Evidence map›Paper›PMID 42890211›Full record

ArticleFrontiers in immunology2026

Early functional maturation of anti-Spike antibodies predicts efficient SARS-CoV-2 RNA clearance.

Danielle A S Rodrigues, Barbara Gabrielle de Araujo, Julia Pestana, Layla de Freitas, Brenda N Ramos, Lendel C da Costa, Matheus V Andrade, Letícia M Raposo, Vicente B T Bozza, Luciana Conde and 14 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2026. 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
–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

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

24 authors.

Danielle A S RodriguesLaboratório de Biologia de Linfócitos, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Barbara Gabrielle de AraujoLaboratório de Biologia de Linfócitos, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Julia PestanaLaboratório de Biologia de Linfócitos, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Layla de FreitasLaboratório de Biologia de Linfócitos, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Brenda N RamosLaboratório de Biologia de Linfócitos, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Lendel C da CostaLaboratório de Virologia Molecular, Departamento de Genética, Instituto de Biologia, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Matheus V AndradeLaboratório de Virologia Molecular, Departamento de Genética, Instituto de Biologia, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Letícia M RaposoCentro de Ciências Exatas e Tecnologia, Universidade Federal do Estado do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Vicente B T BozzaLaboratório de Biologia de Linfócitos, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Luciana CondeLaboratório de Biologia de Linfócitos, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Elena Montes-CobosInstituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Andreza M D S GamaInstituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Vinicius M VidalInstituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Rafael M GalliezNúcleo de Enfrentamento e Estudos de Doenças Infecciosas Emergentes e Reemergentes, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Amilcar TanuriLaboratório de Virologia Molecular, Departamento de Genética, Instituto de Biologia, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Orlando D C FerreiraLaboratório de Virologia Molecular, Departamento de Genética, Instituto de Biologia, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Marcus Vinicius de Mattos SilvaLaboratório de Biotecnologia e Bioengenharia Estrutural, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Ronaldo Mohana-BorgesLaboratório de Biotecnologia e Bioengenharia Estrutural, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Leda R CastilhoLaboratório de Engenharia de Cultivos Celulares, Programa de Engenharia Química, COPPE, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Juliana Echevarria-LimaInstituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Luiza M HigaLaboratório de Virologia Molecular, Departamento de Genética, Instituto de Biologia, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Terezinha M CastineirasNúcleo de Enfrentamento e Estudos de Doenças Infecciosas Emergentes e Reemergentes, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Marcelo T BozzaInstituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
André M ValeLaboratório de Biologia de Linfócitos, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Viral RNA clearance following mild SARS-CoV-2 infection varies considerably among individuals, but the early humoral immune features underlying this heterogeneity remain incompletely understood. Methods: We investigated whether the kinetics and functional maturation of the antibody response were associated with viral RNA clearance in a longitudinal study of 78 healthcare professionals infected with the ancestral Wuhan SARS-CoV-2 strain and followed for up to three years. Participants were stratified according to viral RNA clearance kinetics as nonpersistent (≤21 days) or persistent (>21 days). Humoral responses were longitudinally characterized by seroconversion kinetics, antibody isotypes and IgG subclasses, affinity, cross-variant recognition, and neutralizing activity. Results: Nonpersistent individuals exhibited accelerated seroconversion to Spike and receptor-binding domain antigens within the first 11 days after symptom onset, accompanied by significantly greater neutralizing activity against the ancestral strain. In contrast, persistent individuals displayed delayed seroconversion, prolonged IgM responses, and reduced coordination among IgG subclasses during acute infection, consistent with delayed early humoral maturation. Total immunoglobulin levels did not distinguish the groups, whereas cross-variant antibody recognition during acute infection remained limited and predominantly strain-focused in both groups. During convalescence, durable anti-Spike IgG responses were maintained independently of persistence status, without significant differences in cross-variant breadth. Vaccination robustly enhanced antibody titers, variant recognition, and ACE2-blocking responses in both groups. Discussion: Accelerated functional maturation of the early anti-Spike antibody response, rather than overall antibody magnitude, was associated with efficient SARS-CoV-2 RNA clearance. These findings identify early functional maturation of the humoral response as an immunological correlate of efficient viral clearance and provide mechanistic insight into the immune processes underlying heterogeneous SARS-CoV-2 RNA clearance during mild infection.

Indexed as

Antibodies, ViralCOVID-19RNA, ViralSARS-CoV-2Spike Glycoprotein, CoronavirusAdultAntibodies, NeutralizingFemaleHumansImmunity, HumoralImmunoglobulin GImmunoglobulin MLongitudinal StudiesMaleMiddle AgedSeroconversionAntibodies, NeutralizingAntibodies, ViralImmunoglobulin GImmunoglobulin MRNA, ViralSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2antibody kineticscross-reactivityneutralizing antibodiesSARS-CoV-2vaccinationviral persistence

Identifiers

PMID42890211
PMCPMC13672549

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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.