Department of Dermatology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
The Wistar Institute, Philadelphia, Pennsylvania, USA.
J Invest Dermatol. 2014 Jan;134(1):229-236. doi: 10.1038/jid.2013.279. Epub 2013 Jun 21.
Sézary syndrome (SS) cells express cell surface molecules also found on normal activated CD4 T cells. In an effort to find a more specific surface marker for malignant SS cells, a microarray analysis of gene expression was performed. Results showed significantly increased levels of mRNA for CD164, a sialomucin found on human CD34+ hematopoietic stem cells, and FCRL3, a molecule present on a subset of human natural T regulatory cells. Both markers were increased in CD4 T cells from SS patients compared with healthy donors (HD). Flow cytometry studies confirmed the increased expression of CD164 and FCRL3 primarily on CD4+CD26- T cells of SS patients. Importantly, a statistically significant correlation was found between an elevated percentage of CD4+CD164+ T cells and an elevated percentage of CD4+CD26- T cells in all tested SS patients but not in patients with mycosis fungoides and atopic dermatitis or HD. FCRL3 expression was significantly increased only in patients with high tumor burden. CD4+CD164+ cells displayed cerebriform morphology and their loss correlated with clinical improvement in treated patients. Our results suggest that CD164 can serve as a marker for diagnosis and for monitoring progression of cutaneous T-cell lymphoma (CTCL)/SS and that FCRL3 expression correlates with a high circulating tumor burden.
蕈样肉芽肿/赛扎里综合征(SS)细胞表达正常激活的 CD4 T 细胞上也存在的细胞表面分子。为了寻找恶性 SS 细胞更特异的表面标志物,我们对基因表达进行了微阵列分析。结果显示,在人类 CD34+造血干细胞上发现的唾液酸粘蛋白 CD164 和存在于人类天然 T 调节细胞亚群上的分子 FCRL3 的 mRNA 水平显著增加。与健康供体(HD)相比,SS 患者的 CD4 T 细胞中这两种标志物均增加。流式细胞术研究证实,与健康供体相比,SS 患者 CD4+CD26-T 细胞中 CD164 和 FCRL3 的表达增加。重要的是,在所有检测到的 SS 患者中,均发现 CD4+CD164+T 细胞的百分比升高与 CD4+CD26-T 细胞的百分比升高之间存在统计学显著相关性,但在蕈样肉芽肿和特应性皮炎患者或 HD 中则没有这种相关性。仅在肿瘤负荷高的患者中 FCRL3 表达显著增加。CD4+CD164+细胞呈现脑回样形态,其丢失与治疗患者的临床改善相关。我们的结果表明,CD164 可作为诊断和监测皮肤 T 细胞淋巴瘤(CTCL)/SS 进展的标志物,并且 FCRL3 表达与高循环肿瘤负荷相关。