医学
淋巴增殖性疾病
自身免疫性淋巴增生综合征
免疫学
淋巴增殖性病變
自身免疫性疾病
外周血
疾病
病理
淋巴瘤
抗体
遗传学
细胞凋亡
程序性细胞死亡
Fas受体
生物
作者
Mahnaz Jamee,Samin Sharafian,Narges Eslami,Shideh Namazi Bayegi,Mohammad Keramatipour,Mohamad Nabavi,Sima Shokri,Marjan Shakiba,Bibi Shahin Shamsian,Hassan Abolghasemi,Kurosh Vahidshahi,Ghamartaj Khanbabaee,Shahnaz Armin,Zahra Chavoshzadeh,Mehrnaz Mesdaghi
标识
DOI:10.15586/aei.v52i5.1115
摘要
Elevated level of double-negative T (DNT) cells is a historical hallmark of autoimmune lymphoproliferative syndrome (ALPS) diagnosis. However, the peripheral blood level of DNT cells might also be compromised in autoimmune lymphoproliferative immunodeficiencies (ALPID) other than ALPS, inattention to which would increase the delay in diagnosis of the underlying genetic defect and hinder disease-specific treatment.
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