Evidence map›Paper›PMID 23607394›Full record

ArticleClinical and experimental immunology2013

RGD capsid modification enhances mucosal protective immunity of a non-human primate adenovirus vector expressing Pseudomonas aeruginosa OprF.

A Krause, W Z Whu, J Qiu, D Wafadari, N R Hackett, A Sharma, R G Crystal, S Worgall

Open access · greenAbstract readComparative Study
In one paragraph

Article in Clinical and experimental immunology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. International journal of molecular sciences · 2025
    Review
  3. Article
  4. Immunological considerations in the development ofHuman vaccines & immunotherapeutics · 2020
    Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
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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 1 institution in 1 country.

A KrauseDepartment of Genetic Medicine, Weill Cornell Medical College, New York, NY 10065, USA.
W Z Whu
J Qiu
D Wafadari
N R Hackett
A Sharma
R G Crystal
S Worgall
Cornell University · US

Funding

Immunization Against Pseudomonas aeruginosa by Modified Ad VectorsU01AI069032 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI WORGALL, STEFAN · 2006 to 2010
$2.1M
Immunity Induced by Modified Adenovirus FiberR01AI072238 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI WORGALL, STEFAN · 2007 to 2011
$2.1M
Mucosal Immunization Against P. aeruginosa by Modified Adenovirus VectorsR01AI103341 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI WORGALL, STEFAN · 2013 to 2016
$1.7M
NIAID NIH HHS R01 AI072238NIAID NIH HHS R01 AI103341NIAID NIH HHS R01 AI72238NIAID NIH HHS U01 AI069032
6 · The paper itself

Abstract

Replication-deficient adenoviral (Ad) vectors of non-human serotypes can serve as Ad vaccine platforms to circumvent pre-existing anti-human Ad immunity. We found previously that, in addition to that feature, a non-human primate-based AdC7 vector expressing outer membrane protein F of P. aeruginosa (AdC7OprF) was more potent in inducing lung mucosal and protective immunity compared to a human Ad5-based vector. In this study we analysed if genetic modification of the AdC7 fibre to display an integrin-binding arginine-glycine-aspartic acid (RGD) sequence can further enhance lung mucosal immunogenicity of AdC7OprF. Intratracheal immunization of mice with either AdC7OprF.RGD or AdC7OprF induced robust serum levels of anti-OprF immunoglobulin (Ig)G up to 12 weeks that were higher compared to immunization with the human vectors Ad5OprF or Ad5OprF.RGD. OprF-specific cellular responses in lung T cells isolated from mice immunized with AdC7OprF.RGD and AdC7OprF were similar for T helper type 1 (Th1) [interferon (IFN)-γ in CD8(+) and interleukin (IL)-12 in CD4(+)], Th2 (IL-4, IL-5 and IL-13 in CD4(+)) and Th17 (IL-17 in CD4(+)). Interestingly, AdC7OprF.RGD induced more robust protective immunity against pulmonary infection with P. aeruginosa compared to AdC7OprF or the control Ad5 vectors. The enhanced protective immunity induced by AdC7OprF.RGD was maintained in the absence of alveolar macrophages (AM) or CD1d natural killer T cells. Together, the data suggest that addition of RGD to the fibre of an AdC7-based vaccine is useful to enhance its mucosal protective immunogenicity.

Indexed as

OligopeptidesAdenoviridaeAnimalsCD8-Positive T-LymphocytesCells, CulturedCytokinesFemaleGenetic VectorsHumansImmunity, MucosalImmunoglobulin GLungMiceMice, Inbred C57BLPorinsPrimatesarginyl-glycyl-aspartic acidCytokinesImmunoglobulin GOligopeptidesOmpF proteinPorinsPseudomonas Vaccinesadenoviruslungmucosal immunitypseudomonasRGD

Identifiers

PMID23607394
PMCPMC3722923
OpenAlexW1757371285

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.