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Immune reconstitution syndrome due to BCG in HIV-treated children

Original title: Immune reconstitution syndrome due to BCG in HIV-treated children
  • Edwin Miranda-Choque
    ,
  • Jorge Candela-Herrera
    ,
  • ,
  • Sonia Farfán-Ramos
    ,
  • Aldo Barriga
  • Instituto Nacional de Salud del Niño
    ,
  • Universidad Peruana Cayetano Heredia
    ,
  • University of California Los Angeles
    ,
  • Hospital de Emergencias Pediatricas
Research Output:
Contribution to journal
Article
Peer-review

Open access

Publication Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Pages from-to (Number of pages)

Pages 498-502 (5 pages)

Journal (Volume, Issue Number)

Revista Peruana de Medicina Experimental y Salud Publica (Volume 29, Issue 4)

Publication milestones

  • Published - 2012

Publication status

Published - 2012

ISSN

1726-4634

Publication IDs

  • Scopus: 84873971042

Abstract

The objective of this study is to describe the clinical profile of the immune reconstitution syndrome due to Mycobacterium bovis Bacillus Calmette-Guérin (IRS-BCG) in children with HIV infection who receive highly active antiretroviral treatment (HAART) at Instituto Nacional de Salud del Niño de Lima (National Children's Health Institute of Lima), Peru. A case study was conducted, including 8 children with IRS-BCG, defined as the presence of regional lymphadenopathy or inflammation on the BCG vaccination site with at least one less logarithm in the viral load or immune improvement. All patients had AIDS (C3). The starting median age in HAART was 7.2 months and the event occurred 3 to 11 weeks after the treatment was started. 7 cases showed axillary adenitis. When compared with the Non IRS-BCG group, a significant association between the age at which HAART was started at one year, severe immunodepression, and increased viral load was found. It is concluded that IRS-BCG was related to a rapid clinical progression of the mother-to-child transmitted HIV/AIDS infection, severe immunosuppression and high viral load when the HAART began.

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