Evidence map›Paper›PMID 29473899›Full record

ReviewInternational journal of environmental research and public health2018

Immune Responses to Dengue and Zika Viruses-Guidance for T Cell Vaccine Development.

Claude Roth, Félix G Delgado, Etienne Simon-Lorière, Anavaj Sakuntabhai

Open access · goldAbstract readReview
In one paragraph

Review in International journal of environmental research and public health, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Zika Virus.Pathogens (Basel, Switzerland) · 2020
    Review
  4. Review
  5. Review
  6. Review
  7. Zika Vaccine Development: Current Status.Mayo Clinic proceedings · 2019
    Review
  8. The situation of vaccines for the prevention of infections in adults: An opinion paper on the situation in Spain.Revista espanola de quimioterapia : publicacion oficial de la Sociedad Espanola de Quimioterapia · 2019
    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

4 authors at 1 institution in 2 countries.

Claude RothFunctional Genetics of Infectious Diseases Unit, Institut Pasteur, 75015 Paris, France. claude.roth@pasteur.fr.
Félix G DelgadoFunctional Genetics of Infectious Diseases Unit, Institut Pasteur, 75015 Paris, France. fdelgadot@unbosque.edu.co.ORCID 0000-0002-1734-6855
Etienne Simon-LorièreFunctional Genetics of Infectious Diseases Unit, Institut Pasteur, 75015 Paris, France. etienne.simon-loriere@pasteur.fr.ORCID 0000-0001-8420-7743
Anavaj SakuntabhaiFunctional Genetics of Infectious Diseases Unit, Institut Pasteur, 75015 Paris, France. anavaj.sakuntabhai@pasteur.fr.
Centre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite numerous efforts to identify the molecular and cellular effectors of the adaptive immunity that induce a long-lasting immunity against dengue or Zika virus infection, the specific mechanisms underlying such protective immunity remain largely unknown. One of the major challenges lies in the high level of dengue virus (DENV) seroprevalence in areas where Zika virus (ZIKV) is circulating. In the context of such a pre-existing DENV immunity that can exacerbate ZIKV infection and disease, and given the lack of appropriate treatment for ZIKV infection, there is an urgent need to develop an efficient vaccine against DENV and ZIKV. Notably, whereas several ZIKV vaccine candidates are currently in clinical trials, all these vaccine candidates have been designed to induce neutralizing antibodies as the primary mechanism of immune protection. Given the difficulty to elicit simultaneously high levels of neutralizing antibodies against the different DENV serotypes, and the potential impact of pre-existing subneutralizing antibodies induced upon DENV infection or vaccination on ZIKV infection and disease, additional or alternative strategies to enhance vaccine efficacy, through T cell immunity, are now being considered. In this review, we summarize recent discoveries about cross-reactive B and T cell responses against DENV and ZIKV and propose guidelines for the development of safe and efficient T cell vaccines targeting both viruses.

Indexed as

Adaptive ImmunityAntibodies, NeutralizingAntibodies, ViralCross ReactionsDengueDengue VirusHumansSeroepidemiologic StudiesSerogroupT-LymphocytesVaccinesZika VirusZika Virus InfectionAntibodies, NeutralizingAntibodies, ViralVaccinesdengue virusT cell epitopesvaccinationZika virus

Identifiers

PMID29473899
PMCPMC5858454
OpenAlexW2789532771

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.