From the Divisions of Rheumatic Diseases.
Pulmonary and Critical Care Medicine, Department of Internal Medicine.
J Clin Rheumatol. 2022 Mar 1;28(2):84-88. doi: 10.1097/RHU.0000000000001808.
BACKGROUND/OBJECTIVE: We have limited knowledge regarding characteristics of patients with interstitial pneumonia with autoimmune features (IPAF) that are associated with response to immunosuppression. In this study, we used published IPAF criteria to characterize features associated with response to treatment.
We conducted a single-center medical records review study of 63 IPAF patients to evaluate for serological, clinical, and morphological characteristics that are associated with response to immunosuppression. Response was defined as % relative functional vital capacity decline of less than 10% and absence of death or lung transplant within the first year of continuous immunosuppressive therapy. Nonparametric measures of association and multivariate logistic regression were used to evaluate the relationship between baseline characteristics and immunosuppressive response.
There was a trend of greater progression among men, ever smokers, those negative for antisynthetase antibodies, and those with usual interstitial pneumonia radiographic pattern, but no statistically significant relationship was found between baseline serological, clinical, or morphological features and response to immunosuppression. Patients on combination therapy with mycophenolate mofetil and prednisone had less disease progression (p = 0.018) than those on regimens that did not include both of these medications.
In our cohort, baseline clinical assessment did not identify which patients with IPAF will respond to immunosuppressive therapy. Combination therapy with mycophenolate mofetil and prednisone was associated with lack of disease progression in our IPAF patients, including in IPAF-usual interstitial pneumonia. Further studies are needed to evaluate which IPAF patients would benefit from immunosuppressive therapy, antifibrotic therapy, or a combination of both.
背景/目的:我们对自身免疫特征性间质性肺炎(IPAF)患者的特征及其与免疫抑制反应的相关性知之甚少。本研究使用已发表的 IPAF 标准来描述与治疗反应相关的特征。
我们对 63 例 IPAF 患者进行了单中心病历回顾研究,以评估与免疫抑制反应相关的血清学、临床和形态学特征。将反应定义为连续免疫抑制治疗的前 1 年内,功能残气量的相对下降百分比<10%,且无死亡或肺移植。采用非参数关联度量和多变量逻辑回归来评估基线特征与免疫抑制反应之间的关系。
男性、曾经吸烟者、抗合成酶抗体阴性者和普通间质性肺炎影像学模式者的进展趋势更大,但在基线血清学、临床或形态学特征与免疫抑制反应之间未发现统计学上的显著关系。与不包括这两种药物的方案相比,联合应用霉酚酸酯和泼尼松的患者疾病进展较少(p=0.018)。
在本队列中,基线临床评估未能确定哪些 IPAF 患者对免疫抑制治疗有反应。霉酚酸酯联合泼尼松治疗与我们的 IPAF 患者(包括 IPAF-普通间质性肺炎)的疾病无进展相关。需要进一步研究以评估哪些 IPAF 患者将从免疫抑制治疗、抗纤维化治疗或两者联合治疗中获益。