严重的RAS相关的淋巴增殖性疾病病例,增加了具有非典型特征的αβ双阴性T细胞
Daisuke Kurita1, Norio Shiba2, Takashi Ohya1
1Department of Pediatrics, Yokohama City University Graduate School of Medicine, 3-9, Fukuura, Kanazawa, Yokohama, Kanagawa, 236-0004, Japan.
Journal of clinical immunology
|August 29, 2023
概括
一个儿童的RAS相关白血病扩散性疾病 (RALD) 进展为白血病,其特征是增加双阴性T细胞 (αβDNTs). 这些细胞与Th17相似,在RALD和相关疾病中可能导致炎症和休克.
科学领域:
- 免疫学 免疫学 免疫学
- 血液学 血液学 血液学
- 遗传学 遗传学 是一个
背景情况:
- 自免疫淋巴增殖综合征 (ALPS) 涉及淋巴细胞恒温缺陷和TCRαβ+CD4-CD8-双阴性T细胞 (αβDNTs) 的增加.
- 与RAS相关的白血病扩散性疾病 (RALD) 包括来自KRAS/NRAS变异的疾病,呈现类似的临床过程.
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