Evidence map›Paper›PMID 33932299›Full record

ArticleJournal of medical virology2021

SARS-CoV-2 antibodies: IgA correlates with severity of disease in early COVID-19 infection.

Fainareti N Zervou, Ping Louie, Anna Stachel, Ioannis M Zacharioudakis, Yadira Ortiz-Mendez, Kristen Thomas, Maria E Aguero-Rosenfeld

Open access · bronzeAbstract read
In one paragraph

Article in Journal of medical virology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 2 pooled it
5.9field-weighted citation impact, top 3% 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

56 citing papers in PubMed, 2 syntheses or guidelines pooled it, 98 citations in OpenAlex.

  1. Pooled it
  2. Mucosal immune response in biology, disease prevention and treatment.Signal transduction and targeted therapy · 2025
    Pooled it
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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

7 authors at 2 institutions in 1 country.

Fainareti N ZervouDivision of Infectious Diseases, Department of Medicine, NYU Grossman School of Medicine, New York, New York, USA.ORCID http://orcid.org/0000-0002-6192-7403
Ping LouieDepartment of Medicine, Tisch Hospital Clinical Laboratories, NYU Langone Health, New York, New York, USA.
Anna StachelDepartment of Medicine, Infection Prevention and Control, NYU Langone Health, Tisch Hospital, New York, New York, USA.
Ioannis M ZacharioudakisDivision of Infectious Diseases, Department of Medicine, NYU Grossman School of Medicine, New York, New York, USA.
Yadira Ortiz-MendezDepartment of Medicine, Tisch Hospital Clinical Laboratories, NYU Langone Health, New York, New York, USA.
Kristen ThomasDepartment of Pathology, NYU Grossman School of Medicine, New York, New York, USA.
Maria E Aguero-RosenfeldDivision of Infectious Diseases, Department of Medicine, NYU Grossman School of Medicine, New York, New York, USA.
Tisch Hospital · USNew York University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Timing of detection of immunoglobulin G (IgG), immunoglobulin A (IgA), and immunoglobulin M (IgM) antibodies against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), and their use to support the diagnosis are of increasing interest. We used the Gold Standard Diagnostics ELISA to evaluate the kinetics of SARS-CoV-2 IgG, IgA, and IgM antibodies in sera of 82 hospitalized patients with polymerase chain reaction (PCR)-confirmed coronavirus disease 2019 (COVID-19). Serum samples were collected 1-59 days post-onset of symptoms (PoS) and we examined the association of age, sex, disease severity, and symptoms' duration with antibody levels. We also tested sera of 100 ambulatory hospital employees with PCR-confirmed COVID-19 and samples collected during convalescence, 35-57 days PoS. All but four of the admitted patients (95.1%) developed antibodies to SARS-CoV-2. Antibodies were detected within 7 days PoS; IgA in 60.0%, IgM in 53.3%, and IgG in 46.7% of samples. IgG positivity increased to 100% on Day 21. We did not observe significant differences in the rate of antibody development in regard to age and sex. IgA levels were highest in patients with a severe and critical illness. In multiple regression analyses, only IgA levels were statistically significantly correlated with critical disease (p = .05) regardless of age, sex, and duration of symptoms. Among 100 ambulatory hospital employees who had antibody testing after 4 weeks PoS only 10% had positive IgA antibodies. The most frequently isolated isotype in sera of employees after 30 days PoS was IgG (88%). IgA was the predominant immunoglobulin in early disease and correlated independently with a critical illness. IgG antibodies remained detectable in almost 90% of samples collected up to two months after infection.

Indexed as

AdultAgedAged, 80 and overAntibodies, ViralConvalescenceCOVID-19COVID-19 Serological TestingEnzyme-Linked Immunosorbent AssayFemaleHumansImmunoglobulin AImmunoglobulin GImmunoglobulin MMaleMiddle AgedSARS-CoV-2Antibodies, ViralImmunoglobulin AImmunoglobulin GImmunoglobulin MCOVID-19IgASARS-CoV-2serology

Identifiers

PMID33932299
PMCPMC8242647
OpenAlexW3157463471

What OpenQuestion holds

Textmetadata
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.