Hoffman R W, Greidinger E L
Division of Immunology and Rheumatology, University of Missouri and Department of Veterans Affairs Medical Center, Columbia 64212, USA.
Curr Opin Rheumatol. 2000 Sep;12(5):386-90. doi: 10.1097/00002281-200009000-00006.
A defining feature of mixed connective tissue disease (MCTD) is the presence of antibodies against the U1-ribonucleoprotein (RNP) complex, but other autoantibodies in MCTD have recently been described. Research has also further elucidated the immune responses directed against U1-RNP in humans and in murine models of disease. Hypotheses implicating modified self-antigens and/or infectious agents in the pathogenesis of MCTD have been advanced. Links between the immunologic and clinical phenomena in MCTD are emerging. Longitudinal study of patients with MCTD highlights the impact of pulmonary hypertension on disease outcome.
混合性结缔组织病(MCTD)的一个决定性特征是存在针对U1核糖核蛋白(RNP)复合物的抗体,但最近已发现MCTD中还有其他自身抗体。研究还进一步阐明了人类和疾病小鼠模型中针对U1-RNP的免疫反应。关于修饰的自身抗原和/或感染因子参与MCTD发病机制的假说也已提出。MCTD中免疫现象与临床现象之间的联系正在显现。对MCTD患者的纵向研究突出了肺动脉高压对疾病转归的影响。