EGFR and neoplasm: While our study cannot formally rule out a chemokine mediated influx and subsequent expansion of Treg populations in EGFR overexpressing tumours, the correlation between overexpression of mutated EGFR and CD8 T-cell exclusion (Figure 1) strongly resembled the immune exclusion phenotype driven by the soluble immunomodulatory mediator Transforming Growth Factor beta (TGFβ) [54,55].