Abstract

HIV is the top and tuberculosis is the second leading cause of death from infectious disease worldwide, with an estimated 8.7 million incident cases of tuberculosis and 2.5 million new HIV infections annually. The World Health Organization estimates that HIV prevalence among children with tuberculosis, in countries with moderate to high prevalence, ranges from 10 to 60%. The mechanisms promoting susceptibility of people with HIV to tuberculosis disease are incompletely understood, being likely caused by multifactorial processes.Paediatric tuberculosis and HIV have overlapping clinical manifestations, which could lead to missed or late diagnosis. Although every effort should be made to obtain a microbiologically-confirmed diagnosis in children with tuberculosis, in reality this may only be achieved in a minority, reflecting their paucibacillary nature and the difficulties in obtain samples. Rapid polymerase chain reaction tests, such as Xpert MTB/RIF assay, are increasingly used in children. The use of less or non invasive methods of sample collection, such as naso-pharyngeal aspirates and stool samples for a polymerase chain reaction-based diagnostic test tests and mycobacterial cultures is promising technique in HIV negative and HIV positive children. Anti-tuberculosis treatment should be started immediately at diagnosis with a four drug regimen, irrespective of the disease severity. Moreover, tuberculosis disease in an HIV infected child is considered to be a clinical indication for initiation of antiretroviral treatment. The World Health Organization recommends starting antiretroviral treatment in children as soon as anti-tuberculosis treatment is tolerated and within 2- 8 weeks after initiating it. The treatment of choice depends on the child’s age and availability of age-appropriate formulations, and potential drug interactions and resistance. Treatment of multi-drug resistant tuberculosis in HIV-infected children follows same principles as for HIV uninfected children. There are conflicting results on effectiveness of isoniazid preventive therapy in reducing incidence of tuberculosis disease in children with HIV.ConclusionData on HIV/TB co-infection in children are still lacking. There are on-going large clinical trials on the prevention and treatment of TB/HIV infection in children that hopefully will help to guide an evidence-based clinical practice in both resource-rich and resource-limited settings.

Highlights

  • HIV is the top and tuberculosis is the second leading cause of death from infectious disease worldwide, with an estimated 8.7 million incident cases of tuberculosis and 2.5 million new HIV infections annually

  • Global epidemiology of HIV and TB Worldwide, 2 billion people are estimated to be latently infected with tuberculosis (TB) [1], whilst there are an estimated 35.3 million people living with HIV, 70% of whom live in sub-Saharan Africa (SSA) [2]

  • Close follow up of infants known to be born to HIV-infected mothers and who received Bacillus Calmette–Guérin (BCG) at birth is recommended in order to provide early identification and treatment of any BCG-related complication [31]

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Summary

Conclusion

TB and HIV both represent major threats to public health worldwide. Renewed global interest led to advances in recognising TB/HIV co-infection and understanding the mechanisms promoting susceptibility of HIV-infected people in developing TB disease as part of a multifactorial process [26,27,28,29,30]. There are ongoing large clinical trials (i.e. the PREVENT TB study, SHINE-trial) on the prevention and treatment of TB/ HIV infection in children that should provide new, much needed data on paediatric TB/HIV infection and help to guide evidence-based clinical practice in both resource-rich and resource-limited settings. List of abbreviation used ART: anti-retroviral treatment; BCG: bacillus Calmette– Guérin; dBCG: disseminated BCG disease; ECDC: European Centre for Disease Prevention and Control; EFV: efavirenz; EPTB: extra-pulmonary TB; GA: gastric aspirate; IGRA: interferon-g release assays; IPT: Isoniazide preventing therapy; IRIS: Immune reconstitution inflammatory syndrome; IS: induced sputum; MDR: multi drug resistant; NPA: naso-pharyngeal aspirate; PCR: polymerase chain reaction; SSA: sub-Saharan Africa; TB: tuberculosis; TST: tuberculin skin test; WHO: World Health Organization; XDR: extensively drug resistant.

World Health Organization
Findings
38. European Centre for Disease Prevention and Control
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