Sensitivity of multidrug-resistant tumor cell lines to immunologic effector cells

被引:177
作者
SchmidtWolf, IGH
LEfterova, P
Johnston, V
Scheffold, C
Csipai, M
Mehta, BA
Tsuruo, T
Huhn, D
Negrin, RS
机构
[1] STANFORD UNIV,MED CTR,BONE MARROW TRANSPLANTAT PROGRAM,STANFORD,CA 94305
[2] CTR CANC CHEMOTHERAPY,DIV EXPT CHEMOTHERAPY,TOSHIMA KU,TOKYO,JAPAN
关键词
D O I
10.1006/cimm.1996.0094
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The ability of malignant cells to survive exposure to cytotoxic agents is a major obstacle to cure in patients with cancer. Multidrug resistance and the expression of P-glycoprotein are emerging as a cause of chemotherapy failure. Immunologic effector cells such as lymphokine-activated killer (LAK) cells or cytokine-induced killer (CIK) cells are capable of killing a broad range of tumor cell lines or freshly isolated tumor cells. As demonstrated here, LAK and CIK cells possess a high level of cytotoxic activity against tumor cell lines both resistant and sensitive to chemotherapeutic agents such as doxorubicin or vinblastine. CIK cells possessed a higher level of cytotoxic activity than LAK cells as determined by Cr-51 release and a tumor colony assay. Monoclonal antibodies against P-glycoprotein did not block the lysis of tumor cells resistant to chemotherapy by CIK cells. In contrast, antibodies to LFA-1 and ICAM-1 blocked CIK cell-mediated tumor cell lysis. These data demonstrate that immunological approaches to cancer therapy may be useful in overcoming disease caused by drug resistance. (C) 1996 Academic Press, Inc.
引用
收藏
页码:85 / 90
页数:6
相关论文
共 31 条
[1]   INTERCELLULAR-ADHESION MOLECULE-1 (ICAM-1) HAS A CENTRAL ROLE IN CELL CELL CONTACT-MEDIATED IMMUNE-MECHANISMS [J].
BOYD, AW ;
WAWRYK, SO ;
BURNS, GF ;
FECONDO, JV .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (09) :3095-3099
[2]  
DEUCHARS KL, 1989, SEMIN ONCOL, V16, P156
[3]   LYMPHOKINE-ACTIVATED KILLER CELL PHENOMENON .2. PRECURSOR PHENOTYPE IS SEROLOGICALLY DISTINCT FROM PERIPHERAL LYMPHOCYTES-T, MEMORY CYTO-TOXIC THYMUS-DERIVED LYMPHOCYTES, AND NATURAL-KILLER CELLS [J].
GRIMM, EA ;
RAMSEY, KM ;
MAZUMDER, A ;
WILSON, DJ ;
DJEU, JY ;
ROSENBERG, SA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1983, 157 (03) :884-897
[4]   ISOLATION AND EXPRESSION OF A COMPLEMENTARY-DNA THAT CONFERS MULTIDRUG RESISTANCE [J].
GROS, P ;
BEN-NERIAH, Y ;
CROOP, JM ;
HOUSMAN, DE .
NATURE, 1986, 323 (6090) :728-731
[5]  
HERBERMAN RB, 1986, ANNU REV IMMUNOL, V4, P651, DOI 10.1146/annurev.iy.04.040186.003251
[6]   EXPRESSION OF MDR1 AND MDR3 MULTIDRUG-RESISTANCE GENES IN HUMAN ACUTE AND CHRONIC LEUKEMIAS AND ASSOCIATION WITH STIMULATION OF DRUG ACCUMULATION BY CYCLOSPORINE [J].
HERWEIJER, H ;
SONNEVELD, P ;
BAAS, F ;
NOOTER, K .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1990, 82 (13) :1133-1140
[7]  
IMAMURA N, 1988, BLOOD, V72, P1837
[8]  
KANEKO T, 1993, BLOOD, V81, P1333
[9]  
KRENSKY AM, 1983, J IMMUNOL, V131, P611
[10]  
KUWAZURU Y, 1990, CANCER, V66, P868, DOI 10.1002/1097-0142(19900901)66:5<868::AID-CNCR2820660510>3.0.CO