CBP/p300 drives the differentiation of regulatory T cells through transcriptional and non-transcriptional mechanisms

J Castillo, E Wu, C Lowe, S Srinivasan, R McCord… - Cancer Research, 2019 - AACR
J Castillo, E Wu, C Lowe, S Srinivasan, R McCord, MC Wagle, S Jayakar, MG Edick…
Cancer Research, 2019AACR
Regulatory T cells (Treg) are immunosuppressive and negatively impact response to cancer
immunotherapies. CREB-binding protein (CBP) and p300 are closely related
acetyltransferases and transcriptional coactivators. Here, we evaluate the mechanisms by
which CBP/p300 regulate Treg differentiation and the consequences of CBP/p300 loss-of-
function mutations in follicular lymphoma. Transcriptional and epigenetic profiling identified
a cascade of transcription factors essential for Treg differentiation. Mass spectrometry …
Abstract
Regulatory T cells (Treg) are immunosuppressive and negatively impact response to cancer immunotherapies. CREB-binding protein (CBP) and p300 are closely related acetyltransferases and transcriptional coactivators. Here, we evaluate the mechanisms by which CBP/p300 regulate Treg differentiation and the consequences of CBP/p300 loss-of-function mutations in follicular lymphoma. Transcriptional and epigenetic profiling identified a cascade of transcription factors essential for Treg differentiation. Mass spectrometry analysis showed that CBP/p300 acetylates prostacyclin synthase, which regulates Treg differentiation by altering proinflammatory cytokine secretion by T and B cells. Reduced Treg presence in tissues harboring CBP/p300 loss-of-function mutations was observed in follicular lymphoma. Our findings provide novel insights into the regulation of Treg differentiation by CBP/p300, with potential clinical implications on alteration of the immune landscape.
Significance
This study provides insights into the dynamic role of CBP/p300 in the differentiation of Tregs, with potential clinical implications in the alteration of the immune landscape in follicular lymphoma.
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