Targeted Deletion of CXCR2 in Myeloid Cells Alters the Tumor Immune Environment to Improve Antitumor Immunity

Recruitment of myeloid-derived suppressor cells (MDSC) into the tumor microenvironment (TME) contributes to cancer immune evasion. MDSCs express the chemokine receptor CXCR2, and inhibiting CXCR2 suppresses the recruitment of MDSCs into the tumor and the premetastatic niche. Here, we compared the growth and metastasis of melanoma and breast cancer xenografts in mice exhibiting or not exhibiting targeted deletion of Cxcr2 in myeloid cells (CXCR2(mye Delta/Delta) vs. CXCR2(myeWT)). Detailed analysis of leukocyte populations in peripheral blood and in tumors from CXCR2(mye Delta/Delta) mice revealed that loss of CXCR2 signaling in myeloid cells resulted in reduced intratumoral MDSCs and increased intratumoral CXCL11. The increase in intratumoral CXCL11 was derived in part from tumor-infiltrating B1b cells. The reduction in intratumoral MDSCs coupled with an increase in intratumoral B1b cells expressing CXCL11 resulted in enhanced infiltration and activation of effector CD8(+) T cells in the TME of CXCR2(mye Delta/Delta) mice, accompanied by inhibition of tumor growth in CXCR2(mye Delta/Delta) mice compared with CXCR2(myeWT) littermates. Treatment of tumor-bearing mice with a CXCR2 antagonist (SX-682) also inhibited tumor growth, reduced intratumoral MDSCs, and increased intratumoral Bib cells expressing CXCL11, leading to an increase in activated CD8(+) T cells in the tumor. Depletion of B220(+) cells or depletion of CD8 + T cells reversed the tumor-inhibitory properties in CXCR2(mye Delta/Delta) mice. These data revealed a mechanism by which loss of CXCR2 signaling in myeloid cells modulates antitumor immunity through decreasing MDSCs and enriching CXCL11-producing B lb cells in the TME, which in turn increases CD8(+) T-cell recruitment and activation in tumors.

Automated summary

The inhibition of the CXCR2 signaling pathway can reduce the number of MDSC in the tumor microenvironment, increase CXCL11-expressing B1b cells, and subsequently promote the infiltration and activation of effector CD8(+) T cells in tumors.