Interestingly, according to breast cancer subtype, the sum of abundant TCRB CDR3 clonotypes was significantly increased in TNBC tumors compared to ER-positive tumors (p = 0.004, Figure 4C), suggesting that TNBC may have the unique tumor microenvironment where a subset of T cells could be efficiently expanded after dual blockade of PD-L1 and CTLA-4. The gene discussed is CTLA4; the disease is neoplasm.