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Early versus late BCG vaccination in HIV-1-exposed infants in Uganda: study protocol for a randomized controlled trial
BACKGROUND: Bacillus Calmette-Guérin (BCG) vaccination may have nonspecific effects, i.e., effects on childhood morbidity and mortality that go beyond its effect on the risk of childhood tuberculosis (TB). Though the available scientific literature is mostly from observational studies, and is fraugh...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5374628/ https://www.ncbi.nlm.nih.gov/pubmed/28359325 http://dx.doi.org/10.1186/s13063-017-1881-z |
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author | Nankabirwa, Victoria Tumwine, James K. Namugga, Olive Tylleskär, Thorkild Ndeezi, Grace Robberstad, Bjarne Netea, Mihai G. Sommerfelt, Halvor |
author_facet | Nankabirwa, Victoria Tumwine, James K. Namugga, Olive Tylleskär, Thorkild Ndeezi, Grace Robberstad, Bjarne Netea, Mihai G. Sommerfelt, Halvor |
author_sort | Nankabirwa, Victoria |
collection | PubMed |
description | BACKGROUND: Bacillus Calmette-Guérin (BCG) vaccination may have nonspecific effects, i.e., effects on childhood morbidity and mortality that go beyond its effect on the risk of childhood tuberculosis (TB). Though the available scientific literature is mostly from observational studies, and is fraught with controversy, BCG vaccination at birth may protect infants in high-mortality populations against serious infections other than TB. Yet, other studies indicate that giving BCG later in infancy may modify immune responses to non-TB antigens and potentially enhance immunity, potentially also against tuberculosis (TB). It is unclear whether BCG vaccination very early in life offers adequate protection against TB and other infections among HIV-1-exposed children because even those who remain uninfected with HIV-1 show signs of impaired immunocompetence early in infancy. This study will compare BCG vaccination at birth with BCG vaccination at 14 weeks of age in HIV-1-exposed infants. METHODS: This is an individually randomized controlled trial in 2200 HIV-1-exposed infants. The intervention is BCG vaccination within 24 h of birth while the comparator is BCG given at 14 weeks of age. The study co-primary outcomes are severe illness in the first 14 weeks of life, and production of tumor necrosis factor, interleukin (IL)-1β, IL-6 and interferon-γ in response to mycobacterial and nonmycobacterial antigens. The study is being conducted in three health centers in Uganda. DISCUSSION: A well-timed BCG vaccination could have important nonspecific effects in HIV-1-exposed infants. This trial could inform the development of appropriate timing of BCG vaccination for HIV-1-exposed infants. TRIAL REGISTRATION: ClinicalTrials.gov, identifier: NCT02606526. Registered on 12 November 2015. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13063-017-1881-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5374628 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53746282017-04-03 Early versus late BCG vaccination in HIV-1-exposed infants in Uganda: study protocol for a randomized controlled trial Nankabirwa, Victoria Tumwine, James K. Namugga, Olive Tylleskär, Thorkild Ndeezi, Grace Robberstad, Bjarne Netea, Mihai G. Sommerfelt, Halvor Trials Study Protocol BACKGROUND: Bacillus Calmette-Guérin (BCG) vaccination may have nonspecific effects, i.e., effects on childhood morbidity and mortality that go beyond its effect on the risk of childhood tuberculosis (TB). Though the available scientific literature is mostly from observational studies, and is fraught with controversy, BCG vaccination at birth may protect infants in high-mortality populations against serious infections other than TB. Yet, other studies indicate that giving BCG later in infancy may modify immune responses to non-TB antigens and potentially enhance immunity, potentially also against tuberculosis (TB). It is unclear whether BCG vaccination very early in life offers adequate protection against TB and other infections among HIV-1-exposed children because even those who remain uninfected with HIV-1 show signs of impaired immunocompetence early in infancy. This study will compare BCG vaccination at birth with BCG vaccination at 14 weeks of age in HIV-1-exposed infants. METHODS: This is an individually randomized controlled trial in 2200 HIV-1-exposed infants. The intervention is BCG vaccination within 24 h of birth while the comparator is BCG given at 14 weeks of age. The study co-primary outcomes are severe illness in the first 14 weeks of life, and production of tumor necrosis factor, interleukin (IL)-1β, IL-6 and interferon-γ in response to mycobacterial and nonmycobacterial antigens. The study is being conducted in three health centers in Uganda. DISCUSSION: A well-timed BCG vaccination could have important nonspecific effects in HIV-1-exposed infants. This trial could inform the development of appropriate timing of BCG vaccination for HIV-1-exposed infants. TRIAL REGISTRATION: ClinicalTrials.gov, identifier: NCT02606526. Registered on 12 November 2015. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13063-017-1881-z) contains supplementary material, which is available to authorized users. BioMed Central 2017-03-31 /pmc/articles/PMC5374628/ /pubmed/28359325 http://dx.doi.org/10.1186/s13063-017-1881-z Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Study Protocol Nankabirwa, Victoria Tumwine, James K. Namugga, Olive Tylleskär, Thorkild Ndeezi, Grace Robberstad, Bjarne Netea, Mihai G. Sommerfelt, Halvor Early versus late BCG vaccination in HIV-1-exposed infants in Uganda: study protocol for a randomized controlled trial |
title | Early versus late BCG vaccination in HIV-1-exposed infants in Uganda: study protocol for a randomized controlled trial |
title_full | Early versus late BCG vaccination in HIV-1-exposed infants in Uganda: study protocol for a randomized controlled trial |
title_fullStr | Early versus late BCG vaccination in HIV-1-exposed infants in Uganda: study protocol for a randomized controlled trial |
title_full_unstemmed | Early versus late BCG vaccination in HIV-1-exposed infants in Uganda: study protocol for a randomized controlled trial |
title_short | Early versus late BCG vaccination in HIV-1-exposed infants in Uganda: study protocol for a randomized controlled trial |
title_sort | early versus late bcg vaccination in hiv-1-exposed infants in uganda: study protocol for a randomized controlled trial |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5374628/ https://www.ncbi.nlm.nih.gov/pubmed/28359325 http://dx.doi.org/10.1186/s13063-017-1881-z |
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