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Randomized controlled trial of Hepatitis B virus vaccine in HIV-1-infected patients comparing two different doses

BACKGROUND: Co-infection with hepatitis B virus (HBV) and human immunodeficiency virus (HIV) is not infrequent as both share same route of exposure. The risk of developing chronic hepatitis B virus is 6%, in general population but can reach 10–20% in HBV/HIV co-infected patients. When compared to ge...

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Autores principales: Cornejo-Juárez, Patricia, Volkow-Fernández, Patricia, Escobedo-López, Kenia, Vilar-Compte, Diana, Ruiz-Palacios, Guillermo, Soto-Ramírez, Luis Enrique
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1468419/
https://www.ncbi.nlm.nih.gov/pubmed/16600028
http://dx.doi.org/10.1186/1742-6405-3-9
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author Cornejo-Juárez, Patricia
Volkow-Fernández, Patricia
Escobedo-López, Kenia
Vilar-Compte, Diana
Ruiz-Palacios, Guillermo
Soto-Ramírez, Luis Enrique
author_facet Cornejo-Juárez, Patricia
Volkow-Fernández, Patricia
Escobedo-López, Kenia
Vilar-Compte, Diana
Ruiz-Palacios, Guillermo
Soto-Ramírez, Luis Enrique
author_sort Cornejo-Juárez, Patricia
collection PubMed
description BACKGROUND: Co-infection with hepatitis B virus (HBV) and human immunodeficiency virus (HIV) is not infrequent as both share same route of exposure. The risk of developing chronic hepatitis B virus is 6%, in general population but can reach 10–20% in HBV/HIV co-infected patients. When compared to general population, the response rate to HBV vaccine in HIV-infected patients is diminished, so previous studies have tried to improve this response using variety of schedules, doses and co-administration of immunomodulators. The purpose of this study was to evaluate two doses of recombinant HBV vaccine (10 or 40 μg), IM at 0, 1 and 6 months. Vaccination response was measured 30–50 days after last dose; titers of >9.9 IU/L were considered positive. RESULTS: Seventy-nine patients were included, 48 patients (60.7%) serconverted. Thirty-nine patients (49.3%) received 10 μg vaccine dose, 24 patients (61.5%) seroconverted. Forty patients (50.7%) received 40 μg vaccine dose, 24 (60%) seroconverted. There were no differences between two doses. A statistically significant higher seroconversion rate was found for patients with CD4 cell counts at vaccination ≥ 200 cel/mm3 (33 of 38 patients, 86.8%), compared with those with CD4 < 200 cel/mm3 (15 of 41, 36.6%), [OR 11.44, 95% IC 3.67–35.59, p = 0.003], there were no differences between two vaccine doses. Using the logistic regression model, CD(4 )count <200 cel/mm(3 )were significantly associated with non serologic response (p = 0.003). None other variables such as gender, age, risk exposure for HIV, viral load, type or duration of HAART or AIDS-defining illness, were asociated with seroconversion. CONCLUSION: In this study, an increase dose of HBV vaccine did not show to increase the rate of response in HIV infected subjects. The only significant findings associated to the response rate was that a CD4 count ≥ 200 cel/mm(3), we suggest this threshold at which HIV patients should be vaccinated.
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spelling pubmed-14684192006-05-25 Randomized controlled trial of Hepatitis B virus vaccine in HIV-1-infected patients comparing two different doses Cornejo-Juárez, Patricia Volkow-Fernández, Patricia Escobedo-López, Kenia Vilar-Compte, Diana Ruiz-Palacios, Guillermo Soto-Ramírez, Luis Enrique AIDS Res Ther Research BACKGROUND: Co-infection with hepatitis B virus (HBV) and human immunodeficiency virus (HIV) is not infrequent as both share same route of exposure. The risk of developing chronic hepatitis B virus is 6%, in general population but can reach 10–20% in HBV/HIV co-infected patients. When compared to general population, the response rate to HBV vaccine in HIV-infected patients is diminished, so previous studies have tried to improve this response using variety of schedules, doses and co-administration of immunomodulators. The purpose of this study was to evaluate two doses of recombinant HBV vaccine (10 or 40 μg), IM at 0, 1 and 6 months. Vaccination response was measured 30–50 days after last dose; titers of >9.9 IU/L were considered positive. RESULTS: Seventy-nine patients were included, 48 patients (60.7%) serconverted. Thirty-nine patients (49.3%) received 10 μg vaccine dose, 24 patients (61.5%) seroconverted. Forty patients (50.7%) received 40 μg vaccine dose, 24 (60%) seroconverted. There were no differences between two doses. A statistically significant higher seroconversion rate was found for patients with CD4 cell counts at vaccination ≥ 200 cel/mm3 (33 of 38 patients, 86.8%), compared with those with CD4 < 200 cel/mm3 (15 of 41, 36.6%), [OR 11.44, 95% IC 3.67–35.59, p = 0.003], there were no differences between two vaccine doses. Using the logistic regression model, CD(4 )count <200 cel/mm(3 )were significantly associated with non serologic response (p = 0.003). None other variables such as gender, age, risk exposure for HIV, viral load, type or duration of HAART or AIDS-defining illness, were asociated with seroconversion. CONCLUSION: In this study, an increase dose of HBV vaccine did not show to increase the rate of response in HIV infected subjects. The only significant findings associated to the response rate was that a CD4 count ≥ 200 cel/mm(3), we suggest this threshold at which HIV patients should be vaccinated. BioMed Central 2006-04-06 /pmc/articles/PMC1468419/ /pubmed/16600028 http://dx.doi.org/10.1186/1742-6405-3-9 Text en Copyright © 2006 Cornejo-Juárez et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Cornejo-Juárez, Patricia
Volkow-Fernández, Patricia
Escobedo-López, Kenia
Vilar-Compte, Diana
Ruiz-Palacios, Guillermo
Soto-Ramírez, Luis Enrique
Randomized controlled trial of Hepatitis B virus vaccine in HIV-1-infected patients comparing two different doses
title Randomized controlled trial of Hepatitis B virus vaccine in HIV-1-infected patients comparing two different doses
title_full Randomized controlled trial of Hepatitis B virus vaccine in HIV-1-infected patients comparing two different doses
title_fullStr Randomized controlled trial of Hepatitis B virus vaccine in HIV-1-infected patients comparing two different doses
title_full_unstemmed Randomized controlled trial of Hepatitis B virus vaccine in HIV-1-infected patients comparing two different doses
title_short Randomized controlled trial of Hepatitis B virus vaccine in HIV-1-infected patients comparing two different doses
title_sort randomized controlled trial of hepatitis b virus vaccine in hiv-1-infected patients comparing two different doses
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1468419/
https://www.ncbi.nlm.nih.gov/pubmed/16600028
http://dx.doi.org/10.1186/1742-6405-3-9
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