ArticleThe American journal of pathology1996
Evidence that intestinal intraepithelial lymphocytes are activated cytotoxic T cells in celiac disease but not in giardiasis.
Article in The American journal of pathology, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 20 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
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Who cites it
20 citing papers in PubMed.
- T cell receptors for antigen on intraepithelial cytolytic T lymphocytes in celiac disease engage enterocyte HLA-E and HLA-B.Proceedings of the National Academy of Sciences of the United States of America · 2026Article
- Immune cell dynamics and mechanisms of epithelial injury in celiac disease.Frontiers in immunology · 2026Review
- Bacteria: Potential Make-or-Break Determinants of Celiac Disease.International journal of molecular sciences · 2024Review
- Artificial Intelligence Analysis of Celiac Disease Using an Autoimmune Discovery Transcriptomic Panel Highlighted Pathogenic Genes including BTLA.Healthcare (Basel, Switzerland) · 2022Article
- Giardia lamblia: Laboratory Maintenance, Lifecycle Induction, and Infection of Murine Models.Current protocols in microbiology · 2020Article
- Prolonged Duodenal Mucosal Lymphocyte Alterations in Patients With and Without Postinfectious Functional Gastrointestinal Disorders After Giardia Infection.The Journal of infectious diseases · 2019Article
- Rare Gastric Lesions Associated withJournal of pathology and translational medicine · 2017Review
- The Microbiota Contributes to CD8+ T Cell Activation and Nutrient Malabsorption following Intestinal Infection with Giardia duodenalis.Infection and immunity · 2016Article
- Intestinal γδ T-cell lymphomas are most frequently of type II enteropathy-associated T-cell type.Human pathology · 2013Article
- Gliadin activates HLA class I-restricted CD8+ T cells in celiac disease intestinal mucosa and induces the enterocyte apoptosis.Gastroenterology · 2008Article
- Role of CD8+ and CD4+ T lymphocytes in jejunal mucosal injury during murine giardiasis.Infection and immunity · 2004Article
- Immunohistochemical study of the apoptotic mechanisms in the intestinal mucosa during children's coeliac disease.Virchows Archiv : an international journal of pathology · 2003Article
- Distribution of HLA class I alleles differs in celiac disease patients according to age of onset.Digestive diseases and sciences · 2003Article
- Jejunal brush border microvillous alterations in Giardia muris-infected mice: role of T lymphocytes and interleukin-6.Infection and immunity · 2000Article
- Cytolytic mechanisms of intraepithelial lymphocytes in coeliac disease (CoD).Clinical and experimental immunology · 2000Article
- Selective expansion of intraepithelial lymphocytes expressing the HLA-E-specific natural killer receptor CD94 in celiac disease.Gastroenterology · 2000Article
- Article
- A cytotoxic phenotype does not predict clinical outcome in anaplastic large cell lymphomas.Journal of clinical pathology · 1999Article
- Most CD56+ intestinal lymphomas are CD8+CD5-T-cell lymphomas of monomorphic small to medium size histology.The American journal of pathology · 1998Article
- Intraepithelial lymphocytes in normal human intestine do not express proteins associated with cytolytic function.The American journal of pathology · 1997Article
Corrections and comments
- Erratum issuedKummer, A J [corrected to Kummer, J A]
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
To further define intraepithelial lymphocytes (IELs) in celiac disease (CD) and giardiasis, IELs were probed for the presence of cytolytic granules containing granzyme B (GrB) and T-cell-restricted intracellular antigen (TIA)-1. The expression of TIA-1, GrB, CD3 (T-cell-receptor-associated complex), and Leu-7 (subset of natural killer cells) was studied by a sensitive three-step immunoperoxidase technique. Stained IELs were determined quantitatively, and results were expressed as number of stained IELs per 100 epithelial cells (ECs). The relative content in labeled lamina propria lymphocytes was determined and expressed as the percentage of all lamina propria cells counted. When compared with controls, CD3+ and GrB+ IELs were significantly increased (P < 0.0004) in CD paralleled by an increase in TIA-1+ IELs (P < 0.0004). In CD, the highest numbers of IELs containing GrB were found in subjects with a flat mucosa (median, 38 IELs/100 ECs, P < 0.0004), followed by cases with shortened and blunted villi (median, 8 IELs/100 ECs, P < 0.0004) and, finally, CD patients with an intact villous architecture (median, 0.5 IELs/100 ECs, P < 0.02). Except for cases with giardiasis, Leu-7+ IELs were virtually absent in all groups as were GrB+ IELs in the controls and in subjects with giardiasis. In the lamina propria of CD subjects, GrB+ lymphocytes were also significantly increased (P < 0.001), whereas controls and cases with giardiasis were essentially free of GrB+ cytotoxic T lymphocytes. The percentage of CD3+ lamina propria lymphocytes was nearly equal in all groups. In humans and mice, extensive studies revealed a GrB expression to be absolutely restricted to activated cytotoxic T lymphocytes and natural killer cells. TIA-1, on the other hand, is considered a marker of resting T lymphocytes possessing cytolytic potential. We therefore conclude that IELs are cytotoxic T cells that are in a resting state in the normal small bowel and in giardiasis. In CD, they become activated as suggested by the GrB positivity of their granules.
Indexed as
Identifiers
8623906PMC1861583What OpenQuestion holds
Registered trials
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