Evidence map›Paper›PMID 40170787›Full record

ArticleTransplant international : official journal of the European Society for Organ Transplantation2025

Anti-TNFα as an Adjunctive Therapy in Pancreas and Kidney Transplantation.

Christophe Masset, Benoit Mesnard, Olivia Rousseau, Alexandre Walencik, Ismaël Chelghaf, Magali Giral, Aurélie Houzet, Gilles Blancho, Jacques Dantal, Julien Branchereau and 2 more

Abstract read
In one paragraph

Article in Transplant international : official journal of the European Society for Organ Transplantation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Christophe MassetInstitut de Transplantation-Urologie-Néphrologie (ITUN), Nantes University Hospital, Nantes, France.
Benoit MesnardInstitut de Transplantation-Urologie-Néphrologie (ITUN), Nantes University Hospital, Nantes, France.
Olivia RousseauNantes Université, INSERM, Center for Research in Transplantation and Translational Immunology, UMR 1064, Nantes, France.
Alexandre WalencikLaboratoire Human Leucocyte Antigen (HLA), Etablissement Français du Sang, Nantes, France.
Ismaël ChelghafInstitut de Transplantation-Urologie-Néphrologie (ITUN), Nantes University Hospital, Nantes, France.
Magali GiralInstitut de Transplantation-Urologie-Néphrologie (ITUN), Nantes University Hospital, Nantes, France.
Aurélie HouzetInstitut de Transplantation-Urologie-Néphrologie (ITUN), Nantes University Hospital, Nantes, France.
Gilles BlanchoInstitut de Transplantation-Urologie-Néphrologie (ITUN), Nantes University Hospital, Nantes, France.
Jacques DantalInstitut de Transplantation-Urologie-Néphrologie (ITUN), Nantes University Hospital, Nantes, France.
Julien BranchereauInstitut de Transplantation-Urologie-Néphrologie (ITUN), Nantes University Hospital, Nantes, France.
Claire GarandeauInstitut de Transplantation-Urologie-Néphrologie (ITUN), Nantes University Hospital, Nantes, France.
Diego CantarovichInstitut de Transplantation-Urologie-Néphrologie (ITUN), Nantes University Hospital, Nantes, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The rate of early pancreas allograft failure remains high due to thrombosis but also to severity of rejection episodes. We investigated if adjunct anti-TNFα therapy was safe and could improve outcomes after pancreas transplantation. We investigated all pancreas transplants performed in our institution between 2010 and 2022. Etanercept, an anti TNFα therapy, was added to our standard immunosuppressive regimen since 2017 after approval from our institutional human ethics committee. Pancreas survival, rejection episodes, as well as infectious complications were analyzed. A total of 236 pancreas transplants were included, among whom 87 received Etanercept for induction. In multivariable analysis, after adjustment on confounding variables, pancreas survival did not differ between groups (HR = 0.92, CI 95% = 0.48; 1.73, p = 0.79). However, patients receiving Etanercept presented a significantly lower occurrence of pancreas rejection in multivariate analysis (HR = 0.36, CI 95% = 0.14; 0.95, p = 0.04). Patients receiving Etanercept did not experienced a higher risk of bacterial, fungal, CMV nor BK virus infections compared to the non-treated group. The use of anti-TNFα after pancreas transplantation was safe and did not increase infectious complications. Despite a similar rate of thrombosis, anti-TNFα significantly reduced pancreatic rejection, thus supporting its use among pancreas transplant recipients.

Indexed as

EtanerceptGraft RejectionImmunosuppressive AgentsKidney TransplantationPancreas TransplantationTumor Necrosis Factor-alphaAdultFemaleGraft SurvivalHumansMaleMiddle AgedPostoperative ComplicationsRetrospective StudiesTreatment OutcomeEtanerceptImmunosuppressive AgentsTumor Necrosis Factor-alphaallograft rejectionallograft thrombosisanti-TNFαinflammationischemia/reperfusionpancreas transplantation

Identifiers

PMID40170787
PMCPMC11957988

What Socratic holds

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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 Socratic graph.