Hagn-Meincke Rasmus, Novovic Srdan, Hadi Amer, Jensen Annette B, Drewes Asbjørn M, Krarup Henrik, Frøkjær Jens B, Park Walter G, Jørgensen Peter L, Møller Holger Jon, Deleuran Bent W, Olesen Søren S
Departments of Gastroenterology and Gastrointestinal Surgery and.
Radiology, Hvidovre Hospital, Hvidovre.
Pancreas. 2025 Apr 1;54(4):e331-e339. doi: 10.1097/MPA.0000000000002443.
Activation of type M2 macrophages has been implicated in the pathogenesis of chronic pancreatitis (CP). In a clinical pilot study, we investigated blood-based markers of macrophage activation at different stages of CP.
We performed a cross-sectional analysis of prospectively collected plasma samples from healthy controls and patients with suspected or definitive CP according to the M-ANNHEIM criteria. Plasma concentrations of soluble CD163 (sCD163), soluble CD206 (sCD206), and monocyte chemoattractant protein-1 (MCP-1) were analyzed using enzyme-linked immunosorbent assays. Group and pairwise comparisons of analytes were performed using regression models and area under the receiver operating curves (AUC-ROC).
In total, 73 subjects with CP (28 suspected CP and 45 definitive CP) and 40 controls were included. Compared to controls, the median plasma concentrations of sCD163 ( P = 0.019) and sCD206 ( P = 0.033) were elevated in patients with definitive CP. sCD206 was also elevated in patients with definitive CP ( P = 0.042) compared to suspected CP. ROC analysis revealed the optimal sCD163 cutpoint to distinguish definitive CP from controls was 1.84 mg/mL (AUC-ROC 0.65; 95% confidence interval [CI], 0.54-0.77). The optimal sCD206 cutpoint to distinguish definitive CP from controls was 0.24 mg/mL (AUC-ROC 0.66; 95% CI, 0.54-0.78). MCP-1 concentrations showed no differences across subgroups.
Our study demonstrates that subjects with definitive CP, sampled during a clinically quiescent phase, exhibited increased levels of sCD163 and sCD206. This indicates the presence of activated M2 macrophages in patients with CP at advanced, but not early, clinical stages.
M2型巨噬细胞的激活与慢性胰腺炎(CP)的发病机制有关。在一项临床初步研究中,我们调查了CP不同阶段基于血液的巨噬细胞激活标志物。
我们对根据M-ANNHEIM标准前瞻性收集的健康对照者以及疑似或确诊CP患者的血浆样本进行了横断面分析。使用酶联免疫吸附测定法分析可溶性CD163(sCD163)、可溶性CD206(sCD206)和单核细胞趋化蛋白-1(MCP-1)的血浆浓度。使用回归模型和受试者工作曲线下面积(AUC-ROC)对分析物进行组间和两两比较。
总共纳入了73例CP患者(28例疑似CP和45例确诊CP)和40例对照者。与对照者相比,确诊CP患者的sCD163(P = 0.019)和sCD206(P = 0.033)血浆浓度中位数升高。与疑似CP患者相比,确诊CP患者的sCD206也升高(P = 0.042)。ROC分析显示,区分确诊CP与对照者的最佳sCD163切点为1.84mg/mL(AUC-ROC 0.65;95%置信区间[CI],0.54 - 0.77)。区分确诊CP与对照者的最佳sCD206切点为0.24mg/mL(AUC-ROC 0.66;95%CI,0.54 - 0.78)。MCP-1浓度在各亚组之间无差异。
我们的研究表明,在临床静止期采样的确诊CP患者表现出sCD163和sCD206水平升高。这表明在CP患者的晚期而非早期临床阶段存在活化的M2巨噬细胞。