Wang Siyu, Thitilertdecha Premrutai, Khowawisetsut Ladawan, Maneesawat Theeraporn, Chuansumrit Ampaiwan, Chokephaibulkit Kulkanya, Pattanapanyasat Kovit, Onlamoon Nattawat
Graduate Program in Immunology, Department of Immunology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand.
Siriraj Research Group in Immunobiology and Therapeutic Sciences, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand.
Viruses. 2025 Apr 8;17(4):541. doi: 10.3390/v17040541.
Little is known about the regulation of B cell subpopulations in association with programmed cell death during dengue virus (DENV) infection. Therefore, blood samples from dengue-infected patients and healthy donors were obtained for B cell subset characterization and the analysis of pro-apoptotic CD95 expression in these cell subsets. The results showed that the activated memory (AM) subset in the patients remained unchanged compared to the healthy donors. In contrast, tissue memory (TM) and antibody-secreting cells (ASCs) were notably increased, whereas naïve cells and resting memory (RM) cells were considerably decreased. Although the ASCs maintained comparably high levels of CD95 expression in both groups, significantly increased percentages of CD95-expressing cells in the other B cell subsets were found in the patients. When B cells from the healthy donors were treated with DENV non-structural protein 1 (NS1), the results showed that the NS1 protein at 2 µg/mL could induce CD95 expression and the exposure of phosphatidylserine on the cell membrane in most B cell subsets, except for the RM. This study demonstrates that DENV infection could induce CD95 expression in both activated and resting B cell subsets in all patients. The results also suggest a potential mechanism of apoptotic regulation in B cell subsets through the increased CD95 expression caused by the interaction between the B cells and the NS1 protein.
关于登革病毒(DENV)感染期间与程序性细胞死亡相关的B细胞亚群调节知之甚少。因此,采集了登革热感染患者和健康供体的血样,用于B细胞亚群特征分析以及这些细胞亚群中促凋亡蛋白CD95表达的分析。结果显示,与健康供体相比,患者体内的活化记忆(AM)亚群保持不变。相反,组织记忆(TM)和抗体分泌细胞(ASC)显著增加,而幼稚细胞和静息记忆(RM)细胞则大幅减少。虽然两组中的ASC均维持相对较高水平的CD95表达,但在患者的其他B细胞亚群中,发现表达CD95的细胞百分比显著增加。当用DENV非结构蛋白1(NS1)处理健康供体的B细胞时,结果显示,2 μg/mL的NS1蛋白可诱导大多数B细胞亚群(RM除外)中CD95的表达以及细胞膜上磷脂酰丝氨酸的暴露。本研究表明,DENV感染可在所有患者的活化和静息B细胞亚群中诱导CD95表达。结果还提示了一种B细胞亚群凋亡调节的潜在机制,即通过B细胞与NS1蛋白相互作用导致CD95表达增加来实现。