Dohi Y, Sunada S, Aoki M, Moriguchi A, Okabayashi M, Miyata M, Matsuda H
Department of Bacteriology, Osaka University Medical School, Japan.
Cancer Immunol Immunother. 1993 Jun;36(6):357-63. doi: 10.1007/BF01742251.
The possibility of in vivo removal of metastatic tumour cells from lymph nodes by local intradermal administration of an anti-CD3 monoclonal antibody (mAb) was examined. Murine tumour cells in the lymph nodes were completely eradicated by intradermal injections of the mAb. This treatment was effective for removal of Lewis lung cancer cells from lymph nodes, but not for removal of subcutaneous tumours of this cell line. This treatment induced in vivo cytotoxicity in the regional lymph nodes against the syngeneic tumour cells. The following in vitro studies suggested that the cytotoxicity was probably mediated mainly by CD4+ T cells, with slight participation of CD8+ T cells. Normal lymph node and spleen cells showed cytotoxicity after in vitro incubation with the mAb for 2 days. Cell sorting with a fluorescein-activated cell sorter showed that CD4+ T cells developed during the incubation to lyse syngeneic tumor cells directly by themselves, macrophages not being involved in this tumour cell lysis. The lytic activity was detected in the cellular fractions, but not in the culture supernatants of these T cells. Furthermore, it was completely blocked by specific antiserum for tumour necrosis factor-alpha (TNF alpha). An immunoprecipitation study revealed that these T cells expressed TNF alpha molecules of 26 kDa, but not of 17 kDa, suggesting that tumour cell lysis was caused by membrane-integrated integrated TNF alpha molecules. These results strongly suggest that local administration of anti-CD3 antibody is a very effective and appropriate procedure for eradication of metastatic tumour cells from regional lymph nodes.
研究了通过局部皮内注射抗CD3单克隆抗体(mAb)在体内清除淋巴结中转移性肿瘤细胞的可能性。皮内注射该mAb可完全清除淋巴结中的鼠源肿瘤细胞。这种治疗方法对清除淋巴结中的Lewis肺癌细胞有效,但对清除该细胞系的皮下肿瘤无效。这种治疗在体内诱导区域淋巴结对同基因肿瘤细胞产生细胞毒性。以下体外研究表明,细胞毒性可能主要由CD4 + T细胞介导,CD8 + T细胞有轻微参与。正常淋巴结和脾细胞在与mAb体外孵育2天后表现出细胞毒性。用荧光激活细胞分选仪进行细胞分选显示,CD4 + T细胞在孵育过程中发育,能够直接自行裂解同基因肿瘤细胞,巨噬细胞不参与这种肿瘤细胞裂解。在这些T细胞的细胞组分中检测到裂解活性,但在培养上清液中未检测到。此外,它被肿瘤坏死因子-α(TNFα)的特异性抗血清完全阻断。免疫沉淀研究表明,这些T细胞表达26 kDa的TNFα分子,但不表达17 kDa的TNFα分子,这表明肿瘤细胞裂解是由膜整合的TNFα分子引起的。这些结果强烈表明,局部给予抗CD3抗体是从区域淋巴结中根除转移性肿瘤细胞的一种非常有效且合适的方法。