Evidence map›Paper›PMID 27330321›Full record

ReviewJournal of inflammation research2016

Toll-like receptor cascade and gene polymorphism in host-pathogen interaction in Lyme disease.

Shusmita Rahman, Maria Shering, Nicholas H Ogden, Robbin Lindsay, Alaa Badawi

Open access · goldAbstract readReview
In one paragraph

Review in Journal of inflammation research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.0field-weighted citation impact, top 16% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Exploring the Innate Immunity in Invertebrates.Advances in experimental medicine and biology · 2025
    Review
  3. International journal of molecular sciences · 2024
    Article
  4. Review
  5. Comparison of ruminal microbiota,Frontiers in microbiology · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
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

5 authors at 2 institutions in 1 country.

Shusmita RahmanNational Microbiology Laboratory, Public Health Agency of Canada, Toronto, ON, Canada.
Maria SheringFaculty of Arts and Science, University of Toronto, Toronto, ON, Canada.
Nicholas H OgdenNational Microbiology Laboratory, Public Health Agency of Canada, Saint-Hyacinthe, QC, Canada.
Robbin LindsayNational Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, MB, Canada.
Alaa BadawiNational Microbiology Laboratory, Public Health Agency of Canada, Toronto, ON, Canada.
Public Health Agency of Canada · CAUniversity of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lyme disease (LD) risk occurs in North America and Europe where the tick vectors of the causal agent Borrelia burgdorferi sensu lato are found. It is associated with local and systemic manifestations, and has persistent posttreatment health complications in some individuals. The innate immune system likely plays a critical role in both host defense against B. burgdorferi and disease severity. Recognition of B. burgdorferi, activation of the innate immune system, production of proinflammatory cytokines, and modulation of the host adaptive responses are all initiated by Toll-like receptors (TLRs). A number of Borrelia outer-surface proteins (eg, OspA and OspB) are recognized by TLRs. Specifically, TLR1 and TLR2 were identified as the receptors most relevant to LD. Several functional single-nucleotide polymorphisms have been identified in TLR genes, and are associated with varying cytokines types and synthesis levels, altered pathogen recognition, and disruption of the downstream signaling cascade. These single-nucleotide polymorphism-related functional alterations are postulated to be linked to disease development and posttreatment persistent illness. Elucidating the role of TLRs in LD may facilitate a better understanding of disease pathogenesis and can provide an insight into novel therapeutic targets during active disease or postinfection and posttreatment stages.

Indexed as

Borrelia lipoproteinsgenetic polymorphismshost-pathogen interactionLyme diseaseToll-like receptors

Identifiers

PMID27330321
PMCPMC4898433
OpenAlexW2409100747

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.