Evidence map›Paper›PMID 18081041›Full record

ArticleEuropean journal of immunology2008

Broad T cell immunity to the LcrV virulence protein is induced by targeted delivery to DEC-205/CD205-positive mouse dendritic cells.

Yoonkyung Do, Chae Gyu Park, Young-Sun Kang, Sung Ho Park, Rebecca M Lynch, Haekyung Lee, Bradford S Powell, Ralph M Steinman

Open access · greenAbstract read
In one paragraph

Article in European journal of immunology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

30 citing papers in PubMed, 61 citations in OpenAlex.

  1. Review
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  5. Polymorphism in theFrontiers in immunology · 2019
    Article
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  8. Targeted Delivery ofFrontiers in immunology · 2018
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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

8 authors at 3 institutions in 2 countries.

Yoonkyung DoLaboratory of Cellular Physiology and Immunology and Chris Browne Center for Immunology and Immune Diseases, The Rockefeller University, New York 10065-6399, USA.
Chae Gyu Park
Young-Sun Kang
Sung Ho Park
Rebecca M Lynch
Haekyung Lee
Bradford S Powell
Ralph M Steinman
Rockefeller University · USKonkuk University · KRUnited States Army Medical Research Institute of Infectious Diseases · US

Funding

Viral Pathogenesis and TherapeuticsU54AI057158 · NIAID · WADSWORTH CENTER · PI LEVY, DAVID E · 2003 to 2014
$100.8M
Properties of Mouse of Dendritic Cells and MacrophagesR01AI013013 · NIAID · ROCKEFELLER UNIVERSITY · PI MOJSOV, SVETLANA · 1985 to 2015
$8.9M
PROPERTIES OF MOUSE DENDRITIC CELLS AND MACROPHAGESR37AI013013 · NIAID · ROCKEFELLER UNIVERSITY · PI STEINMAN, RALPH M. · 1986 to 1995
–
NIAID NIH HHS 5 U54 AI057158NIAID NIH HHS AI13013NIAID NIH HHS R01 AI013013NIAID NIH HHS U54 AI057158
6 · The paper itself

Abstract

There is a need for a more efficient vaccine against the bacterium Yersinia pestis, the agent of pneumonic plague. The F1-LcrV (F1-V) subunit vaccine in alhydrogel is known to induce humoral immunity. In this study, we utilized DC to investigate cellular immunity. We genetically engineered the LcrV virulence protein into the anti-DEC-205/CD205 mAb and thereby targeted the conjugated protein directly to mouse DEC-205(+) DC in situ. We observed antigen-specific CD4(+) T cell immunity measured by intracellular staining for IFN-gamma in three different mouse strains (C57BL/6, BALB/c, and C3H/HeJ), while we could not observe such T cell responses with F1-V vaccine in alhydrogel. Using a peptide library for LcrV protein, we identified two or more distinct CD4(+) T cell mimetopes in each MHC haplotype, consistent with the induction of broad immunity. When compared to nontargeted standard protein vaccine, DC targeting greatly increased the efficiency for inducing IFN-gamma-producing T cells. The targeted LcrV protein induced antibody responses to a similar extent as the F1-V subunit vaccine, but Th1-dependent IgG2a and IgG2c isotypes were observed only after anti-DEC-205:LcrV mAb immunization. This study sets the stage for the analysis of functional roles of IFN-gamma-producing T cells in Y. pestis infection.

Indexed as

AnimalsAntibodies, MonoclonalAntibody FormationAntigen PresentationAntigens, BacterialAntigens, CDBlotting, WesternDendritic CellsElectrophoresis, Polyacrylamide GelEpitopes, T-LymphocyteInterferon-gammaLectins, C-TypeLymphocyte ActivationMiceMinor Histocompatibility AntigensPlague VaccineAntibodies, MonoclonalAntigens, BacterialAntigens, CDDEC-205 receptorEpitopes, T-LymphocyteInterferon-gammaLcrV protein, YersiniaLectins, C-TypeMinor Histocompatibility AntigensPlague VaccinePore Forming Cytotoxic ProteinsReceptors, Cell SurfaceRecombinant Fusion Proteins

Identifiers

PMID18081041
PMCPMC2864640
OpenAlexW2008072330

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.