Evidence map›Paper›PMID 39494758›Full record

ArticleTransplant infectious disease : an official journal of the Transplantation Society

Epidemiology of Infections in Lung Transplant Recipients Treated With Belatacept.

Madeleine R Heldman, Jennifer L Saullo, Brandon M Menachem, Julia A Messina, Sana Arif, Julie M Steinbrink, Patrick C K Tam, Manuela Carugati, Cameron R Wolfe, Arthur W Baker and 1 more

Abstract read
In one paragraph

Article in Transplant infectious disease : an official journal of the Transplantation Society. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Belatacept as an alternative immunosuppressive agent for bone marrow-sparing in idiopathic pulmonary fibrosis lung transplant recipients with short telomeres.The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation · 2025
    Article
  2. 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.

Madeleine R HeldmanDepartment of Medicine, Division of Infectious Diseases, Duke University School of Medicine, Durham, North Carolina, USA.ORCID https://orcid.org/0000-0002-9424-1870
Jennifer L SaulloDepartment of Medicine, Division of Infectious Diseases, Duke University School of Medicine, Durham, North Carolina, USA.ORCID https://orcid.org/0000-0002-7684-431X
Brandon M MenachemDepartment of Medicine, Division of Pulmonary, Allergy, and Critical Care Medicine, Duke University School of Medicine, Durham, North Carolina, USA.
Julia A MessinaDepartment of Medicine, Division of Infectious Diseases, Duke University School of Medicine, Durham, North Carolina, USA.ORCID https://orcid.org/0000-0001-6411-198X
Sana ArifDepartment of Medicine, Division of Infectious Diseases, Duke University School of Medicine, Durham, North Carolina, USA.
Julie M SteinbrinkDepartment of Medicine, Division of Infectious Diseases, Duke University School of Medicine, Durham, North Carolina, USA.ORCID https://orcid.org/0000-0003-0771-3647
Patrick C K TamDepartment of Medicine, Division of Infectious Diseases, Duke University School of Medicine, Durham, North Carolina, USA.ORCID https://orcid.org/0000-0003-4602-1889
Manuela CarugatiDepartment of Medicine, Division of Infectious Diseases, Duke University School of Medicine, Durham, North Carolina, USA.ORCID https://orcid.org/0000-0002-3187-5905
Cameron R WolfeDepartment of Medicine, Division of Infectious Diseases, Duke University School of Medicine, Durham, North Carolina, USA.ORCID https://orcid.org/0000-0002-5365-5030
Arthur W BakerDepartment of Medicine, Division of Infectious Diseases, Duke University School of Medicine, Durham, North Carolina, USA.ORCID https://orcid.org/0000-0002-0914-0291
Eileen K MaziarzDepartment of Medicine, Division of Infectious Diseases, Duke University School of Medicine, Durham, North Carolina, USA.ORCID https://orcid.org/0000-0001-7779-9605

Funding

Combined Use of Statistical Process Control and Whole Genome Sequencing to Detect and Investigate Nontuberculous Mycobacterial Clusters and OutbreaksK08AI163462 · NIAID · DUKE UNIVERSITY · PI BAKER, ARTHUR W · 2021 to 2025
$942k
and Infectious DiseasesInternational Society of Lung TransplantationNational Institute of AllergyNIAID NIH HHS K08 AI163462NIH HHS K08-AI163462
6 · The paper itself

Abstract

backgroundBelatacept is a costimulatory blocker that can be used to prevent and treat rejection in lung transplant recipients (LuTRs). The epidemiology of infections in belatacept-treated LuTRs has not been systematically evaluated.

methodsWe performed a single-center retrospective study of all adult LuTRs who received belatacept as prevention or treatment of antibody-mediated rejection (desensitization) or as part of maintenance immunosuppression from January 1, 2011, to June 30, 2022. We assessed the epidemiology of infections that occurred within 12 months following the first belatacept dose.

resultsFifty-two LuTRs received at least one dose of belatacept as either desensitization (n = 32) or maintenance immunosuppression (n = 20). Among 45 patients who were cytomegalovirus (CMV) donor and/or recipient seropositive, nine (20%) developed CMV infection. Seven (77%) CMV infections occurred despite valganciclovir prophylaxis and four (44%) were associated with antiviral resistance. Three (6%) LuTRs developed Epstein-Barr virus (EBV) associated post-transplant lymphoproliferative disorder (PTLD). Twenty-five (48%) LuTRs developed 43 bacterial infections and five (10%) developed proven or probable invasive fungal disease. Incidence rates of viral, bacterial, and fungal infections were similar between the desensitization and maintenance groups: incidence rate ratios (95% confidence interval) were 0.70 (0.32-1.57), 1.31 (0.70-2.46), and 2.82 (0.31-25.2), respectively. Infection/PTLD prompted belatacept discontinuation in eight (15%) patients.

conclusionsIn the first year after belatacept initiation, LuTRs commonly developed CMV infections, EBV+ PTLD, and bacterial infections. Multicenter collaborations are needed to better understand infection risks in LuTRs treated with belatacept.

Indexed as

AbataceptBacterial InfectionsGraft RejectionImmunosuppressive AgentsLung TransplantationAdultAgedCytomegalovirus InfectionsFemaleHumansIncidenceMaleMiddle AgedRetrospective StudiesTransplant RecipientsAbataceptImmunosuppressive AgentsbelataceptCytomegalovirusimmunosuppressioninfectionslung transplant

Identifiers

PMID39494758
PMCPMC11867099

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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.