ThymoSpheres culture: A model to study human polyclonal unconventional T cells

Author:

Billiet Lore1ORCID,Jansen Hanne1,Pille Melissa1,Boehme Lena1ORCID,Sanchez Sanchez Guillem2345,De Cock Laurenz16,Goetgeluk Glenn16,Pascal Eva16,De Munter Stijn16,Deseins Lucas167ORCID,Ingels Joline168,Michiels Thomas16,De Vos Robrecht167,Zolfaghari Amin16,Vandamme Niels910,Roels Jana910ORCID,Kerre Tessa167,Dmitriev Ruslan I.11,Taghon Tom16,Vermijlen David2345,Vandekerckhove Bart168

Affiliation:

1. Department of Diagnostic Sciences Ghent University Ghent Belgium

2. Department of Pharmacotherapy and Pharmaceutics Université Libre de Bruxelles (ULB) Brussels Belgium

3. Institute for Medical Immunology Université Libre de Bruxelles (ULB) Brussels Belgium

4. ULB Center for Research in Immunology (U‐CRI) Université Libre de Bruxelles (ULB) Brussels Belgium

5. WELBIO Department WEL Research Institute Wavre Belgium

6. Cancer Research Institute Ghent (CRIG) Ghent Belgium

7. Department of Internal Medicine and Pediatrics Ghent University Ghent Belgium

8. GMP Unit CellGenTherapies Ghent University Hospital Ghent Belgium

9. VIB Single Cell Core, VIB Ghent Belgium

10. Department of Biomedical Molecular Biology Ghent University Ghent Belgium

11. Tissue Engineering and Biomaterials Group, Department of Human Structure and Repair Ghent University Ghent Belgium

Abstract

AbstractIn vitro cultures remain crucial for studying the fundamental mechanisms of human T‐cell development. Here, we introduce a novel in vitro cultivation system based on ThymoSpheres (TS): dense spheroids consisting of DLL4‐expressing stromal cells and human hematopoietic precursor cells, in the absence of thymic epithelial cells. These spheroids are subsequently cultured at the air–liquid interphase. TS generate large numbers of mature T cells, are easy to manipulate, scalable, and can be repeatably sampled to monitor T‐cell differentiation. The mature T cells generated from primary human hematopoietic precursor cells were extensively characterized using single‐cell RNA and combined T‐cell receptor (TCR) sequencing. These predominantly CD8α T cells exhibit transcriptional and TCR CDR3 characteristics similar to the recently described human polyclonal αβ unconventional T cell (UTC) lineage. This includes the expression of hallmark genes associated with agonist selection, such as IKZF2 (Helios), and the expression of various natural killer receptors. The TCR repertoire of these UTCs is polyclonal and enriched for CDR3‐associated autoreactive features and early rearrangements of the TCR‐α chain. In conclusion, TS cultures offer an intriguing platform to study the development of this human polyclonal UTC lineage and its inducing selection mechanisms.

Funder

Fonds Wetenschappelijk Onderzoek

Stichting Tegen Kanker

Publisher

Wiley

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