Early decrease of T-bet plus B cells during subcutaneous belimumab predicts response to therapy in systemic lupus erythematosus patients

被引:0
|
作者
La Gualana, Francesca [1 ]
Olivieri, Giulio [2 ]
Petriti, Begi [1 ]
Picciariello, Licia [3 ]
Natalucci, Francesco [3 ]
Sciannamea, Maddalena [1 ]
Gragnani, Laura [4 ]
Basile, Umberto [5 ]
Casato, Milvia [1 ]
Spinelli, Francesca Romana [3 ]
Stefanini, Lucia [1 ]
Basili, Stefania [1 ]
Visentini, Marcella [1 ]
Ceccarelli, Fulvia [3 ]
Conti, Fabrizio [3 ]
机构
[1] Sapienza Univ, Dept Translat & Precis Med, Viale Univ 37, I-00185 Rome, Italy
[2] Bambino Gesu Pediat Hosp, IRCCS, Res Unit Clin Immunol & Vaccinol, Rome, Italy
[3] Sapienza Univ Roma, Dipartimento Sci Clin Internist Anestesiolog & Car, Lupus Clin, Rheumatol, Viale Policlin 155, I-00161 Rome, Italy
[4] Univ Pisa, Dept Translat Res & New Technol Med & Surg, Med Sch, Pisa, Italy
[5] Santa Maria Goretti Hosp AUSL Latina, Dept Clin Pathol, Latina, Italy
关键词
Systemic lupus erythematosus; Belimumab; T -bet plus B cells; Biomarker; MIXED CRYOGLOBULINEMIA; SELECTION; ABNORMALITIES; EFFICACY; BAFF; BLYS;
D O I
10.1016/j.imlet.2024.106962
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Systemic lupus erythematosus (SLE) is characterized by B cell dysregulation and expansion of atypical B cells that may correlate with disease manifestations and activity. This study investigated the impact of subcutaneous (sc) Belimumab (BLM) on the peripheral B cell compartment and on the functional properties of CD21low, T-bet+ and CD11c+ atypical B cells, in 21 active SLE patients over a 12-month period. At baseline, active SLE patients displayed reduced unswitched IgM memory B cells and expansion of atypical B cells, compared to healthy donors and to SLE patients in remission. sc BLM therapy promptly restored B cell homeostasis with a reduction of T-bet+ B cells, observed early in patients responsive to therapy. These findings highlight the pathogenic role of T-bet+ B cells in SLE disease and suggest their potential utility as biomarker of clinical response.
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页数:10
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