Selmi Carlo
Division of Rheumatology and Clinical Immunology, Humanitas Clinical and Research Center, via A. Manzoni 56, 20089 Rozzano, Milan, Italy.
BIOMETRA Department, University of Milan, Milan, Italy.
Clin Rev Allergy Immunol. 2015 Oct;49(2):93-9. doi: 10.1007/s12016-015-8504-9.
Our PubMed search for peer-reviewed articles published in the 2014 solar year retrieved a significantly higher number of hits compared to 2013 with a net 28 % increase. Importantly, full articles related to autoimmunity constitute approximately 5 % of immunology articles. We confirm that our understanding of autoimmunity is becoming a translational paradigm with pathogenetic elements rapidly followed by new treatment options. Furthermore, numerous clinical and pathogenetic elements and features are shared among autoimmune diseases, and this is well illustrated in the recent literature. More specifically, the past year witnessed critical revisions of our understanding and management of antiphospholipid syndrome with new exciting data on the pathogenicity of the serum anti-beta2 glycoprotein autoantibody, a better understanding of the current and new treatments for rheumatoid arthritis, and new position papers on important clinical questions such as vaccinations in patients with autoimmune disease, comorbidities, or new classification criteria. Furthermore, data confirming the important connections between innate immunity and autoimmunity via toll-like receptors or the critical role of T regulatory cells in tolerance breakdown and autoimmunity perpetuation were also reported. Lastly, genetic and epigenetic data were provided to confirm that the mosaic of autoimmunity warrants a susceptible individual background which may be geographically determined and contribute to the geoepidemiology of diseases. The 2014 literature in the autoimmunity world should be cumulatively regarded as part of an annus mirabilis in which, on a different level, the 2014 Annual Meeting of the American College of Rheumatology in Boston was attended by over 16,000 participants with over selected 3000 abstracts.
我们在PubMed上搜索2014年发表的同行评审文章,与2013年相比,检索到的命中数显著增加,净增长28%。重要的是,与自身免疫相关的全文约占免疫学文章的5%。我们证实,我们对自身免疫的理解正在成为一种转化范式,发病机制元素迅速出现,随后是新的治疗选择。此外,自身免疫性疾病之间共享许多临床和发病机制元素及特征,最近的文献对此有很好的说明。更具体地说,过去一年见证了我们对抗磷脂综合征的理解和管理的重大修订,关于血清抗β2糖蛋白自身抗体致病性的新的令人兴奋的数据,对类风湿关节炎现有和新治疗方法的更好理解,以及关于自身免疫性疾病患者疫苗接种、合并症或新分类标准等重要临床问题的新立场文件。此外,还报道了通过Toll样受体证实先天免疫与自身免疫之间重要联系的数据,或T调节细胞在耐受性破坏和自身免疫持续中的关键作用。最后,提供了遗传和表观遗传数据,以证实自身免疫的全貌需要一个易感个体背景,这可能由地理因素决定,并有助于疾病的地理流行病学。2014年自身免疫领域的文献应被视为奇迹之年的一部分,在不同层面上,2014年美国风湿病学会在波士顿举行的年会有超过16000名参与者,收到了超过3000篇摘要。