| Literature DB >> 27553405 |
Alejandro Francisco-Cruz1, Dulce Mata-Espinosa2, Octavio Ramos-Espinosa2, Brenda Marquina-Castillo2, Sergio Estrada-Parra3, Zhou Xing4, Rogelio Hernández-Pando5.
Abstract
Tuberculosis (TB), although a curable disease, remains a major cause of morbidity and mortality worldwide. It is necessary to develop a short-term therapy with reduced drug toxicity in order to improve adherence rate and control disease burden. Granulocyte-macrophage colony-stimulating factor (GM-CSF) may be a key cytokine in the treatment of pulmonary TB since it primes the activation and differentiation of myeloid and non-myeloid precursor cells, inducing the release of protective Th1 cytokines. In this work, we administrated by intratracheal route recombinant adenoviruses encoding GM-CSF (AdGM-CSF). This treatment produced significant bacterial elimination when administered in a single dose at 60 days of infection with drug sensitive or drug resistant Mtb strains in a murine model of progressive disease. Moreover, AdGM-CSF combined with primary antibiotics produced more rapid elimination of pulmonary bacterial burdens than conventional chemotherapy suggesting that this form of treatment could shorten the conventional treatment.Entities:
Keywords: Adjunct treatment; Granulocyte-macrophage colony-stimulating factor; Multidrug-resistant tuberculosis; Tuberculosis
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Year: 2016 PMID: 27553405 DOI: 10.1016/j.tube.2016.05.015
Source DB: PubMed Journal: Tuberculosis (Edinb) ISSN: 1472-9792 Impact factor: 3.131