Evidence map›Paper›PMID 24045788›Full record

ArticleHuman vaccines & immunotherapeutics2013

Immunization with cross-conserved H1N1 influenza CD4+ T-cell epitopes lowers viral burden in HLA DR3 transgenic mice.

Leonard Moise, Ryan Tassone, Howard Latimer, Frances Terry, Lauren Levitz, John P Haran, Ted M Ross, Christine M Boyle, William D Martin, Anne S De Groot

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 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

18 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. PromiscuousFrontiers in immunology · 2019
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. 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

10 authors at 4 institutions in 2 countries.

Leonard MoiseEpiVax, Inc.; Providence, RI USA; Institute for Immunology and Informatics; University of Rhode Island; Providence, RI USA.
Ryan TassoneEpiVax, Inc.; Providence, RI USA.
Howard LatimerEpiVax, Inc.; Providence, RI USA.
Frances TerryEpiVax, Inc.; Providence, RI USA.
Lauren LevitzEpiVax, Inc.; Providence, RI USA.
John P HaranBrown University Warren Alpert Medical School; Providence, RI USA.
Ted M RossVaccine & Gene Therapy Institute of Florida; Port Saint Lucie, FL USA.
Christine M BoyleEpiVax, Inc.; Providence, RI USA.
William D MartinEpiVax, Inc.; Providence, RI USA.
Anne S De GrootEpiVax, Inc.; Providence, RI USA; Institute for Immunology and Informatics; University of Rhode Island; Providence, RI USA.
Providence College · USEpiVax (United States) · USUniversity of Rhode Island · USVaccine & Gene Therapy Institute of Florida · US

Funding

Novel H1N1 influenza protection via cross-reactive immunityR21AI090359 · NIAID · EPIVAX, INC. · PI DEGROOT, ANNE SEARLS · 2011 to 2012
$472k
NIAID NIH HHS R21 AI090359NIAID NIH HHS R21AI090359
6 · The paper itself

Abstract

The emergence of the pandemic H1N1 strain of influenza in 2009 was associated with a unique w-shaped age-related susceptibility curve, with higher incidence of morbidity and mortality among young persons and lower incidence among older persons, also observed during the 1918 influenza pandemic. Pre-existing H1N1 antibodies were not cross-reactive with the prior seasonal vaccine, forcing influenza experts to scramble to develop a new vaccine specific for the pandemic virus. We hypothesized that response to T-cell epitopes that are cross-conserved between pandemic H1N1 and the 2008 seasonal influenza vaccine strains might have contributed to partial protection from clinical illness among older adults, despite the lack of cross-reactive humoral immunity. Using immunoinformatics tools, we previously identified hemagglutinin and neuraminidase epitopes that were highly conserved between seasonal and pandemic H1N1. Here, we validated predicted CD4(+) T-cell epitopes for their ability to bind HLA and to stimulate interferon-γ production in peripheral blood mononuclear cells from a cohort of donors presenting with influenza-like illness during the 2009 pandemic and a separate cohort immunized with trivalent influenza vaccine in 2011. A limited-epitope heterologous DNA-prime/peptide-boost vaccine composed of these sequences stimulated immune responses and lowered lung viral loads in HLA DR3 transgenic mice challenged with pandemic 2009 H1N1 influenza. Cross-priming with conserved influenza T-cell epitopes such as these may be critically important to T cell-mediated protection against pandemic H1N1 in the absence of cross-protective antibodies.

Indexed as

AnimalsCD4-Positive T-LymphocytesEpitopes, T-LymphocyteHLA-DR3 AntigenInfluenza A Virus, H1N1 SubtypeInfluenza VaccinesLungMiceMice, TransgenicViral LoadEpitopes, T-LymphocyteHLA-DR3 AntigenInfluenza VaccinesimmunoinformaticsinfluenzapandemicT-cell epitopevaccine

Identifiers

PMID24045788
PMCPMC3906390
OpenAlexW2099665987

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.