Evidence map›Paper›PMID 37636574›Full record

ReviewFrontiers in medicine2023

Sterile inflammation in liver transplantation.

Riley Kahan, Paul L Cray, Nader Abraham, Qimeng Gao, Matthew G Hartwig, Justin J Pollara, Andrew S Barbas

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
4.1field-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

5 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. 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

7 authors at 1 institution in 1 country.

Riley KahanDuke Ex-Vivo Organ Lab (DEVOL)-Division of Abdominal Transplant Surgery, Duke University, Durham, NC, United States.
Paul L CrayDuke Ex-Vivo Organ Lab (DEVOL)-Division of Abdominal Transplant Surgery, Duke University, Durham, NC, United States.
Nader AbrahamDuke Ex-Vivo Organ Lab (DEVOL)-Division of Abdominal Transplant Surgery, Duke University, Durham, NC, United States.
Qimeng GaoDuke Ex-Vivo Organ Lab (DEVOL)-Division of Abdominal Transplant Surgery, Duke University, Durham, NC, United States.
Matthew G HartwigDuke Ex-Vivo Organ Lab (DEVOL)-Division of Abdominal Transplant Surgery, Duke University, Durham, NC, United States.
Justin J PollaraDuke Ex-Vivo Organ Lab (DEVOL)-Division of Abdominal Transplant Surgery, Duke University, Durham, NC, United States.
Andrew S BarbasDuke Ex-Vivo Organ Lab (DEVOL)-Division of Abdominal Transplant Surgery, Duke University, Durham, NC, United States.
Duke University · US

Funding

Improving transplant organ survival through the mitigation of donor-derived mitochondrial damage-associated molecular patternsR01AI153274 · NIAID · DUKE UNIVERSITY · PI BARBAS, ANDREW SERGHIOS, BRENNAN, TODD VICTOR · 2020 to 2023
$1.6M
NIAID NIH HHS R01 AI153274
6 · The paper itself

Abstract

Sterile inflammation is the immune response to damage-associated molecular patterns (DAMPs) released during cell death in the absence of foreign pathogens. In the setting of solid organ transplantation, ischemia-reperfusion injury results in mitochondria-mediated production of reactive oxygen and nitrogen species that are a major cause of uncontrolled cell death and release of various DAMPs from the graft tissue. When properly regulated, the immune response initiated by DAMP-sensing serves as means of damage control and is necessary for initiation of recovery pathways and re-establishment of homeostasis. In contrast, a dysregulated or overt sterile inflammatory response can inadvertently lead to further injury through recruitment of immune cells, innate immune cell activation, and sensitization of the adaptive immune system. In liver transplantation, sterile inflammation may manifest as early graft dysfunction, acute graft failure, or increased risk of immunosuppression-resistant rejection. Understanding the mechanisms of the development of sterile inflammation in the setting of liver transplantation is crucial for finding reliable biomarkers that predict graft function, and for development of therapeutic approaches to improve long-term transplant outcomes. Here, we discuss the recent advances that have been made to elucidate the early signs of sterile inflammation and extent of damage from it. We also discuss new therapeutics that may be effective in quelling the detrimental effects of sterile inflammation.

Indexed as

DAMPS (damage associated molecular pattern molecules)liver diseaseliver transplantmachine perfusionsterile inflammation

Identifiers

PMID37636574
PMCPMC10449546
OpenAlexW4385718305

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.