Evidence map›Paper›PMID 38806623›Full record

ArticleCellular & molecular immunology2024

The protective roles of integrin α4β7 and Amphiregulin-expressing innate lymphoid cells in lupus nephritis.

Seungwon Ryu, Kyung Ah Kim, Jinwoo Kim, Dong Hun Lee, Yong-Soo Bae, Hajeong Lee, Byoung Choul Kim, Hye Young Kim

Abstract read
In one paragraph

Article in Cellular & molecular immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–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

15 citing papers in PubMed.

  1. IgA2Cell reports. Medicine · 2025
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  10. bioRxiv : the preprint server for biology · 2025
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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.

Seungwon RyuDepartment of Microbiology, Gachon University College of Medicine, Incheon, 21999, South Korea.ORCID 0000-0003-2638-5749
Kyung Ah KimDepartment of Nano-Bioengineering, Incheon National University, Incheon, 22012, South Korea.
Jinwoo KimLaboratory of Mucosal Immunology, Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, 03080, South Korea.
Dong Hun LeeDepartment of Dermatology, Seoul National University College of Medicine, Seoul, 03080, South Korea.
Yong-Soo BaeDepartment of Biological Sciences, SRC Center for Immune Research on Non-lymphoid Organs, Sungkyunkwan University, Suwon, 16419, South Korea.ORCID 0000-0002-2233-9449
Hajeong LeeDivision of Nephrology, Department of Internal Medicine, Seoul National University Hospital and Seoul National University College of Medicine, Seoul, 03080, South Korea.
Byoung Choul KimDepartment of Nano-Bioengineering, Incheon National University, Incheon, 22012, South Korea.
Hye Young KimLaboratory of Mucosal Immunology, Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, 03080, South Korea. hykim11@snu.ac.kr.ORCID 0000-0001-5978-512X

Funding

National Research Foundation of Korea (NRF) RS-2023-00211566National Research Foundation of Korea (NRF) SRC 2017R1A5A1014560National Research Foundation of Korea (NRF) SRC 2017R1A5A1014560, RS-2023-00217798 and NRF-2019R1A2C2087574
6 · The paper itself

Abstract

Type 2 innate lymphoid cells (ILC2s) have emerged as key regulators of the immune response in renal inflammatory diseases such as lupus nephritis. However, the mechanisms underlying ILC2 adhesion and migration in the kidney remain poorly understood. Here, we revealed the critical role of integrin α4β7 in mediating renal ILC2 adhesion and function. We found that integrin α4β7 enables the retention of ILC2s in the kidney by binding to VCAM-1, E-cadherin, or fibronectin on structural cells. Moreover, integrin α4β7 knockdown reduced the production of the reparative cytokine amphiregulin (Areg) by ILC2s. In lupus nephritis, TLR7/9 signaling within the kidney microenvironment downregulates integrin α4β7 expression, leading to decreased Areg production and promoting the egress of ILC2s. Notably, IL-33 treatment upregulated integrin α4β7 and Areg expression in ILC2s, thereby enhancing survival and reducing inflammation in lupus nephritis. Together, these findings highlight the potential of targeting ILC2 adhesion as a therapeutic strategy for autoimmune kidney diseases.

Indexed as

AmphiregulinIntegrin alpha4Integrin beta ChainsLupus NephritisLymphocytesAnimalsCell AdhesionCell MovementDisease Models, AnimalFemaleGene Expression RegulationHumansInterleukin-33KidneyMiceProtein BindingAmphiregulinIntegrin alpha4integrin beta7Integrin beta ChainsInterleukin-33Adhesion moleculesAmphiregulinInnate lymphoid cellsIntegrinsKidneyLupus nephritisTissue residency

Identifiers

PMID38806623
PMCPMC11214630

What OpenQuestion holds

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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.