Matches in SemOpenAlex for { <https://semopenalex.org/work/W1975783620> ?p ?o ?g. }
- W1975783620 endingPage "516.e5" @default.
- W1975783620 startingPage "508" @default.
- W1975783620 abstract "BackgroundCeliac disease (CeD) is a common gluten-sensitive autoimmune enteropathy. A gluten-free diet is an effective treatment, but compliance is demanding; hence, new treatment strategies for CeD are required.ObjectiveParasitic helminths hold promise for treating inflammatory disorders, so we examined the influence of experimental hookworm infection on the predicted outcomes of escalating gluten challenges in CeD subjects.MethodsA 52-week study was conducted involving 12 adults with diet-managed CeD. Subjects were inoculated with 20 Necator americanus larvae, and escalating gluten challenges consumed as pasta were subsequently administered: (1) 10 to 50 mg for 12 weeks (microchallenge); (2) 25 mg daily + 1 g twice weekly for 12 weeks (GC-1g); and (3) 3 g daily (60-75 straws of spaghetti) for 2 weeks (GC-3g). Symptomatic, serologic, and histological outcomes evaluated gluten toxicity. Regulatory and inflammatory T cell populations in blood and mucosa were examined.ResultsTwo gluten-intolerant subjects were withdrawn after microchallenge. Ten completed GC-1g, 8 of whom enrolled in and completed GC-3g. Primary outcomes: median villous height-to-crypt depth ratios (2.60-2.63; P = .98) did not decrease as predicted after GC-1g, and the mean IgA-tissue transglutaminase titers declined, contrary to the predicted rise after GC-3g. Secondary outcomes: quality of life scores improved (46.3-40.6; P = .05); celiac symptom indices (24.3-24.3; P = .53), intra-epithelial lymphocyte percentages (32.5-35.0; P = .47), and Marsh scores were unchanged by gluten challenge. Intestinal T cells expressing IFNγ were reduced following hookworm infection (23.9%-11.5%; P = .04), with corresponding increases in CD4+ Foxp3+ regulatory T cells (0.19%-1.12%; P = .001).ConclusionsNecator americanus and gluten microchallenge promoted tolerance and stabilized or improved all tested indices of gluten toxicity in CeD subjects. Celiac disease (CeD) is a common gluten-sensitive autoimmune enteropathy. A gluten-free diet is an effective treatment, but compliance is demanding; hence, new treatment strategies for CeD are required. Parasitic helminths hold promise for treating inflammatory disorders, so we examined the influence of experimental hookworm infection on the predicted outcomes of escalating gluten challenges in CeD subjects. A 52-week study was conducted involving 12 adults with diet-managed CeD. Subjects were inoculated with 20 Necator americanus larvae, and escalating gluten challenges consumed as pasta were subsequently administered: (1) 10 to 50 mg for 12 weeks (microchallenge); (2) 25 mg daily + 1 g twice weekly for 12 weeks (GC-1g); and (3) 3 g daily (60-75 straws of spaghetti) for 2 weeks (GC-3g). Symptomatic, serologic, and histological outcomes evaluated gluten toxicity. Regulatory and inflammatory T cell populations in blood and mucosa were examined. Two gluten-intolerant subjects were withdrawn after microchallenge. Ten completed GC-1g, 8 of whom enrolled in and completed GC-3g. Primary outcomes: median villous height-to-crypt depth ratios (2.60-2.63; P = .98) did not decrease as predicted after GC-1g, and the mean IgA-tissue transglutaminase titers declined, contrary to the predicted rise after GC-3g. Secondary outcomes: quality of life scores improved (46.3-40.6; P = .05); celiac symptom indices (24.3-24.3; P = .53), intra-epithelial lymphocyte percentages (32.5-35.0; P = .47), and Marsh scores were unchanged by gluten challenge. Intestinal T cells expressing IFNγ were reduced following hookworm infection (23.9%-11.5%; P = .04), with corresponding increases in CD4+ Foxp3+ regulatory T cells (0.19%-1.12%; P = .001). Necator americanus and gluten microchallenge promoted tolerance and stabilized or improved all tested indices of gluten toxicity in CeD subjects." @default.
- W1975783620 created "2016-06-24" @default.
- W1975783620 creator A5001125098 @default.
- W1975783620 creator A5004780792 @default.
- W1975783620 creator A5004853564 @default.
- W1975783620 creator A5014706177 @default.
- W1975783620 creator A5015492632 @default.
- W1975783620 creator A5018848802 @default.
- W1975783620 creator A5028375853 @default.
- W1975783620 creator A5038795279 @default.
- W1975783620 creator A5051336225 @default.
- W1975783620 creator A5055957305 @default.
- W1975783620 creator A5056604982 @default.
