Evidence map›Paper›PMID 28947539›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2017

Priming and Activation of Inflammasome by Canarypox Virus Vector ALVAC via the cGAS/IFI16-STING-Type I IFN Pathway and AIM2 Sensor.

Fengliang Liu, Qingli Niu, Xiuzhen Fan, Connie Liu, Jie Zhang, Zhi Wei, Wei Hou, Thirumala-Devi Kanneganti, Merlin L Robb, Jerome H Kim and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

33 citing papers in PubMed, 43 citations in OpenAlex.

  1. Review
  2. CD8Cell reports. Medicine · 2026
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  17. Adenovirus vector-based vaccine for infectious diseases.Drug metabolism and pharmacokinetics · 2022
    Review
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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 6 institutions in 3 countries.

Fengliang LiuDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX 77555.ORCID 0000-0002-5038-5012
Qingli NiuDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX 77555.ORCID 0000-0002-0318-295X
Xiuzhen FanDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX 77555.
Connie LiuDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX 77555.ORCID 0000-0002-8692-8023
Jie ZhangDepartment of Computer Science, New Jersey Institute of Technology, Newark, NJ 07102.ORCID 0000-0003-0242-8812
Zhi WeiDepartment of Computer Science, New Jersey Institute of Technology, Newark, NJ 07102.
Wei HouSchool of Basic Medical Sciences, Wuhan University, Wuhan 430070, China.ORCID 0000-0003-1439-455X
Thirumala-Devi KannegantiImmunology Department, St. Jude Children's Research Hospital, Memphis, TN 38105.ORCID 0000-0002-6395-6443
Merlin L RobbMilitary HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, MD 20910.ORCID 0000-0003-3949-9649
Jerome H KimInternational Vaccine Institute, Seoul 08826, Republic of Korea; and.ORCID 0000-0003-0461-6438
Nelson L MichaelMilitary HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, MD 20910.ORCID 0000-0001-5882-5548
Jiaren SunDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX 77555.ORCID 0000-0001-5084-4437
Lynn SoongDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX 77555.ORCID 0000-0003-3370-3434
Haitao HuDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX 77555; haihu@UTMB.edu.
The University of Texas Medical Branch at Galveston · USNew Jersey Institute of Technology · USWalter Reed Army Institute of Research · USInternational Vaccine Institute · KRSt. Jude Children's Research Hospital · USWuhan University · CN

Funding

Susceptibility of antigen-specific CD4 T cells to HIV: implications for HIV vacciR21AI110214 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI HU, HAITAO · 2014 to 2015
$403k
NIAID NIH HHS R21 AI110214
6 · The paper itself

Abstract

Viral vectors derived from different virus families, including poxvirus (canarypox virus vector ALVAC) and adenovirus (human Ad5 vector), have been widely used in vaccine development for a range of human diseases including HIV/AIDS. Less is known about the mechanisms underlying the host innate response to these vectors. Increasing evidence from clinical vaccine trials testing different viral vectors has suggested the importance of understanding basic elements of host-viral vector interactions. In this study, we investigated the innate interactions of APCs with two commonly used HIV vaccine vectors, ALVAC and Ad5, and identified AIM2 as an innate sensor for ALVAC, triggering strong inflammasome activation in both human and mouse APCs. Microarray and comprehensive gene-knockout analyses (CRISPR/Cas9) identified that ALVAC stimulated the cGAS/IFI16-STING-type I IFN pathway to prime AIM2, which was functionally required for ALVAC-induced inflammasome activation. We also provided evidence that, in contrast to ALVAC, the Ad5 vector itself was unable to induce inflammasome activation, which was related to its inability to stimulate the STING-type I IFN pathway and to provide inflammasome-priming signals. In preconditioned APCs, the Ad5 vector could stimulate inflammasome activation through an AIM2-independent mechanism. Therefore, our study identifies the AIM2 inflammasome and cGAS/IFI16-STING-type I IFN pathway as a novel mechanism for host innate immunity to the ALVAC vaccine vector.

Indexed as

Immunity, InnateAdenoviridaeAnimalsAntigen-Presenting CellsCanarypox virusCRISPR-Cas SystemsCyclic Guanosine Monophosphate-Adenosine Monophosphate SynthaseDNA-Binding ProteinsFemaleGene Knockdown TechniquesGenetic VectorsHumansInterferon Type IMaleMembrane ProteinsMiceAIM2 protein, humanAim2 protein, mousecGAS protein, humancGAS protein, mouseCyclic Guanosine Monophosphate-Adenosine Monophosphate SynthaseDNA-Binding ProteinsIFI16 protein, humanIfi16 protein, mouseInterferon Type IMembrane ProteinsNuclear ProteinsNucleotidyltransferasesPhosphoproteinsSTING1 protein, humanSting1 protein, mouseSTING Protein

Identifiers

PMID28947539
PMCPMC5679316
OpenAlexW2759627343

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.