| Literature DB >> 32556283 |
Marita Bosticardo1, Francesca Pala1, Enrica Calzoni1,2, Ottavia M Delmonte1, Kerry Dobbs1, Cameron L Gardner1,3, Nicolo' Sacchetti1,4,5, Tomoki Kawai1, Elizabeth K Garabedian6, Debbie Draper1, Jenna R E Bergerson1, Suk See DeRavin1, Alexandra F Freeman1, Tayfun Güngör7, Nicholas Hartog8, Steven M Holland1, Donald B Kohn9, Harry L Malech1, Mary Louise Markert10,11, Katja G Weinacht12, Anna Villa4,13, Christopher S Seet14, Amelie Montel-Hagen15, Gay M Crooks15, Luigi D Notarangelo1.
Abstract
The study of early T-cell development in humans is challenging because of limited availability of thymic samples and the limitations of in vitro T-cell differentiation assays. We used an artificial thymic organoid (ATO) platform generated by aggregating a DLL4-expressing stromal cell line (MS5-hDLL4) with CD34+ cells isolated from bone marrow or mobilized peripheral blood to study T-cell development from CD34+ cells of patients carrying hematopoietic intrinsic or thymic defects that cause T-cell lymphopenia. We found that AK2 deficiency is associated with decreased cell viability and an early block in T-cell development. We observed a similar defect in a patient carrying a null IL2RG mutation. In contrast, CD34+ cells from a patient carrying a missense IL2RG mutation reached full T-cell maturation, although cell numbers were significantly lower than in controls. CD34+ cells from patients carrying RAG mutations were able to differentiate to CD4+CD8+ cells, but not to CD3+TCRαβ+ cells. Finally, normal T-cell differentiation was observed in a patient with complete DiGeorge syndrome, consistent with the extra-hematopoietic nature of the defect. The ATO system may help determine whether T-cell deficiency reflects hematopoietic or thymic intrinsic abnormalities and define the exact stage at which T-cell differentiation is blocked.Entities:
Mesh:
Substances:
Year: 2020 PMID: 32556283 PMCID: PMC7322962 DOI: 10.1182/bloodadvances.2020001730
Source DB: PubMed Journal: Blood Adv ISSN: 2473-9529