Evidence map›Paper›PMID 37018795›Full record

ArticleMemorias do Instituto Oswaldo Cruz2023

In vitro immunogenic profile of recombinant SARS-CoV2 S1-RBD peptide in murine macrophage and microglial cells.

Adriano José Maia Chaves Filho, Paloma Marinho Jucá, Michelle Verde Ramo Soares, Caio Andrade de Oliveira, Raul Cavalcante de Sousa, Deniele Bezerra Lós, Remo Castro Russo, Juliana Navarro Ueda Yaochite, Danielle S Macedo

Open access · diamondAbstract read
In one paragraph

Article in Memorias do Instituto Oswaldo Cruz, 2023. 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
0.6field-weighted citation impact, top 31% 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

0 citing papers in PubMed, 3 citations in OpenAlex.

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

9 authors at 2 institutions in 1 country.

Adriano José Maia Chaves FilhoUniversidade Federal do Ceará, Faculdade de Medicina, Departamento de Fisiologia e Farmacologia, Núcleo de Pesquisa e Desenvolvimento de Medicamentos, Laboratório de Neurofarmacologia, Fortaleza, CE, Brasil.
Paloma Marinho JucáUniversidade Federal do Ceará, Faculdade de Medicina, Departamento de Fisiologia e Farmacologia, Núcleo de Pesquisa e Desenvolvimento de Medicamentos, Laboratório de Neurofarmacologia, Fortaleza, CE, Brasil.
Michelle Verde Ramo SoaresUniversidade Federal do Ceará, Faculdade de Medicina, Departamento de Fisiologia e Farmacologia, Núcleo de Pesquisa e Desenvolvimento de Medicamentos, Laboratório de Neurofarmacologia, Fortaleza, CE, Brasil.
Caio Andrade de OliveiraUniversidade Federal do Ceará, Faculdade de Medicina, Departamento de Fisiologia e Farmacologia, Núcleo de Pesquisa e Desenvolvimento de Medicamentos, Laboratório de Neurofarmacologia, Fortaleza, CE, Brasil.
Raul Cavalcante de SousaUniversidade Federal do Ceará, Faculdade de Medicina, Departamento de Fisiologia e Farmacologia, Núcleo de Pesquisa e Desenvolvimento de Medicamentos, Laboratório de Neurofarmacologia, Fortaleza, CE, Brasil.
Deniele Bezerra LósUniversidade Federal do Ceará, Faculdade de Medicina, Departamento de Fisiologia e Farmacologia, Núcleo de Pesquisa e Desenvolvimento de Medicamentos, Laboratório de Neurofarmacologia, Fortaleza, CE, Brasil.
Remo Castro RussoUniversidade Federal de Minas Gerais, Instituto de Ciências Biológicas, Departamento de Fisiologia e Biofísica, Laboratório de Imunologia e Mecânica Pulmonar, Belo Horizonte, MG, Brasil.
Juliana Navarro Ueda YaochiteUniversidade Federal do Ceará, Faculdade de Farmácia, Odontologia e Enfermagem, Departamento de Análises Clínicas, Fortaleza, CE, Brasil.
Danielle S MacedoUniversidade Federal do Ceará, Faculdade de Medicina, Departamento de Fisiologia e Farmacologia, Núcleo de Pesquisa e Desenvolvimento de Medicamentos, Laboratório de Neurofarmacologia, Fortaleza, CE, Brasil.ORCID http://orcid.org/0000-0001-8980-9970
Universidade Federal do Ceará · BRUniversidade Federal de Minas Gerais · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants can infect common mice inducing significant pathological lung lesions and inflammatory responses. This substantially mimics coronavirus disease 19 (COVID-19) infection and pathogenesis in humans.

objectivesTo characterise the effects of recombinant SARS-CoV-2 S1 receptor-binding domain (RBD) peptide in murine macrophage and microglial cells' immune activation compared with classical PAMPs in vitro.

methodsMurine RAW 264.7 macrophages and BV2 microglial cells were exposed to increasing concentrations of the RBD peptide (0.01, 0.05, and 0.1 µg/mL), Lipopolysaccharide (LPS) and Poly(I:C) and evaluated after two and 24 h for significant markers of macrophage activation. We determined the effects of RBD peptide on cell viability, cleaved caspase 3 expressions, and nuclear morphometry analysis.

findingsIn RAW cells, RBD peptide was cytotoxic, but not for BV2 cells. RAW cells presented increased arginase activity and IL-10 production; however, BV2 cells expressed iNOS and IL-6 after RBD peptide exposure. In addition, RAW cells increased cleaved-caspase-3, apoptosis, and mitotic catastrophe after RBD peptide stimulation but not BV2 cells.

conclusionRBD peptide exposure has different effects depending on the cell line, exposure time, and concentration. This study brings new evidence about the immunogenic profile of RBD in macrophage and microglial cells, advancing the understanding of SARS-Cov2 immuno- and neuropathology.

Indexed as

COVID-19AnimalsAntibodies, ViralHumansMacrophagesMiceMicrogliaRecombinant ProteinsRNA, ViralSARS-CoV-2Antibodies, ViralRecombinant ProteinsRNA, Viral

Identifiers

PMID37018795
PMCPMC10065410
OpenAlexW4362499449

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.