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Processing of Bronchoalveolar Lavage Fluid and Matched Blood for Alveolar Macrophage and CD4+ T-cell Immunophenotyping and HIV Reservoir Assessment
Published on: June 23, 2019
Tuberculosis during early antiretroviral-induced immune reconstitution in HIV-infected children
1School of Child and Adolescent Health, Division of Paediatric Medicine, Red Cross War Memorial Children's Hospital, Klipfontein Road, Rondebosch, 7700 Cape Town, South Africa. mzampoli@ich.uct.ac.za
Insights
Tuberculosis (TB) in children with human immunodeficiency virus (HIV) on antiretroviral therapy can present with immune reconstitution inflammatory syndrome. Early diagnosis and management are crucial for better outcomes in these vulnerable patients.
Area of Science:
- Pediatric Infectious Diseases
- Immunology
- Public Health
Background:
- Human immunodeficiency virus (HIV) infection significantly impacts tuberculosis (TB) presentation and management in children.
- Antiretroviral therapy can lead to immune reconstitution, potentially altering the clinical course of concurrent TB.
Purpose of the Study:
- To characterize the clinical manifestations of TB in HIV-infected children during the early stages of immune reconstitution induced by highly active antiretroviral therapy (HAART).
Main Methods:
- A case series design was employed at a referral pediatric hospital in Cape Town, South Africa.
- Clinical data from eleven children with probable or confirmed TB during early HAART were retrospectively analyzed.
Main Results:
- Seven children developed pulmonary TB after a median of 25 days on HAART, with one also having extrapulmonary disease.
- Four patients experienced paradoxical reactions, including one death from suspected tuberculous immune reconstitution pneumonitis.
- Radiographic findings included new or worsening intrathoracic lymphadenopathy, parenchymal infiltrates, and pleural effusions.
Conclusions:
- The clinical presentation of TB in HIV-infected children on early HAART may be influenced by immune reconstitution.
- Improved diagnostic methods for TB in this population are urgently needed.
Setting:
Referral paediatric hospital, Cape Town, South Africa.
Objective:
To describe the clinical manifestations of Mycobacterium tuberculosis (TB) associated disease in human immunodeficiency virus (HIV) infected children during early antiretroviral-induced immune reconstitution.
Design:
Case series.
Results:
Eleven patients with probable or culture confirmed TB were identified. Seven presented after a median 25 (range 8-54) days on highly active antiretroviral therapy (HAART) with pulmonary TB and one also had extra-pulmonary disease. Three of the patients had a prior history of TB and presented with relapse or recurrent disease. Four patients with TB developed a tuberculous paradoxical reaction; one died of suspected tuberculous immune reconstitution pneumonitis. The duration of pre-HAART anti-tuberculosis treatment and antiretroviral treatment ranged from 21 to 59 and 6 to 105 days, respectively, when they presented with a paradoxical reaction. Drug-resistant (isoniazid and rifampicin) TB was cultured from one patient with relapse disease. Chest radiograph features present during immune reconstitution were increasing or new intrathoracic lymphadenopathy, parenchymal infiltrates and pleural effusions.
Conclusion:
This report documents the clinical presentation of TB during the early phase of HAART which may be attributed to HAART-mediated immune reconstitution. More research is needed to improve the accuracy of TB diagnosis in HIV-infected children.
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