Evidence map›Paper›PMID 25287443›Full record

ArticleImmunology and cell biology2015

Overexpression of Jagged-1 combined with blockade of CD40 pathway prolongs allograft survival.

Yingying Lin, Weili Chen, Jiali Li, Guoliang Yan, Chun Li, Ning Jin, Jie Chen, Chang Gao, Pengfei Ma, Shuangyue Xu and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Immunology and cell biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Notch Signaling and Immune Regulation in Alloimmunity.Current transplantation reports · 2016
    Article
  9. Review
  10. Targeting the Notch Pathway to Prevent Rejection.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2016
    Review
  11. Article
  12. 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

11 authors at 1 institution in 1 country.

Yingying LinOrgan Transplantation Institute, Xiamen University, Fujian Province, P.R. China.
Weili ChenOrgan Transplantation Institute, Xiamen University, Fujian Province, P.R. China.
Jiali LiOrgan Transplantation Institute, Xiamen University, Fujian Province, P.R. China.
Guoliang YanBasic Medical Department of Medical College, Xiamen University, Fujian Province, P.R. China.
Chun LiOrgan Transplantation Institute, Xiamen University, Fujian Province, P.R. China.
Ning JinOrgan Transplantation Institute, Xiamen University, Fujian Province, P.R. China.
Jie ChenBasic Medical Department of Medical College, Xiamen University, Fujian Province, P.R. China.
Chang GaoOrgan Transplantation Institute, Xiamen University, Fujian Province, P.R. China.
Pengfei MaOrgan Transplantation Institute, Xiamen University, Fujian Province, P.R. China.
Shuangyue XuOrgan Transplantation Institute, Xiamen University, Fujian Province, P.R. China.
Zhongquan QiOrgan Transplantation Institute, Xiamen University, Fujian Province, P.R. China.
Xiamen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dendritic cells (DCs) have the tolerogenic potential to regulate adaptive immunity and induce allografts acceptance. Here we investigated whether blockade of the CD40 pathway could enhance the immune tolerance induced by DC2.4 cells modified to express Jagged-1 (JAG1-DC) in heart transplantation. Results showed that JAG1-DC treatment combined with anti-CD40L monoclonal antibody (mAb) administration significantly prolonged cardiac allograft survival in mice, with long-term survival (>110 days) of 50% of the allografts in the recipients. The therapy specifically inhibited the immune response, induced alloantigen-specific T-cell hyporesponsiveness, upregulated transforming growth factor-β synthesis and increased the population of regulatory T cells (Tregs) driven by Jagged-1-Notch activation. These results highlight the potential application of gene therapy to induce alloantigen-specific Tregs effectively by providing the Jagged-1 stimulation.

Indexed as

Signal TransductionAllograftsAnimalsCalcium-Binding ProteinsCD40 AntigensCD40 LigandCell LineCell ProliferationDendritic CellsFemaleForkhead Transcription FactorsGraft SurvivalHeart TransplantationImmunosuppression TherapyInflammationIntercellular Signaling Peptides and ProteinsCalcium-Binding ProteinsCD40 AntigensCD40 LigandForkhead Transcription FactorsFoxp3 protein, mouseIntercellular Signaling Peptides and ProteinsJag1 protein, mouseJagged-1 ProteinMembrane ProteinsReceptors, NotchSerrate-Jagged ProteinsTransforming Growth Factor beta

Identifiers

PMID25287443
OpenAlexW2085222677

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.