Evidence map›Paper›PMID 41210940›Full record

ArticleFrontiers in cellular and infection microbiology2025

Lymphocyte loss and plasmacytosis are associated with IL-6- and TNF-producing cells in the spleens of fatal COVID-19 cases.

Bianca Ramos Mesquita, Lilian Verena da Silva Carvalho, Leonardo Cardoso Gomes Baqueiro, Reginaldo Brito, Luma Bahia Figueiredo Pinto, Erina Masayo Alves Hassegawa, Jonathan Luís Magalhães Fontes, Cláudio Pereira Figueira, Eraldo Salustiano de Moura, Maria Brandão Tavares and 3 more

Abstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 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
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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

13 authors.

Bianca Ramos MesquitaLaboratório de Patologia Estrutural e Molecular, Instituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Brazil.
Lilian Verena da Silva CarvalhoInstituto Couto Maia, Bahia State Health Secretary, Salvador, Brazil.
Leonardo Cardoso Gomes BaqueiroLaboratório de Patologia Estrutural e Molecular, Instituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Brazil.
Reginaldo BritoLaboratório de Patologia Estrutural e Molecular, Instituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Brazil.
Luma Bahia Figueiredo PintoLaboratório de Patologia Estrutural e Molecular, Instituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Brazil.
Erina Masayo Alves HassegawaLaboratório de Patologia Estrutural e Molecular, Instituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Brazil.
Jonathan Luís Magalhães FontesLaboratório de Patologia Estrutural e Molecular, Instituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Brazil.
Cláudio Pereira FigueiraLaboratório de Patologia Estrutural e Molecular, Instituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Brazil.
Eraldo Salustiano de MouraHospital do Subúrbio, Bahia State Health Secretary, Salvador, Brazil.
Maria Brandão TavaresHospital do Subúrbio, Bahia State Health Secretary, Salvador, Brazil.
Carla PagliariDepartamento de Patologia, Universidade de São Paulo, Faculdade de Medicina, São Paulo, Brazil.
Geraldo G S OliveiraLaboratório de Patologia Estrutural e Molecular, Instituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Brazil.
Washington L C Dos-SantosLaboratório de Patologia Estrutural e Molecular, Instituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The spleen undergoes changes during acute and chronic infections, which may contribute to immune dysregulation and disease aggravation. In fatal cases of COVID-19, pronounced splenic changes are noted. However, the role played by these alterations in patient mortality remains poorly understood. Objectives: We aim to characterize structural alterations and changes in splenic cell populations in fatal COVID-19 cases, as a potential substrate for immune dysfunction associated with bacterial coinfection and mortality in severe infectious diseases. Methods: In this study, we characterized the histological and cellular changes observed in the spleens of nine patients who died from COVID-19. Spleens from five healthy individuals were used as a reference. Histopathological analysis and immunolabeling techniques were employed to evaluate tissue architecture, cell composition, cytokine production, and cell death. Results: COVID-19-associated changes included atrophy of the white pulp (WP), reduced cellular density in the red pulp (RP), and reticular fiber fragmentation. Leukocyte phenotyping revealed substantial lymphocyte depletion across all splenic compartments, accompanied by plasma cell accumulation. These alterations correlated with increased numbers of IL-6- and TNF-producing cells. Additionally, a high density of TUNEL-positive cells indicated widespread cell death in the spleens of COVID-19 patients. Conclusion: These findings suggest that the spleen contributes to the inflammatory response in

Indexed as

COVID-19Interleukin-6LymphocytesPlasma CellsSpleenTumor Necrosis Factor-alphaAdultAgedFemaleHumansMaleMiddle AgedSARS-CoV-2IL6 protein, humanInterleukin-6Tumor Necrosis Factor-alphaCOVID-19IL-6lymphocyte lossspleen disorganizationTNF

Identifiers

PMID41210940
PMCPMC12588937

What Socratic holds

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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 Socratic graph.