Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2014 Jan-Feb;157(1-2):23-37.
doi: 10.1016/j.imlet.2013.11.003. Epub 2013 Nov 11.

Innate lymphoid cells: new paradigm in immunology of inflammation

Affiliations
Review

Innate lymphoid cells: new paradigm in immunology of inflammation

Vijay Kumar. Immunol Lett. 2014 Jan-Feb.

Abstract

Immune system is well characterized by immunologists into two major arms called innate immunity and adaptive immunity. However, recent advances in the field of immunology has led to the identification of specific immune cells, which lack signature signs of mature lymphocytes (i.e. antigen receptors), yet produce major cytokines (i.e. IFN-γ, IL-4, IL-5, IL-13, IL-9, etc.) of helper T (Th) cell mediated immune response. Therefore, these cells can be represented as the innate counterpart of helper T cells of adaptive immunity and are known as innate lymphoid cells (ILCs). These ILCs comprise of three different groups having different kinds of cells, i.e. group 1 (NK cells and ILC1 cells), group 2 and group 3 ILCs. However, they are also emerging as novel regulators of both chronic as well as acute inflammation induced by infection or caused by sterile inflammation. Therefore, an attempt has been made to highlight the regulatory role of ILCs during inflammation and modulation of these cells as novel tissue protective mechanism.

Keywords: Chemokines; Cytokines; ILCs; Infection; Inflammation; LTi cells.

PubMed Disclaimer

LinkOut - more resources