IMMUNOHISTOCHEMICAL DETECTION OF DOUBLE-STRANDED-RNA-DEPENDENT PROTEIN-KINASE (P68) WITH A NOVEL MONOCLONAL-ANTIBODY TJ4C4 - A CASE-REPORT OF AN AIDS-ASSOCIATED KAPOSIS-SARCOMA TREATED WITH ALPHA-INTERFERON

被引:3
作者
HAINES, GK
GHADGE, GD
COMBS, SG
LESLIE, W
THIMMAPPAYA, B
RADOSEVICH, JA
机构
[1] NORTHWESTERN UNIV,VA LAKESIDE MED CTR,DEPT MED,ALLERGY IMMUNOL SECT,TARRY 3-707,CHICAGO,IL 60611
[2] NORTHWESTERN UNIV,VA LAKESIDE MED CTR,DEPT PATHOL,CHICAGO,IL 60611
[3] NORTHWESTERN UNIV,VA LAKESIDE MED CTR,DEPT MICROBIOL & IMMUNOL,CHICAGO,IL 60611
[4] RUSH MED COLL,DEPT MED,MED ONCOL SECT,CHICAGO,IL 60612
关键词
P68; EIF-2A KINASE; KAPOSIS SARCOMA; INTERFERON-ALPHA; MAB TJ4C4; IMMUNOPEROXIDASE IRON STAIN; AIDS;
D O I
10.1159/000217782
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Double-stranded RNA (dsRNA)-dependent protein kinase (p68) has been shown to be induced by alpha-interferon (IFN-alpha) in mammalian cells. It binds to dsRNA, and is believed to be a factor in the control of both cellular and viral protein synthesis. This report describes the use of a new monoclonal antibody (MAb) TJ4C4, to monitor levels of p68 in a patient with AIDS-associated Kaposi's sarcoma. Using a novel immunoperoxidase/iron staining method, we examined formalin-fixed, paraffin-embedded biopsies prior to, and 4 months after the initiation of IFN therapy. Immunostaining showed low levels (1+ staining) of p68 in the pretreatment tissue, whereas a marked increase (4+ staining) was noted during interferon treatment. This staining suggests an increased level of intracellular p68 expression. This patient has subsequently remained on IFN-alpha therapy and is alive with no evidence of Kaposi's sarcoma, 6 1/2 years after diagnosis. The use of MAb TJ4C4 will greatly facilitate the study of p68 kinase in clinical tissues, and may provide a way to monitor the effects of IFN therapy.
引用
收藏
页码:324 / 329
页数:6
相关论文
共 31 条
  • [1] BERRY MJ, 1985, J BIOL CHEM, V260, P1240
  • [2] BOVI PD, 1986, CANCER RES, V46, P6333
  • [3] BROOKS JJ, 1986, LANCET, V2, P1309
  • [4] COSTA J, 1983, LANCET, V1, P58
  • [5] Enzinger RM., 2011, SOFT TISSUE TUMORS, P1178
  • [6] FISHL MA, 1991, AM J MED, V90, pS2
  • [7] GALABRU J, 1987, J BIOL CHEM, V262, P15538
  • [8] SIMPLE METHOD FOR POLYETHYLENE GLYCOL-PROMOTED HYBRIDIZATION OF MOUSE MYELOMA CELLS
    GEFTER, ML
    MARGULIES, DH
    SCHARFF, MD
    [J]. SOMATIC CELL GENETICS, 1977, 3 (02): : 231 - 236
  • [9] GILL PS, 1990, J BIOL RESP MODIF, V9, P512
  • [10] KAPOSIS SARCOMA AND ITS RELATIONSHIP TO CYTOMEGALO-VIRUS (CMV) .3. CMV DNA AND CMV EARLY ANTIGENS IN KAPOSIS SARCOMA
    GIRALDO, G
    BETH, E
    HUANG, ES
    [J]. INTERNATIONAL JOURNAL OF CANCER, 1980, 26 (01) : 23 - 29