MYCOSIS-FUNGOIDES SKIN-LESIONS CONTAIN CD8+ TUMOR-INFILTRATING LYMPHOCYTES EXPRESSING AN ACTIVATED, MHC-RESTRICTED CYTOTOXIC T-LYMPHOCYTE PHENOTYPE

被引:53
作者
WOOD, GS
EDINGER, A
HOPPE, RT
WARNKE, RA
机构
[1] CASE WESTERN RESERVE UNIV,DEPT ELECT ENGN,CLEVELAND,OH 44106
[2] CASE WESTERN RESERVE UNIV,DEPT OBSTET & GYNAECOL,CLEVELAND,OH 44106
[3] CASE WESTERN RESERVE UNIV,SKIN DIS RES CTR,CLEVELAND,OH 44106
[4] STANFORD UNIV,DEPT RADIAT ONCOL,STANFORD,CA 94305
[5] STANFORD UNIV,DEPT PATHOL,STANFORD,CA 94305
关键词
D O I
10.1111/j.1600-0560.1994.tb00250.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
In prior studies, we showed that most CD8+ cells infiltrating skin lesions of CD3+CD4+ mycosis fungoides were CD3+ T-line-age tumor-infiltrating lymphocytes (TIL) whose overall phenotype was suggestive of MHC-restricted cytotoxic T lymphocytes (CTL). However, their lack of cytotoxic-associated granzyme A mRNA suggested that they might be unactivated CTL precursors. In this study, we used single- and double-label immunohistologic techniques to assess the expression of TIA-1-reactive protein and HLA-DR by these CD8+TIL. Monoclonal antibody TIA-1 recognizes a novel family of proteins expressed preferentially by cytotoxic cells, including some that lack granzyme A. HLA-DR is a marker of T-cell activation. Single-label studies of 32 cases showed that CD8+TIL and TIA-1+ cells constituted a variable minority of the total cellular infiltrate and had a similar distribution. Double-label studies of 14 cases showed that in most instances the aggregate phenotype of the majority of CD8+TIL was CD3+TIA-1+HLA-DR+CD56-CD57-. These findings suggest that many of the CD8+TIL within skin lesions of CD3+CD4+ mycosis fungoides are activated, MHC-restricted CTL.
引用
收藏
页码:151 / 156
页数:6
相关论文
共 19 条
  • [1] ANDERSON P, 1990, J IMMUNOL, V144, P574
  • [2] DIAZ JI, 1991, AM J PATHOL, V139, P503
  • [3] THE IMMUNOHISTOLOGY OF THE PERSISTENT GENERALIZED LYMPHADENOPATHY SYNDROME (PGL)
    GARCIA, CF
    LIFSON, JD
    ENGLEMAN, EG
    SCHMIDT, DM
    WARNKE, RA
    WOOD, GS
    [J]. AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 1986, 86 (06) : 706 - 715
  • [4] HAFFNER AC, 1993, J INVEST DERMATOL, V100, P566
  • [5] IDENTIFICATION AND FUNCTIONAL-CHARACTERIZATION OF A TIA-1-RELATED NUCLEOLYSIN
    KAWAKAMI, A
    TIAN, QS
    DUAN, XC
    STREULI, M
    SCHLOSSMAN, SF
    ANDERSON, P
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (18) : 8681 - 8685
  • [6] EXPRESSION OF T-CELL RECEPTOR ANTIGENS IN MYCOSIS-FUNGOIDES AND INFLAMMATORY SKIN-LESIONS
    MICHIE, SA
    ABEL, EA
    HOPPE, RT
    WARNKE, RA
    WOOD, GS
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1989, 93 (01) : 116 - 120
  • [7] MUELLER C, 1989, EUR J IMMUNOL, V19, P1253
  • [8] MULLER C, 1988, J EXP MED, V167, P1124
  • [9] HLA-DR EXPRESSION ON CYTOTOXIC LYMPHOCYTES-T
    RESS, SR
    STRASSMANN, G
    BACH, FH
    [J]. SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 1985, 22 (05) : 455 - 461
  • [10] HUMAN LYMPHOCYTE-T SUBSETS - FUNCTIONAL-HETEROGENEITY AND SURFACE RECOGNITION STRUCTURES
    ROMAIN, PL
    SCHLOSSMAN, SF
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1984, 74 (05) : 1559 - 1565