Evidence map›Paper›PMID 29844470›Full record

ArticleScientific reports2018

Repeated administration of alpha-galactosylceramide ameliorates experimental lupus nephritis in mice.

Takahiro Uchida, Hiroyuki Nakashima, Akira Yamagata, Seigo Ito, Takuya Ishikiriyama, Masahiro Nakashima, Shuhji Seki, Hiroo Kumagai, Naoki Oshima

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Metabolic signatures of immune cells in chronic kidney disease.Expert reviews in molecular medicine · 2022
    Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Unconventional T cells and kidney disease.Nature reviews. Nephrology · 2021
    Review
  9. Article
  10. Review
  11. Article
  12. Roles of Natural Killer T Cells and Natural Killer Cells in Kidney Injury.International journal of molecular sciences · 2019
    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

9 authors at 1 institution in 1 country.

Takahiro UchidaDepartment of Nephrology and Endocrinology, National Defense Medical College, Tokorozawa, Saitama, Japan. DRI1905@ndmc.ac.jp.
Hiroyuki NakashimaDepartment of Immunology and Microbiology, National Defense Medical College, Tokorozawa, Saitama, Japan.
Akira YamagataDepartment of Nephrology and Endocrinology, National Defense Medical College, Tokorozawa, Saitama, Japan.
Seigo ItoDepartment of Nephrology and Endocrinology, National Defense Medical College, Tokorozawa, Saitama, Japan.ORCID 0000-0001-7080-3157
Takuya IshikiriyamaDepartment of Immunology and Microbiology, National Defense Medical College, Tokorozawa, Saitama, Japan.
Masahiro NakashimaDepartment of Immunology and Microbiology, National Defense Medical College, Tokorozawa, Saitama, Japan.
Shuhji SekiDepartment of Immunology and Microbiology, National Defense Medical College, Tokorozawa, Saitama, Japan.
Hiroo KumagaiDepartment of Nephrology and Endocrinology, National Defense Medical College, Tokorozawa, Saitama, Japan.
Naoki OshimaDepartment of Nephrology and Endocrinology, National Defense Medical College, Tokorozawa, Saitama, Japan.
National Defense Medical College · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lupus nephritis is a crucial complication of systemic lupus erythematosus. In this study, we investigated the roles of mouse natural killer T (NKT) cells in lupus nephritis. From 24 weeks of age, NZB/NZW F1 mice were injected with alpha-galactosylceramide (α-GalCer) or vehicle once a week for four weeks. In the α-GalCer group, the levels of proteinuria and blood urea nitrogen were significantly lower than those in the vehicle group. The histological evaluation showed a decrease in glomerular immune complex deposits and an alleviation of podocyte injury. The proportion of NKT cells in the mononuclear cell (MNC) fraction in the α-GalCer group was significantly decreased in the liver, kidney, and spleen. The proliferation and cytokine production in α-GalCer-stimulated liver MNCs were markedly diminished in the α-GalCer group (anergy). The IFN-γ production in liver MNCs stimulated by concanavalin A or an anti-CD3 antibody did not differ between the two groups, whereas the IL-4 production was significantly lower in the α-GalCer group. In addition, the IgM production in CpG-oligodeoxynucleotide-stimulated spleen MNCs was significantly lower in the α-GalCer group. These results suggest that α-GalCer suppressed Th2 immune responses in NKT cells and B cell function, thereby slowing the progression of lupus nephritis.

Indexed as

AnimalsB-LymphocytesDisease ProgressionDrug Administration ScheduleFemaleGalactosylceramidesImmunoglobulin GInterleukin-4KidneyLupus NephritisMiceNatural Killer T-Cellsalpha-galactosylceramideGalactosylceramidesIl4 protein, mouseImmunoglobulin GInterleukin-4

Identifiers

PMID29844470
PMCPMC5974230
OpenAlexW2805747977

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.