Hellbacher Erik, Sundström Christer, Molin Daniel, Baecklund Eva, Hollander Peter
Department of Medical Sciences, Rheumatology, Uppsala University, S-751 85 Uppsala, Sweden.
Clinical and Experimental Pathology, Department of Immunology, Genetics and Pathology, Uppsala University, SE-752 36 Uppsala, Sweden.
Cancers (Basel). 2022 Mar 15;14(6):1509. doi: 10.3390/cancers14061509.
Current research seeks to identify subgroups of non-Hodgkin lymphoma (NHL) patients responsive to PD-1 blocking agents. Whether patients with pre-existing rheumatic diseases might constitute such a subgroup is unknown. We determined intratumoral expression of PD-1 and its ligands in lymphoma patients with pre-existing rheumatic diseases. We included 215 patients with rheumatoid arthritis (RA), systemic lupus erythematosus (SLE) or Sjögren's syndrome with subsequent lymphoma and 74 diffuse large B-cell lymphoma (DLBCL) controls without rheumatic disease. PD-1 and PD-ligand immunohistochemical markers were applied on tumor tissue microarrays. The number of PD-1+ tumor infiltrating leukocytes (TILs) and proportions of PD-L1+ and PD-L2+ tumor cells and TILs were calculated and correlated with clinical data. Expression of PD-L1 in tumor cells and TILs was highest in classical Hodgkin lymphoma and DLBCL. In DLBCLs, expression of PD-1 in TILs and PD-L1 in tumor cells was similar in RA, SLE and controls. In RA-DLBCL, high expression of PD-L1 in tumor cells was significantly more common in patients with the most severe RA disease and was associated with inferior overall survival in multivariable analysis.
当前的研究旨在确定对PD-1阻断剂有反应的非霍奇金淋巴瘤(NHL)患者亚组。患有既往存在的风湿性疾病的患者是否可能构成这样一个亚组尚不清楚。我们测定了患有既往存在的风湿性疾病的淋巴瘤患者肿瘤内PD-1及其配体的表达。我们纳入了215例患有类风湿关节炎(RA)、系统性红斑狼疮(SLE)或干燥综合征并随后发生淋巴瘤的患者以及74例无风湿性疾病的弥漫性大B细胞淋巴瘤(DLBCL)对照。将PD-1和PD-配体免疫组化标志物应用于肿瘤组织微阵列。计算PD-1+肿瘤浸润白细胞(TIL)的数量以及PD-L1+和PD-L2+肿瘤细胞及TIL的比例,并将其与临床数据相关联。PD-L1在肿瘤细胞和TIL中的表达在经典型霍奇金淋巴瘤和DLBCL中最高。在DLBCL中,RA、SLE患者和对照中TIL中PD-1的表达以及肿瘤细胞中PD-L1的表达相似。在RA-DLBCL中,肿瘤细胞中PD-L1的高表达在患有最严重RA疾病的患者中明显更为常见,并且在多变量分析中与较差的总生存期相关。