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Cathepsin G in Experimental Tuberculosis: Relevance for Antibacterial Protection and Potential for Immunotherapy.
Walter, Kerstin; Steinwede, Kathrin; Aly, Sahar; Reinheckel, Thomas; Bohling, Jennifer; Maus, Ulrich A; Ehlers, Stefan.
Afiliação
  • Walter K; Priority Area Infections, Research Center Borstel, Borstel 23845, Germany; German Center for Infection Research, Thematic Translational Unit Tuberculosis, partner site Borstel, Borstel 23845, Germany; kwalter@fz-borstel.de.
  • Steinwede K; Department of Experimental Pneumology, Hannover Medical School, Hannover 30625, Germany;
  • Aly S; Medical Clinic for Infection Biology and Pneumology, Charité University Medicine Berlin, Berlin 13353, Germany; and.
  • Reinheckel T; Institute of Molecular Medicine and Cell Research, University of Freiburg, Freiburg 79104, Germany.
  • Bohling J; Department of Experimental Pneumology, Hannover Medical School, Hannover 30625, Germany;
  • Maus UA; Department of Experimental Pneumology, Hannover Medical School, Hannover 30625, Germany;
  • Ehlers S; Priority Area Infections, Research Center Borstel, Borstel 23845, Germany; German Center for Infection Research, Thematic Translational Unit Tuberculosis, partner site Borstel, Borstel 23845, Germany;
J Immunol ; 195(7): 3325-33, 2015 Oct 01.
Article em En | MEDLINE | ID: mdl-26320257
ABSTRACT
Neutrophil serine proteases, such as cathepsin G (CG) and neutrophil elastase (NE), have been implicated in the protective response against infections, including experimental mycobacterial infections. The goal of this study was to explore the role of CG in immunocompetent mice challenged aerogenically with Mycobacterium tuberculosis. We used genetically CG- or CG/NE-deficient mice to define the importance of these neutrophil serine proteases for antibacterial protection, granulomatous response, and survival. In addition, we explored the effect of intratracheally delivered liposomally encapsulated CG/NE as a therapeutic approach early during M. tuberculosis infection. Our data show that the presence of CG or CG/NE prolongs survival in M. tuberculosis-infected mice. However, CG is not directly involved in antibacterial defenses, and exogenous intratracheal administration of CG combined with NE does not reduce bacterial loads in the lungs of M. tuberculosis-infected mice.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tuberculose / Elastase de Leucócito / Catepsina G / Mycobacterium tuberculosis Limite: Animals Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tuberculose / Elastase de Leucócito / Catepsina G / Mycobacterium tuberculosis Limite: Animals Idioma: En Ano de publicação: 2015 Tipo de documento: Article