Intracellular Major Histocompatibility Complex Class II and C-X-C Motif Chemokine Ligand 10-Expressing Neutrophils Indicate the State of Anti-Tumor Activity Induced by <i>Bacillus Calmette–Guérin</i>
Yuji Takeda,
Tomoyuki Kato,
Saima Sabrina,
Sei Naito,
Hiromi Ito,
Naoto Emi,
Yuya Kuboki,
Yuki Takai,
Hiroki Fukuhara,
Masaki Ushijima,
Takafumi Narisawa,
Mayu Yagi,
Hidenori Kanno,
Toshihiko Sakurai,
Hayato Nishida,
Akemi Araki,
Yoshitaka Shimotai,
Mikako Nagashima,
Yusuke Nouchi,
Shinichi Saitoh,
Hidetoshi Nara,
Norihiko Tsuchiya,
Hironobu Asao
Affiliations
Yuji Takeda
Department of Immunology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan
Tomoyuki Kato
Department of Urology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan
Saima Sabrina
Department of Immunology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan
Sei Naito
Department of Urology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan
Hiromi Ito
Department of Urology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan
Naoto Emi
Department of Immunology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan
Yuya Kuboki
Department of Urology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan
Yuki Takai
Department of Urology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan
Hiroki Fukuhara
Department of Urology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan
Masaki Ushijima
Department of Urology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan
Takafumi Narisawa
Department of Urology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan
Mayu Yagi
Department of Urology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan
Hidenori Kanno
Department of Urology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan
Toshihiko Sakurai
Department of Urology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan
Hayato Nishida
Department of Urology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan
Akemi Araki
Department of Immunology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan
Yoshitaka Shimotai
Department of Infectious Diseases, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan
Mikako Nagashima
Department of Immunology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan
Yusuke Nouchi
Department of Immunology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan
Shinichi Saitoh
Department of Immunology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan
Hidetoshi Nara
Department of Biological Sciences, Faculty of Science and Engineering, Ishinomaki Senshu University, Miyagi 986-8580, Japan
Norihiko Tsuchiya
Department of Urology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan
Hironobu Asao
Department of Immunology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan
(1) Background: Inflammatory responses induce the formation of both anti-tumor and pro-tumor neutrophils known as myeloid-derived suppressor cells (MDSCs). Intermittent intravesical infusion of Bacillus Calmette–Guérin (BCG) is an established cancer immunotherapy for non-muscle-invasive bladder cancer (NMIBC). However, the types of neutrophils induced via the inflammatory response to both tumor-bearing and BCG remain unclear. (2) Methods: We therefore analyzed neutrophil dynamics in the peripheral blood and urine of patients with NMIBC who received BCG therapy. Further, we analyzed the effects of BCG in a mouse intraperitoneal tumor model. (3) Results: BCG therapy induced the formation of CXCL10 and MHC class II-positive neutrophils in the urine of patients with NMIBC but did not induce MDSC formation. CXCL10- and MHC class II-expressing neutrophils were detected in peritoneal exudate cells formed after BCG administration. Partial neutrophil depletion using an anti-Ly6G antibody suppressed the upregulation of CXCL10 and MHC class II in neutrophils and reversed the anti-tumor activity of BCG in mouse models. (4) Conclusions: These results indicated that intracellular MHC class II- and CXCL10-expressing neutrophils indicate the state of anti-tumor activity induced via BCG. The status of neutrophils in mixed inflammation of immunosuppressive and anti-tumor responses may therefore be useful for evaluating immunological systemic conditions.