Use este identificador para citar ou linkar para este item: http://hdl.handle.net/1843/78301
Tipo: Artigo de Periódico
Título: Panoramic snapshot of serum soluble mediator interplay in pregnant women with convalescent covid-19: an exploratory study
Autor(es): Geraldo Magela Fernandes
Lizandra Moura Paravidine Sasaki
Gabriela Profírio Jardim-Santos
Heidi Luise Schulte
Felipe Motta
Ângelo Pereira da Silva
Aleida Oliveira de Carvalho
Yacara Ribeiro Pereira
Caroline de Oliveira Alves
Otávio de Toledo Nóbrega
David Alves de Araújo Júnior
Lizandra Moura Paravidine Sasaki
Dayde Lane Mendonça-Silva
Karina Nascimento Costa
Maria Eduarda Canellas de Castro
Lucas Lauand
Rodrigo de Resende Nery
Rosana Tristão
Patricia Shu Kurizky
Otávio de Toledo Nóbrega
Laila Salmen Espindola
Luiz Cláudio Gonçalves de Castro
Patrícia Nessralla Alpoim
Lara Carvalho Godoi
Luci Maria Sant Ana Dusse
Jordana Grazziela Alves Coelho-Dos-Reis
Laurence Rodrigues do Amaral
Matheus de Souza Gomes
Pedro Luiz Lima Bertarini
Joaquim Pedro Brito-de-Sousa
Ismael Artur da Costa-Rocha
Ana Carolina Campi-Azevedo
Vanessa Peruhype-Magalhães
Andrea Teixeira-Carvalho
Alberto Moreno Zaconeta
Alexandre Anderson de Sousa Munhoz Soares
Valéria Valim
Ciro Martins Gomes
Cleandro Pires de Albuquerque
Olindo Assis Martins-Filho
Licia Maria Henrique da Mota
Resumo: Abstract Introduction: SARS-CoV-2 infection during pregnancy can induce changes in the maternal immune response, with effects on pregnancy outcome and offspring. This is a cross-sectional observational study designed to characterize the immunological status of pregnant women with convalescent COVID-19 at distinct pregnancy trimesters. The study focused on providing a clear snapshot of the interplay among serum soluble mediators. Methods: A sample of 141 pregnant women from all prenatal periods (1st, 2nd and 3rd trimesters) comprised patients with convalescent SARS-CoV-2 infection at 3-20 weeks after symptoms onset (COVID, n=89) and a control group of pre-pandemic non-infected pregnant women (HC, n=52). Chemokine, pro-inflammatory/regulatory cytokine and growth factor levels were quantified by a high-throughput microbeads array. Results: In the HC group, most serum soluble mediators progressively decreased towards the 2nd and 3rd trimesters of pregnancy, while higher chemokine, cytokine and growth factor levels were observed in the COVID patient group. Serum soluble mediator signatures and heatmap analysis pointed out that the major increase observed in the COVID group related to pro-inflammatory cytokines (IL-6, TNF-α, IL-12, IFN-γ and IL-17). A larger set of biomarkers displayed an increased COVID/HC ratio towards the 2nd (3x increase) and the 3rd (3x to 15x increase) trimesters. Integrative network analysis demonstrated that HC pregnancy evolves with decreasing connectivity between pairs of serum soluble mediators towards the 3rd trimester. Although the COVID group exhibited a similar profile, the number of connections was remarkably lower throughout the pregnancy. Meanwhile, IL-1Ra, IL-10 and GM-CSF presented a preserved number of correlations (≥5 strong correlations in HC and COVID), IL-17, FGF-basic and VEGF lost connectivity throughout the pregnancy. IL-6 and CXCL8 were included in a set of acquired attributes, named COVID-selective (≥5 strong correlations in COVID and <5 in HC) observed at the 3rd pregnancy trimester. Discussion and conclusion: From an overall perspective, a pronounced increase in serum levels of soluble mediators with decreased network interplay between them demonstrated an imbalanced immune response in convalescent COVID-19 infection during pregnancy that may contribute to the management of, or indeed recovery from, late complications in the post-symptomatic phase of the SARS-CoV-2 infection in pregnant women.
Assunto: Covi-19
Gravidez
Idioma: eng
País: Brasil
Editor: Universidade Federal de Minas Gerais
Sigla da Instituição: UFMG
Departamento: FAR - DEPARTAMENTO DE ANÁLISES CLÍNICAS E TOXICOLÓGICAS
ICB - DEPARTAMENTO DE MICROBIOLOGIA
Tipo de Acesso: Acesso Aberto
Identificador DOI: 10.3389/fimmu.2023.1176898
URI: http://hdl.handle.net/1843/78301
Data do documento: 11-Abr-2023
metadata.dc.url.externa: https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2023.1176898/full
metadata.dc.relation.ispartof: Frontiers in Immunology
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