Evidence map›Paper›PMID 20536563›Full record

ReviewImmunological reviews2010

TIM genes: a family of cell surface phosphatidylserine receptors that regulate innate and adaptive immunity.

Gordon J Freeman, Jose M Casasnovas, Dale T Umetsu, Rosemarie H DeKruyff

Open access · greenAbstract readReview
In one paragraph

Review in Immunological reviews, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 379 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
379citing papers in PubMed, 4 pooled it
11.5field-weighted citation impact, top 1% 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

379 citing papers in PubMed, 4 syntheses or guidelines pooled it, 605 citations in OpenAlex.

  1. Pooled it
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  4. Pooled it
  5. Plasma KIM-1 Is Associated with Recurrence Risk after Nephrectomy for Localized Renal Cell Carcinoma: A Trial of the ECOG-ACRIN Research Group (E2805).Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Trial
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  7. Review
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  10. Article
  11. TIM-3 in Cardiovascular Disease.Current heart failure reports · 2026
    Review
  12. Article
  13. Immune checkpoint molecules beyond PD-1 and CTLA-4: emerging targets in autoimmune diseases and cancer immunotherapy.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Review
  14. Article
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319 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

4 authors at 1 institution in 1 country.

Gordon J FreemanDepartment of Medical Oncology, Dana-Farber Cancer Institute, and Department of Medicine, Harvard Medical School, Boston, MA, USA. gordon_freeman@dfci.harvard.edu
Jose M Casasnovas
Dale T Umetsu
Rosemarie H DeKruyff
Dana-Farber Cancer Institute · US

Funding

TIM recognition of phosphatidylserine regulates innate and adaptive immunityP01AI054456 · NIAID · STANFORD UNIVERSITY · PI FREEMAN, GORDON JAMES · 2003 to 2014
$12.8M
Immune Tolerance/Immune Deviation Protect Against AsthmaR01HL069507 · NHLBI · STANFORD UNIVERSITY · PI DEKRUYFF, ROSEMARIE H · 2001 to 2004
$1.4M
NHLBI NIH HHS HL069507NHLBI NIH HHS R01 HL069507NIAID NIH HHS P01 AI054456
6 · The paper itself

Abstract

The TIM (T cell/transmembrane, immunoglobulin, and mucin) gene family plays a critical role in regulating immune responses, including allergy, asthma, transplant tolerance, autoimmunity, and the response to viral infections. The unique structure of TIM immunoglobulin variable region domains allows highly specific recognition of phosphatidylserine (PtdSer), exposed on the surface of apoptotic cells. TIM-1, TIM-3, and TIM-4 all recognize PtdSer but differ in expression, suggesting that they have distinct functions in regulating immune responses. TIM-1, an important susceptibility gene for asthma and allergy, is preferentially expressed on T-helper 2 (Th2) cells and functions as a potent costimulatory molecule for T-cell activation. TIM-3 is preferentially expressed on Th1 and Tc1 cells, and generates an inhibitory signal resulting in apoptosis of Th1 and Tc1 cells. TIM-3 is also expressed on some dendritic cells and can mediate phagocytosis of apoptotic cells and cross-presentation of antigen. In contrast, TIM-4 is exclusively expressed on antigen-presenting cells, where it mediates phagocytosis of apoptotic cells and plays an important role in maintaining tolerance. TIM molecules thus provide a functional repertoire for recognition of apoptotic cells, which determines whether apoptotic cell recognition leads to immune activation or tolerance, depending on the TIM molecule engaged and the cell type on which it is expressed.

Indexed as

Adaptive ImmunityImmunity, InnateAnimalsApoptosisBinding SitesDendritic CellsGenetic Association StudiesGenetic LinkageHepatitis A Virus Cellular Receptor 1Hepatitis A Virus Cellular Receptor 2HumansImmune SystemImmune ToleranceMembrane GlycoproteinsMembrane ProteinsModels, MolecularHAVCR1 protein, humanHAVCR2 protein, humanHepatitis A Virus Cellular Receptor 1Hepatitis A Virus Cellular Receptor 2Membrane GlycoproteinsMembrane Proteinsphosphatidylserine receptorPhosphatidylserinesReceptors, Cell SurfaceReceptors, VirusTIMD4 protein, human

Identifiers

PMID20536563
PMCPMC2914464
OpenAlexW2167717479

What OpenQuestion holds

Textmetadata
LicenceTDM
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.