Evidence map›Paper›PMID 42097357›Full record

ArticleAmerican journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons2026

De novo belatacept-based immunosuppression is not associated with increased risk of invasive fungal infection in kidney transplant recipients.

Emily M Eichenberger, Geeta M Karadkhele, Payas Vasanth, Christian Larsen

Abstract read
In one paragraph

Article in American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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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

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5 · Who and what money

Authors and funding

4 authors.

Emily M EichenbergerDivision of Infectious Disease, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia, USA. Electronic address: Emily.m.eichenberger@emory.edu.
Geeta M KaradkheleDepartment of Surgery, Emory University School of Medicine, Atlanta, Georgia, USA.
Payas VasanthDivision of Transplant Nephrology, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia, USA.
Christian LarsenDepartment of Surgery, Emory University School of Medicine, Atlanta, Georgia, USA.

Funding

Immune biomarkers to predict outcomes in solid organ transplant patients with bloodstream infectionsK23AI175676 · NIAID · EMORY UNIVERSITY · PI Emily M. Eichenberger · 2024 to 2026
$589k
NIAID NIH HHS K23 AI175676
6 · The paper itself

Abstract

The risk of invasive fungal infection (IFI) in kidney transplant recipients (KTRs) receiving de novo belatacept-based immunosuppression remains incompletely understood. We conducted a single-center retrospective cohort study of adult KTRs receiving de novo belatacept- or tacrolimus-based immunosuppression between 2016 and 2025. Cumulative incidence of IFI was estimated using competing-risks methods with death as a competing event and compared using Gray's test. Associations between immunosuppression and IFI risk were evaluated using a cause-specific Cox model, with thymoglobulin and high-dose steroids modeled as time-dependent covariates. A prespecified propensity score-matched cohort was analyzed to address selection bias. Associations between IFI and mortality were assessed using time-dependent Cox proportional hazards models. Among 2729 KTRs, 1875 (68.7%) received belatacept and 854 (31.3%) tacrolimus. The 1-year cumulative incidence of IFI was 1.4% in belatacept-treated patients vs 1.8% in tacrolimus-treated patients (P = .47). Belatacept compared with tacrolimus was not associated with IFI (hazard ratio, 0.87; 95% confidence interval, 0.54-1.39). IFI was associated with mortality (hazard ratio, 5.03; 95% confidence interval, 3.12-8.09). Similar results were observed in the propensity score-matched cohort. De novo belatacept-based immunosuppression does not confer increased risk of IFI, and routine antifungal prophylaxis may not be necessary.

Indexed as

AbataceptGraft RejectionImmunosuppression TherapyImmunosuppressive AgentsInvasive Fungal InfectionsKidney Failure, ChronicKidney TransplantationPostoperative ComplicationsAdultFemaleFollow-Up StudiesGraft SurvivalHumansIncidenceMaleMiddle AgedAbataceptImmunosuppressive Agentsbelataceptinvasive fungal infectionkidney transplant

Identifiers

PMID42097357
PMCPMC13251877

What OpenQuestion holds

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Registered trials

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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.