Generation of MC-38 adenocarcinoma tumor-specific tumor infiltrating lymphocytes by murine anti-CD3 antibody and recombinant interleukin-2.

Molecular biotherapy Pub Date : 1991-03-01
R Lafreniere, K Borkenhagen, L D Bryant
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Abstract

The growth, in vitro cytolytic activity and phenotype of murine MC-38 adenocarcinoma tumor infiltrating lymphocytes (TILs) stimulated with anti-CD3 monoclonal antibody (mAb) and recombinant interleukin-2 (RIL-2) as compared to RIL-2 alone was investigated. When assayed for growth, anti-CD3 mAb + RIL-2 MC-38 TILs demonstrated an enhanced proliferative activity compared to RIL-2 alone (fold expansion, 16,228 and 365,713 compared to 112 and 5594, culture times: 55 and 118 days, experiments 1 and 2, respectively). TILs cultured with anti-CD3 mAb alone demonstrated little expansion (fold expansion 6 and 3, experiments 1 and 2, respectively). Early during culture, the anti-CD3 mAb + RIL-2 MC-38 expanded TILs demonstrated broad cytolytic activity (LU: day 17, against MCA-102: greater than 125, YAC-1: greater than 125, MC-38, greater than 125). This lytic picture reversed with time with increasing specificity demonstrated against MC-38 (LU: day 53, MCA-102: less than 1, YAC-1: less than 1, MC-38: 8). TILs expanded with RIL-2 alone demonstrated more lysis of the YAC-1 target and little lysis of the other targets.(ABSTRACT TRUNCATED AT 250 WORDS)

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用小鼠抗cd3抗体和重组白细胞介素-2诱导MC-38腺癌肿瘤特异性肿瘤浸润淋巴细胞。
用抗cd3单克隆抗体(mAb)和重组白细胞介素-2 (RIL-2)刺激小鼠MC-38腺癌肿瘤浸润淋巴细胞(TILs)的生长、体外细胞溶解活性和表型,并与单独使用il -2进行比较。当检测生长时,anti-CD3 mAb + RIL-2 MC-38 TILs比单独使用RIL-2表现出更强的增殖活性(扩增倍数分别为16,228和365,713倍,分别为112和5594倍,培养时间分别为55和118天,实验1和2)。单独使用抗cd3单抗培养的til几乎没有扩增(分别为实验1和实验2的6倍扩增和3倍扩增)。在培养早期,抗cd3 mAb + RIL-2 MC-38扩增TILs表现出广泛的细胞溶解活性(LU: 17天,抗MCA-102:大于125,抗YAC-1:大于125,抗MC-38,大于125)。随着时间的推移,这一裂解图与MC-38相反,显示出对MC-38的特异性增加(LU: 53天,MCA-102:小于1,YAC-1:小于1,MC-38: 8)。RIL-2单独扩增的TILs显示出对YAC-1靶点的裂解更多,而对其他靶点的裂解很少。(摘要删节250字)
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