Second, although this study mainly explored the clinical translational value of blocking CD24 and CD47 signals to increase the anti‐tumor immune response of macrophages, this study also found that, in addition to macrophages, the cervical cancer microenvironment was rich in infiltration of dendritic cells, NK cells, and CD8+ T cells (Figure 2A). The gene discussed is CD8A; the disease is cervical carcinoma.