Modulation of TCR signalling components occurs prior to positive selection and lineage commitment in iNKT cells

Abstract

AbstractiNKT cells play a critical role in controlling the strength and character of adaptive and innate immune responses. Their unique functional characteristics are induced by a transcriptional program initiated by positive selection mediated by CD1d expressed by CD4+CD8+ (double positive, DP) thymocytes. Here, using a novel Vα14 TCR transgenic strain bearing greatly expanded numbers of CD24hiCD44loNKT cells, we examined transcriptional events in four immature thymic iNKT cell subsets. A transcriptional regulatory network approach identified transcriptional changes in proximal components of the TCR signalling cascade in DP NKT cells. Subsequently, positive and negative selection, and lineage commitment, occurred at the transition from DP NKT to CD4 NKT. Thus, this study introduces previously unrecognised steps in early NKT cell development, and separates the events associated with modulation of the T cell signalling cascade prior to changes associated with positive selection and lineage commitment.

Checkpoint CD24 function on tumor and immunotherapy

“…In addition, the high expression of CD24 on tumor cells can inhibit TCR and BCR-related kinases through the binding of Siglec-10 on the surface of B cells and T cells. As a result, the activation of TCR and BCR is blocked, ultimately promoting tumor immune escape ( 28 , 29 ).…”