Hysa Elvis, Campitiello Rosanna, Sammorì Silvia, Gotelli Emanuele, Cere Andrea, Pesce Giampaola, Pizzorni Carmen, Paolino Sabrina, Sulli Alberto, Smith Vanessa, Cutolo Maurizio
Laboratory of Experimental Rheumatology and Academic Division of Clinical Rheumatology, Department of Internal Medicine, University of Genoa, San Martino Polyclinic, 16132 Genoa, Italy.
Autoimmunity Laboratory, Department of Internal Medicine, University of Genoa, 16132 Genoa, Italy.
Antibodies (Basel). 2023 Jan 4;12(1):3. doi: 10.3390/antib12010003.
Specific autoantibodies and nailfold videocapillaroscopy (NVC) findings are serum and morphological diagnostic hallmarks of systemic sclerosis (SSc) as well as useful biomarkers which stratify the microvascular progression and prognosis of patients.
The aim of our narrative review is to provide an update and overview of the link between SSc-related autoantibodies, used in clinical practice, and microvascular damage, evaluated by NVC, by exploring the interaction between these players in published studies. A narrative review was conducted by searching relevant keywords related to this field in Pubmed, Medline and EULAR/ACR conference abstracts with a focus on the findings published in the last 5 years.
Our search yielded 13 clinical studies and 10 pre-clinical studies. Most of the clinical studies (8/13, 61.5%) reported a significant association between SSc-related autoantibodies and NVC patterns: more specifically anti-centromere autoantibodies (ACA) were associated more often with an "Early" NVC pattern, whereas anti-topoisomerase autoantibodies (ATA) more frequently showed an "Active" or "Late" NVC pattern. Five studies, instead, did not find a significant association between specific autoantibodies and NVC findings. Among the pre-clinical studies, SSc-related autoantibodies showed different mechanisms of damage towards both endothelial cells, fibroblasts and smooth muscle vascular cells.
The clinical and laboratory evidence on SSc-related autoantibodies and microvascular damage shows that these players are interconnected. Further clinical and demographic factors (e.g., age, sex, disease duration, treatment and comorbidities) might play an additional role in the SSc-related microvascular injury whose progression appears to be complex and multifactorial.
特异性自身抗体和甲襞微血管镜检查(NVC)结果是系统性硬化症(SSc)的血清学和形态学诊断标志,也是对患者微血管病变进展和预后进行分层的有用生物标志物。
我们的叙述性综述旨在通过探索已发表研究中这些因素之间的相互作用,对临床实践中使用的SSc相关自身抗体与通过NVC评估的微血管损伤之间的联系进行更新和概述。通过在PubMed、Medline和EULAR/ACR会议摘要中搜索与该领域相关的关键词进行叙述性综述,重点关注过去5年发表的研究结果。
我们的搜索产生了13项临床研究和10项临床前研究。大多数临床研究(8/13,61.5%)报告了SSc相关自身抗体与NVC模式之间存在显著关联:更具体地说,抗着丝点自身抗体(ACA)更常与“早期”NVC模式相关,而抗拓扑异构酶自身抗体(ATA)更频繁地表现为“活动期”或“晚期”NVC模式。相反,有五项研究未发现特定自身抗体与NVC结果之间存在显著关联。在临床前研究中,SSc相关自身抗体对内皮细胞、成纤维细胞和平滑肌血管细胞均表现出不同的损伤机制。
关于SSc相关自身抗体和微血管损伤的临床和实验室证据表明,这些因素相互关联。进一步的临床和人口统计学因素(如年龄、性别、病程、治疗和合并症)可能在SSc相关微血管损伤中起额外作用,其进展似乎是复杂的且多因素的。