Evidence map›Paper›PMID 34878034›Full record

ArticleClinics (Sao Paulo, Brazil)

SARS-CoV-2 recombinant proteins stimulate distinct cellular and humoral immune response profiles in samples from COVID-19 convalescent patients.

Laís Teodoro da Silva, Marina Mazzilli Ortega, Bruna Tiaki Tiyo, Isabelle Freire Tabosa Viana, Tayná Evily de Lima, Tania Regina Tozetto-Mendoza, Luanda Mara da Silva Oliveira, Franciane Mouradian Emidio Teixeira, Roberto Dias Lins, Alexandre de Almeida and 3 more

Open access · goldAbstract read
In one paragraph

Article in Clinics (Sao Paulo, Brazil). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

5 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
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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

13 authors at 2 institutions in 1 country.

Laís Teodoro da SilvaLaboratorio de Investigacao Medica em Dermatologia e Imunodeficiencias (LIM 56), Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, SP, BR.ORCID http://orcid.org/0000-0001-8542-802X
Marina Mazzilli OrtegaLaboratorio de Investigacao Medica em Dermatologia e Imunodeficiencias (LIM 56), Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, SP, BR.ORCID http://orcid.org/0000-0003-3258-8315
Bruna Tiaki TiyoLaboratorio de Investigacao Medica em Dermatologia e Imunodeficiencias (LIM 56), Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, SP, BR.ORCID http://orcid.org/0000-0002-8107-9536
Isabelle Freire Tabosa VianaDepartamento de Virologia, Instituto Aggeu Magalhaes, Fundacao Oswaldo Cruz, Recife, PE, BR.ORCID http://orcid.org/0000-0003-4648-6635
Tayná Evily de LimaDepartamento de Virologia, Instituto Aggeu Magalhaes, Fundacao Oswaldo Cruz, Recife, PE, BR.ORCID http://orcid.org/0000-0002-4609-1433
Tania Regina Tozetto-MendozaLaboratorio de Virologia (LIM-52), Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, SP, BR.ORCID http://orcid.org/0000-0002-5659-1052
Luanda Mara da Silva OliveiraLaboratorio de Investigacao Medica em Dermatologia e Imunodeficiencias (LIM 56), Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, SP, BR.ORCID http://orcid.org/0000-0003-0903-8219
Franciane Mouradian Emidio TeixeiraLaboratorio de Investigacao Medica em Dermatologia e Imunodeficiencias (LIM 56), Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, SP, BR.ORCID http://orcid.org/0000-0001-5622-903X
Roberto Dias LinsDepartamento de Virologia, Instituto Aggeu Magalhaes, Fundacao Oswaldo Cruz, Recife, PE, BR.ORCID http://orcid.org/0000-0002-3983-8025
Alexandre de AlmeidaLaboratorio de Investigacao Medica em Dermatologia e Imunodeficiencias (LIM 56), Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, SP, BR.ORCID http://orcid.org/0000-0002-1694-5450
Maria Cassia Mendes-CorreaLaboratorio de Virologia (LIM-52), Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, SP, BR.ORCID http://orcid.org/0000-0001-5655-8108
Alberto Jose da Silva DuarteLaboratorio de Investigacao Medica em Dermatologia e Imunodeficiencias (LIM 56), Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, SP, BR.ORCID http://orcid.org/0000-0002-8707-4904
Telma Miyuki OshiroLaboratorio de Investigacao Medica em Dermatologia e Imunodeficiencias (LIM 56), Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, SP, BR.ORCID http://orcid.org/0000-0002-8791-9233
Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo · BRFundação Oswaldo Cruz · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesIn this preliminary study we investigated cellular and humoral immune responses to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antigens in blood samples from 14 recovered coronavirus disease 2019 (COVID-19) patients and compared them to those in samples from 12 uninfected/unvaccinated volunteers.

methodsCellular immunity was assessed by intracellular detection of IFN-γ in CD3+ T lymphocytes after stimulation with SARS-CoV-2 spike (S1), nucleocapsid (NC), or receptor-binding domain (RBD) recombinant proteins or overlapping peptide pools covering the sequence of SARS-CoV-2 spike, membrane and nucleocapsid regions. The humoral response was examined by ELISAs and/or chemiluminescence assays for the presence of serum IgG antibodies directed to SARS-CoV-2 proteins.

resultsWe observed differences between humoral and cellular immune profiles in response to stimulation with the same proteins. Assays of IgG antibodies directed to SARS-CoV-2 NC, RBD and S1/S2 recombinant proteins were able to differentiate convalescent from uninfected/unvaccinated groups. Cellular immune responses to SARS-CoV-2 protein stimuli did not exhibit a specific response, as T cells from both individuals with no history of contact with SARS-CoV-2 and from recovered donors were able to produce IFN-γ.

conclusionsDetermination of the cellular immune response to stimulation with a pool of SARS-CoV-2 peptides but not with SARS-CoV-2 proteins is able to distinguish convalescent individuals from unexposed individuals. Regarding the humoral immune response, the screening for serum IgG antibodies directed to SARS-CoV-2 proteins has been shown to be specific for the response of recovered individuals.

Indexed as

COVID-19SARS-CoV-2Antibodies, ViralHumansImmunity, HumoralRecombinant ProteinsSpike Glycoprotein, CoronavirusAntibodies, ViralRecombinant ProteinsSpike Glycoprotein, Coronavirus

Identifiers

PMID34878034
PMCPMC8610223
OpenAlexW3217085289

What OpenQuestion holds

Textmetadata
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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.