Evidence map›Paper›PMID 42515585›Full record

ArticleViruses2026

Cytokine and Lymphocyte Profiles in COVID-19 Patients with Cancer: Implications for Disease Severity and Clinical Outcomes.

Marina M Burlá, Karina L Silva, Bárbara C Peixoto, Livia R Goes, Isaclaudia Azevedo-Quintanilha, Fernando A Bozza, Marcelo A Soares, Andreia C de Melo, Eugenio D Hottz, Patricia T Bozza and 1 more

Abstract read
In one paragraph

Article in Viruses, 2026. 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

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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

11 authors.

Marina M BurláProgram of Immunology and Tumor Biology, Brazilian National Cancer Institute (INCA), Rio de Janeiro 20231-050, RJ, Brazil.ORCID 0000-0002-4899-9082
Karina L SilvaProgram of Immunology and Tumor Biology, Brazilian National Cancer Institute (INCA), Rio de Janeiro 20231-050, RJ, Brazil.
Bárbara C PeixotoProgram of Immunology and Tumor Biology, Brazilian National Cancer Institute (INCA), Rio de Janeiro 20231-050, RJ, Brazil.ORCID 0000-0002-8228-0194
Livia R GoesProgram of Genetics and Tumor Virology, Brazilian National Cancer Institute (INCA), Rio de Janeiro 20231-050, RJ, Brazil.
Isaclaudia Azevedo-QuintanilhaLaboratory of Immunopharmacology, Oswaldo Cruz Institute (IOC), Oswaldo Cruz Foundation (FIOCRUZ), Rio de Janeiro 21040-361, RJ, Brazil.
Fernando A BozzaIntensive Care Medicine Laboratory, National Institute of Infectiology (INI), Oswaldo Cruz Foundation (FIOCRUZ), Rio de Janeiro 21040-361, RJ, Brazil.ORCID 0000-0003-4878-0256
Marcelo A SoaresProgram of Genetics and Tumor Virology, Brazilian National Cancer Institute (INCA), Rio de Janeiro 20231-050, RJ, Brazil.ORCID 0000-0002-9013-2570
Andreia C de MeloDivision of Clinical Research and Technological Development, Brazilian National Cancer Institute (INCA), Rio de Janeiro 20231-050, RJ, Brazil.ORCID 0000-0002-1201-4333
Eugenio D HottzLaboratory of Immunothrombosis, Department of Biochemistry, Federal University of Juiz de Fora (UFJF), Juiz de Fora 36036-330, MG, Brazil.
Patricia T BozzaLaboratory of Immunopharmacology, Oswaldo Cruz Institute (IOC), Oswaldo Cruz Foundation (FIOCRUZ), Rio de Janeiro 21040-361, RJ, Brazil.
João P B ViolaProgram of Immunology and Tumor Biology, Brazilian National Cancer Institute (INCA), Rio de Janeiro 20231-050, RJ, Brazil.ORCID 0000-0002-0698-3146

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 311926/2021-5 and 311686/2019-2Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro 210.168/2020, 210.150/2020, 211.126/2021 and 200.568/2023
6 · The paper itself

Abstract

Patients with cancer are at increased risk of severe outcomes from COVID-19. Yet, the immunological determinants underlying this vulnerability remain incompletely understood, particularly in low- and middle-income settings. Moreover, the impact of the severe viral disease surge and its compensatory mechanisms, such as stressed myelopoiesis, on this population needs further elucidation. This study aims to characterize the cytokine and lymphocyte profiles of cancer patients with COVID-19, correlate these profiles with disease severity, and compare them to those of non-cancer patients with COVID-19. Plasma cytokine, chemokine, and growth factor levels were quantified using Luminex technology, and immune cell subsets were characterized by flow cytometry. A total of 67 patients were analyzed: 40 with cancer (26 mild cases and 14 severe cases) and 27 without cancer (12 mild cases and 15 severe cases). Clinical outcomes showed an 86% mortality rate in cancer patients due to severe COVID-19. This contrasted with a 3.8% mortality rate in cancer patients with mild COVID-19, all unrelated to the infection. Our findings revealed elevated CXCL10 (IP-10) and reduced MIF levels in cancer patients with COVID-19, distinguished by disease severity. Compared with that in cancer patients with mild COVID-19, the level of CXCL10 in cancer patients with severe COVID-19 was further elevated. Additionally, cancer patients with COVID-19 presented reduced CD3

Indexed as

COVID-19CytokinesLymphocytesNeoplasmsAdultAgedFemaleHumansKiller Cells, NaturalMaleMiddle AgedSARS-CoV-2Severity of Illness IndexT-Cell ExhaustionT-Lymphocytes, RegulatoryCytokinescancerCOVID-19CXCL10/IP-10MIFNK cellsT-cell exhaustionT lymphocyteTreg cells

Identifiers

PMID42515585
PMCPMC13431523

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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.