Khoder Ahmad, Alsuliman Abdullah, Basar Rafet, Sobieski Catherine, Kondo Kayo, Alousi Amin Majid, Szydlo Richard, Muftuoglu Muharrem, Shaim Hila, Apperley Jane F, Gokdemir Elif, Cooper Nichola, Mehta Rohtesh S, Marin David, Champlin Richard, Shpall Elizabeth, Rezvani Katayoun
Department of Haematology, Imperial College London, London, United Kingdom.
Stem Cell Transplantation and Cellular Therapy, University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Front Immunol. 2018 Jan 12;8:1937. doi: 10.3389/fimmu.2017.01937. eCollection 2017.
Chronic graft-versus-host disease (cGvHD) remains a major complication of allogeneic hematopoietic stem cell transplantation (HSCT). A number of studies support a role for B cells in the pathogenesis of cGvHD. In this study, we report the presence of an expanded population of CD19+CD21- B cells with features of exhaustion in the peripheral blood of patients with cGvHD. CD21- B cells were significantly increased in patients with active cGvHD compared to patients without cGvHD and healthy controls (median 12.2 versus 2.12 versus 3%, respectively; < 0.01). Compared with naïve (CD27-CD21+) and classical memory (CD27+CD21+) B cells, CD19+CD21- B cells in cGvHD were CD10 negative, CD27 negative and CD20hi, and exhibited features of exhaustion, including increased expression of multiple inhibitory receptors such as FCRL4, CD22, CD85J, and altered expression of chemokine and adhesion molecules such as CD11c, CXCR3, CCR7, and CD62L. Moreover, CD21- B cells in cGvHD patients were functionally exhausted and displayed poor proliferative response and calcium mobilization in response to B-cell receptor triggering and CD40 ligation. Finally, the frequencies of circulating CD21- B cells correlated with cGvHD severity in patients after HSCT. Our study further characterizes B cells in chronic cGVHD and supports the use of CD21-CD27-CD10- B cell frequencies as a biomarker of disease severity.
慢性移植物抗宿主病(cGvHD)仍然是异基因造血干细胞移植(HSCT)的主要并发症。多项研究支持B细胞在cGvHD发病机制中发挥作用。在本研究中,我们报告了cGvHD患者外周血中存在一群扩增的具有耗竭特征的CD19⁺CD21⁻ B细胞。与无cGvHD的患者及健康对照相比,活动性cGvHD患者的CD21⁻ B细胞显著增加(中位数分别为12.2%、2.12%和3%;P<0.01)。与幼稚(CD27⁻CD21⁺)和经典记忆(CD27⁺CD21⁺)B细胞相比,cGvHD患者的CD19⁺CD21⁻ B细胞CD10阴性、CD27阴性且CD20高表达,并表现出耗竭特征,包括多种抑制性受体如FCRL4、CD22、CD85J表达增加,以及趋化因子和黏附分子如CD11c、CXCR3、CCR7和CD62L表达改变。此外,cGvHD患者的CD21⁻ B细胞功能耗竭,对B细胞受体触发和CD40连接的增殖反应及钙动员能力较差。最后,HSCT后患者循环CD21⁻ B细胞的频率与cGvHD严重程度相关。我们的研究进一步明确了慢性cGVHD中的B细胞特征,并支持将CD21⁻CD27⁻CD10⁻ B细胞频率作为疾病严重程度的生物标志物。