Extrafollicular IgD-CD27-CXCR5-CD11c-DN3 B cells infiltrate inflamed tissues in autoimmune fibrosis and in severe COVID-19

被引:25
作者
Allard-Chamard, Hugues [1 ,2 ]
Kaneko, Naoki [1 ,3 ]
Bertocchi, Alice [1 ]
Sun, Na [1 ]
Boucau, Julie [1 ]
Kuo, Hsiao-Hsuan [1 ]
Farmer, Jocelyn R. [1 ]
Perugino, Cory [1 ,4 ]
Mahajan, Vinay S. [1 ]
Murphy, Samuel J. H. [1 ]
Premo, Katherine [1 ]
Diefenbach, Thomas [1 ]
Ghebremichael, Musie [1 ]
Yuen, Grace [1 ]
Kotta, Alekhya [1 ]
Akman, Zafer [1 ]
Lichterfeld, Mathias [1 ,6 ]
Walker, Bruce D. [1 ,7 ,8 ]
Yu, Xu G. [3 ]
Moriyama, Masafumi [3 ]
Maehara, Takashi [1 ,3 ]
Nakamura, Seiji [3 ]
Stone, John H. [4 ]
Padera, Robert F. [5 ]
Pillai, Shiv [1 ]
机构
[1] MIT & Harvard, Ragon Inst MGH, Cambridge, MA 02139 USA
[2] Univ Sherbrooke, Fac med & Sci Sante, Ctr Rech Clin Etienne Le Bel, Div Rheumatol, Sherbrooke, PQ J1K 2R1, Canada
[3] Kyushu Univ, Fac Dent Sci, Div Maxillofacial Diagnost & Surg Sci, Sect Oral & Maxillofacial Oncol, Fukuoka, Japan
[4] Massachusetts Gen Hosp, Div Rheumatol Allergy & Immunol, Boston, MA 02114 USA
[5] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
[6] Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
[7] Howard Hughes Med Inst, Chevy Chase, MD 20815 USA
[8] MIT, Inst Med Engn & Sci, Dept Biol, Cambridge, MA 02139 USA
来源
CELL REPORTS | 2023年 / 42卷 / 06期
关键词
B cell depletion in disease; COVID-19; pathogenesis; CP: Immunology; DN3 B cells; double-negative B cells; extrafollicular B cells; IgG4-related disease; inflammatory fibrosis; T-B collaboration in disease;
D O I
10.1016/j.celrep.2023.112630
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Although therapeutic B cell depletion dramatically resolves inflammation in many diseases in which anti-bodies appear not to play a central role, distinct extrafollicular pathogenic B cell subsets that accumulate in disease lesions have hitherto not been identified. The circulating immunoglobulin D (IgD)-CD27- CXCR5-CD11c+ DN2 B cell subset has been previously studied in some autoimmune diseases. A distinct IgD-CD27-CXCR5-CD11c- DN3 B cell subset accumulates in the blood both in IgG4-related disease, an autoimmune disease in which inflammation and fibrosis can be reversed by B cell depletion, and in severe COVID-19. These DN3 B cells prominently accumulate in the end organs of IgG4-related disease and in lung lesions in COVID-19, and double-negative B cells prominently cluster with CD4+ T cells in these lesions. Extrafollicular DN3 B cells may participate in tissue inflammation and fibrosis in autoimmune fibrotic dis-eases, as well as in COVID-19.
引用
收藏
页数:16
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