ArticleAlcoholism, clinical and experimental research2008
Chronic ethanol consumption decreases murine Langerhans cell numbers and delays migration of Langerhans cells as well as dermal dendritic cells.
Article in Alcoholism, clinical and experimental research, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.
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29 citing papers in PubMed, 46 citations in OpenAlex.
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- Recombinant human milk fat globule-EGF factor VIII (rhMFG-E8) as a therapy for sepsis after acute exposure to alcohol.Molecular medicine (Cambridge, Mass.) · 2019Article
- Alcohol, aging, and innate immunity.Journal of leukocyte biology · 2017Review
- Skin Immunization Obviates Alcohol-Related Immune Dysfunction.Biomolecules · 2015Article
- Chronic ethanol feeding increases the severity of Staphylococcus aureus skin infections by altering local host defenses.Journal of leukocyte biology · 2015Article
- Alcohol's Effects on Lung Health and Immunity.Alcohol research : current reviews · 2015Review
- Alcohol Use As a Risk Factor in Infections and Healing: A Clinician's Perspective.Alcohol research : current reviews · 2015Review
- Pathogenesis of alcoholic liver disease: role of oxidative metabolism.World journal of gastroenterology · 2014Review
- Chronic ethanol exposure selectively inhibits the influenza-specific CD8 T cell response during influenza a virus infection.Alcoholism, clinical and experimental research · 2014Article
- Chronic ethanol feeding induces subset loss and hyporesponsiveness in skin T cells.Alcoholism, clinical and experimental research · 2014Article
- Mechanisms by which chronic ethanol feeding impairs the migratory capacity of cutaneous dendritic cells.Alcoholism, clinical and experimental research · 2013Article
- Alcoholic lung injury: metabolic, biochemical and immunological aspects.Toxicology letters · 2013Review
- Alcohol and inflammation and infection: clinical and experimental systems--summary of the 2010 Alcohol and Immunology Research Interest Group Meeting.Alcohol (Fayetteville, N.Y.) · 2012Article
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Authors and funding
6 authors at 1 institution in 1 country.
Funding
Abstract
backgroundChronic alcoholics experience increased incidence and severity of infections, the mechanism of which is incompletely understood. Dendritic cells (DC) migrate from peripheral locations to lymph nodes (LN) to initiate adaptive immunity against infection. Little is known about how chronic alcohol exposure affects skin DC numbers or migration.
methodsMice received 20% EtOH in the drinking water for up to 35 weeks. Baseline Langerhans cell (LC) and dermal DC (dDC) numbers were enumerated by immunofluorescence (IF). LC repopulation after inflammation was determined following congenic bone marrow (BM) transplant and ultraviolet (UV) irradiation. Net LC loss from epidermis was determined by IF following TNF-alpha or CpG stimulation. LC and dDC migration into LN was assessed by flow cytometry following epicutaneous FITC administration.
resultsChronic EtOH consumption caused a baseline reduction in LC but not dDC numbers. The deficit was not corrected following transplantation with non-EtOH-exposed BM and UV irradiation, supporting the hypothesis that the defect is intrinsic to the skin environment rather than LC precursors. Net loss of LC from epidermis following inflammation was greatly reduced in EtOH-fed mice versus controls. Ethanol consumption for at least 4 weeks led to delayed LC migration into LN, and consumption for at least 8 weeks led to delayed dDC migration into LN following epicutaneous FITC application.
conclusionsChronic EtOH consumption causes decreased density of epidermal LC, which likely results in decreased epidermal immunosurveillance. It also results in altered migratory responsiveness and delayed LC and dDC migration into LN, which likely delays activation of adaptive immunity. Decreased LC density at baseline appears to be the result of an alteration in the skin environment rather than an intrinsic LC defect. These findings provide novel mechanisms to at least partially explain why chronic alcoholics are more susceptible to infections, especially those following skin penetration.
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