Evidence map›Paper›PMID 27846813›Full record

ArticleBMC nephrology2016

Granulocyte colony-stimulating factor treatment ameliorates lupus nephritis through the expansion of regulatory T cells.

Ji-Jing Yan, Enkthuya Jambaldorj, Jae-Ghi Lee, Joon Young Jang, Jung Min Shim, Miyeun Han, Tai Yeon Koo, Curie Ahn, Jaeseok Yang

Open access · goldAbstract read
In one paragraph

Article in BMC nephrology, 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
2.4field-weighted citation impact, top 12% 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

10 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Skin-kidney crosstalk in SLE.Nature reviews. Rheumatology · 2021
    Article
  7. Review
  8. Review
  9. Regulatory T cells in renal disease.Clinical & translational immunology · 2018
    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

9 authors at 2 institutions in 1 country.

Ji-Jing YanTransplantation Research Institute, Seoul National University College of Medicine, Seoul, 03080, Republic of Korea.
Enkthuya JambaldorjTransplantation Research Institute, Seoul National University College of Medicine, Seoul, 03080, Republic of Korea.
Jae-Ghi LeeTransplantation Research Institute, Seoul National University College of Medicine, Seoul, 03080, Republic of Korea.
Joon Young JangTransplantation Research Institute, Seoul National University College of Medicine, Seoul, 03080, Republic of Korea.
Jung Min ShimTransplantation Research Institute, Seoul National University College of Medicine, Seoul, 03080, Republic of Korea.
Miyeun HanDepartment of Internal Medicine, Seoul National University College of Medicine, Seoul, 03080, Republic of Korea.
Tai Yeon KooTransplantation Center, Seoul National University Hospital, Seoul, 03080, Republic of Korea.
Curie AhnDepartment of Internal Medicine, Seoul National University College of Medicine, Seoul, 03080, Republic of Korea.
Jaeseok YangTransplantation Research Institute, Seoul National University College of Medicine, Seoul, 03080, Republic of Korea. jcyjs@dreamwiz.com.
Seoul National University · KRSeoul National University Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGranulocyte colony-stimulating factor (G-CSF) can induce regulatory T cells (Tregs) as well as myeloid-derived suppressor cells (MDSCs). Despite the immune modulatory effects of G-CSF, results of G-CSF treatment in systemic lupus erythematosus are still controversial. We therefore investigated whether G-CSF can ameliorate lupus nephritis and studied the underlying mechanisms.

methodsNZB/W F1 female mice were treated with G-CSF or phosphate-buffered saline for 5 consecutive days every week from 24 weeks of age, and were analyzed at 36 weeks of age.

resultsG-CSF treatment decreased proteinuria and serum anti-dsDNA, increased serum complement component 3 (C3), and attenuated renal tissue injury including deposition of IgG and C3. G-CSF treatment also decreased serum levels of BUN and creatinine, and ultimately decreased mortality of NZB/W F1 mice. G-CSF treatment induced expansion of CD4

conclusionsG-CSF treatment ameliorated lupus nephritis through the preferential expansion of CD4

Indexed as

AnimalsFemaleGranulocyte Colony-Stimulating FactorLupus NephritisMiceT-Lymphocytes, RegulatoryGranulocyte Colony-Stimulating FactorGranulocyte colony-stimulating factorLupus nephritisRegulatory T cells

Identifiers

PMID27846813
PMCPMC5111287
OpenAlexW2549593825

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.