Generation and characterization of a monoclonal antibody that recognizes an activation antigen expressed by a majority of adherent lymphokine-activated killer cells

被引:2
|
作者
Chan, CS [1 ]
Kane, KP [1 ]
机构
[1] Univ Alberta, Dept Med Microbiol & Immunol, Fac Med, Edmonton, AB T6G 2S2, Canada
来源
HYBRIDOMA | 2000年 / 19卷 / 01期
关键词
D O I
10.1089/027245700315798
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In an attempt to generate murine natural killer (NK) cell-specific monoclonal antibodies (MAbs) by immunizing Balb/c mice with C57BL/6 (B6) A-LAKs, we have isolated a hybridoma, CS/NicT.2, which secretes an IgM that recognizes a majority of B6 and B6 Rag-1(-/-) A-LAKs. The CS/NicT.2 antigen is highly expressed by A-LAKs, but only at extremely low levels on resting splenocytes, suggesting that its expression is tightly associated with IL-2 activation, Among the cell lines examined, only CTLL-2 expresses the CS/NicT.2 antigen at relatively high levels. A low level of CS/NicT.2 staining is also detected on resting allo-specific cytotoxic T lymphocytes (CTL) clones, AB.1 and C11. In addition, a similar low level of CS/NicT.2 staining is detected on the T-helper cell line HT-2, The CS/NicT.2 antigen is upregulated by ionomycin but not by phorbol 12-myristate 13-acetate (PMA). For the CTL clones examined, CS/NicT.2 staining is also dramatically increased by anti-TCRbeta or anti-CD3(epsilon) stimulation, Protease treatments of CTLL-2 show that this antigen is proteinase K sensitive, but relatively resistant to trypsin digestion. Furthermore, the CS/NicT.2 antigen exhibits a relatively fast turnover rate as assessed by proteinase K and cycloheximide treatments of CTLL-2, suggesting that the CS/NicT.2 antigen may have a short half-life on the cell surface.
引用
收藏
页码:49 / 61
页数:13
相关论文
共 50 条
  • [41] MURINE LYMPHOKINE-ACTIVATED KILLER (LAK) CELLS - PHENOTYPIC CHARACTERIZATION OF THE PRECURSOR AND EFFECTOR-CELLS
    YANG, JC
    MULE, JJ
    ROSENBERG, SA
    JOURNAL OF IMMUNOLOGY, 1986, 137 (02): : 715 - 722
  • [42] TISSUE DISTRIBUTION OF ADOPTIVELY TRANSFERRED ADHERENT LYMPHOKINE-ACTIVATED KILLER-CELLS ASSESSED BY DIFFERENT CELL LABELS
    BASSE, P
    HERBERMAN, RB
    HOKLAND, M
    GOLDFARB, RH
    CANCER IMMUNOLOGY IMMUNOTHERAPY, 1992, 34 (04) : 221 - 227
  • [43] CHARACTERIZATION OF LYMPHOKINE-ACTIVATED KILLER (LAK) CELLS FROM HUMAN INTESTINAL-MUCOSA
    HOGAN, PG
    HAPEL, AJ
    DOE, WF
    AUSTRALIAN AND NEW ZEALAND JOURNAL OF MEDICINE, 1986, 16 (01): : 168 - 168
  • [44] ADHERENT LYMPHOKINE-ACTIVATED KILLER-CELLS SUPPRESS AUTOLOGOUS HUMAN NORMAL BONE-MARROW PROGENITORS
    MILLER, JS
    VERFAILLIE, C
    MCGLAVE, P
    BLOOD, 1991, 77 (11) : 2389 - 2395
  • [45] ANTI-IDIOTYPE ANTIBODY REACTIVE WITH A TARGET MOLECULE FOR MOUSE LYMPHOKINE-ACTIVATED KILLER CELLS
    SATO, N
    MASUKO, T
    NISHIMURA, T
    KATO, K
    HASHIMOTO, Y
    CELLULAR IMMUNOLOGY, 1989, 121 (02) : 217 - 224
  • [46] GENERATION OF NATURAL-KILLER CELLS AND LYMPHOKINE-ACTIVATED KILLER CELLS IN HUMAN AB SERUM OR FETAL BOVINE SERUM
    IMIR, T
    GIBBS, DL
    SIBBITT, WL
    BANKHURST, AD
    CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1985, 36 (03): : 289 - 296
  • [47] A NEW APPROACH TO GENERATING ANTITUMOR EFFECTORS FOR ADOPTIVE IMMUNOTHERAPY USING HUMAN ADHERENT LYMPHOKINE-ACTIVATED KILLER CELLS
    MELDER, RJ
    WHITESIDE, TL
    VUJANOVIC, NL
    HISERODT, JC
    HERBERMAN, RB
    CANCER RESEARCH, 1988, 48 (12) : 3461 - 3469
  • [48] STUDIES OF VARIOUS CULTURE CONDITIONS FOR THE GENERATION OF LYMPHOKINE-ACTIVATED KILLER CELLS IN CLINICAL-TRIALS
    COZE, C
    COMBARET, V
    PHILIP, I
    GASPARD, M
    PHILIP, T
    FAVROT, MC
    LYMPHOKINE RESEARCH, 1988, 7 (03): : 296 - 296
  • [49] INTESTINAL LYMPHOKINE-ACTIVATED KILLER (LAK) CELLS - CYTOTOXICITY FOR COLON CANCER-CELLS AND MODULATION OF THEIR GENERATION
    HOGAN, PG
    HAPEL, AJ
    GIBSON, PR
    DOE, WF
    AUSTRALIAN AND NEW ZEALAND JOURNAL OF MEDICINE, 1986, 16 (04): : 612 - 612
  • [50] INTESTINAL LYMPHOKINE-ACTIVATED KILLER (LAK) CELLS - CYTOTOXICITY FOR COLON CANCER-CELLS AND MODULATION OF THEIR GENERATION
    HOGAN, PG
    HAPEL, AJ
    DOE, WF
    GASTROENTEROLOGY, 1986, 90 (05) : 1462 - 1462