GAMMA-DELTA T-CELL ANTIGEN RECEPTORS EXPRESSED ON TUMOR-INFILTRATING LYMPHOCYTES FROM PATIENTS WITH SOLID TUMORS

被引:48
作者
NANNO, M [1 ]
SEKI, H [1 ]
MATHIOUDAKIS, G [1 ]
SUZUKI, R [1 ]
ITOH, K [1 ]
IOANNIDES, CG [1 ]
SUZUKI, S [1 ]
CHEN, PF [1 ]
PLATSOUCAS, CD [1 ]
机构
[1] UNIV TEXAS, MD ANDERSON CANC CTR,DEPT IMMUNOL,BOX 178, 1515 HOLCOMBE BLVD, HOUSTON, TX 77030 USA
关键词
D O I
10.1002/eji.1830220310
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The expression of gamma/delta-T cell antigen receptors (TcR) in T cell lines or clones derived from tumor-infiltrating lymphocytes (TIL) from patients with solid tumors was investigated. Gamma/delta-TcR T cell lines were derived from TIL from patients with Wilms tumor, sarcoma or metastatic melanoma by stimulation with autologous tumor cells alone and recombinant interleukin 2 and they exhibited nonspecific cytotoxicity against autologous and allogeneic tumor cells, or cells of the K562 or the MEL21 tumor cell lines. Two T cell lines were derived from a patient with Wilms tumor. One of them expressed a non-disulfide-linked gamma/delta-TcR using the 60-kDa gamma-chain,whereas, the other expressed a disulfide-linked gamma/delta TcR. A T cell line was derived from a patient with sarcoma and expressed a disulfide-linked gamma/delta-TcR, whereas, a T cell line derived from a patient with melanoma expressed a non-disulfide-linked gamma-chain of 62 kDa. Several T cell clones were developed from patients with metastatic melanoma or Wilms tumor and expressed either disulfide- or non-disulfide-linked gamma/delta-TcR. Northern analysis of RNA from certain of these clones revealed a full-length gamma-chain transcript, whereas, the alpha or beta-chain transcripts were either absent or truncated. These T cell clones exhibited nonspecific cytotoxicity. Both disulfide- and non-disulfide-linked TIL T cell lines and clones expressed the delta-TCS1 determinant. Gamma/delta-TcR+ cells in freshly prepared TIL from these patients were present in low proportions (< 5%) and their delta-TCS1/delta-1 ratios were within the range observed in the peripheral blood of normal donors. These results demonstrate that both disulfide- and non-disulfide-linked gamma/delta-TcR are expressed on T cell lines and clones derived from TIL from solid tumors. Non-disulfide-linked gamma/delta-TcR using the 56-66-kDa gamma-chain are frequently found on TIL-derived T cell lines and clones. These 56-66-kDa gamma-chains are rarely expressed on T cell lines or clones derived from peripheral blood lymphocytes of normal donors.
引用
收藏
页码:679 / 687
页数:9
相关论文
共 63 条
[1]   LYSIS OF AUTOLOGOUS MELANOMA-CELLS BY TUMOR-INFILTRATING LYMPHOCYTES - ASSOCIATION WITH CLINICAL-RESPONSE [J].
AEBERSOLD, P ;
HYATT, C ;
JOHNSON, S ;
HINES, K ;
KORCAK, L ;
SANDERS, M ;
LOTZE, M ;
TOPALIAN, S ;
YANG, J ;
ROSENBERG, SA .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1991, 83 (13) :932-937
[2]   FUNCTIONAL GAMMA-CHAIN ASSOCIATED T-CELL RECEPTORS ON CEREBROSPINAL-FLUID DERIVED NATURAL-KILLER LIKE T-CELL CLONES [J].
ANG, SL ;
SEIDMAN, JG ;
PETERMAN, GM ;
DUBY, AD ;
BENJAMIN, D ;
LEE, SJ ;
HAFLER, DA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1987, 165 (05) :1453-1458
[3]  
BALCH CM, 1990, ARCH SURG-CHICAGO, V125, P200
[4]   IMMUNOCHEMICAL PROOF THAT A NOVEL REARRANGING GENE ENCODES THE T-CELL RECEPTOR-DELTA SUBUNIT [J].
BAND, H ;
HOCHSTENBACH, F ;
MCLEAN, J ;
HATA, S ;
KRANGEL, MS ;
BRENNER, MB .
SCIENCE, 1987, 238 (4827) :682-684
[5]   A FUNCTIONAL T3 MOLECULE ASSOCIATED WITH A NOVEL HETERODIMER ON THE SURFACE OF IMMATURE HUMAN THYMOCYTES [J].
BANK, I ;
DEPINHO, RA ;
BRENNER, MB ;
CASSIMERIS, J ;
ALT, FW ;
CHESS, L .
NATURE, 1986, 322 (6075) :179-181
[6]  
BELLDEGRUN A, 1989, J IMMUNOL, V142, P4520
[7]  
BELLDEGRUN A, 1988, CANCER RES, V48, P206
[8]   A T-CELL RECEPTOR GAMMA-CD3 COMPLEX FOUND ON CLONED FUNCTIONAL LYMPHOCYTES [J].
BORST, J ;
VANDEGRIEND, RJ ;
VANOOSTVEEN, JW ;
ANG, SL ;
MELIEF, CJ ;
SEIDMAN, JG ;
BOLHUIS, RLH .
NATURE, 1987, 325 (6106) :683-688
[9]   2 SUBSETS OF HUMAN LYMPHOCYTES-T EXPRESSING GAMMA-ANTIGEN DELTA-ANTIGEN RECEPTOR ARE IDENTIFIABLE BY MONOCLONAL-ANTIBODIES DIRECTED TO 2 DISTINCT MOLECULAR-FORMS OF THE RECEPTOR [J].
BOTTINO, C ;
TAMBUSSI, G ;
FERRINI, S ;
CICCONE, E ;
VARESE, P ;
MINGARI, MC ;
MORETTA, L ;
MORETTA, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 168 (02) :491-505
[10]  
BRENNER MB, 1987, J IMMUNOL, V138, P1502