Department of Diabetes and Endocrinology, Japanese Red Cross Wakayama Medical Center, Wakayama, Japan.
The First Department of Medicine, Wakayama Medical University, Wakayama, Japan.
Endocrinol Metab (Seoul). 2022 Feb;37(1):84-95. doi: 10.3803/EnM.2021.1282. Epub 2022 Feb 28.
Type 1 diabetes mellitus induced by immune-checkpoint inhibitors (ICI-T1DM) is a rare critical entity. However, the etiology of ICI-T1DM remains unclear.
In order to elucidate risk factors for ICI-T1DM, we evaluated the clinical course and immunological status of patients with ICI-T1DM who had been diagnosed during 2016 to 2021.
Seven of 871 (0.8%, six men and one woman) patients developed ICI-T1DM. We revealed that the allele frequencies of human leukocyte antigen (HLA)-DPA102:02 and DPB105:01 were significantly higher in the patients with ICI-T1DM In comparison to the controls who received ICI (11/14 vs. 10/26, P=0.022; 11/14 vs. 7/26, P=0.0027, respectively). HLA-DRB104:05, which has been found to be a T1DM susceptibility allele in Asians, was also observed as a high-risk allele for ICI-T1DM. The significance of the HLA-DPB105:01 and DRB1*04:05 alleles was confirmed by an analysis of four additional patients. The absolute/relative neutrophil count, neutrophils-lymphocyte ratio, and neutrophil-eosinophil ratio increased, and the absolute lymphocyte count and absolute/relative eosinophil count decreased at the onset as compared with 6 weeks before. In two patients, alterations in cytokines and chemokines were found at the onset.
Novel high-risk HLA alleles and haplotypes were identified in ICI-T1DM, and peripheral blood factors may be utilized as biomarkers.
免疫检查点抑制剂(ICI)引起的 1 型糖尿病(ICI-T1DM)是一种罕见的危急病症。然而,ICI-T1DM 的病因仍不清楚。
为了阐明 ICI-T1DM 的危险因素,我们评估了 2016 年至 2021 年期间诊断出的 ICI-T1DM 患者的临床过程和免疫状态。
871 例患者中有 7 例(0.8%,6 名男性和 1 名女性)发生 ICI-T1DM。我们发现,与接受 ICI 的对照组相比(11/14 比 10/26,P=0.022;11/14 比 7/26,P=0.0027),ICI-T1DM 患者的人类白细胞抗原(HLA)-DPA102:02 和 DPB105:01 等位基因频率显著更高。在亚洲人中已被发现为 1 型糖尿病易感等位基因的 HLA-DRB104:05 也被观察为 ICI-T1DM 的高危等位基因。另外 4 名患者的分析证实了 HLA-DPB105:01 和 DRB1*04:05 等位基因的意义。与发病前 6 周相比,发病时绝对/相对中性粒细胞计数、中性粒细胞-淋巴细胞比值和中性粒细胞-嗜酸性粒细胞比值增加,而绝对淋巴细胞计数和绝对/相对嗜酸性粒细胞计数减少。在两名患者中,发病时发现细胞因子和趋化因子的改变。
在 ICI-T1DM 中发现了新的高危 HLA 等位基因和单倍型,外周血因子可用作生物标志物。