Evidence map›Paper›PMID 35364615›Full record

ArticleAllergy2022

Autoantibodies in COVID-19 correlate with antiviral humoral responses and distinct immune signatures.

Patrick Taeschler, Carlo Cervia, Yves Zurbuchen, Sara Hasler, Christian Pou, Ziyang Tan, Sarah Adamo, Miro E Raeber, Esther Bächli, Alain Rudiger and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Allergy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 3 pooled it
6.1field-weighted citation impact, top 2% of its field
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

35 citing papers in PubMed, 3 syntheses or guidelines pooled it, 61 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Autoantibodies against type I interferons in COVID-19 infection: A systematic review and meta-analysis.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2023
    Pooled it
  4. Review
  5. Observational
  6. Article
  7. A Systemic Lupus Erythematosus Incidence Surveillance Report Among DoD Beneficiaries During the COVID-19 Pandemic.Federal practitioner : for the health care professionals of the VA, DoD, and PHS · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article
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

16 authors at 6 institutions in 3 countries.

Patrick TaeschlerDepartment of Immunology, University Hospital Zurich, Zurich, Switzerland.ORCID 0000-0003-0522-7629
Carlo CerviaDepartment of Immunology, University Hospital Zurich, Zurich, Switzerland.ORCID 0000-0001-7120-8739
Yves ZurbuchenDepartment of Immunology, University Hospital Zurich, Zurich, Switzerland.ORCID 0000-0001-5387-9950
Sara HaslerDepartment of Immunology, University Hospital Zurich, Zurich, Switzerland.ORCID 0000-0001-7357-9090
Christian PouScience for Life Laboratory, Department of Women's and Children's Health, Karolinska Institutet, Solna, Sweden.ORCID 0000-0003-3932-788X
Ziyang TanScience for Life Laboratory, Department of Women's and Children's Health, Karolinska Institutet, Solna, Sweden.ORCID 0000-0002-7205-4978
Sarah AdamoDepartment of Immunology, University Hospital Zurich, Zurich, Switzerland.ORCID 0000-0002-6161-3156
Miro E RaeberDepartment of Immunology, University Hospital Zurich, Zurich, Switzerland.ORCID 0000-0003-2609-0246
Esther BächliClinic for Internal Medicine, Hirslanden Klinik St. Anna, Lucerne, Switzerland.ORCID 0000-0003-4887-7576
Alain RudigerDepartment of Medicine, Limmattal Hospital, Schlieren, Switzerland.ORCID 0000-0001-7943-7624
Melina Stüssi-HelblingClinic for Internal Medicine, City Hospital Triemli Zurich, Zurich, Switzerland.ORCID 0000-0002-7896-6644
Lars C HuberClinic for Internal Medicine, City Hospital Triemli Zurich, Zurich, Switzerland.ORCID 0000-0001-5378-4716
Petter BrodinScience for Life Laboratory, Department of Women's and Children's Health, Karolinska Institutet, Solna, Sweden.ORCID 0000-0002-8103-0046
Jakob NilssonDepartment of Immunology, University Hospital Zurich, Zurich, Switzerland.ORCID 0000-0001-5091-8133
Elsbeth Probst-MüllerDepartment of Immunology, University Hospital Zurich, Zurich, Switzerland.ORCID 0000-0002-9046-4196
Onur BoymanDepartment of Immunology, University Hospital Zurich, Zurich, Switzerland.ORCID 0000-0001-8279-5545
University of Zurich · CHScience for Life Laboratory · SETriemli Hospital · CHHirslanden Klinik St. Anna · CHKarolinska University Hospital · SESpital Limmattal · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSeveral autoimmune features occur during coronavirus disease 2019 (COVID-19), with possible implications for disease course, immunity, and autoimmune pathology. In this study, we longitudinally screened for clinically relevant systemic autoantibodies to assess their prevalence, temporal trajectory, and association with immunity, comorbidities, and severity of COVID-19.

methodsWe performed highly sensitive indirect immunofluorescence assays to detect antinuclear antibodies (ANA) and antineutrophil cytoplasmic antibodies (ANCA), along with serum proteomics and virome-wide serological profiling in a multicentric cohort of 175 COVID-19 patients followed up to 1 year after infection, eleven vaccinated individuals, and 41 unexposed controls.

resultsCompared with healthy controls, similar prevalence and patterns of ANA were present in patients during acute COVID-19 and recovery. However, the paired analysis revealed a subgroup of patients with transient presence of certain ANA patterns during acute COVID-19. Furthermore, patients with severe COVID-19 exhibited a high prevalence of ANCA during acute disease. These autoantibodies were quantitatively associated with higher SARS-CoV-2-specific antibody titers in COVID-19 patients and in vaccinated individuals, thus linking autoantibody production to increased antigen-specific humoral responses. Notably, the qualitative breadth of antibodies cross-reactive with other coronaviruses was comparable in ANA-positive and ANA-negative individuals during acute COVID-19. In autoantibody-positive patients, multiparametric characterization demonstrated an inflammatory signature during acute COVID-19 and alterations of the B-cell compartment after recovery.

conclusionHighly sensitive indirect immunofluorescence assays revealed transient autoantibody production during acute SARS-CoV-2 infection, while the presence of autoantibodies in COVID-19 patients correlated with increased antiviral humoral immune responses and inflammatory immune signatures.

Indexed as

AutoantibodiesCOVID-19Antibodies, Antineutrophil CytoplasmicAntibodies, AntinuclearAntiviral AgentsHumansImmunity, HumoralSARS-CoV-2Antibodies, Antineutrophil CytoplasmicAntibodies, AntinuclearAntiviral AgentsAutoantibodiesantinuclear antibodiesautoantibodiesCOVID-19SARS-CoV-2VirScan

Identifiers

PMID35364615
PMCPMC9111424
OpenAlexW4226340491

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.