1Institute for Genetic Medicine, Newcastle University, and Newcastle Hospitals NHS Trust, Newcastle upon Tyne, United Kingdom.
2Thyroid Research Group, School of Medicine, Cardiff University, Cardiff, United Kingdom.
Thyroid. 2019 Jul;29(7):1003-1011. doi: 10.1089/thy.2019.0036. Epub 2019 Jun 13.
Graves' disease is one of the most common autoimmune conditions, but treatment remains imperfect. This study explores the first-in-human use of antigen-specific immunotherapy with a combination of two thyrotropin receptor (TSHR) peptides (termed ATX-GD-59) in Graves' hyperthyroidism. Twelve participants (11 female) with previously untreated mild to moderate Graves' hyperthyroidism were enrolled in a Phase I open label trial to receive 10 doses of ATX-GD-59 administered intradermally over an 18-week period. Adverse events, tolerability, changes in serum free thyroid hormones, and TSHR autoantibodies were measured. Ten subjects received all 10 doses of ATX-GD-59, five (50%) of whom had free triiodothyronine within the reference interval by the 18-week visit. Two further subjects had improved free thyroid hormones by the end of the study (7/10 responders), whereas three subjects showed worsening thyrotoxicosis during the study. Serum TSHR autoantibody concentrations reduced during the study and correlated with changes in free thyroid hormones ( = 0.85, = 0.002 for TSHR autoantibody vs. free triiodothyronine). Mild injection-site swelling and pain were the most common adverse events. These preliminary data suggest that ATX-GD-59 is a safe and well-tolerated treatment. The improvement in free thyroid hormones in 70% of subjects receiving the medication suggests potential efficacy as a novel treatment for Graves' hyperthyroidism.
格雷夫斯病是最常见的自身免疫性疾病之一,但治疗仍不完善。本研究探讨了使用两种促甲状腺激素受体(TSHR)肽(称为 ATX-GD-59)的抗原特异性免疫疗法在格雷夫斯甲亢中的首次人体应用。 12 名(11 名女性)未经治疗的轻度至中度格雷夫斯甲亢患者参加了一项 I 期开放标签试验,以在 18 周内接受 10 次 ATX-GD-59 皮内给药。测量不良反应、耐受性、血清游离甲状腺激素和 TSHR 自身抗体的变化。 10 名受试者接受了所有 10 剂 ATX-GD-59,其中 5 名(50%)在 18 周时游离三碘甲状腺原氨酸在参考范围内。另外两名受试者在研究结束时游离甲状腺激素有所改善(10 名应答者中的 7 名),而 3 名受试者在研究期间出现甲状腺毒症恶化。研究期间血清 TSHR 自身抗体浓度降低,并与游离甲状腺激素的变化相关( = 0.85, = 0.002 用于 TSHR 自身抗体与游离三碘甲状腺原氨酸)。轻度注射部位肿胀和疼痛是最常见的不良反应。 这些初步数据表明 ATX-GD-59 是一种安全且耐受良好的治疗方法。在接受药物治疗的 70%的受试者中,游离甲状腺激素的改善表明其作为一种新型格雷夫斯甲亢治疗方法具有潜在疗效。