Avdeeva A S, Aleksankin A P, Chetina E V, Gorbunova Yu N, Popkova T V, Markova G A, Panafidina T A, Nasonov E L
Nasonova Research Institute of Rheumatology, Moscow, Russia.
Avtsyn Research Institute of Human Morphology of Petrovsky National Research Center of Surgery, Moscow, Russia.
Dokl Biochem Biophys. 2025 May 11. doi: 10.1134/S1607672925700073.
to evaluate subpopulations of B lymphocytes and features of interferon (IFN) status in patients with systemic lupus erythematosus (SLE), to clarify the relationship of immunological parameters with clinical manifestations of the disease.
: A total of 139 patients (123 women (88%) and 16 men (12%)) with a definite diagnosis of SLE were included in the analysis. The disease duration was 3.0 [0.3; 12.0] years, SLEDAI-2K 7 [4; 11] points, SDI 0 [0; 1] points. Immunophenotyping of peripheral blood lymphocytes, including determination of B cells, the general population of memory B cells, non-switched and switched memory B cells, naive, transient B cells, and plasmablasts was carried out using multicolor flow cytometry. IFN status was assessed by the expression of IFN-stimulated genes (MX1, RSAD2, and EPSTI1) using real-time polymerase chain reaction.
. Two immunological "patterns" were identified-the prevailing immunological mechanism of the pathogenesis of the disease (SLE) with predominant activation of type I IFN and with predominant activation of the B-cell component of the immune system. The immunological phenotype with activation of type I IFN was associated with high immunological activity, predominant skin damage, and leukopenia, whereas the phenotype with predominant activation of the B-cell component was associated with damage to the kidneys and nervous system.
. The results of the work suggest a wide variety of immune mechanisms underlying the pathogenesis of SLE. It is possible to identify a number of leading molecular "patterns" of the pathogenesis of the disease, which must be taken into account to select an effective "targeted" drug.
评估系统性红斑狼疮(SLE)患者的B淋巴细胞亚群及干扰素(IFN)状态特征,以阐明免疫参数与疾病临床表现之间的关系。
共纳入139例确诊为SLE的患者(123例女性(88%)和16例男性(12%))进行分析。病程为3.0[0.3;12.0]年,SLEDAI-2K评分为7[4;11]分,SDI评分为0[0;1]分。采用多色流式细胞术对外周血淋巴细胞进行免疫表型分析,包括测定B细胞、记忆B细胞总体、未转换和转换记忆B细胞、幼稚B细胞、瞬时B细胞和浆母细胞。通过实时聚合酶链反应检测IFN刺激基因(MX1、RSAD2和EPSTI1)的表达来评估IFN状态。
确定了两种免疫“模式”——疾病(SLE)发病机制中占主导地位的免疫机制,一种是I型IFN主要激活,另一种是免疫系统的B细胞成分主要激活。I型IFN激活的免疫表型与高免疫活性、主要的皮肤损伤和白细胞减少有关,而B细胞成分主要激活的表型与肾脏和神经系统损伤有关。
该研究结果提示SLE发病机制存在多种免疫机制。有可能确定该疾病发病机制的一些主要分子“模式”,在选择有效的“靶向”药物时必须予以考虑。