检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:Nadir Kadri Syivie Amu llen lacobaeus Erik Boberg Katarina Le Blanc
机构地区:[1]Department of Laboratory Medicine,Karolinska Institutet,Stockholm,Sweden [2]Department of Clinical Neuroscience,Division of Neurology,Karolinska Institute and Karolinska University Hospital,Stockholm,Sweden [3]Department of Haematology,Karolinska University Hospital,Stockholm,Sweden [4]Department of Cell Therapies and Allogeneic Stem Cell Transplantation Karolinska University Hospital,Stockholm,Sweden
出 处:《Cellular & Molecular Immunology》2023年第6期613-625,共13页中国免疫学杂志(英文版)
摘 要:Graft versus host disease(GvHD)is the clinical condition in which bone marrow-derived mesenchymal stromal cells(MsCs)have been most frequently studied.In this review,we summarize the experience from clinical trials that have paved the way to translation.While MsC-based therapy has shown an exceptional safety profile,identifying potency assays and disease biomarkers that reliably predict the capacity of a specific MSC batch to alleviate GvHD has been difficult.As GvHD diagnosis and staging are based solely on clinical criteria,individual patients recruited in the same clinical trial may have vastly different underlying biology,obscuring trial outcomes and making it difficult to determine the benefit of MsCs in subgroups of patients.An accumulating body of evidence indicates the importance of considering not only the cell product but also patient-specific biomarkers and/or immune characteristics in determining MSC responsiveness.A mode of action where intravascular MSC destruction is followed by monocyte-efferocytosis-mediated skewing of the immune repertoire in a permissive inflammatory environment would both explain why cell engraftment is irrelevant for MsC efficacy and stress the importance of biologic differences between responding and nonresponding patients.We recommend a combined analysis of clinical outcomes and both biomarkers of disease activity and MSC potency assays to identify patients with GvHD who are likely to benefit from MSC therapy.
关 键 词:MSC GVHD Hematological malignancies acute GVHD chronic GVHD
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:3.16.75.169