Evidence map›Paper›PMID 34614112›Full record

ArticleClinics (Sao Paulo, Brazil)2021

Association between circulating exhausted CD4+ T cells with poor meningococcal C conjugate vaccine antibody response in HIV-infected children and adolescents.

Giselle P Silva, Wania F Pereira-Manfro, Priscilla R Costa, Dayane A Costa, Bianca Ferreira, Daniela M Barreto, Ana Cristina C Frota, Cristina B Hofer, Carlos M Figueredo, Barbara Coelho and 2 more

Open access · goldAbstract read
In one paragraph

Article in Clinics (Sao Paulo, Brazil), 2021. 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
0.1field-weighted citation impact, top 55% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  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

12 authors at 4 institutions in 2 countries.

Giselle P SilvaDepartamento de Microbiologia, Imunologia e Parasitologia, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ, BR.ORCID 0000-0001-8469-4019
Wania F Pereira-ManfroDepartamento de Microbiologia, Imunologia e Parasitologia, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ, BR.ORCID 0000-0003-0166-8144
Priscilla R CostaDivisao de Imunologia Clinica e Alergia, Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo, SP, BR.ORCID 0000-0001-6812-4999
Dayane A CostaDivisao de Imunologia Clinica e Alergia, Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo, SP, BR.ORCID 0000-0002-6350-7648
Bianca FerreiraInstituto de Puericultura e Pediatria Martagão Gesteira, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, BR.ORCID 0000-0002-9056-5034
Daniela M BarretoInstituto de Puericultura e Pediatria Martagão Gesteira, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, BR.ORCID 0000-0001-5051-0357
Ana Cristina C FrotaInstituto de Puericultura e Pediatria Martagão Gesteira, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, BR.ORCID 0000-0002-2825-4374
Cristina B HoferInstituto de Puericultura e Pediatria Martagão Gesteira, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, BR.ORCID 0000-0001-8633-0913
Carlos M FigueredoDepartamento de Periodontia, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ, BR.ORCID 0000-0003-0222-9231
Barbara CoelhoDepartamento de Periodontia, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ, BR.ORCID 0000-0001-9501-3944
Esper G KallasDivisao de Imunologia Clinica e Alergia, Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo, SP, BR.ORCID 0000-0003-2026-6925
Lucimar G MilagresDepartamento de Microbiologia, Imunologia e Parasitologia, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ, BR.ORCID 0000-0002-0860-818X
Griffith University · AUHospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo · BRUniversidade do Estado do Rio de Janeiro · BRUniversidade Federal do Rio de Janeiro · BR

Funding

Immunogenicity of meningococcal C conjugate vaccine in HIV infected childrenR01TW008397 · FIC · FEDERAL UNIVERSITY OF RIO DE JANEIRO · PI HOFER, CRISTINA BARROSO · 2009 to 2013
$250k
FIC NIH HHS R01 TW008397
6 · The paper itself

Abstract

objectivesTo investigate the expression levels of surface markers of activation (CD38 and HLA-DR), inhibition (PD-1, TIGIT and CD57) and co-stimulation (CD28 and CD127) on CD4+ T cells of children/adolescents with vertical HIV infection (HI patients) and HIV-uninfected (HU) controls vaccinated with the meningococcal C conjugate vaccine (MCC).

methodsHI patients (n=12), aged 8-17 years, were immunized with two MCC injections, while HU controls (n=9), aged 5.3-10.7 years, received a single MCC dose (as per national recommendation at the time of this study, a single MCC vaccine dose should be given for healthy children and youth aged 1-18 years). The HI patients were categorized according to the combined antiretroviral therapy (cART) treatment. Blood samples were obtained before vaccination, after priming, and after the administration of a booster dose of vaccine to determine the serum bactericidal antibody (SBA) titers and the expression levels of surface markers on CD4+ T cells by flow cytometry. The levels of serum cytokines, IL-4 and CXCL-13 were also measured using Luminex kits.

resultsThe co-expression of the TIGIT-HLA-DR-CD38 molecules increased in the CD4+ T cells of HI patients/no-cART who also showed a lower frequency of CD127+CD28+ CD4+ T cells than HI patients/cART and HU group subjects. There were significant negative correlations between the frequency of exhausted CD4+ T cells and the SBA response. IL-4 levels were higher in HI patients/cART and positively correlated with SBA titers but negatively associated with the expression of exhaustion markers. Moreover, the CXCL-13 levels were positively correlated with the exhausted CD4+ T cells.

conclusionThe results of our study suggest that the co-expression of exhaustion markers and/or loss of co-stimulatory molecules influence the SBA response in HI patients.

Indexed as

HIV InfectionsMeningococcal VaccinesAdolescentAntibody FormationCD4-Positive T-LymphocytesChildHumansMeningococcal Vaccinesserogroup C meningococcal conjugate vaccine

Identifiers

PMID34614112
PMCPMC8449930
OpenAlexW3199985150

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.