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Tuberculosis and HIV—An Update on the “Cursed Duet” in Children

HIV and tuberculosis (TB) often occur together with each exacerbating the other. Improvements in vertical transmission prevention has reduced the number of HIV-infected children being born and early antiretroviral therapy (ART) protects against tuberculosis. However, with delayed HIV diagnosis, HIV-...

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Autores principales: Fry, Samantha H.-L., Barnabas, Shaun L., Cotton, Mark F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7073470/
https://www.ncbi.nlm.nih.gov/pubmed/32211351
http://dx.doi.org/10.3389/fped.2019.00159
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author Fry, Samantha H.-L.
Barnabas, Shaun L.
Cotton, Mark F.
author_facet Fry, Samantha H.-L.
Barnabas, Shaun L.
Cotton, Mark F.
author_sort Fry, Samantha H.-L.
collection PubMed
description HIV and tuberculosis (TB) often occur together with each exacerbating the other. Improvements in vertical transmission prevention has reduced the number of HIV-infected children being born and early antiretroviral therapy (ART) protects against tuberculosis. However, with delayed HIV diagnosis, HIV-infected infants often present with tuberculosis co-infection. The number of HIV exposed uninfected children has increased and these infants have high exposure to TB and may be more immunologically vulnerable due to HIV exposure in utero. Bacillus Calmette-Guérin (BCG) immunization shortly after birth is essential for preventing severe TB in infancy. With early infant HIV diagnosis and ART, disseminated BCG is no longer an issue. TB prevention therapy should be implemented for contacts of a source case and for all HIV-infected individuals over a year of age. Although infection can be identified through skin tests or interferon gamma release assays, the non-availability of these tests should not preclude prevention therapy, once active TB has been excluded. Therapeutic options have moved from isoniazid only for 6–9 months to shorter regimens. Prevention therapy after exposure to a source case with resistant TB should also be implemented, but should not prevent pivotal prevention trials already under way. A microbiological diagnosis for TB remains the gold standard because of increasing drug resistance. Antiretroviral therapy for rifampicin co-treatment requires adaptation for those on lopinavir-ritonavir, which requires super-boosting with additional ritonavir. For those with drug resistant TB, the main problems are identification and overlapping toxicity between antiretroviral and anti-TB therapy. In spite of renewed focus and improved interventions, infants are still vulnerable to TB.
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spelling pubmed-70734702020-03-24 Tuberculosis and HIV—An Update on the “Cursed Duet” in Children Fry, Samantha H.-L. Barnabas, Shaun L. Cotton, Mark F. Front Pediatr Pediatrics HIV and tuberculosis (TB) often occur together with each exacerbating the other. Improvements in vertical transmission prevention has reduced the number of HIV-infected children being born and early antiretroviral therapy (ART) protects against tuberculosis. However, with delayed HIV diagnosis, HIV-infected infants often present with tuberculosis co-infection. The number of HIV exposed uninfected children has increased and these infants have high exposure to TB and may be more immunologically vulnerable due to HIV exposure in utero. Bacillus Calmette-Guérin (BCG) immunization shortly after birth is essential for preventing severe TB in infancy. With early infant HIV diagnosis and ART, disseminated BCG is no longer an issue. TB prevention therapy should be implemented for contacts of a source case and for all HIV-infected individuals over a year of age. Although infection can be identified through skin tests or interferon gamma release assays, the non-availability of these tests should not preclude prevention therapy, once active TB has been excluded. Therapeutic options have moved from isoniazid only for 6–9 months to shorter regimens. Prevention therapy after exposure to a source case with resistant TB should also be implemented, but should not prevent pivotal prevention trials already under way. A microbiological diagnosis for TB remains the gold standard because of increasing drug resistance. Antiretroviral therapy for rifampicin co-treatment requires adaptation for those on lopinavir-ritonavir, which requires super-boosting with additional ritonavir. For those with drug resistant TB, the main problems are identification and overlapping toxicity between antiretroviral and anti-TB therapy. In spite of renewed focus and improved interventions, infants are still vulnerable to TB. Frontiers Media S.A. 2019-04-25 /pmc/articles/PMC7073470/ /pubmed/32211351 http://dx.doi.org/10.3389/fped.2019.00159 Text en Copyright © 2019 Fry, Barnabas and Cotton. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
Fry, Samantha H.-L.
Barnabas, Shaun L.
Cotton, Mark F.
Tuberculosis and HIV—An Update on the “Cursed Duet” in Children
title Tuberculosis and HIV—An Update on the “Cursed Duet” in Children
title_full Tuberculosis and HIV—An Update on the “Cursed Duet” in Children
title_fullStr Tuberculosis and HIV—An Update on the “Cursed Duet” in Children
title_full_unstemmed Tuberculosis and HIV—An Update on the “Cursed Duet” in Children
title_short Tuberculosis and HIV—An Update on the “Cursed Duet” in Children
title_sort tuberculosis and hiv—an update on the “cursed duet” in children
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7073470/
https://www.ncbi.nlm.nih.gov/pubmed/32211351
http://dx.doi.org/10.3389/fped.2019.00159
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