Collections / bia-s-biad859

bia-s-biad859

Datasets2
Size~4.2 GB
AssayPhenoCycler
Samplehuman · pancreas
KindPublication
Flag a data issue
10.7554/elife.100535 ↗
Python · sddb client
from sddb import Catalog

cohort = Catalog().collection("bia-s-biad859")
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="bia-s-biad859")
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 bia-s-biad859 --dest data/

Licenses: 2 CC0 1.0

The extra-islet pancreas supports autoimmunity in human type 1 diabetes.

In autoimmune type 1 diabetes (T1D), immune cells infiltrate and destroy the islets of Langerhans - islands of endocrine tissue dispersed throughout the pancreas. However, the contribution of cellular programs outside islets to insulitis is unclear. Here, using CO-Detection by indEXing (CODEX) tissue imaging and cadaveric pancreas samples, we simultaneously examine islet and extra-islet inflammation in human T1D. We identify four sub-states of inflamed islets characterized by the activation profiles of CD8<sup>+</sup>T cells enriched in islets relative to the surrounding tissue. We further find that the extra-islet space of lobules with extensive islet-infiltration differs from the extra-islet space of less infiltrated areas within the same tissue section. Finally, we identify lymphoid structures away from islets enriched in CD45RA<sup>+</sup> T cells - a population also enriched in one of the inflamed islet sub-states. Together, these data help define the coordination between islets and the extra-islet pancreas in the pathogenesis of human T1D.

Open in Vitessce
PhenoCycler
Human pancreas
S-BIAD859:6371v1:reg002
human pancreas type 1 diabetes mellitus 2.1 GB 57,248 cells silver CC0 1.0
TechnologyPhenoCycler
Organismhuman
Tissuepancreas
Conditiontype 1 diabetes mellitus
Size2.1 GB
Cells57,248
silver CC0 1.0 Open in Vitessce
Open in Vitessce
PhenoCycler
Human pancreas
S-BIAD859:6371v1:reg001
human pancreas type 1 diabetes mellitus 2.1 GB 50,567 cells silver CC0 1.0
TechnologyPhenoCycler
Organismhuman
Tissuepancreas
Conditiontype 1 diabetes mellitus
Size2.1 GB
Cells50,567
silver CC0 1.0 Open in Vitessce

Cite this collection

doi.org/10.7554/elife.100535 ↗
BibTeX
@article{Barlow_2025,
  title = {The extra-islet pancreas supports autoimmunity in human type 1 diabetes},
  volume = {13},
  ISSN = {2050-084X},
  url = {http://dx.doi.org/10.7554/elife.100535},
  DOI = {10.7554/elife.100535},
  journal = {eLife},
  publisher = {eLife Sciences Publications, Ltd},
  author = {Barlow, Graham L and Schürch, Christian M and Bhate, Salil S and Phillips, Darci J and Young, Arabella and Dong, Shen and Martinez, Hunter A and Kaber, Gernot and Nagy, Nadine and Ramachandran, Sasvath and Meng, Janet and Korpos, Eva and Bluestone, Jeffrey A and Nolan, Garry P and Bollyky, Paul L},
  year = {2025},
  month = Apr
}