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New pathways of protective and pathological host defense to mycobacteria

期刊

TRENDS IN MICROBIOLOGY
卷 20, 期 9, 页码 419-428

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.tim.2012.06.002

关键词

tuberculosis; leprosy; T cells; innate immunity; genome wide screens; inflammation; protection

资金

  1. Netherlands' Organization of Scientific Research (NWO)
  2. Royal Netherlands' Academy of Arts and Sciences (KNAW)
  3. WOTRO/NACCAP
  4. Bill and Melinda Gates Foundation Grand Challenges in Global Health [GC6 74, GC12 82]
  5. EDCTP (AE-TBC project)
  6. Top Institute Pharma
  7. Netherlands Leprosy Relief Foundation
  8. Turing Foundation
  9. European Union's Seventh Framework Programme (FP7) for project NEWTBVAC
  10. European Union's Seventh Framework Programme (FP7) for project IDEA
  11. European Union's Seventh Framework Programme (FP7) for project ADITEC [280873]

向作者/读者索取更多资源

Recent studies have uncovered new mechanisms by which the human immune system attempts to control infection and how pathogens elude these mechanisms. Mycobacterial infections are prime examples of chronic battle fields between host and pathogens. The study of tuberculosis and related mycobacterial infectious diseases such as leprosy have greatly aided in deciphering mechanisms of immune mediated protection and pathology in humans. Here we review recent insights into the role of newly discovered T cell subsets including Th17, Tregs and nonclassically restricted T cells in adaptive immunity to mycobacteria. The role of newly discovered innate immune mechanisms in tuberculosis and leprosy along with recent results from 'unbiased' genome-wide and functional genetic approaches, are deciphering critical host pathways in human infectious disease.

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