Cited by 45Immune Response and Inflammationinterferon and immune responsesImmunotherapy and Immune Responses

Sequence-Specific Sensing of Nucleic Acids

Open access
Vabret, Nicolas, Bhardwaj, Nina, Greenbaum, Benjamin D.·2017·Trends in Immunology

Abstract

Innate immune cells are endowed with many nucleic acid receptors, but the role of sequence in the detection of foreign organisms remains unclear. Can sequence patterns influence recognition? In addition, how can we infer those patterns from sequence data? Here, we detail recent computational and experimental evidence associated with sequence-specific sensing. We review the mechanisms underlying the detection and discrimination of foreign sequences from self. We also describe quantitative approaches used to infer the stimulatory capacity of a given pathogen nucleic acid species, and the influence of sequence-specific sensing on host-pathogen coevolution, including endogenous sequences of foreign origin. Finally, we speculate how further studies of sequence-specific sensing will be useful to improve vaccine design, gene therapy and cancer treatment.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1016/j.it.2016.10.006

Cites

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • Although GTCGTT has been proposed as an optimal human TLR9 activating sequence, other sequences of CpG ODN are also activating and questions remain regarding the potency of activation through sequence context, TLR secondary structure, and cell type.

    “Although GTCGTT has been proposed as an optimal human TLR9 activating sequence, other sequences of CpG ODN are also activating and questions remain regarding the potency of activation through sequence context, TLR secondary structure, and cell type [96][97][98].”

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

The citation lists haven’t been fetched yet

References 95 · Cited by 45

Authors
Vabret, N., Bhardwaj, N., & Greenbaum, B. D.
Affiliations
Tisch Cancer Institute (US)
Corresponding author
  • Vabret, Nicolas
  • Greenbaum, Benjamin D.
Venue
Trends in Immunology
Publisher
Elsevier BV
Published
2017-01
Volume
38
Issue
1
Pages
53-65
ISSN
1471-4906 (ISSN-L)
OpenAlex
W2553460399
Cited by
45
References
95
Citations by year
2025: 4 · 2024: 2 · 2023: 3 · 2022: 8 · 2021: 4 · 2020: 3 · 2019: 7 · 2018: 9 · 2017: 5
FWCI
0.68
Type
journal article
Language
en
Open access
Locations
  • Trends in Immunology (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • National Cancer Institute (P01CA087497, R01CA180913, P30CA196521)
  • National Institute of Allergy and Infectious Diseases (R01AI081848)
Topics
  • Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
  • Life Sciences › Immunology and Microbiology › Immunology › interferon and immune responses
  • Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
Keywords
innate immunity, pattern recognition receptors, host-pathogen coevolution, vaccine design, gene therapy, cancer immunotherapy
MeSH terms
Animals, Autoantigens, Base Sequence, Biological Evolution, Humans, Immunity, Innate, Nucleic Acids, Computational Biology, Receptors, Pattern Recognition, Host-Pathogen Interactions

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review