The immune system in multiple myeloma and precursor states: Lessons and implications for immunotherapy and interception

被引:23
|
作者
Dhodapkar, Madhav, V [1 ]
机构
[1] Emory Univ, Winship Canc Inst, Dept Hematol & Med Oncol, Atlanta, GA 30332 USA
关键词
T-CELLS; BONE-MARROW; DENDRITIC CELLS; SUPPRESSOR-CELLS; MONOCLONAL GAMMOPATHY; ANTITUMOR IMMUNITY; REGULATORY CELLS; PLASMA-CELLS; TUMOR; MICROENVIRONMENT;
D O I
10.1002/ajh.26752
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Multiple myeloma (MM) and its precursor monoclonal gammopathy of undetermined significance (MGUS) are distinct disorders that likely originate in the setting of chronic immune activation. Evolution of these lesions is impacted by cross-talk with both innate and adaptive immune systems of the host. Harnessing the immune system may, therefore, be an attractive strategy to prevent clinical malignancy. While clinical MM is characterized by both regional and systemic immune suppression and paresis, immune-based approaches, particularly redirecting T cells have shown remarkable efficacy in MM patients. Optimal application and sequencing of these new immune therapies and their integration into clinical MM management may depend on the underlying immune status, in turn impacted by host, tumor, and environmental features. Immune therapies carry the potential to achieve durable unmaintained responses and cures in MM.
引用
收藏
页码:S4 / S12
页数:9
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