Evidence map›Paper›PMID 23324399›Full record

ArticleHuman vaccines & immunotherapeutics2013

Relevance of a pre-existing measles immunity prior immunization with a recombinant measles virus vector.

Marlyse C Knuchel, René R Marty, Teldja Neige Azzouz Morin, Orhan Ilter, Armando Zuniga, Hussein Y Naim

Open access · bronzeAbstract read
In one paragraph

Article in Human vaccines & immunotherapeutics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

26 citing papers in PubMed, 34 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. A next-generation intranasal trivalent MMS vaccine induces durable and broad protection against SARS-CoV-2 variants of concern.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  6. Review
  7. Review
  8. Vaccines platforms and COVID-19: what you need to know.Tropical diseases, travel medicine and vaccines · 2022
    Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. 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

6 authors at 6 institutions in 4 countries.

Marlyse C KnuchelCurrent affiliations: Bussigny, Switzerland.
René R Marty
Teldja Neige Azzouz Morin
Orhan Ilter
Armando Zuniga
Hussein Y Naim
Ferarihs · CHGlobal Vaccines (United States) · USInstitution de Lavigny · CHSanofi (France) · FRVifor Pharma (Switzerland) · CHZHAW Zurich University of Applied Sciences · CH

Funding

RECOMBINANT YELLOW FEVER VIRUS AS A CANDIDATE AIDS VACCINEP01AI046007 · NIAID · UNIVERSITY OF ZURICH · PI FEINBERG, MARK B. · 1999 to 2003
$6.7M
Mechanisms of Avian Hepadnavirus ReplicationR01AI060018 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI LOEB, DANIEL D · 2005 to 2008
$1.4M
NIAID NIH HHS AI46007NIAID NIH HHS N01 AI060018NIAID NIH HHS P01 AI046007
6 · The paper itself

Abstract

Measles virus (MV) vectors are promising candidates for designing new recombinant vaccines since the parental live vaccines have a well-known safety and efficacy record. Like all viral vectors, the MV vector efficacy in inducing a protecting immune answer could be affected by the pre-existing immunity among the human population. In order to determine the optimal immunization route and regimen, we mimicked a MV pre-immunity by passively administrating MV neutralizing antibodies (MV-nAb) prior intramuscular (i.m.) and/or intranasal (i.n.) immunization with recombinant MV expressing the SIV-gag antigen (rMV-SIVgag). Our results revealed that 500 mIU of MV-nAb allowed the induction of a humoral and cellular immune response against the vector and the transgene, while higher titers of the MV-nAb were significantly inhibitory. In a prime-boost regimen, in the presence of MV-nAb, the intranasal-intramuscular (i.n.-i.m.) or intramuscular-intramuscular (i.m.-i.m.) routes induced higher humoral immune responses against the vector and the transgene (SIV-gag). In naive animals, cellular immune response was significantly higher by i.m. immunization; however, MV pre-immunity did not seem to affect the cellular immune response after an i.n. immunization.   In summary, we show that a pre-existing immunity of up to 500 mIU anti-MV neutralizing antibodies had little effect on the replication of rMV and did not inhibit the induction of significant humoral and cellular immune responses in immune-competent mice.

Indexed as

Drug CarriersAdministration, IntranasalAnimalsAntibodies, NeutralizingAntibodies, ViralGenetic VectorsHumansImmunity, CellularImmunizationInjections, IntramuscularMeaslesMeasles virusMiceVaccines, SyntheticViral VaccinesAntibodies, NeutralizingAntibodies, ViralDrug CarriersVaccines, SyntheticViral Vaccinesimmune competent miceimmunization routemeaslespre-existing immunityrecombinant virusreverse geneticsSIVvaccine

Identifiers

PMID23324399
PMCPMC3891717
OpenAlexW2050416479

What OpenQuestion holds

Textmetadata
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.