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Adjuvant interferon gamma in patients with drug – resistant pulmonary tuberculosis: a pilot study
BACKGROUND: Tuberculosis (TB) is increasing in the world and drug-resistant (DR) disease beckons new treatments. METHODS: To evaluate the action of interferon (IFN) gamma as immunoadjuvant to chemotherapy on pulmonary DR-TB patients, a pilot, open label clinical trial was carried out in the Cuban re...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2004
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC529257/ https://www.ncbi.nlm.nih.gov/pubmed/15500691 http://dx.doi.org/10.1186/1471-2334-4-44 |
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author | Suárez-Méndez, Roberto García-García, Idrian Fernández-Olivera, Norma Valdés-Quintana, Magalys Milanés-Virelles, María T Carbonell, Dalia Machado-Molina, Delfina Valenzuela-Silva, Carmen M López-Saura, Pedro A |
author_facet | Suárez-Méndez, Roberto García-García, Idrian Fernández-Olivera, Norma Valdés-Quintana, Magalys Milanés-Virelles, María T Carbonell, Dalia Machado-Molina, Delfina Valenzuela-Silva, Carmen M López-Saura, Pedro A |
author_sort | Suárez-Méndez, Roberto |
collection | PubMed |
description | BACKGROUND: Tuberculosis (TB) is increasing in the world and drug-resistant (DR) disease beckons new treatments. METHODS: To evaluate the action of interferon (IFN) gamma as immunoadjuvant to chemotherapy on pulmonary DR-TB patients, a pilot, open label clinical trial was carried out in the Cuban reference ward for the management of this disease. The eight subjects existing in the country at the moment received, as in-patients, 1 × 10(6 )IU of recombinant human IFN gamma intramuscularly, daily for one month and then three times per week up to 6 months as adjuvant to the indicated chemotherapy, according to their antibiograms and WHO guidelines. Sputum samples collection for direct smear observation and culture as well as routine clinical and thorax radiography assessments were done monthly. RESULTS: Sputum smears and cultures became negative for acid-fast-bacilli before three months of treatment in all patients. Lesion size was reduced at the end of 6 months treatment; the lesions disappeared in one case. Clinical improvement was also evident; body mass index increased in general. Interferon gamma was well tolerated. Few adverse events were registered, mostly mild; fever and arthralgias prevailed. CONCLUSIONS: These data suggest that IFN gamma is useful and well tolerated as adjunctive therapy in patients with DR-TB. Further controlled clinical trials are encouraged. |
format | Text |
id | pubmed-529257 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-5292572004-11-19 Adjuvant interferon gamma in patients with drug – resistant pulmonary tuberculosis: a pilot study Suárez-Méndez, Roberto García-García, Idrian Fernández-Olivera, Norma Valdés-Quintana, Magalys Milanés-Virelles, María T Carbonell, Dalia Machado-Molina, Delfina Valenzuela-Silva, Carmen M López-Saura, Pedro A BMC Infect Dis Research Article BACKGROUND: Tuberculosis (TB) is increasing in the world and drug-resistant (DR) disease beckons new treatments. METHODS: To evaluate the action of interferon (IFN) gamma as immunoadjuvant to chemotherapy on pulmonary DR-TB patients, a pilot, open label clinical trial was carried out in the Cuban reference ward for the management of this disease. The eight subjects existing in the country at the moment received, as in-patients, 1 × 10(6 )IU of recombinant human IFN gamma intramuscularly, daily for one month and then three times per week up to 6 months as adjuvant to the indicated chemotherapy, according to their antibiograms and WHO guidelines. Sputum samples collection for direct smear observation and culture as well as routine clinical and thorax radiography assessments were done monthly. RESULTS: Sputum smears and cultures became negative for acid-fast-bacilli before three months of treatment in all patients. Lesion size was reduced at the end of 6 months treatment; the lesions disappeared in one case. Clinical improvement was also evident; body mass index increased in general. Interferon gamma was well tolerated. Few adverse events were registered, mostly mild; fever and arthralgias prevailed. CONCLUSIONS: These data suggest that IFN gamma is useful and well tolerated as adjunctive therapy in patients with DR-TB. Further controlled clinical trials are encouraged. BioMed Central 2004-10-22 /pmc/articles/PMC529257/ /pubmed/15500691 http://dx.doi.org/10.1186/1471-2334-4-44 Text en Copyright © 2004 Suárez-Méndez et al; licensee BioMed Central Ltd. |
spellingShingle | Research Article Suárez-Méndez, Roberto García-García, Idrian Fernández-Olivera, Norma Valdés-Quintana, Magalys Milanés-Virelles, María T Carbonell, Dalia Machado-Molina, Delfina Valenzuela-Silva, Carmen M López-Saura, Pedro A Adjuvant interferon gamma in patients with drug – resistant pulmonary tuberculosis: a pilot study |
title | Adjuvant interferon gamma in patients with drug – resistant pulmonary tuberculosis: a pilot study |
title_full | Adjuvant interferon gamma in patients with drug – resistant pulmonary tuberculosis: a pilot study |
title_fullStr | Adjuvant interferon gamma in patients with drug – resistant pulmonary tuberculosis: a pilot study |
title_full_unstemmed | Adjuvant interferon gamma in patients with drug – resistant pulmonary tuberculosis: a pilot study |
title_short | Adjuvant interferon gamma in patients with drug – resistant pulmonary tuberculosis: a pilot study |
title_sort | adjuvant interferon gamma in patients with drug – resistant pulmonary tuberculosis: a pilot study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC529257/ https://www.ncbi.nlm.nih.gov/pubmed/15500691 http://dx.doi.org/10.1186/1471-2334-4-44 |
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