Evidence map›Paper›PMID 26068236›Full record

ReviewInternational journal of molecular sciences2015

Roles of B Cell-Intrinsic TLR Signals in Systemic Lupus Erythematosus.

Kongyang Ma, Jingyi Li, Yongfei Fang, Liwei Lu

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 9% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 44 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Regulation of Toll-like receptor-mediated inflammatory response by microRNA-152-3p-mediated demethylation of MyD88 in systemic lupus erythematosus.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2021
    Article
  17. Review
  18. Frontiers in cellular and infection microbiology · 2021
    Article
  19. Toll-Like Receptor as a Potential Biomarker in Renal Diseases.International journal of molecular sciences · 2020
    Review
  20. 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

4 authors at 3 institutions in 2 countries.

Kongyang MaDepartment of Pathology and Center of Infection and Immunology, Shenzhen Institute of Research and Innovation, The University of Hong Kong, Hong Kong, China. kongyang@hku.hk.
Jingyi LiDepartment of Rheumatology, Southwest Hospital, Third Military Medical University, Chongqing 400038, China. lijingyi_tmmu@yahoo.com.
Yongfei FangDepartment of Rheumatology, Southwest Hospital, Third Military Medical University, Chongqing 400038, China. fangyongfeitmmu@hotmail.com.
Liwei LuDepartment of Pathology and Center of Infection and Immunology, Shenzhen Institute of Research and Innovation, The University of Hong Kong, Hong Kong, China. liweilu@hku.hk.
Army Medical University · CNCity University of Hong Kong, Shenzhen Research Institute · CNUniversity of Hong Kong · HK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Toll-like receptors (TLRs) are a large family of pattern recognition receptors. TLR signals are involved in the pathogenesis of systemic lupus erythematosus. Mouse and human B cells constitutively express most TLRs. Many B cell subpopulations are highly responsive to certain TLR ligation, including B-1 B cells, transitional B cells, marginal zone B cells, germinal center B cell and memory B cells. The B cell-intrinsic TLR signals play critical roles during lupus process. In this review, roles of B cell-intrinsic TLR2, 4, 7, 8 and 9 signals are discussed during lupus pathogenesis in both mouse model and patients. Moreover, mechanisms underlying TLR ligation-triggered B cell activation and signaling pathways are highlighted.

Indexed as

Signal TransductionAnimalsB-LymphocytesHumansLupus Erythematosus, SystemicToll-Like ReceptorsToll-Like Receptorsanti-nuclear autoantibody (ANA)B-1 B cellsgerminal center B cells (GC B cells)marginal zone B cells (MZ B cells)memory B cellsmyeloid differentiation primary response gene 88 (MyD88)systemic lupus erythematosus (SLE)toll-like receptor (TLR)transitional B cellsUnc-93 Homolog B1 (C. elegans) (Unc93b1)

Identifiers

PMID26068236
PMCPMC4490487
OpenAlexW1604232547

What OpenQuestion holds

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LicenceCC BY
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.