Evidence map›Paper›PMID 40657748›Full record

ArticleJournal of proteome research2025

Considerations and Software for Successful Immune Cell Deconvolution Using Proteomics Data.

Måns Zamore, Sergio Mosquim Junior, Sebastian L Andree, Can Altunbulakli, Malin Lindstedt, Fredrik Levander

Abstract read
In one paragraph

Article in Journal of proteome research, 2025. 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. Article
  2. Observational
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

6 authors.

Måns ZamoreDepartment of Immunotechnology, Lund University, SE-22363 Lund, Sweden.ORCID 0000-0002-8108-1097
Sergio Mosquim JuniorDepartment of Immunotechnology, Lund University, SE-22363 Lund, Sweden.
Sebastian L AndreeDepartment of Immunotechnology, Lund University, SE-22363 Lund, Sweden.
Can AltunbulakliDepartment of Immunotechnology, Lund University, SE-22363 Lund, Sweden.
Malin LindstedtDepartment of Immunotechnology, Lund University, SE-22363 Lund, Sweden.
Fredrik LevanderDepartment of Immunotechnology, Lund University, SE-22363 Lund, Sweden.ORCID 0000-0002-0710-9792

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inferring the cell-type composition of bulk samples can provide biological insight. While bulk transcriptomics data has been extensively used for this purpose, the use of proteomics data has remained unexplored until recently. This study evaluates computational approaches for estimating immune cell composition using bulk sample proteomics data. Leveraging defined immune cell populations and simulated mixtures, we assess the impact of preprocessing methods and software tools on cell deconvolution outcomes. Our findings demonstrate the feasibility of using proteomics data for cell-type deconvolution, with Pearson correlations for estimated proportions in simulated sample mixtures above 0.9 when employing optimal missing value imputation and reference matrix generation parameters. We further provide an R package, proteoDeconv, to facilitate the preprocessing of proteomics data for deconvolution and parsing of results. This study highlights the feasibility of using proteomics for analyzing cell-type composition in biological samples.

Indexed as

ProteomicsSoftwareComputational BiologyHumanscell-type deconvolutionimmune cellsimmune infiltrationLC-MS/MSproteomics

Identifiers

PMID40657748
PMCPMC12322953

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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.