Evidence map›Paper›PMID 26697973›Full record

Trial reportHuman vaccines & immunotherapeutics2015

Assessment of immune responses to H5N1 inactivated influenza vaccine among individuals previously primed with H5N2 live attenuated influenza vaccine.

Larisa Rudenko, Anatoly Naykhin, Svetlana Donina, Daniil Korenkov, Galina Petukhova, Irina Isakova-Sivak, Igor Losev, Marina Stukova, Mariana Erofeeva, Alexandra Nikiforova and 2 more

Open access · hybridAbstract readClinical Trial
In one paragraph

Trial report in Human vaccines & immunotherapeutics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

12 citing papers in PubMed, 30 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. 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 3 institutions in 3 countries.

Larisa Rudenkoa Institute of Experimental Medicine ; Saint Petersburg , Russia.
Anatoly Naykhina Institute of Experimental Medicine ; Saint Petersburg , Russia.
Svetlana Doninaa Institute of Experimental Medicine ; Saint Petersburg , Russia.
Daniil Korenkova Institute of Experimental Medicine ; Saint Petersburg , Russia.
Galina Petukhovaa Institute of Experimental Medicine ; Saint Petersburg , Russia.
Irina Isakova-Sivaka Institute of Experimental Medicine ; Saint Petersburg , Russia.
Igor Loseva Institute of Experimental Medicine ; Saint Petersburg , Russia.
Marina Stukovab Research Institute of Influenza ; Saint Petersburg , Russia.
Mariana Erofeevab Research Institute of Influenza ; Saint Petersburg , Russia.
Alexandra Nikiforovac Department of Preclinical Trials, Microge ; Moscow , Russia.
Maureen Powerd PATH ; Seattle , WA USA.
Jorge Floresa Institute of Experimental Medicine ; Saint Petersburg , Russia.
Czech Academy of Sciences, Institute of Experimental Medicine · CZResearch Institute of Influenza · RUSeattle University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During the past decade, a number of H5 subtype influenza vaccines have been developed and tested in clinical trials, but most of them induced poor serum antibody responses prompting the evaluation of novel vaccination approaches. One of the most promising ones is a "prime-boost" strategy, which could result in the induction of prompt and robust immune responses to a booster influenza vaccine following priming with homologous or heterologous vaccine strains. In our study we evaluated immunogenicity of an adjuvanted A(H5N1) inactivated influenza vaccine (IIV) in healthy adult subjects who received A(H5N2) live attenuated influenza vaccine (LAIV) 1.5 years earlier and compared this with a group of naïve subjects. We found that priming with A(H5N2) LAIV induced a long-lasting B-cell immunological memory against influenza A(H5N1) virus, which was brought on by more prompt and vigorous antibody production to a single dose of A(H5N1) IIV in the primed group, compared to the naïve controls. Thus, by day 28 after the first booster dose, the hemagglutination inhibition and neutralizing (MN) antibody titer rises were 17.2 and 30.8 in the primed group, compared to 2.3 and 8.0 in the control group, respectively. The majority (79%) of the primed individuals achieved seroprotective MN antibody titers at 7 days after the first dose of the IIV. All LAIV-primed volunteers had MN titers ≥ 1:40 by Day 28 after one dose of IIV, whereas only 58% subjects from the naïve control group developed similar immune responses at this time point. The second A(H5N1) IIV dose did not increase the immune response in the LAIV-primed group, whereas 2 doses of IIV were required for naïve volunteers to develop significant immune responses. These findings were of special significance since Russian-based LAIV technology has been licensed to WHO, through whom the vaccine has been provided to vaccine manufacturers in India, China and Thailand - countries particularly vulnerable to a pandemic influenza. The results of our study will be useful to inform the development of vaccination strategies in these countries in the event of a pandemic.

Indexed as

AdultAntibodies, NeutralizingAntibodies, ViralAntibody FormationB-LymphocytesCross ReactionsFemaleHemagglutination Inhibition TestsHumansImmunization, SecondaryImmunoglobulin AImmunoglobulin GImmunologic MemoryInfluenza A Virus, H5N1 SubtypeInfluenza A Virus, H5N2 SubtypeInfluenza VaccinesAntibodies, NeutralizingAntibodies, ViralImmunoglobulin AImmunoglobulin GInfluenza VaccinesVaccines, AttenuatedVaccines, Inactivatedclinical trialH5 avian influenza virusesinactivated influenza vaccinelive attenuated influenza vaccinememory immune responseprime-boost strategysafety

Identifiers

PMID26697973
PMCPMC5054797
OpenAlexW2211764956

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.