Collections / Synovial Th17 transdifferentiation into exTh17 sustains chronic IL-17-independent inflammatory arthritis [Visium]

Synovial Th17 transdifferentiation into exTh17 sustains chronic IL-17-independent inflammatory arthritis [Visium]

Rheumatoid arthritis (RA) is the most common systemic autoimmune disease. T helper 17 (Th17) cells are found in the inflamed synovium in RA and believed to play a pathogenic role. However, IL-17 targeted interventions have shown limited efficacy in established RA. Inflammation can induce Th17 transdifferentiation into IL-17 negative Th1 or Tr1 like exTh17. To assess the potential phenotype and role of exTh17 in inflammatory arthritis, we performed Th17 fate mapping studies in the SKG mouse model of RA. We generated triTh17-SKG (IL-17Cre.IfngYFP.Il10eGFP.R26tdTomfl.Zap70SKG) mice and leveraged them to show that in arthritic mice synovial Th17 transdifferentiate into IFNγ- and IL-10- exTh17 which become the most prominent CD4 population in chronic arthritis. These exTh17 cells are more arthritogenic than Th17, and able to sustain arthritis that is IL-17 independent but enriched with IL-6 and TNF, two known RA-promoting cytokines. Synovial exTh17 present a unique gene signature including upregulation of CD44 and S1PR4 that has correlates in the profile of CD4 T cells found in human RA synovium. We further demonstrate that a crosstalk with synoviocytes and S1P signaling promote Th17-exTh17 conversion and that CD44 – another known target for RA- is necessary for the arthritogenic effect of exTh17. Our study suggests that the synoviocyte expansion which occurs during RA progression can drive progressive conversion of Th17 into exTh17, which in turn sustain inflammation that has hallmarks of human established RA.

Datasets2
Size~20.3 MB
AssayVisium
Samplehuman · synovial membrane of synovial joint
KindOther
Flag a data issue
PMID:41202149 ↗
Python · sddb client
from sddb import Catalog

cohort = Catalog().collection("geo-gse232734")
cohort.members        # the 2 datasets as a table

print(cohort.licenses())              # check the terms before you download

sdatas = cohort.to_dict()             # {uid: SpatialData}, cached locally
# or keep the .zarr files in a folder of your choice:
# sdatas = cohort.to_dict(dest="data/")
Python · lamindb

Needs pip install lamindb and network access to the Lamin database, which is limited during the alpha. If it fails, use the Client tab.

import lamindb as ln

db = ln.DB("scverse/spatialdata-db")
coll = db.Collection.get(key="geo-gse232734")
coll.ordered_artifacts.to_dataframe()   # the 2 members, ordered

# download every member .zarr to the local cache:
paths = [a.cache() for a in coll.ordered_artifacts.all()]
Shell
# sddb client: download every member .zarr into data/
sddb-cli download --collection geo-gse232734 --dest data/

Licenses: 2 NCBI GEO policy

Open in Vitessce
Visium
Human synovial membrane of synovial joint
GSM7372755
human synovial membrane of synovial joint rheumatoid arthritis 12.0 MB 1,878 spots bronze H&E NCBI GEO policy
TechnologyVisium
Organismhuman
Tissuesynovial membrane of synovial joint
Conditionrheumatoid arthritis
Size12.0 MB
Spots1,878
bronze H&E NCBI GEO policy Open in Vitessce
Open in Vitessce
Visium
Human synovial membrane of synovial joint
GSM7372756
human synovial membrane of synovial joint rheumatoid arthritis 8.3 MB 836 spots bronze H&E NCBI GEO policy
TechnologyVisium
Organismhuman
Tissuesynovial membrane of synovial joint
Conditionrheumatoid arthritis
Size8.3 MB
Spots836
Magnificationother · 5.968 µm/px
bronze H&E NCBI GEO policy Open in Vitessce

Cite this collection

doi.org/10.1126/sciimmunol.adm7800 ↗
BibTeX
@article{Zoccheddu_2025,
  title = {T
                    <sub>H</sub>
                    17 cells converted into exT
                    <sub>H</sub>
                    17 cells sustain rheumatoid-like IL-17–independent inflammatory arthritis},
  volume = {10},
  ISSN = {2470-9468},
  url = {http://dx.doi.org/10.1126/sciimmunol.adm7800},
  DOI = {10.1126/sciimmunol.adm7800},
  number = {113},
  journal = {Science Immunology},
  publisher = {American Association for the Advancement of Science (AAAS)},
  author = {Zoccheddu, Martina and Suga, Kensuke and Seng, Amara and Svensson, Mattias N. D. and Dutta, Paramita and Panahandeh, Sanaz and Makinde, Hadijat-Kubura Moradeke and Ro, Myungja and Wang, Yizhou and Kim, Hyobin and Mikulski, Zbigniew and Dobaczewska, Katarzyna and Ingegnoli, Francesca and Minsha, Ruth and Seagrist, John F. and Carns, Mary and Aren, Kathleen and Dominguez, Salina and Khan, Mohammad Daud and Denn, Angela and Caporali, Roberto and Randelli, Pietro Simone and McBride, David A. and Mandelin, Arthur M. and Cuda, Carla Marie and Wang, Zhiping Paul and Moore, Jason H. and Shah, Nisarg J. and Won, Kyoung Jae and Winter, Deborah R. and Ay, Ferhat and Perlman, Harris and Bottini, Nunzio},
  year = {2025},
  month = Nov
}