Evidence map›Paper›PMID 40855359›Full record

ArticleScientific reports2025

High throughput tear proteomics with data independent acquisition enables biomarker discovery in allergic conditions.

América Vera-Montecinos, Claudio Carril Pardo, Mauricio Hernández, Pablo Saldivia, Guillermo Nourdin, Roberto Elizondo-Vega, Evelyn Sánchez, Sofía Amulef, Elard Koch, Cristian Vargas and 1 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Exploratory proteomic characterization ofFrontiers in pharmacology · 2026
    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.

América Vera-MontecinosDepartamento de Ciencias Biológicas y Químicas, Facultad de Ciencias, Universidad San Sebastián, sede Concepción, Concepción, Chile.
Claudio Carril PardoLaboratorio de Neuroinmunología, Facultad de Ciencias, Universidad San Sebastián, sede Concepción, Concepción, Chile.
Mauricio HernándezDivision of Biotechnology, MELISA Institute, San Pedro de la Paz, Concepción, Chile.
Pablo SaldiviaFundación de Investigación San Ramon, San Pedro de la Paz, Concepción, Chile.
Guillermo NourdinDivision of Biotechnology, MELISA Institute, San Pedro de la Paz, Concepción, Chile.
Roberto Elizondo-VegaLaboratorio de Biología Celular, Departamento de Biología Celular, Facultad de Ciencias Biológicas, Universidad de Concepción, Concepción, Chile.
Evelyn SánchezEscuela de Tecnología Médica, Facultad de Ciencias, Universidad San Sebastián, sede Concepción, Concepción, Chile.
Sofía AmulefLaboratorio de Neuroinmunología, Facultad de Ciencias, Universidad San Sebastián, sede Concepción, Concepción, Chile.
Elard KochDivision of Biotechnology, MELISA Institute, San Pedro de la Paz, Concepción, Chile.
Cristian VargasDivision of Biotechnology, MELISA Institute, San Pedro de la Paz, Concepción, Chile.
Karina OyarceLaboratorio de Neuroinmunología, Facultad de Ciencias, Universidad San Sebastián, sede Concepción, Concepción, Chile. Karina.oyarce@uss.cl.

Funding

Fundación de Investigación San Ramón (FISAR) CLA-025025-1
6 · The paper itself

Abstract

The search for pathological biomarkers in biological fluids that can provide valuable insight into an individual's health status, is a relevant area of research for multiple pathologies. Currently, the use of proteomics for the identification of differences in protein expression profiles between samples from healthy subjects and patients, has emerged as a powerful strategy to improve the current diagnosis of various pathologies or propose novel therapeutic approaches. Among the biological fluids from which new pathological biomarkers can be identified, tear secretion is highly attractive, since it can be collected non-invasively and could better concentrate proteins that sensitively reflect allergic responses, owing to their exposure to environmental factors and its connection to the respiratory system. Despite its potential, tear fluid remains underexplored, offering significant research opportunities. In this study, we collected human tear samples using the Shirmer Test from healthy and allergic individuals. Our optimized workflow, combining sample preparation and high-throughput proteomics using the data-independent acquisition (DIA) strategy, identified 2542 proteins and enabled the successful differentiation of the two groups. We identified 99 differentially expressed proteins. Our results show the feasibility of protein analysis in human tear samples, highlighting tears as a highly sensitive fluid for detecting health conditions. Data are available via ProteomeXchange with identifier PXD067099.

Indexed as

BiomarkersEye ProteinsHypersensitivityProteomeProteomicsTearsAdultFemaleHumansMaleBiomarkersEye ProteinsProteometear proteinsBiomarkersDiaPASEFHigh-throughput proteomicsTear secretion

Identifiers

PMID40855359
PMCPMC12379103

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.