Evidence map›Paper›PMID 35837409›Full record

ArticleFrontiers in immunology2022

Plasmablast Expansion Following the Tetravalent, Live-Attenuated Dengue Vaccine Butantan-DV in DENV-Naïve and DENV-Exposed Individuals in a Brazilian Cohort.

Cássia G T Silveira, Diogo M Magnani, Priscilla R Costa, Vivian I Avelino-Silva, Michael J Ricciardi, Maria do Carmo S T Timenetsky, Raphaella Goulart, Carolina A Correia, Mariana P Marmorato, Lilian Ferrari and 8 more

Registry-linked trialAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01696422 (Phase II, Step-wise, Randomized, Double-blind, Controlled Clinical Trial for Safety and Immunogenicity Evaluation of a Lyophilized Formulation of Dengue 1,2,3,4), which is not on this map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–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.

NCT01696422 phase2unknown statusnot on this map

Phase II, Step-wise, Randomized, Double-blind, Controlled Clinical Trial for Safety and Immunogenicity Evaluation of a Lyophilized Formulation of Dengue 1,2,3,4 (Attenuated) Vaccine in Healthy Adults

TypeinterventionalSponsorButantan InstituteRan2013 to 2020Enrolled300ConditionsDengueArmsDengue 1,2,3,4 (attenuated) vaccine, TetraVax-DV Vaccine - Admixture TV003, Placebo
3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Research progress of mosquito-borne virus mRNA vaccines.Molecular therapy. Methods & clinical development · 2025
    Review
  3. Review
  4. Review
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

18 authors.

Cássia G T SilveiraDivision of Clinical Immunology and Allergy, School of Medicine, University of São Paulo, São Paulo, Brazil.
Diogo M MagnaniDepartment of Pathology, University of Miami Miller School of Medicine, Miami, FL, United States.
Priscilla R CostaDivision of Clinical Immunology and Allergy, School of Medicine, University of São Paulo, São Paulo, Brazil.
Vivian I Avelino-SilvaDepartment of Infectious and Parasitic Diseases, School of Medicine, University of São Paulo, São Paulo, Brazil.
Michael J RicciardiDepartment of Pathology, University of Miami Miller School of Medicine, Miami, FL, United States.
Maria do Carmo S T TimenetskyVirology Centre, Instituto Adolfo Lutz, São Paulo, Brazil.
Raphaella GoulartDivision of Clinical Immunology and Allergy, School of Medicine, University of São Paulo, São Paulo, Brazil.
Carolina A CorreiaDivision of Clinical Immunology and Allergy, School of Medicine, University of São Paulo, São Paulo, Brazil.
Mariana P MarmoratoDivision of Clinical Immunology and Allergy, School of Medicine, University of São Paulo, São Paulo, Brazil.
Lilian FerrariDivision of Clinical Immunology and Allergy, School of Medicine, University of São Paulo, São Paulo, Brazil.
Zelinda B NakagawaDivision of Clinical Immunology and Allergy, School of Medicine, University of São Paulo, São Paulo, Brazil.
Claudia TomiyamaDivision of Clinical Immunology and Allergy, School of Medicine, University of São Paulo, São Paulo, Brazil.
Helena TomiyamaDivision of Clinical Immunology and Allergy, School of Medicine, University of São Paulo, São Paulo, Brazil.
Jorge KalilDivision of Clinical Immunology and Allergy, School of Medicine, University of São Paulo, São Paulo, Brazil.
Ricardo PalaciosDivision of Clinical Trials and Pharmacovigilance, Instituto Butantan, São Paulo, Brazil.
Alexander R PreciosoDivision of Clinical Trials and Pharmacovigilance, Instituto Butantan, São Paulo, Brazil.
David I WatkinsDepartment of Pathology, University of Miami Miller School of Medicine, Miami, FL, United States.
Esper G KallásDivision of Clinical Immunology and Allergy, School of Medicine, University of São Paulo, São Paulo, Brazil.

Funding

A multi-tiered approach to develop validated assays to predict efficacy of a tetravalent live attenuated Dengue Virus vaccine in Phase II and Phase III clinical trialsR01AI125202 · NIAID · EMORY UNIVERSITY · PI SEKALY, RAFICK PIERRE · 2016 to 2020
$5.3M
NIAID NIH HHS R01 AI125202
6 · The paper itself

Abstract

An effective vaccine against the dengue virus (DENV) should induce a balanced, long-lasting antibody (Ab) response against all four viral serotypes. The burst of plasmablasts in the peripheral blood after vaccination may reflect enriched vaccine-specific Ab secreting cells. Here we characterize the acute plasmablast responses from naïve and DENV-exposed individuals following immunization with the live attenuated tetravalent (LAT) Butantan DENV vaccine (Butantan-DV). The frequency of circulating plasmablasts was determined by flow cytometric analysis of fresh whole blood specimens collected from 40 participants enrolled in the Phase II Butantan-DV clinical trial (NCT01696422) before and after (days 6, 12, 15 and 22) vaccination. We observed a peak in the number of circulating plasmablast at day 15 after vaccination in both the DENV naïve and the DENV-exposed vaccinees. DENV-exposed vaccinees experienced a significantly higher plasmablast expansion. In the DENV-naïve vaccinees, plasmablasts persisted for approximately three weeks longer than among DENV-exposed volunteers. Our findings indicate that the Butantan-DV can induce plasmablast responses in both DENV-naïve and DENV-exposed individuals and demonstrate the influence of pre-existing DENV immunity on Butantan DV-induced B-cell responses.

Indexed as

Dengue VaccinesDengue VirusAntibodies, ViralBrazilHumansVaccines, AttenuatedAntibodies, ViralDengue VaccinesVaccines, Attenuateddenguedengue infectiondengue vaccinehumoral responseplasmablast

Identifiers

PMID35837409
PMCPMC9274664

What Socratic holds

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LicenceCC BY
Read underepoch 390

Registered trials

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 Socratic graph.