Evidence map›Paper›PMID 28775077›Full record

ArticleCirculation2018

Chronic Rejection of Cardiac Allografts Is Associated With Increased Lymphatic Flow and Cellular Trafficking.

Lindsey A Edwards, Anna K Nowocin, Nazila V Jafari, Lucy L Meader, Kathryn Brown, Aurélien Sarde, Carolyn Lam, Alex Murray, Wilson Wong

Open access · bronzeAbstract read
In one paragraph

Article in Circulation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.2field-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

27 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
  2. Article
  3. Cardiac Lymphatics Predict Survival After Heart Transplantation.Journal of the American Heart Association · 2026
    Article
  4. Article
  5. Review
  6. Best practices of heart transplantation in mice.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2025
    Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Role of Lymphangiogenesis in Cardiac Repair and Regeneration.Methodist DeBakey cardiovascular journal · 2023
    Review
  15. Review
  16. Review
  17. Article
  18. Review
  19. Article
  20. miR-21 antagonism reprograms macrophage metabolism and abrogates chronic allograft vasculopathy.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2021
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Lindsey A EdwardsMRC Centre for Transplantation, King's College London, Guy's Hospital, United Kingdom (L.A.E., A.K.N., N.V.J., L.L.M., K.B., A.S., C.L., A.M., W.W.) wilson.wong@kcl.ac.uk lindsey.edwards@kcl.ac.uk.
Anna K NowocinMRC Centre for Transplantation, King's College London, Guy's Hospital, United Kingdom (L.A.E., A.K.N., N.V.J., L.L.M., K.B., A.S., C.L., A.M., W.W.).
Nazila V JafariMRC Centre for Transplantation, King's College London, Guy's Hospital, United Kingdom (L.A.E., A.K.N., N.V.J., L.L.M., K.B., A.S., C.L., A.M., W.W.).
Lucy L MeaderMRC Centre for Transplantation, King's College London, Guy's Hospital, United Kingdom (L.A.E., A.K.N., N.V.J., L.L.M., K.B., A.S., C.L., A.M., W.W.).
Kathryn BrownMRC Centre for Transplantation, King's College London, Guy's Hospital, United Kingdom (L.A.E., A.K.N., N.V.J., L.L.M., K.B., A.S., C.L., A.M., W.W.).
Aurélien SardeMRC Centre for Transplantation, King's College London, Guy's Hospital, United Kingdom (L.A.E., A.K.N., N.V.J., L.L.M., K.B., A.S., C.L., A.M., W.W.).
Carolyn LamMRC Centre for Transplantation, King's College London, Guy's Hospital, United Kingdom (L.A.E., A.K.N., N.V.J., L.L.M., K.B., A.S., C.L., A.M., W.W.).
Alex MurrayMRC Centre for Transplantation, King's College London, Guy's Hospital, United Kingdom (L.A.E., A.K.N., N.V.J., L.L.M., K.B., A.S., C.L., A.M., W.W.).
Wilson WongMRC Centre for Transplantation, King's College London, Guy's Hospital, United Kingdom (L.A.E., A.K.N., N.V.J., L.L.M., K.B., A.S., C.L., A.M., W.W.) wilson.wong@kcl.ac.uk lindsey.edwards@kcl.ac.uk.
Guy's Hospital · GBKing's College London · GBSt Thomas' Hospital · GB

Funding

British Heart Foundation PG/13/29/30121Medical Research Council MR/J006742/1Wellcome Trust
6 · The paper itself

Abstract

backgroundCardiac transplantation is an excellent treatment for end-stage heart disease. However, rejection of the donor graft, in particular, by chronic rejection leading to cardiac allograft vasculopathy, remains a major cause of graft loss. The lymphatic system plays a crucial role in the alloimmune response, facilitating trafficking of antigen-presenting cells to draining lymph nodes. The encounter of antigen-presenting cells with T lymphocytes in secondary lymphoid organs is essential for the initiation of alloimmunity. Donor lymphatic vessels are not anastomosed to that of the recipient during transplantation. The pathophysiology of lymphatic disruption is unknown, and whether this disruption enhances or hinders the alloimmune responses is unclear. Although histological analysis of lymphatic vessels in donor grafts can yield information on the structure of the lymphatics, the function following cardiac transplantation is poorly understood.

methodsUsing single-photon emission computed tomography/computed tomography lymphoscintigraphy, we quantified the lymphatic flow index following heterotrophic cardiac transplantation in a murine model of chronic rejection.

resultsTen weeks following transplantation of a minor antigen (HY) sex-mismatched heart graft, the lymphatic flow index was significantly increased in comparison with sex-matched controls. Furthermore, the enhanced lymphatic flow index correlated with an increase in donor cells in the mediastinal draining lymph nodes; increased lymphatic vessel area; and graft infiltration of CD4

conclusionsChronic rejection results in increased lymphatic flow from the donor graft to draining lymph nodes, which may be a factor in promoting cellular trafficking, alloimmunity, and cardiac allograft vasculopathy.

Indexed as

Cell MovementHeart TransplantationAllograftsAnimalsChronic DiseaseDisease Models, AnimalFemaleGraft RejectionGraft SurvivalH-2 AntigensHistocompatibilityLymphLymphangiogenesisLymphatic VesselsLymphoscintigraphyMaleH-2 Antigensimmune systeminflammationrejectiontransplantation

Identifiers

PMID28775077
PMCPMC5737875
OpenAlexW2743696349

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.