Evidence map›Paper›PMID 26852268›Full record

ReviewTrends in microbiology2016

Harnessing the Prokaryotic Adaptive Immune System as a Eukaryotic Antiviral Defense.

Aryn A Price, Arash Grakoui, David S Weiss

Abstract readReview
In one paragraph

Review in Trends in microbiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

  1. Review
  2. Review
  3. Production of CFTR-ΔF508 Rabbits.Frontiers in genetics · 2020
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. 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

3 authors.

Aryn A PriceDepartment of Microbiology and Immunology, Microbiology and Molecular Genetics Program, Emory University, Atlanta, GA 30329, USA; Emory Vaccine Center, Emory University, Atlanta, GA 30329, USA; Yerkes National Primate Research Center, Emory University, Atlanta, GA 30329, USA.
Arash GrakouiEmory Vaccine Center, Emory University, Atlanta, GA 30329, USA; Yerkes National Primate Research Center, Emory University, Atlanta, GA 30329, USA; Division of Infectious Diseases, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia 30329, USA. Electronic address: arash.grakoui@emory.edu.
David S WeissEmory Vaccine Center, Emory University, Atlanta, GA 30329, USA; Yerkes National Primate Research Center, Emory University, Atlanta, GA 30329, USA; Division of Infectious Diseases, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia 30329, USA. Electronic address: david.weiss@emory.edu.

Funding

Yerkes National Primate Research Center Role of type-I IFN in regulating COVID-19 induced inflammation and pathogenesisP51OD011132 · OD · EMORY UNIVERSITY · PI Joon Sup Lee · 2012 to 2026
$167.0M
YNPRC NHP CLINICAL MEDICINE RESIDENCY PROGRAM - SUPPLEMENTP51RR000165 · NCRR · EMORY UNIVERSITY · PI ALTMAN, JOHN DAVID · 1985 to 2011
$114.0M
Mechanisms of hepatitis C virus persistenceR01AI070101 · NIAID · EMORY UNIVERSITY · PI GRAKOUI, ARASH · 2006 to 2016
$3.9M
T cell compartmentalization and antiviral responseR01AI124680 · NIAID · EMORY UNIVERSITY · PI GRAKOUI, ARASH, ZHU, CHENG · 2016 to 2020
$3.2M
CRISPR/Cas systems in bacterial gene regulation and virulenceR01AI110701 · NIAID · EMORY UNIVERSITY · PI WEISS, DAVID S · 2014 to 2018
$2.2M
Host and viral determinants of hepatitis C virus macaque infectionR21AI118337 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI EVANS, MATTHEW J, GRAKOUI, ARASH · 2015 to 2016
$499k
NCRR NIH HHS P51 RR000165NCRR NIH HHS P51RR000165NIAID NIH HHS 1R21AI118337NIAID NIH HHS R01 AI070101NIAID NIH HHS R01AI070101NIAID NIH HHS R01 AI110701NIAID NIH HHS R01-AI110701NIAID NIH HHS R01 AI124680NIAID NIH HHS R01AI124680NIAID NIH HHS R21 AI118337NIH HHS P51 OD011132NIH HHS P51OD011132
6 · The paper itself

Abstract

Clustered, regularly interspaced, short palindromic repeats - CRISPR-associated (CRISPR-Cas) systems - are sequence-specific RNA-directed endonuclease complexes that bind and cleave nucleic acids. These systems evolved within prokaryotes as adaptive immune defenses to target and degrade nucleic acids derived from bacteriophages and other foreign genetic elements. The antiviral function of these systems has now been exploited to combat eukaryotic viruses throughout the viral life cycle. Here we discuss current advances in CRISPR-Cas9 technology as a eukaryotic antiviral defense.

Indexed as

Adaptive ImmunityAnimalsBacteriophagesClustered Regularly Interspaced Short Palindromic RepeatsEukaryotic CellsGeminiviridaeHepatitis B virusHIVHumansImmune SystemModels, MolecularPapillomaviridaeProkaryotic CellsVirusesantiviralCas9HBVHCVHIVvirus

Identifiers

PMID26852268
PMCPMC4808413

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.