López-Albaitero Andrés, Ferris Robert L
Department of Otolaryngology, University of Pittsburgh Cancer Institute, Pittsburgh, PA, USA.
Arch Otolaryngol Head Neck Surg. 2007 Dec;133(12):1277-81. doi: 10.1001/archotol.133.12.1277.
To determine if the epidermal growth factor receptor (EGFR)-specific monoclonal antibodies (mAbs) cetuximab or panitumumab mediate in vitro immune activation against squamous cell carcinoma of the head and neck (SCCHN) cell lines.
In vitro study.
Basic science research laboratory.
Squamous cell carcinoma of the head and neck cell lines were treated with the Food and Drug Administration-approved EGFR-specific mAbs cetuximab or panitumumab in the presence or absence of peripheral blood mononuclear cells from healthy donors.
Cetuximab and panitumumab were compared in terms of their cytotoxic effects, ability to induce apoptosis, bind to EGFR, and block phosphorylation of this receptor in SCCHN cell lines.
We demonstrate that both cetuximab and panitumumab have similar levels of EGFR binding, induction of apoptosis, cell lysis, and inhibition of phospho-EGFR in SCCHN cell lines, suggesting similar direct effects. However, neither of these mAbs demonstrated in vitro antitumor activity when used alone. In contrast, in the presence of peripheral blood lymphocytes, either of them can mediate antibody-dependent cell cytotoxicity in vitro when used in doses similar to those found in patients receiving them clinically.
We propose that antibody-dependent cell cytotoxicity may constitute an important antitumor mechanism that could contribute to overall clinical effectiveness of EGFR-specific antibodies.
确定表皮生长因子受体(EGFR)特异性单克隆抗体(mAb)西妥昔单抗或帕尼单抗是否介导针对头颈部鳞状细胞癌(SCCHN)细胞系的体外免疫激活。
体外研究。
基础科学研究实验室。
在有或没有健康供体外周血单个核细胞存在的情况下,用美国食品药品监督管理局批准的EGFR特异性mAb西妥昔单抗或帕尼单抗处理头颈部鳞状细胞癌细胞系。
比较西妥昔单抗和帕尼单抗在SCCHN细胞系中的细胞毒性作用、诱导凋亡的能力、与EGFR的结合以及对该受体磷酸化的阻断作用。
我们证明,西妥昔单抗和帕尼单抗在SCCHN细胞系中具有相似水平的EGFR结合、凋亡诱导、细胞裂解和磷酸化EGFR抑制作用,提示有相似的直接作用。然而,单独使用时这两种mAb均未表现出体外抗肿瘤活性。相反,在有外周血淋巴细胞存在的情况下,当以与临床接受治疗的患者体内相似的剂量使用时,它们中的任何一种都能在体外介导抗体依赖性细胞毒性。
我们提出,抗体依赖性细胞毒性可能构成一种重要的抗肿瘤机制,这可能有助于EGFR特异性抗体的整体临床疗效。