Skip to main navigation Skip to search Skip to main content

Correction: Cancer immunotherapies transition endothelial cells into HEVs that generate TCF1+ T lymphocyte niches through a feed-forward loop

  • Yichao Hua
  • , Gerlanda Vella
  • , Florian Rambow
  • , Elizabeth Allen
  • , Asier Antoranz Martinez
  • , Marie Duhamel
  • , Akira Takeda
  • , Sirpa Jalkanen
  • , Steffie Junius
  • , Ann Smeets
  • , David Nittner
  • , Stefanie Dimmeler
  • , Thomas Hehlgans
  • , Adrian Liston
  • , Francesca Maria Bosisio
  • , Giuseppe Floris
  • , Damya Laoui
  • , Maija Hollmén
  • , Diether Lambrechts
  • , Pascal Merchiers
  • Jean-Christophe Marine, Susan Schlenner, Gabriele Bergers

Research output: Contribution to journalArticlepeer-review

9 Citations (Scopus)
60 Downloads (Pure)

Abstract

(Cancer Cell 40, 1600–1618; December 12, 2022) In this article, the authors demonstrated that antiangiogenic immunotherapies differentiate postcapillary venules into high-endothelial venules (HEVs) that foster permissive TCF1 + T lymphocyte niches. In the introduction, they mistakenly stated that HEVs express L-Selectin/CD62L, while HEVs express the sulphated and glycosylated ligands for L-Selectin/CD62L. The original article has been corrected online. The authors regret this error and apologize for any confusion this might have caused.

Original languageEnglish
Pages (from-to)226-226
Number of pages1
JournalCancer Cell
Volume41
Issue number1
DOIs
Publication statusPublished - 9 Jan 2023

Bibliographical note

Publisher Copyright:
© 2022 The Author(s)

Copyright:
Copyright 2023 Elsevier B.V., All rights reserved.

Fingerprint

Dive into the research topics of 'Correction: Cancer immunotherapies transition endothelial cells into HEVs that generate TCF1+ T lymphocyte niches through a feed-forward loop'. Together they form a unique fingerprint.

Cite this