Menter Thomas, Bodmer-Haecki Andrea, Dirnhofer Stephan, Tzankov Alexandar
Institute of Pathology, University Hospital Basel, 4031 Basel, Switzerland; Department of Histopathology, Hammersmith Hospital Campus, Imperial College Healthcare NHS Trust, W12 0HS London, United Kingdom.
Institute of Pathology, University Hospital Basel, 4031 Basel, Switzerland.
Hum Pathol. 2016 Aug;54:17-24. doi: 10.1016/j.humpath.2016.03.005. Epub 2016 Apr 1.
Activation of the programmed death 1 (PD1)/PD1 ligand (PDL1) pathway is important for tumor cells to escape from immune control. The clinical efficacy of therapeutic modulation of the PD1-PDL1 pathway has been recently shown in classical Hodgkin lymphoma (cHL), but little is known about the frequency and diagnostic and prognostic importance of PDL1 expression in lymphomas. The available anti-PDL1 antibody clones E1L3N and SP142 were compared, and a large cohort of Hodgkin lymphomas (n=280) and B-cell lymphomas (n=619) was examined for PDL1 using E1L3N. The results were correlated with the expression of other phenotypic markers, interphase fluorescence in situ hybridization data of the 9p24.1 region (PDL1 locus), and the clinical outcome. PDL1 was expressed on more than 5% of tumor cells in 70% of cHL, 54% of nodular lymphocyte-predominant Hodgkin lymphoma, and 35% of primary mediastinal B-cell lymphomas; in the latter, PDL1 expression correlated with PDL1 gains (ρ=0.573). PDL1 was expressed in 31% of primary diffuse large B-cell lymphomas (DLBCLs), whereas most other entities did not express PDL1. In cHL, expression of PDL1 correlated with increased numbers of granzyme+ T cells (ρ=0.251) and CD68+ macrophages (ρ=0.221) but with decreased numbers of FoxP3+ T cells (ρ=0.145). In activated B-cell-like DLBCL, PDL1 positively correlated with PD1+ T cells, whereas an inverse correlation with FoxP3+ T cells was seen in the germinal center B-cell-like DLBCL. PDL1 expression can be diagnostically valuable in some gray zones around DLBCL and cHL; it identifies an "immune escape" cluster of cHL and activated B-cell-like DLBCL with increased granzyme+ and PD1+ T cells and macrophages and decreased regulatory T cells.
程序性死亡1(PD1)/PD1配体(PDL1)通路的激活对肿瘤细胞逃避免疫控制至关重要。最近在经典型霍奇金淋巴瘤(cHL)中已显示出调节PD1-PDL1通路治疗的临床疗效,但关于淋巴瘤中PDL1表达的频率及其诊断和预后意义知之甚少。对现有的抗PDL1抗体克隆E1L3N和SP142进行了比较,并使用E1L3N检测了一大组霍奇金淋巴瘤(n = 280)和B细胞淋巴瘤(n = 619)中的PDL1。将结果与其他表型标志物的表达、9p24.1区域(PDL1基因座)的间期荧光原位杂交数据以及临床结局相关联。在70%的cHL、54%的结节性淋巴细胞为主型霍奇金淋巴瘤和35%的原发性纵隔B细胞淋巴瘤中,超过5%的肿瘤细胞表达PDL1;在后者中,PDL1表达与PDL1扩增相关(ρ = 0.573)。31%的原发性弥漫性大B细胞淋巴瘤(DLBCL)表达PDL1,而大多数其他实体不表达PDL1。在cHL中,PDL1表达与颗粒酶+ T细胞数量增加(ρ = 0.251)和CD68+巨噬细胞数量增加(ρ = 0.221)相关,但与FoxP3+ T细胞数量减少(ρ = 0.145)相关。在活化B细胞样DLBCL中,PDL1与PD1+ T细胞呈正相关,而在生发中心B细胞样DLBCL中与FoxP3+ T细胞呈负相关。PDL1表达在DLBCL和cHL周围的一些灰色地带可能具有诊断价值;它可识别出cHL和活化B细胞样DLBCL的“免疫逃逸”集群,其颗粒酶+和PD1+ T细胞以及巨噬细胞数量增加,调节性T细胞数量减少。