噬血细胞性淋巴组织细胞增多症
耐火材料(行星科学)
无容量
医学
免疫学
病毒
内科学
病毒学
免疫疗法
免疫系统
生物
天体生物学
疾病
作者
Pengpeng Liu,Xiangyu Pan,Chong Chen,Ting Niu,Xiao Shuai,Jian Wang,Xuelan Chen,Jiazhuo Liu,Yong Guo,Liping Xie,Yu Wu,Yu Liu,Ting Liu
出处
期刊:Blood
[American Society of Hematology]
日期:2020-01-08
卷期号:135 (11): 826-833
被引量:91
标识
DOI:10.1182/blood.2019003886
摘要
Epstein-Barr virus (EBV)-associated hemophagocytic lymphohistiocytosis (EBV-HLH) is a life-threatening hyperinflammatory syndrome triggered by EBV infection. It often becomes relapsed or refractory (r/r), given that etoposide-based regimens cannot effectively clear the virus. r/r EBV-HLH is invariably lethal in adults without allogeneic hematopoietic stem cell transplantation. Here, we performed a retrospective analysis of 7 r/r EBV-HLH patients who were treated with nivolumab on a compassionate-use basis at West China Hospital. All 7 patients tolerated the treatment and 6 responded to it. Five of them achieved and remained in clinical complete remission with a median follow-up of 16 months (range, 11.4-18.9 months). Importantly, both plasma and cellular EBV-DNAs were completely eradicated in 4 patients. Single-cell RNA-sequencing analysis showed that HLH syndrome was associated with hyperactive monocytes/macrophages and ineffective CD8 T cells with a defective activation program. Nivolumab treatment expanded programmed death protein-1-positive T cells and restored the expression of HLH-associated degranulation and costimulatory genes in CD8 T cells. Our data suggest that nivolumab, as a monotherapy, provides a potential cure for r/r EBV-HLH, most likely by restoring a defective anti-EBV response.
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