Kim Young Jae, Won Chong Hyun, Lee Mi Woo, Choi Jee Ho, Chang Sung Eun, Lee Woo Jin
Department of Dermatology, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Korea.
J Clin Med. 2020 Aug 3;9(8):2500. doi: 10.3390/jcm9082500.
The association between tumor-associated macrophages (TAMs) and the expression of immune checkpoint molecules has not been well described in cutaneous melanoma. We evaluated the correlations between the expression of markers of TAMs, cluster of differentiation 163 (CD163), and immune checkpoint molecules, programmed cell death protein-1 (PD-1), and lymphocyte activating gene-3 (LAG-3). We also determined their relationships with the clinicopathological features and disease outcomes in melanoma. Diagnostic tissues collected from melanoma patients were evaluated using immunohistochemistry for CD163, PD-1, and LAG-3 expression. CD163 expression positively correlated with PD-1 and LAG-3 expression. High expression of both CD163 and PD-1 expressions was significantly associated with negative prognostic factors and worse prognosis than high expression of the single markers. High co-expression of CD163 and LAG-3 was associated with poor clinicopathological indexes of melanoma and worse survival compared to the high expression of the single markers. The expression of immune checkpoint molecules PD-1 and LAG-3 positively correlated with the M2-TAM density in melanoma tissue. Simultaneous high M2-TAM density and immune checkpoint molecules expression acted as independent poor prognostic factors in cutaneous melanoma.
肿瘤相关巨噬细胞(TAM)与免疫检查点分子的表达之间的关联在皮肤黑色素瘤中尚未得到充分描述。我们评估了TAM标志物分化簇163(CD163)的表达与免疫检查点分子程序性细胞死亡蛋白1(PD-1)和淋巴细胞激活基因3(LAG-3)之间的相关性。我们还确定了它们与黑色素瘤临床病理特征和疾病预后的关系。使用免疫组织化学评估从黑色素瘤患者收集的诊断组织中CD163、PD-1和LAG-3的表达。CD163表达与PD-1和LAG-3表达呈正相关。与单一标志物的高表达相比,CD163和PD-1的高表达均与不良预后因素和更差的预后显著相关。与单一标志物的高表达相比,CD163和LAG-3的高共表达与黑色素瘤不良临床病理指标和更差的生存率相关。免疫检查点分子PD-1和LAG-3的表达与黑色素瘤组织中M2-TAM密度呈正相关。同时高M2-TAM密度和免疫检查点分子表达是皮肤黑色素瘤独立的不良预后因素。