Evidence map›Paper›PMID 19036823›Full record

ArticleJournal of virology2009

Incorporation of CD40 ligand into the envelope of pseudotyped single-cycle Simian immunodeficiency viruses enhances immunogenicity.

Fan-ching Lin, Yue Peng, Leslie A Jones, Paulo H Verardi, Tilahun D Yilma

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Fan-ching LinInternational Laboratory of Molecular Biology for Tropical Disease Agents, School of Veterinary Medicine, University of California, Davis, California 95616, USA.
Yue Peng
Leslie A Jones
Paulo H Verardi
Tilahun D Yilma
University of California, Davis · US

Funding

Innate Immunomodulating Genes of Smallpox VaccinesU01AI066344 · NIAID · UNIVERSITY OF CALIFORNIA DAVIS · PI YILMA, TILAHUN D · 2005 to 2009
$1.7M
INDUCTION OF MUCOSAL IMMUNITY WITH RECOMBINANT VACCINESR01AI047025 · NIAID · UNIVERSITY OF CALIFORNIA DAVIS · PI YILMA, TILAHUN D · 2000 to 2002
$1.4M
A Safer and More Efficacious Smallpox VaccineR01AI054951 · NIAID · UNIVERSITY OF CALIFORNIA DAVIS · PI YILMA, TILAHUN D · 2003 to 2005
$1.3M
Safer and More Efficacious Recombinant AIDS VaccinesR21AI053811 · NIAID · UNIVERSITY OF CALIFORNIA DAVIS · PI YILMA, TILAHUN D · 2002 to 2003
$446k
SMART Virus Vectors with a Built-in Safety MechanismR21AI059185 · NIAID · UNIVERSITY OF CALIFORNIA DAVIS · PI VERARDI, PAULO H. · 2004 to 2005
$408k
NIAID NIH HHS AI047025NIAID NIH HHS AI053811NIAID NIH HHS AI054951NIAID NIH HHS AI059185NIAID NIH HHS AI066344NIAID NIH HHS R01 AI054951NIAID NIH HHS R21 AI053811NIAID NIH HHS R21 AI059185NIAID NIH HHS U01 AI066344
6 · The paper itself

Abstract

A vaccine for the prevention of human immunodeficiency virus (HIV) infection is desperately needed to control the AIDS pandemic. To address this problem, we developed vesicular stomatitis virus glycoprotein-pseudotyped replication-defective simian immunodeficiency viruses (dSIVs) as an AIDS vaccine strategy. The dSIVs retain characteristics of a live attenuated virus without the drawbacks of potential virulence caused by replicating virus. To improve vaccine immunogenicity, we incorporated CD40 ligand (CD40L) into the dSIV envelope. CD40L is one of the most potent stimuli for dendritic cell (DC) maturation and activation. Binding of CD40L to its receptor upregulates expression of major histocompatibility complex class I, class II, and costimulatory molecules on DCs and increases production of proinflammatory cytokines and chemokines, especially interleukin 12 (IL-12). This cytokine polarizes CD4(+) T cells to Th1-type immune responses. DC activation and mixed lymphocyte reaction (MLR) studies were performed to evaluate the immunogenicity of CD40L-dSIV in vitro. Expression levels of CD80, CD86, HLA-DR, and CD54 on DCs transduced with the dSIV incorporating CD40L (CD40L-dSIV) were significantly higher than on those transduced with dSIV. Moreover, CD40L-dSIV-transduced DCs expressed up to 10-fold more IL-12 than dSIV-transduced DCs. CD40L-dSIV-transduced DCs enhanced proliferation and gamma interferon secretion by naive T cells in an MLR. In addition, CD40L-dSIV-immunized mice exhibited stronger humoral and cell-mediated immune responses than dSIV-vaccinated animals. The results show that incorporating CD40L into the dSIV envelope significantly enhances immunogenicity. As a result, CD40L-dSIVs can be strong candidates for development of a safe and highly immunogenic AIDS vaccine.

Indexed as

AnimalsAntibodies, ViralBlotting, WesternCD40 LigandCD4-Positive T-LymphocytesCell ProliferationElectrophoresis, Polyacrylamide GelEnzyme-Linked Immunosorbent AssayFemaleHeLa CellsHumansImmunity, CellularInterferon-gammaLymphocyte ActivationMiceSimian Immunodeficiency VirusAntibodies, ViralCD40 LigandInterferon-gamma

Identifiers

PMID19036823
PMCPMC2620918
OpenAlexW2068929579

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.