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慢性淋巴细胞性脉络丛脑膜炎病毒感染期间造血移植后淋巴细胞重建的动力学

Dynamics of Lymphocyte Reconstitution After Hematopoietic Transplantation During Chronic Lymphocytic Choriomeningitis Virus Infection.

作者信息

Bhattacharyya Mitra, Penaloza-MacMaster Pablo

机构信息

Department of Microbiology-Immunology, Feinberg School of Medicine, Northwestern University , Chicago, Illinois.

出版信息

AIDS Res Hum Retroviruses. 2018 May;34(5):430-438. doi: 10.1089/AID.2017.0251. Epub 2018 Apr 18.

Abstract

Bone marrow transplantation is a treatment for various cancers and genetic diseases, and the only case of a cured HIV infection involved the use of this clinical procedure, highlighting the potential use of this therapy for curing many chronic diseases. However, little is known about how chronic viral infection influences lymphocyte reconstitution after bone marrow transplantation. To address this, we infected mice with chronic lymphocytic choriomeningitis virus, and performed bone marrow transplantation to assess lymphocyte reconstitution. Interestingly, we observed that adoptively transferred marrow cells exhibited preferential B cell differentiation in chronically infected mice. Moreover, donor marrow cells that were adoptively transferred into chronically infected mice differentiated into virus-specific CD8 T cells that were able to expand after PD-L1 blockade. Taken together, our data show that chronic viral infection induces a biased differentiation of bone marrow stem cells into B cells, and that exhausted virus-specific CD8 T cells generated de novo in this setting are rescuable by PD-1 blockade. These data contribute to the understanding of how chronic viral infection impacts lymphocyte reconstitution, and may provide valuable information to improve current hematopoietic transplantation regimens in chronically infected hosts.

摘要

骨髓移植是治疗多种癌症和遗传疾病的方法,治愈HIV感染的唯一案例涉及这一临床程序的使用,这凸显了该疗法治愈多种慢性疾病的潜在用途。然而,关于慢性病毒感染如何影响骨髓移植后的淋巴细胞重建,人们知之甚少。为了解决这个问题,我们用慢性淋巴细胞性脉络丛脑膜炎病毒感染小鼠,并进行骨髓移植以评估淋巴细胞重建。有趣的是,我们观察到,在慢性感染的小鼠中,过继转移的骨髓细胞表现出优先的B细胞分化。此外,过继转移到慢性感染小鼠体内的供体骨髓细胞分化为病毒特异性CD8 T细胞,这些细胞在阻断PD-L1后能够扩增。综上所述,我们的数据表明,慢性病毒感染诱导骨髓干细胞偏向分化为B细胞,并且在这种情况下新产生的耗竭性病毒特异性CD8 T细胞可通过阻断PD-1进行挽救。这些数据有助于理解慢性病毒感染如何影响淋巴细胞重建,并可能为改善慢性感染宿主当前的造血移植方案提供有价值的信息。

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