Kitamura K, Takahashi T, Miyagaki T, Yamaoka N, Tsurumi H, Ohtsuji E, Kamiguchi M, Noguchi A, Yamaguchi T
First Department of Surgery, Kyoto Prefectural University of Medicine.
Jpn J Cancer Res. 1992 Jul;83(7):769-74. doi: 10.1111/j.1349-7006.1992.tb01978.x.
The murine monoclonal antibody (Mab) A7 conjugated to neocarzinostatin (A7-NCS) was injected intratumorally (IT) into tumor bearing nude mice. Its pharmacokinetics and tumoricidal effects were compared in the high, moderate and low antigen expressing xenograft for SW1116, WiDr and KB tumor-bearing nude mice, respectively. When injected IT into nude mice, [125I]A7-NCS was retained in the tumors according to the degree of antigen expression; it was also disseminated into the blood inverse proportion to the antigen expression. Addition of an excess amount of Mab A7 reduced [125I]-A7-NCS accumulation in SW1116 xenograft and elevated the [125I]A7-NCS concentration in the circulation. Complete tumor reduction was found in all 5 mice with SW1116 tumor, and 2 of 5 mice with WiDr tumor. However, only incomplete tumor suppression was observed in mice with the KB tumor. The significant tumor reduction in SW1116 bearing nude mice was attenuated when excess of Mab A7 was simultaneously administered with A7-NCS. These findings indicate that A7-NCS was localized in the target tumors and exerted its tumoricidal effects depending on the degree of antigen-antibody interaction when administered IT. Thus, A7-NCS can be used successfully in vivo for local therapy, auguring new and promising applications for local cancer therapy.
将与新制癌菌素(A7-NCS)偶联的鼠单克隆抗体(Mab)A7瘤内注射(IT)到荷瘤裸鼠体内。分别在高、中、低抗原表达的SW1116、WiDr和KB荷瘤裸鼠异种移植模型中比较其药代动力学和杀瘤效果。当瘤内注射到裸鼠体内时,[125I]A7-NCS根据抗原表达程度保留在肿瘤中;它也与抗原表达成反比地扩散到血液中。加入过量的单克隆抗体A7可减少[125I]-A7-NCS在SW1116异种移植瘤中的蓄积,并提高循环中[125I]A7-NCS的浓度。在所有5只携带SW1116肿瘤的小鼠和5只携带WiDr肿瘤的小鼠中有2只发现肿瘤完全消退。然而,在携带KB肿瘤的小鼠中仅观察到不完全的肿瘤抑制。当过量的单克隆抗体A7与A7-NCS同时给药时,携带SW1116的裸鼠中显著的肿瘤消退减弱。这些发现表明,A7-NCS在瘤内给药时定位于靶肿瘤,并根据抗原-抗体相互作用程度发挥其杀瘤作用。因此,A7-NCS可成功用于体内局部治疗,为局部癌症治疗带来新的、有前景的应用。