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Group 2 innate Lymphoid Cells in Pulmonary immunity and Tissue Homeostasis

Journal

FRONTIERS IN IMMUNOLOGY
Volume 9, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2018.00840

Keywords

group 2 innate lymphoid cells; respiratory tract; innate immune responses; lung physiology; pulmonary microenvironment

Categories

Funding

  1. Canadian Institutes of Health Research (CIHR)
  2. Natural Sciences and Engineering Research Council (NSERC)
  3. Canadian Foundation of Innovation (CFI)
  4. CIHR New Investigator Award
  5. Fonds de recherche du Quebec Sante (FRQS)
  6. Canadian Institutes of Health Research
  7. German National Academy of Sciences Leopoldina
  8. American Association of Immunologists Careers in Immunology Fellowship Program

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Group 2 innate lymphoid cells (ILC2) represent an evolutionary rather old but only recently identified member of the family of innate lymphoid cells and have received much attention since their detailed description in 2010. They can orchestrate innate as well as adaptive immune responses as they interact with and influence several immune and non-immune cell populations. Moreover, ILC2 are able to rapidly secrete large amounts of type 2 cytokines that can contribute to protective but also detrimental host immune responses depending on timing, location, and physiological context. Interestingly, ILC2, despite their scarcity, are the dominant innate lymphoid cell population in the lung, indicating a key role as first responders and amplifiers upon immune challenge at this site. In addition, the recently described tissue residency of ILC2 further underlines the importance of their respective microenvironment. In this review, we provide an overview of lung physiology including a description of the most prominent pulmonary resident cells together with a review of known and potential ILC2 interactions within this unique environment. We will further outline recent observations regarding pulmonary ILC2 during immune challenge including respiratory infections and discuss different models and approaches to study ILC2 biology in the lung.

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