- W1975783620 creator A5063583921 @default.
- W1975783620 creator A5072690991 @default.
- W1975783620 creator A5076303778 @default.
- W1975783620 date "2015-02-01" @default.
- W1975783620 modified "2023-10-10" @default.
- W1975783620 title "Experimental hookworm infection and gluten microchallenge promote tolerance in celiac disease" @default.
- W1975783620 cites W1964907966 @default.
- W1975783620 cites W1969157979 @default.
- W1975783620 cites W1970421062 @default.
- W1975783620 cites W1973648078 @default.
- W1975783620 cites W1975230280 @default.
- W1975783620 cites W1979413298 @default.
- W1975783620 cites W1982500490 @default.
- W1975783620 cites W1991861037 @default.
- W1975783620 cites W2004490581 @default.
- W1975783620 cites W2027141686 @default.
- W1975783620 cites W2034563187 @default.
- W1975783620 cites W2035831689 @default.
- W1975783620 cites W2040480374 @default.
- W1975783620 cites W2042261171 @default.
- W1975783620 cites W2048327989 @default.
- W1975783620 cites W2048821674 @default.
- W1975783620 cites W2053486923 @default.
- W1975783620 cites W2067375084 @default.
- W1975783620 cites W2072129671 @default.
- W1975783620 cites W2079451660 @default.
- W1975783620 cites W2084159240 @default.
- W1975783620 cites W2085233320 @default.
- W1975783620 cites W2090205875 @default.
- W1975783620 cites W2102201378 @default.
- W1975783620 cites W2103468078 @default.
- W1975783620 cites W2105614110 @default.
- W1975783620 cites W2111076992 @default.
- W1975783620 cites W2112923677 @default.
- W1975783620 cites W2116239493 @default.
- W1975783620 cites W2134199230 @default.
- W1975783620 cites W2138178372 @default.
- W1975783620 cites W2143252307 @default.
- W1975783620 cites W2143905974 @default.
- W1975783620 cites W2146868709 @default.
- W1975783620 cites W2158758405 @default.
- W1975783620 doi "https://doi.org/10.1016/j.jaci.2014.07.022" @default.
- W1975783620 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/25248819" @default.
- W1975783620 hasPublicationYear "2015" @default.
- W1975783620 type Work @default.
- W1975783620 sameAs 1975783620 @default.
- W1975783620 citedByCount "143" @default.
- W1975783620 countsByYear W19757836202015 @default.
- W1975783620 countsByYear W19757836202016 @default.
- W1975783620 countsByYear W19757836202017 @default.
- W1975783620 countsByYear W19757836202018 @default.
- W1975783620 countsByYear W19757836202019 @default.
- W1975783620 countsByYear W19757836202020 @default.
- W1975783620 countsByYear W19757836202021 @default.
- W1975783620 countsByYear W19757836202022 @default.
- W1975783620 countsByYear W19757836202023 @default.
- W1975783620 crossrefType "journal-article" @default.
- W1975783620 hasAuthorship W1975783620A5001125098 @default.
- W1975783620 hasAuthorship W1975783620A5004780792 @default.
- W1975783620 hasAuthorship W1975783620A5004853564 @default.
- W1975783620 hasAuthorship W1975783620A5014706177 @default.
- W1975783620 hasAuthorship W1975783620A5015492632 @default.
- W1975783620 hasAuthorship W1975783620A5018848802 @default.
- W1975783620 hasAuthorship W1975783620A5028375853 @default.
- W1975783620 hasAuthorship W1975783620A5038795279 @default.
- W1975783620 hasAuthorship W1975783620A5051336225 @default.
- W1975783620 hasAuthorship W1975783620A5055957305 @default.
- W1975783620 hasAuthorship W1975783620A5056604982 @default.
- W1975783620 hasAuthorship W1975783620A5063583921 @default.
- W1975783620 hasAuthorship W1975783620A5072690991 @default.
- W1975783620 hasAuthorship W1975783620A5076303778 @default.
- W1975783620 hasBestOaLocation W19757836201 @default.
- W1975783620 hasConcept C126322002 @default.
- W1975783620 hasConcept C142724271 @default.
- W1975783620 hasConcept C165901193 @default.
- W1975783620 hasConcept C178498320 @default.
- W1975783620 hasConcept C181199279 @default.
- W1975783620 hasConcept C203014093 @default.
- W1975783620 hasConcept C2776336767 @default.
- W1975783620 hasConcept C2776677957 @default.
- W1975783620 hasConcept C2777047024 @default.
- W1975783620 hasConcept C2777364306 @default.
- W1975783620 hasConcept C2778426112 @default.
- W1975783620 hasConcept C2779134260 @default.
- W1975783620 hasConcept C3019118998 @default.