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Comparison of gene profile of WT, STAT3 KO and STAT3koPD-1ko donor T cells in the liver of allogenetic HCT mouse recepients

ABSTRACT: Comparison of gene profile of WT, STAT3 KO and STAT3koPD-1ko donor T cells in the liver of allogenetic HCT mouse recepients

PROVIDER: PRJNA885777 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR21765360.fastq.gz	Fastqsanger.gz
	SRR21765361.fastq.gz	Fastqsanger.gz
	SRR21765362.fastq.gz	Fastqsanger.gz
	SRR21765363.fastq.gz	Fastqsanger.gz
	SRR21765364.fastq.gz	Fastqsanger.gz

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Comparison of gene profile of WT, STAT3 KO donor T cells in the spleen of allogenetic HCT mouse recepients

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Project description:Abundant donor cytotoxic T cells that attack normal host organs remain a major problem for patients receiving allogeneic hematopoietic cell transplantation (Allo-HCT). Despite an increase in our knowledge of the pathobiology of acute graft versus host disease (aGvHD), the mechanisms regulating the proliferation and function of donor T cells remain unclear. Here, we show that activated donor T cells express galectin-3 (Gal-3) after allo-HCT. In both major and minor histocompatibility–mismatched models of murine aGvHD, expression of Gal-3 is associated with decreased T cell activation and suppression of the secretion of effector cytokines including IFN-γ and GM-CSF. Mechanistically, Gal-3 results in activation of NFAT signaling which can induce T cell exhaustion. Gal-3 overexpression in human T cells prevents severe disease by suppressing cytotoxic T cells in xenogeneic aGvHD models. Together these data identify the Gal-3-dependent regulatory pathway in donor T cells as a critical component of inflammation in aGvHD.

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