1991
DOI: 10.1016/0168-8278(91)90930-a
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Jejunal immunoglobulin secretion in alcoholic patients with and without cirrhosis

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Cited by 13 publications
(7 citation statements)
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“…It was reported that patients with decompensated cirrhosis had reduced intestinal secretion of IgA compared with those with compensated cirrhosis. 83 By contrast, two other investigations showed no differences in the levels of IgA secretion 84 and IgA-secreting plasma cells. 85 To date, no studies have evaluated the changes in GALT related to chronic alcohol consumption and how ethanol and/or its metabolites could impact intestinal lymphoid structures and functions.…”
Section: Open Accessmentioning
confidence: 83%
“…It was reported that patients with decompensated cirrhosis had reduced intestinal secretion of IgA compared with those with compensated cirrhosis. 83 By contrast, two other investigations showed no differences in the levels of IgA secretion 84 and IgA-secreting plasma cells. 85 To date, no studies have evaluated the changes in GALT related to chronic alcohol consumption and how ethanol and/or its metabolites could impact intestinal lymphoid structures and functions.…”
Section: Open Accessmentioning
confidence: 83%
“…In one study, patients with decompensated cirrhosis had reduced intestinal secretion of IgA compared to compensated alcohol-associated cirrhosis [71]. By contrast, two other studies reported similar levels of IgA secretion [72] and IgA-secreting plasma cells [73]. Characterization of IgA levels with different methods as well as characterization of IgA-plasma cells at different stages of ALD and possible impact of a period of abstinence before admission may partially explain these conflicting observations.…”
Section: Plasma Cellsmentioning
confidence: 97%
“…4). A decreased number of ileal goblet cells 108 , reduced mucus thickness in the ileum and colon 108,109 , a possible decrease in intestinal SIgA 110,111 , downregulation of small intestinal and colonic tight junction proteins 108,109 , and compromised Paneth cell function with decreased expression of AMPs 112,113 all contribute to impaired gut barrier function as observed in patients with cirrhosis and in experimental models. As a result, translocation of microbial products and live bacteria to mLNs add to mucosal, hepatic and systemic inflammation in liver disease (reviewed previously 114 ) 113,115,116 .…”
Section: Review Articlementioning
confidence: 99%