Demir Selcan, Sag Erdal, Dedeoglu Fatma, Ozen Seza
Division of Pediatric Rheumatology, Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey.
Division of Immunology, Rheumatology Program, Boston Children's Hospital, Boston, MA, United States.
Front Pediatr. 2018 Dec 3;6:377. doi: 10.3389/fped.2018.00377. eCollection 2018.
Autoinflammatory diseases (AID) are diseases of the innate immune system, characterized by recurrent episodes of localized or systemic inflammation. Vasculitis may accompany AID. The causes of the association of vasculitis with monogenic AID are still debated. Among the monogenic AID, Familial Mediterranean Fever (FMF) is the most common. IgA-related vasculitis (IgAV) and Polyarteritis Nodosa (PAN) involving small and/or medium-sized vessels have an increased frequency among FMF patients. There are also case reports revealing vasculitic features in Cryopyrin-Associated Periodic Fever Syndrome (CAPS), Tumor Necrosis Factor Receptor-Associated Periodic Syndrome (TRAPS), Mevalonate Kinase Deficiency (MKD), also known as Hyper IgD syndrome (HIDS), Deficiency of IL-1 Receptor Antagonist (DIRA) and Pyogenic Arthritis, Pyoderma gangrenosum, and Acne (PAPA) patients. Central nervous system vasculitis and vasculopathy have been reported in DIRA and PAPA patients whereas small vessel involvement affecting skin has been reported in CAPS, TRAPS, and MKD patients. Alternatively, vasculitis can also be a leading feature especially in the recently defined monogenic AID (Otulipenia, Deficiency of Adenosine Deaminase 2-DADA2, Haploinsufficiency of A20) and interferonopathies (STING-associated vasculopathy with onset in infancy-SAVI). DADA2 often presents as a PAN-like disease. In otulipenia, patients have painful subcutaneous nodules caused by septal panniculitis with small and medium vessel vasculitis. Haploinsufficiency of A20 (also called Familial Behcet-like Autoinflammatory Syndrome) results in a phenotype very similar to the variable vessel vasculitis of Behcet's disease with recurrent oral-genital ulcers, in addition to, skin rash, uveitis, and polyarthritis. SAVI is an autoinflammatory vasculopathy with increased Interferon (IFN) signature, causing severe skin lesions resulting in ulceration, necrosis, and in some cases, amputation. Behcet's Disease (BD) is a multifactorial polygenic AID characterized by recurrent attacks of oral-genital ulcers, skin lesions, uveitis and a unique vasculitis affecting both arteries and veins of all sizes. Many clinical features overlap with other autoinflammatory diseases and overexpression of proinflammatory cytokines is an important feature of the disease.
自身炎症性疾病(AID)是先天性免疫系统疾病,其特征为局部或全身性炎症反复发作。血管炎可能伴随AID出现。血管炎与单基因AID关联的原因仍存在争议。在单基因AID中,家族性地中海热(FMF)最为常见。在FMF患者中,与IgA相关的血管炎(IgAV)和累及小血管和/或中血管的结节性多动脉炎(PAN)发病率增加。也有病例报告显示,在冷吡啉相关周期性发热综合征(CAPS)、肿瘤坏死因子受体相关周期性综合征(TRAPS)、甲羟戊酸激酶缺乏症(MKD,也称为高IgD综合征(HIDS))、白细胞介素-1受体拮抗剂缺乏症(DIRA)以及化脓性关节炎、坏疽性脓皮病和痤疮(PAPA)患者中存在血管炎特征。DIRA和PAPA患者曾有中枢神经系统血管炎和血管病变的报告,而CAPS、TRAPS和MKD患者曾有影响皮肤的小血管受累的报告。另外,血管炎也可能是主要特征,尤其是在最近定义的单基因AID(奥图普尼亚病、腺苷脱氨酶2缺乏症-DADA2、A20单倍剂量不足)和干扰素病(婴儿期起病的STING相关血管病变-SAVI)中。DADA2常表现为类似PAN的疾病。在奥图普尼亚病中,患者因间隔性脂膜炎伴小血管和中血管血管炎而出现疼痛性皮下结节。A20单倍剂量不足(也称为家族性白塞氏样自身炎症综合征)导致的表型与白塞氏病的可变血管性血管炎非常相似,除反复出现口腔生殖器溃疡外,还有皮疹、葡萄膜炎和多关节炎。SAVI是一种自身炎症性血管病变,具有增加的干扰素(IFN)特征,可导致严重皮肤病变,进而出现溃疡、坏死,在某些情况下还会导致截肢。白塞氏病(BD)是一种多因素多基因AID,其特征为口腔生殖器溃疡、皮肤病变、葡萄膜炎反复发作,以及一种独特的累及各种大小动静脉的血管炎。许多临床特征与其他自身炎症性疾病重叠,促炎细胞因子的过度表达是该疾病的一个重要特征。