Evidence map›Paper›PMID 22947140›Full record

ArticleVaccine2012

Induction of pulmonary mucosal immune responses with a protein vaccine targeted to the DEC-205/CD205 receptor.

Yoonkyung Do, Arnaud M Didierlaurent, Seongho Ryu, Hyein Koh, Chae Gyu Park, Steven Park, David S Perlin, Bradford S Powell, Ralph M Steinman

Abstract read
In one paragraph

Article in Vaccine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

24 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
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  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Targeted Delivery ofFrontiers in immunology · 2018
    Article
  12. Article
  13. Article
  14. Article
  15. Plague Vaccines: Status and Future.Advances in experimental medicine and biology · 2016
    Review
  16. Review
  17. Innate receptors and cellular defense against pulmonary infections.Journal of immunology (Baltimore, Md. : 1950) · 2014
    Review
  18. Article
  19. Article
  20. 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

9 authors at 4 institutions in 1 country.

Yoonkyung DoLaboratory of Cellular Physiology and Immunology and Chris Browne Center, The Rockefeller University, New York, NY 10065, United States. doy@unist.ac.kr
Arnaud M Didierlaurent
Seongho Ryu
Hyein Koh
Chae Gyu Park
Steven Park
David S Perlin
Bradford S Powell
Ralph M Steinman
Rockefeller University · USRutgers, The State University of New Jersey · USCornell University · USUnited States Department of the Army · US

Funding

Viral Pathogenesis and TherapeuticsU54AI057158 · NIAID · WADSWORTH CENTER · PI LIPKIN, W. IAN · 2003 to 2014
$100.8M
Properties of Mouse of Dendritic Cells and MacrophagesR01AI013013 · NIAID · ROCKEFELLER UNIVERSITY · PI MOJSOV, SVETLANA · 1985 to 2015
$8.9M
Improved plague vaccine by targeting dendritic cell subsetsR21AI082331 · NIAID · ROCKEFELLER UNIVERSITY · PI DO, YOONKYUNG · 2009 to 2010
$465k
PROPERTIES OF MOUSE DENDRITIC CELLS AND MACROPHAGESR37AI013013 · NIAID · ROCKEFELLER UNIVERSITY · PI STEINMAN, RALPH M. · 1986 to 1995
–
NIAID NIH HHS 1 R21 AI082331-01NIAID NIH HHS 5 U54 AI057158NIAID NIH HHS AI13013NIAID NIH HHS R01 AI013013NIAID NIH HHS R21 AI082331NIAID NIH HHS U54 AI057158
6 · The paper itself

Abstract

It is of great interest to develop a pneumonic plague vaccine that would induce combined humoral and cellular immunity in the lung. Here we investigate a novel approach based on targeting of dendritic cells using the DEC-205/CD205 receptor (DEC) via the intranasal route as way to improve mucosal cellular immunity to the vaccine. Intranasal administration of Yersinia pestis LcrV (V) protein fused to anti-DEC antibody together with poly IC as an adjuvant induced high frequencies of IFN-γ secreting CD4(+) T cells in the airway and lung as well as pulmonary IgG and IgA antibodies. Anti-DEC:LcrV was more efficient to induce IFN-γ/TNF-α/IL-2 secreting polyfunctional CD4(+) T cells when compared to non-targeted soluble protein vaccine. In addition, the intranasal route of immunization with anti-DEC:LcrV was associated with improved survival upon pulmonary challenge with the virulent CO92 Y. pestis. Taken together, these data indicate that targeting dendritic cells via the mucosal route is a potential new avenue for the development of a mucosal vaccine against pneumonic plague.

Indexed as

Immunity, MucosalAdjuvants, ImmunologicAdministration, IntranasalAnimalsAntibodies, BacterialAntigens, BacterialAntigens, CDCD4-Positive T-LymphocytesDendritic CellsImmunity, CellularImmunity, HumoralImmunoglobulin AImmunoglobulin GInterferon-gammaLectins, C-TypeLungAdjuvants, ImmunologicAntibodies, BacterialAntigens, BacterialAntigens, CDDEC-205 receptorImmunoglobulin AImmunoglobulin GInterferon-gammaLcrV protein, YersiniaLectins, C-TypeMinor Histocompatibility AntigensPlague VaccinePoly I-CPore Forming Cytotoxic ProteinsReceptors, Cell Surface

Identifiers

PMID22947140
PMCPMC3461253
OpenAlexW2053764072

What OpenQuestion holds

Textmetadata
LicenceTDM
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.