AI Article Synopsis

  • Chronic alcohol abuse negatively impacts the immune system, increasing vulnerability to infections and cancer by affecting both innate and adaptive immunity, particularly B cells.
  • Long-term alcohol exposure in a mouse model shows a decline in B cell numbers and their ability to produce effective antibodies, paralleling human chronic alcoholism.
  • Various advanced methods are used to study B cell abnormalities in these ethanol-consuming mice, including assessments of B cell status in bone marrow, tests for B cell activation, and experiments examining the overall immune response.

Article Abstract

Chronic alcohol abuse leads to multiple defects in the immune system, leading to an increased risk of infectious disease and malignancy. Immune lesions encompass both the innate and adaptive arms and include deficiencies in the B-cell compartment. Long-term alcoholics exhibit loss of B cells in the periphery and diminished ability to generate protective antibodies. To better mimic the chronic alcoholic patient, our group has used an ethanol-in-drinking-water mouse model. Mice consuming alcohol in this manner progressively develop a range of immune abnormalities, including defects in humoral immunity. To document and explore B-cell lesions in ethanol-consuming mice, our laboratory has used a broad panel of technologies. These include protocols to define the physical state of B cells in the bone marrow and periphery, in vitro approaches to test B-cell activation potential and in vivo experiments to document the humoral competence of the host. These key techniques are detailed in the present chapter.

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http://dx.doi.org/10.1007/978-1-59745-242-7_20DOI Listing

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