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Microbiota-mediated inflammation and antimicrobial defense in the intestine.
Caballero, Silvia; Pamer, Eric G.
Afiliación
  • Caballero S; Immunology Program, Sloan Kettering Institute, Infectious Diseases Service, Memorial Sloan Kettering Cancer Center, New York, NY 10065; email: pamere@mskcc.org.
Annu Rev Immunol ; 33: 227-56, 2015.
Article en En | MEDLINE | ID: mdl-25581310
ABSTRACT
The diverse microbial populations constituting the intestinal microbiota promote immune development and differentiation, but because of their complex metabolic requirements and the consequent difficulty culturing them, they remained, until recently, largely uncharacterized and mysterious. In the last decade, deep nucleic acid sequencing platforms, new computational and bioinformatics tools, and full-genome characterization of several hundred commensal bacterial species facilitated studies of the microbiota and revealed that differences in microbiota composition can be associated with inflammatory, metabolic, and infectious diseases, that each human is colonized by a distinct bacterial flora, and that the microbiota can be manipulated to reduce and even cure some diseases. Different bacterial species induce distinct immune cell populations that can play pro- and anti-inflammatory roles, and thus the composition of the microbiota determines, in part, the level of resistance to infection and susceptibility to inflammatory diseases. This review summarizes recent work characterizing commensal microbes that contribute to the antimicrobial defense/inflammation axis.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Resistencia a la Enfermedad / Microbioma Gastrointestinal / Gastroenteritis / Mucosa Intestinal Tipo de estudio: Etiology_studies Límite: Animals / Humans Idioma: En Revista: Annu Rev Immunol Año: 2015 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Resistencia a la Enfermedad / Microbioma Gastrointestinal / Gastroenteritis / Mucosa Intestinal Tipo de estudio: Etiology_studies Límite: Animals / Humans Idioma: En Revista: Annu Rev Immunol Año: 2015 Tipo del documento: Article