Evidence map›Paper›PMID 41459516›Full record

ArticleFrontiers in immunology2025

Autoantibodies in long COVID in a black/mixed population compared with recovered and pre-pandemic controls.

Jessica de Jesus Silva, Laila Sampaio Horta, Sayonara Melo Viana, Ana Beatriz Cazé, Isabela S Oliveira, Mariana M Pereira, Natalie Antas Nascimento, Blenda de Jesus Pereira, Ícaro Bonyek-Silva, Sara Nunes de Oliveira Araújo and 13 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 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

23 authors.

Jessica de Jesus Silva *Laboratório de Medicina e Saúde Pública de Precisão, Fundação Oswaldo Cruz, Salvador, Brazil.
Laila Sampaio Horta *Laboratório de Medicina e Saúde Pública de Precisão, Fundação Oswaldo Cruz, Salvador, Brazil.
Sayonara Melo Viana *Laboratório de Medicina e Saúde Pública de Precisão, Fundação Oswaldo Cruz, Salvador, Brazil.
Ana Beatriz CazéUniversidade Federal da Bahia, Salvador, Brazil.
Isabela S OliveiraUniversidade Federal da Bahia, Salvador, Brazil.
Mariana M PereiraUniversidade Federal da Bahia, Salvador, Brazil.
Natalie Antas NascimentoUniversidade Federal da Bahia, Salvador, Brazil.
Blenda de Jesus PereiraLaboratório de Medicina e Saúde Pública de Precisão, Fundação Oswaldo Cruz, Salvador, Brazil.
Ícaro Bonyek-SilvaLaboratório de Medicina e Saúde Pública de Precisão, Fundação Oswaldo Cruz, Salvador, Brazil.
Sara Nunes de Oliveira AraújoLaboratório de Medicina e Saúde Pública de Precisão, Fundação Oswaldo Cruz, Salvador, Brazil.
Ananda Isis Lima de MarinhoLaboratório de Medicina e Saúde Pública de Precisão, Fundação Oswaldo Cruz, Salvador, Brazil.
Juqueline Rocha CristalLaboratório de Medicina e Saúde Pública de Precisão, Fundação Oswaldo Cruz, Salvador, Brazil.
Vishal RaoMicrobiology Department, Icahn School of Medicine, Mount Sinai Hospital, New York City, NY, United States.
Camila CoelhoMicrobiology Department, Icahn School of Medicine, Mount Sinai Hospital, New York City, NY, United States.
Thiago Cerqueira-SilvaLaboratório de Medicina e Saúde Pública de Precisão, Fundação Oswaldo Cruz, Salvador, Brazil.
Kelen Cristina Ribeiro MalmegrimSchool of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil.
Aquiles CamelierPost-covid outpatient Clinic at Octavio Mangabeira Hospital, Salvador, Brazil.
Cristina Ribeiro de Barros CardosoSchool of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil.
Natalia Machado TavaresLaboratório de Medicina e Saúde Pública de Precisão, Fundação Oswaldo Cruz, Salvador, Brazil.
Manoel Barral-NettoLaboratório de Medicina e Saúde Pública de Precisão, Fundação Oswaldo Cruz, Salvador, Brazil.
Aldina BarralLaboratório de Medicina e Saúde Pública de Precisão, Fundação Oswaldo Cruz, Salvador, Brazil.
Cynara BarbosaUniversidade Federal da Bahia, Salvador, Brazil.
Viviane Sampaio BoaventuraLaboratório de Medicina e Saúde Pública de Precisão, Fundação Oswaldo Cruz, Salvador, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Long COVID (LC), a clinical condition marked by persistent and new symptoms after infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), affects up to 10-20% of infected individuals. Although autoimmunity has been proposed as a key mechanism, the specific role of circulating autoantibodies in LC remains unclear. We characterized the autoantibody profiles in individuals with LC and assessed their association with persistent post-COVID symptoms, in comparison to recovered patients and pre-pandemic healthy controls (PPHC). Methods: We analyzed 17 autoantibodies in a cohort of 220 pre-pandemic controls and 291 COVID-19 patients, targeting self-antigens. Of those, 237 patients presented symptoms for a month or more after the onset of SARS-CoV-2 infection (long COVID patients), and 54 individuals recovered from the initial infection without chronic symptoms. Autoantibody frequencies and associations with clinical variables were assessed using logistic regression and subgroup analyses. Results: Autoantibody prevalence was higher in recovered individuals (37%) than in LC patients (24%) or PPHC (19%). While certain autoantibodies such as a-cardiolipin (a-CL) IgM, a-AML IgG, a-SSA IgG and a-SSB IgG were elevated in some COVID-19 patients, they were not significantly different in LC. The most frequently detected autoantibody was a-CL IgM, found across all groups and especially in individuals that fully recovered from COVID-19. However, a-CL did not differentiate individuals with long COVID or correlate with symptom persistence but was associated with the occurrence of dysphagia and anorexia as symptoms. No correlation was observed between autoantibody presence and disease severity. Discussion: These findings do not support a primary pathogenic role for the evaluated autoantibodies in LC and emphasize the need for longitudinal studies to explore their temporal dynamics and interaction with other immunological or clinical factors involved in post-COVID-19 conditions.

Indexed as

AutoantibodiesCOVID-19Post-Acute COVID-19 SyndromeAdultAgedBlack PeopleFemaleHumansMaleMiddle AgedAutoantibodiesanti-cardiolipinautoantibodiesbiomarkersCOVID-19long Covid

Identifiers

PMID41459516
PMCPMC12738873

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