Nishio Junko, Sato Hiroshi, Watanabe Eri, Masuoka Hiroaki, Aoki Kotaro, Kawazoe Mai, Wakiya Risa, Yamada Soichi, Muraoka Sei, Masuoka Shotaro, Hayashi Tomoki, Mizutani Satoshi, Yamada Zento, Koshiba Keiko, Irita Izumi, Kanaji Miwa, Furukawa Karin, Yajima Nobuyuki, Dobashi Hiroaki, Hirose Wataru, Ishii Yoshikazu, Suda Wataru, Nanki Toshihiro
Division of Rheumatology, Department of Internal Medicine, Toho University School of Medicine, 6-11-1 Omori-Nishi, Ota-ku, Tokyo, 143-8541, Japan.
Department of Immunopathology and Immunoregulation, Toho University School of Medicine, 5-21-16 Omori-Nishi, Ota-ku, Tokyo, 143-8540, Japan.
Sci Rep. 2024 Dec 30;14(1):32076. doi: 10.1038/s41598-024-83835-0.
Altered gut microbiota is linked to systemic lupus erythematosus (SLE), but its association with disease development, disease activity, and post-intervention changes remains unclear. We compared new-onset SLE (NOSLE, n = 25), SLE in remission (RemSLE, n = 30), and healthy controls (HC, n = 30) cross-sectionally and conducted the first longitudinal analysis of NOSLE patients (n = 22) from pre-intervention to remission over 12 months. Significant β-diversity differences were observed in both NOSLE and RemSLE compared to HC, but not between NOSLE and RemSLE. Only four operational taxonomic units (OTUs) were enriched in NOSLE versus HC. However, 26 OTUs, including butyrate-producing bacteria (BPB), were depleted, and seven (including five BPBs) remained depleted in RemSLE compared to HC. OTUs positively and negatively correlated with disease activity were also identified. Longitudinal analysis revealed a reversal of several OTUs altered at onset and an increase in Streptococci, unrelated to the disease. Significant β-diversity differences were observed in patients with anti-SSA or anti-RNP antibodies and those with complement reduction compared to their counterparts. Our study identified gut microbiota alterations, including BPB depletion, in SLE regardless of onset or remission status, bacteria linked to disease activity, and a reversal of disease-associated bacteria along with the enrichment of Streptococci through intervention.
肠道微生物群的改变与系统性红斑狼疮(SLE)有关,但其与疾病发展、疾病活动及干预后变化之间的关联仍不明确。我们对新发SLE患者(NOSLE,n = 25)、缓解期SLE患者(RemSLE,n = 30)和健康对照者(HC,n = 30)进行了横断面比较,并对22例NOSLE患者从干预前到12个月缓解期进行了首次纵向分析。与HC相比,NOSLE和RemSLE均观察到显著的β多样性差异,但NOSLE与RemSLE之间未观察到差异。与HC相比,NOSLE中仅4个可操作分类单元(OTU)富集。然而,26个OTU,包括产丁酸菌(BPB)减少,与HC相比,RemSLE中有7个OTU(包括5个BPB)仍减少。还确定了与疾病活动呈正相关和负相关的OTU。纵向分析显示,发病时改变的几个OTU出现逆转,且链球菌增加,这与疾病无关。与相应对照相比,抗SSA或抗RNP抗体阳性及补体降低的患者观察到显著的β多样性差异。我们的研究确定了SLE患者肠道微生物群的改变,包括BPB减少,无论发病或缓解状态如何,均存在与疾病活动相关的细菌,以及通过干预疾病相关细菌的逆转和链球菌的富集。