Evidence map›Paper›PMID 21906254›Full record

ReviewAmerican journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons2011

The emerging role of the TIM molecules in transplantation.

M Y Yeung, M McGrath, N Najafian

Open access · hybridAbstract readReview
In one paragraph

Review in American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

26 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Elevated PD-L1 and PECAM-1 as Diagnostic Biomarkers of Acute Rejection in Lung Transplantation.Transplant international : official journal of the European Society for Organ Transplantation · 2024
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Inhibition of TIM-4 protects against cerebral ischaemia-reperfusion injury.Journal of cellular and molecular medicine · 2020
    Article
  12. Article
  13. Article
  14. Tim-3 Up-regulation in Patients with Gastric Cancer and Peptic Ulcer DiseaseAsian Pacific journal of cancer prevention : APJCP · 2017
    Article
  15. Article
  16. Review
  17. [Effect of inhibiting TIM-4 function in Kupffer cells on liver graft rejection in mice].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2016
    Article
  18. Negative CD4 + TIM-3 signaling confers resistance against cold preservation damage in mouse liver transplantation.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2015
    Article
  19. Article
  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

3 authors at 2 institutions in 1 country.

M Y YeungTransplantation Research Center, Brigham and Women's Hospital and Children's Hospital, Harvard Medical School, Boston, MA, USA.
M McGrath
N Najafian
Brigham and Women's Hospital · USHarvard University · US

Funding

The Role of TIM-1: TIM-4 Pathway in Allograft Rejection and ToleranceR01AI070820 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI SAYEGH, MOHAMED H · 2007 to 2011
$2.1M
TIM-3: Galectin-9: A Novel Regulatory Pathway of Alloimmune ActivationR56AI089777 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI NAJAFIAN, NADER · 2011 to 2011
$312k
NIAID NIH HHS R01 AI070820NIAID NIH HHS R01AI070820NIAID NIH HHS R56 AI089777
6 · The paper itself

Abstract

Since their discovery in 2001, the T-cell immunoglobulin mucin (TIM) family members have been shown to play important roles in the regulation of immune responses. The TIM family comprises of eight genes in the mouse, three of which are conserved in humans (TIM-1, TIM-3 and TIM-4). Initially, TIM-1 and TIM-3 were thought to be expressed solely on T cells. However, emerging data suggest a much broader expression pattern where their presence on APCs confers differing functions, including the ability to mediate phagocytosis. In contrast, TIM-4 is exclusively expressed on APCs. Together, the TIM molecules provide a functional repertoire for determining the fate of T-cell activation and differentiation. To date, much of the knowledge about the TIM family members has been garnered from the models of asthma, allergy and autoimmunity. More recently, data from experimental models of transplantation demonstrate that TIM family members also have a key role in alloimmunity. This review will serve to highlight the emerging data regarding this unique family of molecules and to identify their potential in transplantation tolerance.

Indexed as

TransplantationAnimalsHumansMiceMucinsMucins

Identifiers

PMID21906254
PMCPMC3205957
OpenAlexW1519297113

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.