Evidence map›Paper›PMID 23509365›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2013

Polyinosinic-polycytidylic acid is the most effective TLR adjuvant for SIV Gag protein-induced T cell responses in nonhuman primates.

Haesun Park, Lauren Adamson, Tae Ha, Karl Mullen, Shoko I Hagen, Arys Nogueron, Andrew W Sylwester, Michael K Axthelm, Al Legasse, Michael Piatak and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
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

39 citing papers in PubMed, 1 synthesis or guideline pooled it, 55 citations in OpenAlex.

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  12. Vaccine nanodiscs plus polyICLC elicit robust CD8+ T cell responses in mice and non-human primates.Journal of controlled release : official journal of the Controlled Release Society · 2021
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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

14 authors at 5 institutions in 1 country.

Haesun ParkDepartment of Pathology, Vaccine and Gene Therapy Institute, and Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, OR 97006, USA.
Lauren Adamson
Tae Ha
Karl Mullen
Shoko I Hagen
Arys Nogueron
Andrew W Sylwester
Michael K Axthelm
Al Legasse
Michael Piatak
Jeffrey D Lifson
Juliana M McElrath
Louis J Picker
Robert A Seder
Oregon Health & Science University · USOregon National Primate Research Center · USScience Applications International Corporation (United States) · USFred Hutch Cancer Center · USNational Institutes of Health Clinical Center · US

Funding

Optimization Of HIV Specific Immune Responses In VivoZIAAI005016 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI SEDER, ROBERT A · 2009 to 2018
$31.2M
Optimization Of HIV Specific Immune Responses In VivoZ01AI005016 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI SEDER, ROBERT A · 2002 to 2008
$1.2M
Intramural NIH HHS Z01 AI005016Intramural NIH HHS ZIA AI005016
6 · The paper itself

Abstract

Prime-boost immunization with heterologous vaccines elicits potent cellular immunity. In this study, we assessed the influence of various TLR ligands on SIV Gag-specific T cell immunity and protection following prime-boost immunization. Rhesus macaques (RMs) were primed with SIV Gag protein emulsified in Montanide ISA51 with or without TLR3 (polyinosinic-polycytidylic acid [poly-IC]), TLR4 (monophosphoryl lipid A), TLR7/8 (3M-012), TLR9 (CpG), or TLR3 (poly-IC) combined with TLR7/8 ligands, then boosted with replication defective adenovirus 5 expressing SIV Gag (rAd5-Gag). After priming, RMs that received SIV Gag protein plus poly-IC developed significantly higher frequencies of SIV Gag-specific CD4(+) Th1 responses in blood and bronchoalveolar lavage (BAL) fluid lymphocytes compared with all other adjuvants, and low-level SIV Gag-specific CD8(+) T cell responses. After the rAd5-Gag boost, the magnitude and breadth of SIV Gag-specific CD8(+) T cell responses were significantly increased in RM primed with SIV Gag protein plus poly-IC, with or without the TLR7/8 ligand, or CpG. However, the anamnestic, SIV Gag-specific CD8(+) T cell response to SIVmac251 challenge was not significantly enhanced by SIV Gag protein priming with any of the adjuvants. In contrast, the anamnestic SIV Gag-specific CD4(+) T cell response in BAL was enhanced by SIV Gag protein priming with poly-IC or CpG, which correlated with partial control of early viral replication after SIVmac251 challenge. These results demonstrate that prime-boost vaccination with SIV Gag protein/poly-IC improves magnitude, breadth, and durability of CD4(+) T cell immune responses, which could have a role in the control of SIV viral replication.

Indexed as

Adjuvants, ImmunologicAnimalsEpitopes, T-LymphocyteGene Products, gagMacaca mulattaMannitolOleic AcidsPoly I-CReceptors, Antigen, T-CellSimian Immunodeficiency VirusT-Lymphocyte SubsetsAdjuvants, ImmunologicEpitopes, T-LymphocyteGene Products, gagMannitolmontanide ISA 51Oleic AcidsPoly I-CReceptors, Antigen, T-Cell

Identifiers

PMID23509365
PMCPMC3622154
OpenAlexW2111052723

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.