Evidence map›Paper›PMID 20375595›Full record

ArticleJournal of innate immunity2009

TRIF, and TRIF-interacting TLRs differentially modulate several adenovirus vector-induced immune responses.

D M Appledorn, S Patial, S Godbehere, N Parameswaran, A Amalfitano

Open access · bronzeAbstract read
In one paragraph

Article in Journal of innate immunity, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

27 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Adenovirus vector-based vaccine for infectious diseases.Drug metabolism and pharmacokinetics · 2022
    Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Rhoptry antigens asClinical and experimental vaccine research · 2019
    Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Helper-Dependent Adenoviral Vectors.Journal of genetic syndromes & gene therapy · 2011
    Article
  19. Article
  20. 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

5 authors at 1 institution in 1 country.

D M AppledornDepartment of Microbiology and Molecular Genetics, Michigan State University, East Lansing, MI 48823, USA.
S Patial
S Godbehere
N Parameswaran
A Amalfitano
Michigan State University · US

Funding

RNA TRASFECTED DENDRITIC CELLS FOR CANCER IMMUNOTHERAPYP01CA078673 · NCI · DUKE UNIVERSITY · PI MORSE, MICHAEL A · 1999 to 2008
$13.2M
Adenovirus vectors and complement systemR01DK069884 · NIDDK · MICHIGAN STATE UNIVERSITY · PI AMALFITANO, ANDREA NA · 2005 to 2007
$775k
NCI NIH HHS P01 CA078673NIDDK NIH HHS R01 DK069884NIDDK NIH HHS R01DK-069884
6 · The paper itself

Abstract

The use of Adenovirus (Ad)-based vectors has proven to be a useful platform for the development of gene therapy and vaccine protocols. The immunological mechanisms underlying these properties need to be identified and understood to foster safer, more efficacious use of this important gene transfer platform. Our recent studies have confirmed an important role for MyD88 dependent toll-like receptor (TLR) pathways as mediators of these responses. In this study, we confirm that TLR3, TLR4 and TRIF (TIR-domain-containing adapter-inducing interferon-beta) can also have augmentative or inhibitory roles during Ad-induced immune responses. Importantly, our studies revealed that TLR4 acts to suppress several aspects of the Ad-induced innate immune response, a finding not previously reported for this TLR in any model system. In addition, using MyD88 and TRIF double knockout mice, we demonstrate that the MyD88 and TRIF adaptor proteins can play either additive or redundant roles in mediating certain aspects of Ad vector-induced innate and adaptive immune responses. Furthering this complexity, our model system strongly suggests that non-TLR based systems must not only exist, but also have a significant role to play during Ad vector-mediated induction of adaptive immune responses.

Indexed as

Genetic TherapyAdaptive ImmunityAdaptor Proteins, Vesicular TransportAdenoviridaeAnimalsComplement System ProteinsGenetic VectorsImmunity, InnateMiceMice, Inbred C57BLMice, KnockoutMyeloid Differentiation Factor 88Toll-Like Receptor 3Toll-Like Receptor 4Transduction, GeneticAdaptor Proteins, Vesicular TransportComplement System ProteinsMyd88 protein, mouseMyeloid Differentiation Factor 88Ticam1 protein, mouseTLR3 protein, mouseTlr4 protein, mouseToll-Like Receptor 3Toll-Like Receptor 4

Identifiers

PMID20375595
PMCPMC2853581
OpenAlexW2024437693

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.