Analytical study of the clinical response to two distinct adoptive immunotherapies for advanced hepatocellular carcinoma: Comparison between LAK cell and CTL therapy

被引:33
作者
Haruta, I
Yamauchi, K
Aruga, A
Komatsu, T
Takasaki, K
Hayashi, N
Hanyu, F
机构
[1] TOKYO WOMENS MED COLL,INST GASTROENTEROL,DIV MED,SHINJUKU KU,TOKYO 162,JAPAN
[2] TOKYO WOMENS MED COLL,INST GASTROENTEROL,DIV SURG,SHINJUKU KU,TOKYO 162,JAPAN
[3] YOKOHAMA NATL HOSP,DEPT GASTROENTEROL,YOKOHAMA,KANAGAWA,JAPAN
来源
JOURNAL OF IMMUNOTHERAPY | 1996年 / 19卷 / 03期
关键词
adoptive immunotherapy; LAK cells; cytotoxic T cells; hepatocellular carcinoma;
D O I
10.1097/00002371-199605000-00006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To evaluate the effect of two distinct adoptive immunotherapies, tumor-specific cytotoxic T-cell (CTL) therapy and lymphokine-activated killer (LAK) cell therapy, the clinical responses of patients with stage IV primary hepatocellular carcinoma (HCC) treated with these therapies were studied. Of 18 patients treated with CTL, 3 had complete regression (CR), 2 had partial regression, and 3 had minor regression (MR). Their median survival was 21 months after the end of therapy, and 1 CR patient survived for > 6 years. On the other hand, in the LAK-cell-treated group of eight patients, four had MR and their median survival was only 2 months, No survival was observed 27 months after the end of LAK cell therapy. These results indicate that tumor-specific CTL therapy is more effective than LAK cell therapy and that it might be a promising therapeutic tool for advanced HCC patients.
引用
收藏
页码:218 / 223
页数:6
相关论文
共 22 条
[1]  
[Anonymous], PRIMARY LIVER CANC J
[2]   INDUCTION OF AUTOLOGOUS TUMOR-SPECIFIC CYTOTOXIC T-CELLS IN PATIENTS WITH LIVER-CANCER - CHARACTERIZATIONS AND CLINICAL UTILIZATION [J].
ARUGA, A ;
YAMAUCHI, K ;
TAKASAKI, K ;
FURUKAWA, T ;
HANYU, F .
INTERNATIONAL JOURNAL OF CANCER, 1991, 49 (01) :19-24
[3]  
BEAHRS OH, 1988, MANUAL STAGING CANC, P88
[4]   INCREASED VASCULAR-PERMEABILITY IN ORGANS MEDIATED BY THE SYSTEMIC ADMINISTRATION OF LYMPHOKINE-ACTIVATED KILLER CELLS AND RECOMBINANT INTERLEUKIN-2 IN MICE [J].
ETTINGHAUSEN, SE ;
PURI, RK ;
ROSENBERG, SA .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1988, 80 (03) :177-188
[5]  
Ichino Y, 1985, Auris Nasus Larynx, V12 Suppl 2, pS226
[6]   IMMUNOTHERAPY OF HEPATOCELLULAR-CARCINOMA WITH AUTOLOGOUS LYMPHOKINE-ACTIVATED KILLER CELLS AND OR RECOMBINANT INTERLEUKIN-2 [J].
ISHIKAWA, T ;
IMAWARI, M ;
MORIYAMA, T ;
OHNISHI, S ;
MATSUHASHI, N ;
SUZUKI, G ;
TAKAKU, F .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 1988, 114 (03) :283-290
[7]  
ISSERBACHER KJ, 1994, PRINCIPLES INTERNAL, P1495
[8]   TRANSCATHETER ARTERIAL INJECTION OF AUTOLOGOUS LYMPHOKINE-ACTIVATED KILLER (LAK) CELLS INTO PATIENTS WITH LIVER CANCERS [J].
KOMATSU, T ;
YAMAUCHI, K ;
FURUKAWA, T ;
OBATA, H .
JOURNAL OF CLINICAL IMMUNOLOGY, 1990, 10 (03) :167-174
[9]   AUGMENTATION OF HUMAN CYTO-TOXIC LYMPHOCYTES-T AGAINST AUTOLOGOUS TUMOR BY A FACTOR RELEASED FROM HUMAN MONOCYTIC LEUKEMIA-CELL LINE [J].
MAEDA, N ;
HAMASATO, S ;
MIYAZAWA, H ;
TAKATA, M ;
YAMAMOTO, H ;
FUJIMOTO, S .
JAPANESE JOURNAL OF CANCER RESEARCH, 1989, 80 (06) :537-545
[10]  
MATORY YL, 1985, J BIOL RESP MODIF, V4, P377