Evidence map›Paper›PMID 17222534›Full record

ArticleJournal of autoimmunity2006

T cell targeting and phagocytosis of apoptotic biliary epithelial cells in primary biliary cirrhosis.

Jorge Allina, Bin Hu, Daniel M Sullivan, Maria Isabel Fiel, Swan N Thung, Steven F Bronk, Robert C Huebert, Judy van de Water, Nicholas F LaRusso, M E Gershwin and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of autoimmunity, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

42 citing papers in PubMed, 92 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Myeloid Cells and Chronic Liver Disease: a Comprehensive Review.Clinical reviews in allergy & immunology · 2018
    Review
  7. Review
  8. Review
  9. Article
  10. Primary biliary cirrhosis: From bench to bedside.World journal of gastrointestinal pharmacology and therapeutics · 2015
    Review
  11. Review
  12. Review
  13. Review
  14. Molecular mechanisms of hepatic apoptosis.Cell death & disease · 2014
    Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Cutting-edge issues in primary biliary cirrhosis.Clinical reviews in allergy & immunology · 2012
    Review
  20. Article
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

12 authors at 4 institutions in 1 country.

Jorge AllinaDepartment of Medicine, The Mount Sinai School of Medicine, New York, NY, USA.
Bin Hu
Daniel M Sullivan
Maria Isabel Fiel
Swan N Thung
Steven F Bronk
Robert C Huebert
Judy van de Water
Nicholas F LaRusso
M E Gershwin
Gregory J Gores
Joseph A Odin
Icahn School of Medicine at Mount Sinai · USMayo Clinic · USUniversity of California, Davis · USNational Institutes of Health · US

Funding

MECHANISMS AND PATHOGENESIS OF PRIMARY BILIARY CIRRHOSISR37DK039588 · NIDDK · UNIVERSITY OF CALIFORNIA DAVIS · PI GERSHWIN, MERRILL E · 2001 to 2010
$3.5M
MECHANISMS AND PATHOGENESIS OF PRIMARY BILIARY CIRRHOSISR01DK039588 · NIDDK · UNIVERSITY OF CALIFORNIA DAVIS · PI GERSHWIN, MERRILL E · 1988 to 2015
$2.0M
Advanced Microscopy Shared Resource FacilityR24CA095823 · NCI · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI FRIEDRICH, VICTOR LOUIS · 2002 to 2006
$1.3M
Role of Apoptotic Cholangiocytes in PBCK08DK059653 · NIDDK · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI ODIN, JOSEPH · 2001 to 2005
$638k
NCI NIH HHS 1 R24 CA095823-01NCI NIH HHS R24 CA095823NIDDK NIH HHS DK 39588NIDDK NIH HHS DK59653NIDDK NIH HHS K08 DK059653NIDDK NIH HHS R01 DK039588NIDDK NIH HHS R37 DK039588
6 · The paper itself

Abstract

Primary biliary cirrhosis (PBC) is characterized by loss of tolerance against ubiquitously expressed mitochondrial autoantigens followed by biliary and salivary gland epithelial cell (BEC and SGEC) destruction by autoreactive T cells. It is unclear why BECs and SGECs are targeted. Previous work demonstrated that the reduced form of the major PBC autoantigen predominated in apoptotic BECs and SGECs as opposed to an oxidized form in other apoptotic cells. This led to the hypothesis that presentation of novel self-peptides from phagocytosed apoptotic BECs might contribute to BEC targeting by autoreactive T cells. The effect of autoantigen redox status on self-peptide formation was examined along with the phagocytic ability of BECs. Oxidation of PBC autoantigens first was shown to be due to protein S-glutathionylation of lipoyllysine residues. Absence of protein S-glutathionylation generated novel self-peptides and affected T cell recognition of a lipoyllysine containing peptide. Liver biopsy staining revealed BEC phagocytosis of apoptotic BECs (3.74+/-2.90% of BEC) was present in PBC (7 of 7 cases) but not in normal livers (0 of 3). BECs have the ability to present novel mitochondrial self-peptides derived from phagocytosed apoptotic BECs. Apoptotic cell phagocytosis by non-professional phagocytes may influence the tissue specificity of autoimmune diseases.

Indexed as

AnimalsApoptosisAutoantigensCathepsin BDihydrolipoyllysine-Residue AcetyltransferaseEpithelial CellsFemaleGlutathioneHeLa CellsHumansLiver Cirrhosis, BiliaryLysineMiceOxidation-ReductionPeptide HydrolasesPhagocytosisAutoantigensCathepsin BDihydrolipoyllysine-Residue AcetyltransferaseGlutathionelipoyllysineLysinePeptide HydrolasesThioctic Acid

Identifiers

PMID17222534
PMCPMC6200357
OpenAlexW2051104655

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.