Evidence map›Paper›PMID 42123631›Full record

SynthesisInternational journal of molecular sciences2026

ELISPOT as a Functional for Biomarker Study in Cancer Immunotherapy: Applications and Future Directions.

Laura R Fernández Castro, Matias Regiart, Francisco Gabriel Ortega-Sánchez, Rodrigo Rodríguez, Gonzalo Tortella, Martín A Fernández-Baldo

Abstract readSystematic Review
In one paragraph

Synthesis in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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.

Laura R Fernández CastroGENYO, Centre for Genomics and Oncological Research, Pfizer/University of Granada/Andalusian Regional Government PTS, Avenida de la Ilustración, 114, 18016 Granada, Spain.
Matias RegiartDepartamento de Química, Instituto de Química San Luis (INQUISAL), Universidad Nacional de San Luis, CONICET, Ejército de Los Andes 950, San Luis D5700BWS, Argentina.
Francisco Gabriel Ortega-SánchezGENYO, Centre for Genomics and Oncological Research, Pfizer/University of Granada/Andalusian Regional Government PTS, Avenida de la Ilustración, 114, 18016 Granada, Spain.ORCID 0000-0003-0563-2237
Rodrigo RodríguezFacultad de Ingeniería, Instituto de Ciencias Aplicadas, Universidad Autónoma de Chile, Temuco 4810101, Chile.ORCID 0000-0003-0991-5939
Gonzalo TortellaCentro de Excelencia en Investigación Biotecnológica Aplicada al Medio Ambiente (CIBAMA), Facultad de Ingeniería y Ciencias, Universidad de La Frontera, Av. Francisco Salazar 01145, Temuco 4811230, Chile.ORCID 0000-0001-7069-7454
Martín A Fernández-BaldoDepartamento de Química, Instituto de Química San Luis (INQUISAL), Universidad Nacional de San Luis, CONICET, Ejército de Los Andes 950, San Luis D5700BWS, Argentina.ORCID 0000-0003-0385-2391

Funding

Agencia Nacional de Promoción Científica y Tecnológica PICT-2021-GRF-TI-00136Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET) PIP-11220200100033COInstituto de Salud Carlos III (ISCIII) PI22_01275, CP23/00134, DTS23_00030Universidad de Granada P32/22/02Universidad Nacional de San Luis PROICO 02-2220
6 · The paper itself

Abstract

The Enzyme-Linked ImmunoSpot (ELISPOT) assay is a highly sensitive and widely used technique for assessing antigen-specific cellular immune responses in cancer research. By enabling the quantification of cytokine secretion at the single-cell level, particularly interferon gamma (IFN-γ), ELISPOT provides a functional readout of T cell activity with applications in both preclinical and clinical settings. This systematic review presents a structured qualitative synthesis of 78 studies investigating the use of ELISPOT in cancer immunotherapy, including cancer vaccines, oncolytic viruses, cellular therapies, immune checkpoint inhibitors, and biomarker development. Studies were selected following PRISMA guidelines from PubMed, Scopus, and Embase, focusing on both clinical and preclinical research with translational relevance. The evidence indicates that ELISPOT is widely used to validate tumor-associated antigens and neoantigens, monitor antigen-specific T cell responses during cancer immunotherapy, including immune checkpoint blockade, cancer vaccines, and adoptive cell therapies, and characterize antigen-specific T cell function. However, only a limited subset of studies establishes direct associations between ELISPOT responses and clinically meaningful outcomes. In addition, substantial variability in assay protocols and reporting criteria limits cross-study comparability and reproducibility. Overall, ELISPOT remains a valuable tool for immune monitoring in cancer research. Still, its implementation as a clinically validated biomarker requires further standardization, prospective validation, and integration with complementary analytical approaches.

Indexed as

Biomarkers, TumorEnzyme-Linked Immunospot AssayImmunotherapyNeoplasmsAnimalsCancer VaccinesHumansInterferon-gammaT-LymphocytesBiomarkers, TumorCancer VaccinesInterferon-gammabiomarkerscancer researchenzyme-linked immunospot assay (ELISPOT)immunotherapy

Identifiers

PMID42123631
PMCPMC13164536

What OpenQuestion holds

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LicenceCC BY
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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.