Innate lymphocytes: Role in alcohol-induced immune dysfunction

Alcohol use is known to alter the function of both innate and adaptive immune cells, such as neutrophils, macrophages, B cells, and T cells. Immune dysfunction has been associated with alcohol-induced end-organ damage. The role of innate lymphocytes in alcohol-associated pathogenesis has become a fo...

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Published in:Frontiers in immunology Vol. 13; p. 934617
Main Authors: Ruiz-Cortes, Karla, Villageliu, Daniel N., Samuelson, Derrick R.
Format: Journal Article
Language:English
Published: Frontiers Media S.A 29-08-2022
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Summary:Alcohol use is known to alter the function of both innate and adaptive immune cells, such as neutrophils, macrophages, B cells, and T cells. Immune dysfunction has been associated with alcohol-induced end-organ damage. The role of innate lymphocytes in alcohol-associated pathogenesis has become a focus of research, as liver-resident natural killer (NK) cells were found to play an important role in alcohol-associated liver damage pathogenesis. Innate lymphocytes play a critical role in immunity and homeostasis; they are necessary for an optimal host response against insults including infections and cancer. However, the role of innate lymphocytes, including NK cells, natural killer T (NKT) cells, mucosal associated invariant T (MAIT) cells, gamma delta T cells, and innate lymphoid cells (ILCs) type 1–3, remains ill-defined in the context of alcohol-induced end-organ damage. Innate-like B lymphocytes including marginal zone B cells and B-1 cells have also been identified; however, this review will address the effects of alcohol misuse on innate T lymphocytes, as well as the consequences of innate T-lymphocyte dysfunction on alcohol-induced tissue damage.
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Reviewed by: Luc Van Kaer, Vanderbilt University Medical Center, United States; Barbara L Kee, The University of Chicago, United States; Hui Peng, University of Science and Technology of China, China
Edited by: Jochen Mattner, University of Erlangen Nuremberg, Germany
This article was submitted to Nutritional Immunology, a section of the journal Frontiers in Immunology
These authors have contributed equally to this work
ISSN:1664-3224
1664-3224
DOI:10.3389/fimmu.2022.934617