Kim Chaeyeon, Han Mina, Kim Gamin, Son Wonrak, Kim Jeongah, Gil Minchan, Rhee Yong-Hee, Sim Nam Suk, Kim Chang Gon, Kim Hye Ryun
Division of Medical Oncology, Department of Internal Medicine, Yonsei University College of Medicine, 50-1 Yonsei-ro, Seodaemun-gu, Seoul, 03722, Republic of Korea.
Department of Oncology, Yonsei University College of Medicine, Seoul, Republic of Korea.
Cancer Immunol Immunother. 2025 Mar 10;74(4):144. doi: 10.1007/s00262-025-03959-8.
Head and neck squamous cell carcinoma (HNSCC) presents a significant therapeutic challenge because of the limited effectiveness of current treatments including immunotherapy and chemotherapy. This study investigated the potential of a novel combination therapy using allogeneic natural killer (NK) cells and cetuximab, an anti-epidermal growth factor receptor monoclonal antibody, to enhance anti-tumor efficacy in HNSCC. Allogeneic NK cells were tested against HNSCC cells in vitro and NOG (NOD/Shi-scid/IL-2Rγ null) xenograft mouse models for cytotoxicity. In vitro assays demonstrated enhanced cytotoxicity against HNSCC cells when NK cells were combined with cetuximab, a phenomenon attributed to antibody-dependent cellular cytotoxicity. In vivo, the combination therapy exhibited a significant anti-tumor effect compared to either monotherapy, with high NK cell infiltration and cytotoxic activity in the tumor microenvironment. Tumor infiltration by NK cells was confirmed using flow cytometry and immunohistochemistry, highlighting the increased presence of NK cells (CD3 CD56). These findings suggest that combination allogeneic NK cells and cetuximab could be a potential therapeutic modality for HNSCC and provide a foundation for future clinical trials to improve patient outcomes.
头颈部鳞状细胞癌(HNSCC)由于包括免疫疗法和化疗在内的当前治疗方法效果有限,带来了重大的治疗挑战。本研究调查了使用同种异体自然杀伤(NK)细胞和西妥昔单抗(一种抗表皮生长因子受体单克隆抗体)的新型联合疗法在HNSCC中增强抗肿瘤疗效的潜力。在体外针对HNSCC细胞以及在NOG(NOD/Shi-scid/IL-2Rγ基因敲除)异种移植小鼠模型中测试了同种异体NK细胞的细胞毒性。体外试验表明,当NK细胞与西妥昔单抗联合使用时,对HNSCC细胞的细胞毒性增强,这一现象归因于抗体依赖性细胞毒性。在体内,与单一疗法相比,联合疗法表现出显著的抗肿瘤作用,在肿瘤微环境中有高NK细胞浸润和细胞毒性活性。使用流式细胞术和免疫组织化学证实了NK细胞的肿瘤浸润,突出了NK细胞(CD3 CD56)存在的增加。这些发现表明,同种异体NK细胞和西妥昔单抗联合使用可能是HNSCC的一种潜在治疗方式,并为未来改善患者预后的临床试验奠定了基础。