Evidence map›Paper›PMID 29719256›Full record

ArticleCell reports2018

STING-Activating Adjuvants Elicit a Th17 Immune Response and Protect against Mycobacterium tuberculosis Infection.

Erik Van Dis, Kimberly M Sogi, Chris S Rae, Kelsey E Sivick, Natalie H Surh, Meredith L Leong, David B Kanne, Ken Metchette, Justin J Leong, Jacob R Bruml and 8 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 89 papers.

0numbers the graph read from it
0cells of the map it votes in
89citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

89 citing papers in PubMed, 128 citations in OpenAlex.

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  9. AFrontiers in immunology · 2026
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29 more citing papers are in PubMed but not listed here.

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

18 authors at 4 institutions in 2 countries.

Erik Van DisMolecular and Cell Biology, Division of Immunology and Pathogenesis, University of California, Berkeley, Berkeley, CA 94720, USA.
Kimberly M SogiSchool of Public Health, Division of Infectious Disease and Vaccinology, University of California, Berkeley, Berkeley, CA 94720, USA.
Chris S RaeAduro Biotech, Inc., 740 Heinz Avenue, Berkeley, CA 94710, USA.
Kelsey E SivickAduro Biotech, Inc., 740 Heinz Avenue, Berkeley, CA 94710, USA.
Natalie H SurhAduro Biotech, Inc., 740 Heinz Avenue, Berkeley, CA 94710, USA.
Meredith L LeongAduro Biotech, Inc., 740 Heinz Avenue, Berkeley, CA 94710, USA.
David B KanneAduro Biotech, Inc., 740 Heinz Avenue, Berkeley, CA 94710, USA.
Ken MetchetteAduro Biotech, Inc., 740 Heinz Avenue, Berkeley, CA 94710, USA.
Justin J LeongAduro Biotech, Inc., 740 Heinz Avenue, Berkeley, CA 94710, USA.
Jacob R BrumlAduro Biotech, Inc., 740 Heinz Avenue, Berkeley, CA 94710, USA.
Vivian ChenSchool of Public Health, Division of Infectious Disease and Vaccinology, University of California, Berkeley, Berkeley, CA 94720, USA.
Kartoosh HeydariLKS Flow Cytometry Core, Cancer Research Laboratory, University of California, Berkeley, Berkeley, CA 94720, USA.
Nathalie CadieuxAeras, 1405 Research Blvd., Rockville, MD 20850, USA.
Tom EvansVaccitech Limited, King Charles House, Park End Street, Oxford OX1 1JD, UK.
Sarah M McWhirterAduro Biotech, Inc., 740 Heinz Avenue, Berkeley, CA 94710, USA.
Thomas W DubenskyAduro Biotech, Inc., 740 Heinz Avenue, Berkeley, CA 94710, USA.
Daniel A PortnoyMolecular and Cell Biology, Division of Immunology and Pathogenesis, University of California, Berkeley, Berkeley, CA 94720, USA; School of Public Health, Division of Infectious Disease and Vaccinology, University of California, Berkeley, Berkeley, CA 94720, USA.
Sarah A StanleyMolecular and Cell Biology, Division of Immunology and Pathogenesis, University of California, Berkeley, Berkeley, CA 94720, USA; School of Public Health, Division of Infectious Disease and Vaccinology, University of California, Berkeley, Berkeley, CA 94720, USA. Electronic address: sastanley@berkeley.edu.
Aduro BioTech (United States) · USUniversity of California, Berkeley · USAeras · USVaccitech (United Kingdom) · GB

Funding

The role of Listeria cyclic-di-AMP during infection and immunityP01AI063302 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI STANLEY, SARAH A · 2004 to 2025
$45.5M
THE MOLECULAR BASIS OF CELL FUNCTIONT32GM007232 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI BILDER, DAVID, UNAL, ELCIN · 1985 to 2022
$36.4M
Listeria Hemolysis and Escape From a VacuoleR01AI027655 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI DANIEL A PORTNOY · 1993 to 2026
$10.1M
Immunology & Pathogenesis Program Training GrantT32AI100829 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI Gregory M Barton, ELLEN A ROBEY · 2012 to 2026
$4.7M
Metabolic regulation of macrophage function during M. tuberculosis infectionR01AI113270 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI STANLEY, SARAH A · 2015 to 2024
$3.8M
Listeria-based vaccines engineered to modulate the innate immune systemR56AI091976 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI PORTNOY, DANIEL A · 2011 to 2011
$355k
NIAID NIH HHS P01 AI063302NIAID NIH HHS R01 AI027655NIAID NIH HHS R01 AI113270NIAID NIH HHS R56 AI091976NIAID NIH HHS T32 AI100829NIGMS NIH HHS T32 GM007232
6 · The paper itself

Abstract

There are a limited number of adjuvants that elicit effective cell-based immunity required for protection against intracellular bacterial pathogens. Here, we report that STING-activating cyclic dinucleotides (CDNs) formulated in a protein subunit vaccine elicit long-lasting protective immunity to Mycobacterium tuberculosis in the mouse model. Subcutaneous administration of this vaccine provides equivalent protection to that of the live attenuated vaccine strain Bacille Calmette-Guérin (BCG). Protection is STING dependent but type I IFN independent and correlates with an increased frequency of a recently described subset of CXCR3-expressing T cells that localize to the lung parenchyma. Intranasal delivery results in superior protection compared with BCG, significantly boosts BCG-based immunity, and elicits both Th1 and Th17 immune responses, the latter of which correlates with enhanced protection. Thus, a CDN-adjuvanted protein subunit vaccine has the capability of eliciting a multi-faceted immune response that results in protection from infection by an intracellular pathogen.

Indexed as

Adjuvants, ImmunologicAnimalsBCG VaccineDisease Models, AnimalImmunity, CellularMembrane ProteinsMiceMice, KnockoutMycobacterium tuberculosisSTING ProteinTh17 CellsTh1 CellsTuberculosis, PulmonaryVaccines, SubunitAdjuvants, ImmunologicBCG VaccineMembrane ProteinsSting1 protein, mouseSTING ProteinVaccines, Subunitcyclic dinucleotidesMycobacterium tuberculosisTh17vaccine adjuvant

Identifiers

PMID29719256
PMCPMC6003617
OpenAlexW2802363905

What OpenQuestion holds

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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.