Department of Rheumatology and Clinical Immunology.
Department of Respiratory Medicine.
Rheumatology (Oxford). 2020 Nov 1;59(11):3284-3292. doi: 10.1093/rheumatology/keaa123.
Rapidly progressive interstitial lung disease (RP-ILD) with poor prognosis often accompanies anti-melanoma differentiation-associated gene 5 (MDA5)-positive DM. Combined immunosuppressive therapy, including glucocorticoids, calcineurin inhibitors and intravenous cyclophosphamide (IVCY) is reportedly effective in DM with RP-ILD, but some patients remain resistant to therapy. We examined the utility of plasma exchange (PE) in such intractable cases and investigated the prognostic factors of the disease.
Thirty-eight anti-MDA5-positive DM-ILD patients who received the combined immunosuppressive therapy were retrospectively reviewed. Their serum cytokines were evaluated by multiplex assay before treatment. The patients were divided into two groups: those who achieved remission without exacerbation of respiratory dysfunction (n = 25, group A) and those who progressed to hypoxemia during the treatment (n = 13, group B).
PE was carried out in eight group B patients, but none of group A. Five of the eight treated with PE survived, while the five untreated patients died (P =0.04). Higher neutrophil lymphocyte ratio, higher serum ferritin, hypoxemia, high-resolution computed tomography (HRCT) score before treatment and increase of Krebs von Lungen-6 (KL-6) in the first 4 weeks of the treatment were the prognostic factors for disease progression. Serum cytokines such as IL-1, IL-6, IL-8, IL-10, IL-12p70, IL-18 and sCD163 levels were higher in group B than group A.
PE should be an effective adjuvant treatment in anti-MDA5-positive DM with RP-ILD. Assessment of basal laboratory tests or monocyte/macrophage-derived cytokines and the increase of KL-6, HRCT score and hypoxemia may help us to predict intractable cases and to make early treatment decisions regarding PE in anti-MDA5-positive DM.
伴有预后不良的快速进展性间质性肺病(RP-ILD)常伴有抗黑色素瘤分化相关基因 5(MDA5)阳性皮肌炎(DM)。据报道,包括糖皮质激素、钙调磷酸酶抑制剂和静脉环磷酰胺(IVCY)在内的联合免疫抑制疗法对伴有 RP-ILD 的 DM 有效,但有些患者对治疗仍有抵抗力。我们检查了血浆置换(PE)在这种难治性病例中的效用,并研究了疾病的预后因素。
回顾性分析 38 例接受联合免疫抑制治疗的抗 MDA5 阳性 DM-ILD 患者。在治疗前通过多重分析评估其血清细胞因子。患者分为两组:无呼吸功能恶化的缓解组(n=25,A 组)和治疗期间进展为低氧血症组(n=13,B 组)。
B 组 8 例患者进行了 PE,但 A 组无一例。PE 治疗的 5 例存活,而未治疗的 5 例死亡(P=0.04)。更高的中性粒细胞与淋巴细胞比值、更高的血清铁蛋白、低氧血症、治疗前高分辨率计算机断层扫描(HRCT)评分以及治疗前 4 周 KL-6 的增加是疾病进展的预后因素。B 组的血清细胞因子如白细胞介素 1(IL-1)、白细胞介素 6(IL-6)、白细胞介素 8(IL-8)、白细胞介素 10(IL-10)、白细胞介素 12p70(IL-12p70)、白细胞介素 18(IL-18)和可溶性 CD163 水平高于 A 组。
PE 应成为抗 MDA5 阳性伴有 RP-ILD 的皮肌炎的有效辅助治疗方法。评估基础实验室检查或单核细胞/巨噬细胞衍生细胞因子以及 KL-6、HRCT 评分和低氧血症的增加可能有助于我们预测难治性病例,并对抗 MDA5 阳性皮肌炎中 PE 的治疗做出早期决策。