Evidence map›Paper›PMID 38722858›Full record

ArticlePloS one2024

Comprehensive analysis of early T cell responses to acute Zika Virus infection during the first epidemic in Bahia, Brazil.

Assia Samri, Antonio Carlos Bandeira, Luana Leandro Gois, Carlos Gustavo Regis Silva, Alice Rousseau, Aurelien Corneau, Nadine Tarantino, Christopher Maucourant, Gabriel Andrade Nonato Queiroz, Vincent Vieillard and 5 more

Abstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

15 authors.

Assia SamriSorbonne-Université, Inserm 1135, CNRS ERL8255, Centre d'immunologie et des Maladies Infectieuses, Cimi, Paris, France.ORCID 0000-0002-2610-9915
Antonio Carlos BandeiraSecretaria de Saúde da Bahia, Salvador, Bahia, Brazil.ORCID 0000-0002-7273-8376
Luana Leandro GoisInstituto Gonçalo Moniz, Fundação Oswaldo Cruz (FIOCRUZ), Salvador, Brazil.
Carlos Gustavo Regis SilvaEscola Bahiana de Medicina e Saúde Pública (EBMSP), Salvador, Brazil.
Alice RousseauSorbonne-Université, Inserm 1135, CNRS ERL8255, Centre d'immunologie et des Maladies Infectieuses, Cimi, Paris, France.
Aurelien CorneauFaculté de Médecine Pierre et Marie Curie, Plateforme de Cytométrie (CyPS), UMS30-LUMIC, Paris, France.
Nadine TarantinoSorbonne-Université, Inserm 1135, CNRS ERL8255, Centre d'immunologie et des Maladies Infectieuses, Cimi, Paris, France.
Christopher MaucourantSorbonne-Université, Inserm 1135, CNRS ERL8255, Centre d'immunologie et des Maladies Infectieuses, Cimi, Paris, France.
Gabriel Andrade Nonato QueirozInstituto Gonçalo Moniz, Fundação Oswaldo Cruz (FIOCRUZ), Salvador, Brazil.
Vincent VieillardSorbonne-Université, Inserm 1135, CNRS ERL8255, Centre d'immunologie et des Maladies Infectieuses, Cimi, Paris, France.
Hans YsselSorbonne-Université, Inserm 1135, CNRS ERL8255, Centre d'immunologie et des Maladies Infectieuses, Cimi, Paris, France.ORCID 0000-0001-7454-1836
Gubio Soares CamposDepartamento de Biointeração, Instituto de Ciências da Saúde, Universidade Federal da Bahia, Salvador, Brazil.
Silvia SardiDepartamento de Biointeração, Instituto de Ciências da Saúde, Universidade Federal da Bahia, Salvador, Brazil.
Brigitte AutranSorbonne-Université, Inserm 1135, CNRS ERL8255, Centre d'immunologie et des Maladies Infectieuses, Cimi, Paris, France.
Maria Fernanda Rios GrassiInstituto Gonçalo Moniz, Fundação Oswaldo Cruz (FIOCRUZ), Salvador, Brazil.ORCID 0000-0002-7356-5569

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn most cases, Zika virus (ZIKV) causes a self-limited acute illness in adults, characterized by mild clinical symptoms that resolve within a few days. Immune responses, both innate and adaptive, play a central role in controlling and eliminating virus-infected cells during the early stages of infection.

aimTo test the hypothesis that circulating T cells exhibit phenotypic and functional activation characteristics during the viremic phase of ZIKV infection.

methodsA comprehensive analysis using mass cytometry was performed on peripheral blood mononuclear cells obtained from patients with acute ZIKV infection (as confirmed by RT-PCR) and compared with that from healthy donors (HD). The frequency of IFN-γ-producing T cells in response to peptide pools covering immunogenic regions of structural and nonstructural ZIKV proteins was quantified using an ELISpot assay.

resultsCirculating CD4+ and CD8+ T lymphocytes from ZIKV-infected patients expressed higher levels of IFN-γ and pSTAT-5, as well as cell surface markers associated with proliferation (Ki-67), activation ((HLA-DR, CD38) or exhaustion (PD1 and CTLA-4), compared to those from HD. Activation of CD4+ and CD8+ memory T cell subsets, including Transitional Memory T Cells (TTM), Effector Memory T cells (TEM), and Effector Memory T cells Re-expressing CD45RA (TEMRA), was prominent among CD4+ T cell subset of ZIKV-infected patients and was associated with increased levels of IFN-γ, pSTAT-5, Ki-67, CTLA-4, and PD1, as compared to HD. Additionally, approximately 30% of ZIKV-infected patients exhibited a T cell response primarily directed against the ZIKV NS5 protein.

conclusionCirculating T lymphocytes spontaneously produce IFN-γ and express elevated levels of pSTAT-5 during the early phase of ZIKV infection whereas recognition of ZIKV antigen results in the generation of virus-specific IFN-γ-producing T cells.

Indexed as

CD8-Positive T-LymphocytesInterferon-gammaZika VirusZika Virus InfectionAdultBrazilCD4-Positive T-LymphocytesEpidemicsFemaleHumansLymphocyte ActivationMaleMiddle AgedT-LymphocytesYoung AdultInterferon-gamma

Identifiers

PMID38722858
PMCPMC11081376

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.