Evidence map›Paper›PMID 40486112›Full record

ReviewJHLT open2025

Pharmacodynamics monitoring after lung transplantation.

Manuel Lopez-Meseguer, Marta Zapata-Ortega, Cristina Berastegui Garcia, Marta Andreu Casas, Paula Barquero Dueñas, Victor Monforte, Carlos Bravo, Susana Gomez-Olles, Berta Saez-Gimenez, Eva Revilla-Lopez

Abstract readReview
In one paragraph

Review in JHLT open, 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

10 authors.

Manuel Lopez-MeseguerRespiratory Department, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
Marta Zapata-OrtegaLaboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of Chronic Diseases and Metabolism, KU Leuven, Leuven, Belgium.
Cristina Berastegui GarciaRespiratory Department, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
Marta Andreu CasasRespiratory Department, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
Paula Barquero DueñasRespiratory Department, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
Victor MonforteRespiratory Department, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
Carlos BravoRespiratory Department, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
Susana Gomez-OllesRespiratory Department, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
Berta Saez-GimenezRespiratory Department, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
Eva Revilla-LopezRespiratory Department, Hospital Universitari Vall d'Hebron, Barcelona, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Defining the optimal dosage of immunosuppressive drugs remains a significant challenge for solid organ transplant recipients, particularly for lung transplant recipients, who face an increased risk of infection. In these patients, it is crucial to carefully balance immunosuppression to ensure efficacy, prevent rejection, and minimize toxicity. Although the limitations of therapeutic drug monitoring have been widely discussed, pharmacodynamics monitoring has not reached the clinical practice. This review aims to evaluate the various methodologies available for monitoring the effects of immunosuppression in individual patients. While the initial focus was on directly assessing the impact of immunosuppressive treatments, we found limited evidence in this area. Instead, much of the available research is focused on predicting specific outcomes and indirectly assessing immunosuppression needs in lung transplant recipients. In this review, we provide an overview of the different methodologies that can be utilized to enhance the personalization of immunosuppressive therapy following lung transplantation. These include enzymatic monitoring, T-cell mediated functional assays, monitoring of lymphocyte subsets, gene expression profiling, and viral load measurements. Each of these approaches may contribute to a more tailored and effective immunosuppressive strategy for lung transplant recipients.

Indexed as

functional assaysimmunosuppressionNFATpharmacodynamicsTorque teno virus

Identifiers

PMID40486112
PMCPMC12142548

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.