Type I interferon suppresses type II interferon-triggered human anti-mycobacterial responses

  • Rosane M B Teles
  • , Thomas G Graeber
  • , Stephan R Krutzik
  • , Dennis Montoya
  • , Mirjam Schenk
  • , Delphine J Lee
  • , Evangelia Komisopoulou
  • , Kindra Kelly-Scumpia
  • , Rene Chun
  • , Shankar S Iyer
  • , Euzenir N Sarno
  • , Thomas H Rea
  • , Martin Hewison
  • , John S Adams
  • , Stephen J Popper
  • , David A Relman
  • , Steffen Stenger
  • , Barry R Bloom
  • , Genhong Cheng
  • , Robert L Modlin

Research output: Contribution to journalArticlepeer-review

257 Citations (Scopus)

Abstract

Type I interferons (IFN-α and IFN-β) are important for protection against many viral infections, whereas type II interferon (IFN-γ) is essential for host defense against some bacterial and parasitic pathogens. Study of IFN responses in human leprosy revealed an inverse correlation between IFN-β and IFN-γ gene expression programs. IFN-γ and its downstream vitamin D-dependent antimicrobial genes were preferentially expressed in self-healing tuberculoid lesions and mediated antimicrobial activity against the pathogen Mycobacterium leprae in vitro. In contrast, IFN-β and its downstream genes, including interleukin-10 (IL-10), were induced in monocytes by M. leprae in vitro and preferentially expressed in disseminated and progressive lepromatous lesions. The IFN-γ-induced macrophage vitamin D-dependent antimicrobial peptide response was inhibited by IFN-β and by IL-10, suggesting that the differential production of IFNs contributes to protection versus pathogenesis in some human bacterial infections.

Original languageEnglish
Pages (from-to)1448-53
Number of pages6
JournalScience
Volume339
Issue number6126
DOIs
Publication statusPublished - 22 Mar 2013

Keywords

  • 25-Hydroxyvitamin D3 1-alpha-Hydroxylase
  • Antimicrobial Cationic Peptides
  • Humans
  • Interferon-beta
  • Interferon-gamma
  • Interleukin-10
  • Leprosy, Lepromatous
  • Leprosy, Tuberculoid
  • Microbial Viability
  • Monocytes
  • Mycobacterium leprae
  • RNA, Messenger
  • Receptors, Calcitriol
  • Transcriptome
  • Tuberculosis
  • Up-Regulation
  • beta-Defensins

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