Evidence map›Paper›PMID 31795353›Full record

ReviewInternational journal of molecular sciences2019

Multiple Functions of B Cells in the Pathogenesis of Systemic Lupus Erythematosus.

Kongyang Ma, Wenhan Du, Xiaohui Wang, Shiwen Yuan, Xiaoyan Cai, Dongzhou Liu, Jingyi Li, Liwei Lu

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed, 2 pooled it
–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

60 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Review
  5. Review
  6. Review
  7. The H159Y Variant of the BAFF-R Gene (International journal of molecular sciences · 2026
    Article
  8. Importance of B cells (Review).International journal of molecular medicine · 2026
    Review
  9. Review
  10. Article
  11. Review
  12. [Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2025
    Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Review
  19. Article
  20. 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

8 authors.

Kongyang MaDepartment of Rheumatology and Immunology, Second Clinical Medical College of Jinan University, Shenzhen People's Hospital, Shenzhen 518000, China.
Wenhan DuDepartment of Pathology and Shenzhen Institute of Research and Innovation, The University of Hong Kong, Hong Kong 999077, China.
Xiaohui WangDepartment of Pathology and Shenzhen Institute of Research and Innovation, The University of Hong Kong, Hong Kong 999077, China.
Shiwen YuanDepartment of Rheumatology, Guangzhou First People's Hospital, School of Medicine, South China University of Technology, Guangzhou, 510000, China.ORCID 0000-0002-0919-6252
Xiaoyan CaiDepartment of Rheumatology, Guangzhou First People's Hospital, School of Medicine, South China University of Technology, Guangzhou, 510000, China.
Dongzhou LiuDepartment of Rheumatology and Immunology, Second Clinical Medical College of Jinan University, Shenzhen People's Hospital, Shenzhen 518000, China.
Jingyi LiDepartment of Rheumatology and Immunology, Southwest Hospital, The First Hospital Affiliated to The Army Medical University, Chongqing 400038, China.ORCID 0000-0002-5344-3679
Liwei LuDepartment of Pathology and Shenzhen Institute of Research and Innovation, The University of Hong Kong, Hong Kong 999077, China.

Funding

National Natural Science Foundation of China 91842304; 81771761; 81771735Sanming Project of Medicine in Shenzhen SZSM201512019
6 · The paper itself

Abstract

Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by excessive autoantibody production and multi-organ involvement. Although the etiology of SLE still remains unclear, recent studies have characterized several pathogenic B cell subsets and regulatory B cell subsets involved in the pathogenesis of SLE. Among pathogenic B cell subsets, age-associated B cells (ABCs) are a newly identified subset of autoreactive B cells with T-bet-dependent transcriptional programs and unique functional features in SLE. Accumulation of T-bet

Indexed as

AgingAnimalsB-LymphocytesCytokinesGene Regulatory NetworksHumansLupus Erythematosus, SystemicToll-Like ReceptorsTranscriptional ActivationCytokinesToll-Like Receptorsage-associated B cells (ABCs)autoreactive B cellsregulatory B cells (Bregs)systemic lupus erythematosus (SLE)

Identifiers

PMID31795353
PMCPMC6929160

What OpenQuestion holds

Textmetadata
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.