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CISH controls bacterial burden early after infection with Mycobacterium tuberculosis in mice.
Carow, Berit; Gao, Yu; Terán, Graciela; Yang, Xuexian O; Dong, Chen; Yoshimura, Akihiko; Rottenberg, Martin E.
Afiliação
  • Carow B; Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, 17177 Stockholm, Sweden.
  • Gao Y; Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, 17177 Stockholm, Sweden.
  • Terán G; Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, 17177 Stockholm, Sweden; Immunoparasitology Unit, Universidad Mayor de San Andrés, La Paz, Bolivia.
  • Yang XO; Department of Molecular Genetics and Microbiology, University of New Mexico School of Medicine, Albuquerque, NM 87131, USA.
  • Dong C; Institute for Immunology and School of Medicine, Tsinghua University, Beijing 100084, China.
  • Yoshimura A; Department of Microbiology and Immunology, Keio University School of Medicine, Tokyo 160-8582, Japan.
  • Rottenberg ME; Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, 17177 Stockholm, Sweden. Electronic address: Martin.Rottenberg@ki.se.
Tuberculosis (Edinb) ; 107: 175-180, 2017 12.
Article em En | MEDLINE | ID: mdl-29050767
ABSTRACT
CISH gene has been associated with increased susceptibility to human tuberculosis. We found that cish-/- mice had higher M. tuberculosis load in spleens and lungs up to 2.5 weeks after infection but not later compared to controls. Cish mRNA levels were increased in lungs at early and late time points after M. tuberculosis infection. In relation, the titers of inos and tnf mRNA in lungs were reduced early after infection of cish-/- mice. The transfer of cish-/- and control T cells conferred rag1-/- mice similar protection to infection with M. tuberculosis. Macrophages showed increased cish mRNA levels after M. tuberculosis infection in vitro. However, mycobacterial uptake and growth in cish-/- and control macrophages was similar. Thus, we here show that CISH mediates control of M. tuberculosis in mice early after infection via regulation of innate immune mechanisms.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Tuberculose Pulmonar / Proteínas Supressoras da Sinalização de Citocina / Pulmão / Mycobacterium tuberculosis Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Tuberculose Pulmonar / Proteínas Supressoras da Sinalização de Citocina / Pulmão / Mycobacterium tuberculosis Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2017 Tipo de documento: Article