| Literature DB >> 28837367 |
Piero Ruscitti1, Paola Cipriani1, Paola Di Benedetto1, Vasiliky Liakouli1, Francesco Carubbi1, Onorina Berardicurti1, Francesco Ciccia2, Giuliana Guggino2, Giovanni Triolo2, Roberto Giacomelli1.
Abstract
INTRODUCTION: Macrophage activation syndrome (MAS) is a severe, hyperinflammatory life-threatening syndrome, generally complicating different rheumatic diseases. Despite the severity of the disease, little is known about the pathogenic mechanisms and, thus, possible targeted therapies in the management of these patients. Areas covered: In this review, we aimed to update the current pathogenic knowledge of MAS, during rheumatic diseases, focusing mainly on immunologic abnormalities and on new possible therapeutic strategies. Expert commentary: The difficult pathogenic scenario of MAS, in which genetic defects, predisposing diseases, and triggers are mixed together with the high mortality rate, make it difficult to manage these patients. Although most efforts have been focused on investigating the disease in children, in recent years, several studies are trying to elucidate the possible pathogenic mechanism in adult MAS patients. In this context, genetic and immunological studies might lead to advances in the knowledge of pathogenic mechanisms and possible new therapeutic targets. In the future, the results of ongoing clinical trials are awaited in order to improve the management and, thus, the survival of these patients.Entities:
Keywords: Macrophage activation syndrome; adult onset Still’s disease; cytokine; hyperferritinemic syndrome; inflammation; macrophage; systemic juvenile idiopathic arthritis
Mesh:
Year: 2017 PMID: 28837367 DOI: 10.1080/1744666X.2017.1372194
Source DB: PubMed Journal: Expert Rev Clin Immunol ISSN: 1744-666X Impact factor: 4.473