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They concluded that the risk-edited cells increased a T cell activation profile following non-specific TCR engagement, which mimicked the observations exhibited by PTPN22 knockout cells, suggesting the risk variant acts as a loss-of-function mutant that reduces the ability of LYP to inhibit TCR activation ( PTPN22 variant has also been shown to increase total Treg and nave Treg subgroups in T1D patients compared to healthy controls, which is counterintuitive in the context of T1D ( in vivo models to compare the Treg population frequency when comparing the R620W variant to an appropriate control

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