immune reconstitution in an HIV patientDiagnostic Microbiology and Infectious Disease
immune reconstitution inflammatory syndrome; pediatric HAART; pediatric HIV
© 2009 Lippincott Williams & Wilkins, Inc.
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