Mitsui Takeki, Maekawa Izuru, Yamane Arito, Ishikawa Tomomi, Koiso Hiromi, Yokohama Akihiko, Handa Hiroshi, Matsushima Takafumi, Tsukamoto Norifumi, Murakami Hirokazu, Nojima Yoshihisa, Karasawa Masamitsu
Department of Medicine and Clinical Science, Graduate School of Medicine, Gunma University, Maebashi, Japan.
Br J Haematol. 2004 Jul;126(1):55-62. doi: 10.1111/j.1365-2141.2004.05005.x.
We analysed the cell surface expression of chemokine receptors and natural killer receptors (NKRs) in addition to conventional T- and natural killer (NK)-cell markers in patients with lymphoproliferative disease of granular lymphocytes (LDGL), and compared results between NK- and T-LDGL subgroups. The subjects of this study were 15 LDGL patients: four NK-LDGL and 11 T-LDGL [six CD8(+) T-cell receptor (TCR) alphabeta(+), four CD4(+) TCRalphabeta(+) and one CD8(+) TCRgammadelta(+)] cases. Flow cytometric analysis showed that the expanding cells had a common phenotype, CD45RA(+) CD27(-) CD28(-) CCR7(-), in NK- and T-LDGL patients irrespective of differences in TCR status. There were no marked differences in the expression patterns of chemokine receptors between NK- and T-LDGL patients. Although restricted NKR subsets were expressed on both NK- and T-large granular lymphocytes (LGLs), CD94 was the most widely expressed marker. These findings may be unique to cells of LDGL cases, because normal CD56(dim) NK cells frequently express killer cell immunoglobulin-like receptors. Furthermore, analysis of NKR expression was repeated over an interval of more than 6 months, and fluctuations of NKR repertoire in the LGL clones were minimal.
我们分析了颗粒淋巴细胞增殖性疾病(LDGL)患者细胞表面趋化因子受体和自然杀伤受体(NKRs)的表达情况,以及传统T细胞和自然杀伤(NK)细胞标志物的表达情况,并比较了NK-LDGL和T-LDGL亚组之间的结果。本研究的对象为15例LDGL患者:4例NK-LDGL和11例T-LDGL[6例CD8(+)T细胞受体(TCR)αβ(+)、4例CD4(+)TCRαβ(+)和1例CD8(+)TCRγδ(+)]病例。流式细胞术分析显示,无论TCR状态如何,NK-LDGL和T-LDGL患者中扩增的细胞具有共同的表型,即CD45RA(+)CD27(-)CD28(-)CCR7(-)。NK-LDGL和T-LDGL患者之间趋化因子受体的表达模式没有明显差异。虽然NK和T大颗粒淋巴细胞(LGLs)上均表达有限的NKR亚群,但CD94是表达最广泛的标志物。这些发现可能是LDGL病例细胞所特有的,因为正常的CD56(dim)NK细胞经常表达杀伤细胞免疫球蛋白样受体。此外,在超过6个月的时间间隔内重复进行NKR表达分析,LGL克隆中NKR库的波动最小。