Although several studies have also shown increasing peripheral CD4+ T helper cells and Tregs and increasing PD-1 expression levels on Tregs after cTACE, it remains unclear whether these alterations represent an impaired response to residual tumor cells or an immunological state of surveillance and regulation.[49], [50], [51] Early evidence suggests a link between the upregulation of Tregs and the expression of inhibitory molecules such as PD-1 and CTLA-4 after cTACE, which may exert tumor-mediated immunosuppression.52 Here, CD4 is linked to neoplasm.