Evidence map›Paper›PMID 33717066›Full record

ArticleFrontiers in immunology2021

Interleukin-22 From Type 3 Innate Lymphoid Cells Aggravates Lupus Nephritis by Promoting Macrophage Infiltration in Lupus-Prone Mice.

Lingzhen Hu, Jingyi Hu, Liheng Chen, Yi Zhang, Qingqing Wang, Xuyan Yang

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

21 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. Innate Lymphoid Cells Are the Rheostat of Immune Response in the Kidney.Journal of cellular and molecular medicine · 2025
    Review
  10. Review
  11. Review
  12. IL-22, a vital cytokine in autoimmune diseases.Clinical and experimental immunology · 2024
    Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. ILC3: a case of conflicted identity.Frontiers in immunology · 2023
    Review
  19. 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

6 authors at 2 institutions in 1 country.

Lingzhen HuDepartment of Rheumatology, Second Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, China.
Jingyi HuLaboratory of Immunology, College of Medicine, Institute of Basic Medical Sciences, Zhejiang University, Hangzhou, China.
Liheng ChenDepartment of Rheumatology, Second Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, China.
Yi ZhangDepartment of Rheumatology, Second Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, China.
Qingqing WangLaboratory of Immunology, College of Medicine, Institute of Basic Medical Sciences, Zhejiang University, Hangzhou, China.
Xuyan YangDepartment of Rheumatology, Second Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, China.
Second Affiliated Hospital of Zhejiang University · CNZhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lupus nephritis (LN) is one of the most severe manifestations of systemic lupus erythematosus (SLE). Our previous studies demonstrated increased serum and renal Interleukin (IL)-22 in LN patients and MRL/lpr mice. This study investigated the role of IL-22 and its mechanism in LN. Here, we found that IL-22 was mainly produced by type 3 innate lymphoid cells (ILC3) in kidney of MRL/lpr mice. The systemic illness and local renal lesion were significantly alleviated in IL-22 or IL-22R gene knockout (KO) mice (IL-22 KO or IL-22R KO MRL/lpr mice) than control mice (MRL/lpr mice). IL-22 KO or IL-22R KO MRL/lpr mice had significantly slighter infiltration of macrophage in kidney than MRL/lpr mice. Consistently, by RNA-Seq, the expression of (CC motif) ligand 2 (CCL2) and (CXC motif) ligand 10 (CXCL10) was decreased in kidney of KO mice compared with control mice. By immunoblotting, significantly increased levels of STAT3 phosphorylation were found in the kidney of control mice compared to KO mice.

Indexed as

Immunity, InnateAnimalsAutoantibodiesBiomarkersChemokine CCL2Chemokine CXCL10Complement System ProteinsEpithelial CellsFemaleHumansImmunophenotypingInterleukin-22InterleukinsKidneyLupus NephritisLymphocytesAutoantibodiesBiomarkersChemokine CCL2Chemokine CXCL10Complement System ProteinsInterleukin-22interleukin-22 receptorInterleukinsReceptors, InterleukinSTAT3 protein, humanSTAT3 Transcription Factorinterleukin-22interleukin-22 receptorlupus nephritismacrophagesystemic lupus erythematosus

Identifiers

PMID33717066
PMCPMC7953152
OpenAlexW3134083427

What OpenQuestion holds

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LicenceCC BY
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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.