Evidence map›Paper›PMID 41259457›Full record

ArticleBrazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas2025

Detection of autoantibodies in severe COVID-19 patients two years after hospital discharge.

E M B Hi, C C R Bianchi, R B Gritte, P H A Klauss, N F S M Leal, I S de Oliveira, M F C B de Barros, F G Soriano, R Curi, M C C Machado

Abstract read
In one paragraph

Article in Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
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

10 authors.

E M B HiLaboratório de Emergências Clínicas, Departamento de Clínica Médica, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brasil.ORCID http://orcid.org/0000-0002-8795-9534
C C R BianchiLaboratório de Emergências Clínicas, Departamento de Clínica Médica, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brasil.ORCID http://orcid.org/0009-0000-6463-6778
R B GritteLaboratório de Emergências Clínicas, Departamento de Clínica Médica, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brasil.ORCID http://orcid.org/0000-0002-2935-7922
P H A KlaussLaboratório de Emergências Clínicas, Departamento de Clínica Médica, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brasil.ORCID http://orcid.org/0009-0006-9737-3082
N F S M LealCurso de Biomedicina, Centro Universitário Lusíada, Santos, SP, Brasil.ORCID http://orcid.org/0009-0000-5188-932X
I S de OliveiraFaculdade de Farmácia, Universidade Federal da Bahia, Salvador, BA, Brasil.ORCID http://orcid.org/0009-0009-3856-4702
M F C B de BarrosLaboratório de Emergências Clínicas, Departamento de Clínica Médica, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brasil.ORCID http://orcid.org/0000-0002-6459-7825
F G SorianoLaboratório de Emergências Clínicas, Departamento de Clínica Médica, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brasil.ORCID http://orcid.org/0000-0003-4898-0135
R CuriPrograma de Pós-Graduação Interdisciplinar em Ciências da Saúde, Universidade Cruzeiro do Sul, São Paulo, SP, Brasil.ORCID http://orcid.org/0000-0001-5095-9154
M C C MachadoLaboratório de Emergências Clínicas, Departamento de Clínica Médica, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brasil.ORCID http://orcid.org/0000-0002-0729-1635

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

After SARS-CoV-2 infection, severe COVID-19 may develop with persistent sequelae, even after hospital discharge. This condition may result from tissue damage or immune alterations caused by the virus, including immune dysregulation, hyperinflammation, loss of immune tolerance, excessive neutrophil extracellular trap (NET) production, and antibody cross-reactivity (molecular mimicry), which can promote autoantibody development. This study evaluated autoantibody expression in patients with long COVID-19 and its potential relationship with symptoms. Conducted in Baixada Santista, São Paulo, Brazil, the study involved 55 participants aged 21-85 years who had tested positive for SARS-CoV-2. Blood samples were collected two years post-discharge, and serum was analyzed for inflammatory and autoimmune markers, including antinuclear antibody (ANA), rheumatoid factor (RF), anti-cyclic citrullinated peptide (anti-CCP), procalcitonin (PCT), Venereal Disease Research Laboratory test (VDRL), and C-reactive protein (CRP). Results were compared to a control group of 21 individuals who never tested positive for COVID-19. Among severe COVID-19 patients, 26 reacted to ANA, 16 to VDRL, 2 had elevated RF, 12 had increased PCT, and 11 had high CRP, whereas the control group showed no reactive results. Anti-CCP values were not significant. Findings suggest that hyperinflammation may contribute to autoimmunity, particularly in cases of reactive ANA levels, linking COVID-19 symptoms to autoimmune responses.

Indexed as

AutoantibodiesCOVID-19AdultAgedAged, 80 and overAntibodies, AntinuclearBiomarkersBrazilCase-Control StudiesC-Reactive ProteinFemaleHumansMaleMiddle AgedPatient DischargeProcalcitoninAntibodies, AntinuclearAutoantibodiesBiomarkersC-Reactive ProteinProcalcitoninRheumatoid Factor

Identifiers

PMID41259457
PMCPMC12622924

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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.