Evidence map›Paper›PMID 9202073›Full record

ArticleThe Journal of clinical investigation1997

Intestinal epithelial cells use two distinct pathways for HLA class II antigen processing.

R M Hershberg, P E Framson, D H Cho, L Y Lee, S Kovats, J Beitz, J S Blum, G T Nepom

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
4.5field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

68 citing papers in PubMed, 221 citations in OpenAlex.

  1. Review
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  12. Non-zero-sum microbiome immune system interactions.European journal of immunology · 2021
    Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Host-Derived Serine Protease Inhibitor 6 Provides Granzyme B-Independent Protection of Intestinal Epithelial Cells in Murine Graft-versus-Host Disease.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2018
    Article
  19. Article
  20. Review

8 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

R M HershbergImmunology and Diabetes Programs, Virginia Mason Research Center, Seattle, Washington 98101, USA. hersh@u.washington.edu
P E Framson
D H Cho
L Y Lee
S Kovats
J Beitz
J S Blum
G T Nepom
Virginia Mason Medical Center · USIndiana University – Purdue University Indianapolis · USUniversity of Washington · US

Funding

REGULATION OF ANTIGEN PRESENTATION BY ACIDIC PROTEASESR01AI033418 · NIAID · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI BLUM, JANICE S · 1993 to 2001
$498k
GENETIC DETERMINANTS OF ANTIGEN PRESENTATIONR01AI038913 · NIAID · BENAROYA RESEARCH INST AT VIRGINIA MASON · PI NEPOM, GERALD T · 1996 to 1998
–
NIAID NIH HHS AI33418NIAID NIH HHS AI38913NIDDK NIH HHS DK94017
6 · The paper itself

Abstract

Intestinal epithelial cells express a low level of HLA class II molecules constitutively, with elevated levels seen in the setting of mucosal inflammation including inflammatory bowel disease. The ability of intestinal epithelial cells to act as antigen presenting cells for alphabeta CD4(+) T lymphocytes was examined through a molecular analysis of the HLA class II antigen processing pathway. We have shown that intestinal epithelial cells contain abundant constitutive levels of the cathepsin proteases proven to function in HLA class II mediated antigen presentation. Activation of these cells by gamma-IFN induced the expression of invariant chain and HLA-DM alphabeta, thus facilitating the formation of compact, SDS-stable HLA- DR alphabeta heterodimers. Using HLA-DR-restricted T cells and retroviral mediated gene transfer of HLA-DR alleles into the intestinal epithelial cell lines HT-29 and T84, we demonstrated efficient antigen processing and presentation to CD4(+) T lymphocytes in the presence of the proinflammatory cytokine gamma-IFN. The class II processing pathway and presentation in the presence of gamma-IFN was indistinguishable from that observed with a conventional antigen presenting cell. Antigen processing also occurred in intestinal epithelial cells in the absence of gamma-IFN, and in contrast to that seen after stimulation with gamma-IFN, required high concentration of antigen and was not inhibited by the protease inhibitor leupeptin. These data suggest the use of two distinct pathways of HLA class II antigen processing in enterocytes with differential immunomodulatory properties in the presence or absence of mucosal inflammation.

Indexed as

EndopeptidasesHistocompatibility Antigens Class IICathepsin BCathepsin HCathepsin LCathepsinsCD4-Positive T-LymphocytesColonic NeoplasmsCysteine EndopeptidasesDimerizationDNA PrimersHLA-D AntigensHLA-DQ AntigensHLA-DR AntigensHumansInterferon-gammaCathepsin BCathepsin HCathepsin LCathepsinsCTSH protein, humanCTSL protein, humanCysteine EndopeptidasesDNA PrimersEndopeptidasesH2-M antigensHistocompatibility Antigens Class IIHLA-D AntigensHLA-DM antigensHLA-DQ AntigensHLA-DR AntigensInterferon-gammaleupeptinLeupeptinsProtease InhibitorsRecombinant Proteins

Identifiers

PMID9202073
PMCPMC508181
OpenAlexW2024511093

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.