Service d'Immunologie-hématologie et Rhumatologie pédiatrique, Institut Imagine, Hôpital Necker, Assistance Publique Hôpitaux de Paris, France & Centre National de Référence RAISE, 149 rue de Sèvres, 75015 Paris, France.
Service d'Immunologie Biologique, Groupe Hospitalier Universitaire Paris-Sud, Hôpital Kremlin Bicêtre, Assistance Publique-Hôpitaux de Paris (AP-HP), Le Kremlin Bicêtre, France; INSERM -UMR_S996, Université Paris-Saclay, Clamart, France.
Semin Arthritis Rheum. 2019 Jun;48(6):1014-1018. doi: 10.1016/j.semarthrit.2018.09.002. Epub 2018 Sep 17.
To investigate the relationship of clinical response of Juvenile Idiopathic Arthritis (JIA) to etanercept (ETN) with ETN levels, and the presence of anti-drug antibodies to ETN (ADAb).
Prospective study of JIA patients under 18 years old. Clinical and pharmacological data were collected at two visits. JIA clinical inactivity and activity were assessed according to the Wallace criteria and to the Juvenile Arthritis Disease Activity Score (JADAS). ETN and ADAb serum levels assessments were determined using ELISA-based assays.
126 patients were enrolled. The median duration of ETN treatment at inclusion was 569 days (range 53-2340). ADAb were undetectable (<10 ng/ml) in 171/218 (78%) samples and were > 25 ng/mL in 2/218 samples. No significant relationship between ETN concentration and the clinical inactivity status and JIA activity was found using either univariate logistic regression or multiple logistic regression analysis, adjusted on one individual descriptors, time since diagnosis, time of sampling, use of corticosteroids or methotrexate and classification of JIA. No correlation was found between the remission status and the detection of ADAb.
This study did not demonstrate any correlation between JIA activity and circulating ETN levels in a large population of patients with JIA previously treated with ETN for at least 1.5 months. As described for adults, our study confirms that ETN is marginally immunogenic in pediatric patients. These results do not support the clinical usefulness of a monitoring of ADAb or ETN concentrations for the management of this group of JIA patients if they fail to achieve clinical inactive disease.
研究幼年特发性关节炎(JIA)患者接受依那西普(ETN)治疗后的临床反应与 ETN 水平及抗 ETN 抗体(ADAb)的关系。
这是一项针对 18 岁以下 JIA 患者的前瞻性研究。在两次就诊时收集临床和药理学数据。根据 Wallace 标准和幼年特发性关节炎疾病活动评分(JADAS)评估 JIA 的临床缓解和活动情况。采用 ELISA 法检测 ETN 和 ADAb 血清水平。
共纳入 126 例患者。纳入时 ETN 治疗的中位时间为 569 天(范围 53-2340)。在 218 份样本中,171 份(78%)ADAb 检测不到(<10ng/ml),2 份(1%)ADAb>25ng/ml。在单变量逻辑回归或多变量逻辑回归分析中,均未发现 ETN 浓度与临床缓解状态和 JIA 活动之间存在显著关系,调整了一个个体描述符、诊断后时间、采样时间、皮质类固醇或甲氨蝶呤的使用以及 JIA 的分类。缓解状态与 ADAb 的检测也没有相关性。
本研究未在先前接受 ETN 治疗至少 1.5 个月的 JIA 患者大人群中显示 JIA 活性与循环 ETN 水平之间存在任何相关性。与成人的描述一致,我们的研究证实 ETN 在儿科患者中具有轻微的免疫原性。如果这些 JIA 患者未能达到临床缓解,这些结果不支持 ADAb 或 ETN 浓度监测在这类患者管理中的临床实用性。