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Donor T-cell alloreactivity against host thymic epithelium limits T-cell development after bone marrow transplantation.


ABSTRACT: Acute graft-versus-host disease (aGVHD) impairs thymus-dependent T-cell regeneration in recipients of allogeneic bone marrow transplants through yet to be defined mechanisms. Here, we demonstrate in mice that MHC-mismatched donor T cells home into the thymus of unconditioned recipients. There, activated donor T cells secrete IFN-gamma, which in turn stimulates the programmed cell death of thymic epithelial cells (TECs). Because TECs themselves are competent and sufficient to prime naive allospecific T cells and to elicit their effector function, the elimination of host-type professional antigen-presenting cells (APCs) does not prevent donor T-cell activation and TEC apoptosis, thus precluding normal thymopoiesis in transplant recipients. Hence, strategies that protect TECs may be necessary to improve immune reconstitution following allogeneic bone marrow transplantation.

SUBMITTER: Hauri-Hohl MM 

PROVIDER: S-EPMC1874583 | biostudies-literature | 2007 May

REPOSITORIES: biostudies-literature

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Donor T-cell alloreactivity against host thymic epithelium limits T-cell development after bone marrow transplantation.

Hauri-Hohl Mathias M MM   Keller Marcel P MP   Gill Jason J   Hafen Katrin K   Pachlatko Esther E   Boulay Thomas T   Peter Annick A   Holländer Georg A GA   Krenger Werner W  

Blood 20070109 9


Acute graft-versus-host disease (aGVHD) impairs thymus-dependent T-cell regeneration in recipients of allogeneic bone marrow transplants through yet to be defined mechanisms. Here, we demonstrate in mice that MHC-mismatched donor T cells home into the thymus of unconditioned recipients. There, activated donor T cells secrete IFN-gamma, which in turn stimulates the programmed cell death of thymic epithelial cells (TECs). Because TECs themselves are competent and sufficient to prime naive allospec  ...[more]

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