Novel monoclonal antibodies: A really specific therapy for light chain amyloidosis

被引:1
|
作者
Del Giudice, Maria Livia [1 ,2 ]
Galimberti, Sara [1 ]
Buda, Gabriele [1 ]
机构
[1] Univ Pisa, Dept Clin & Expt Med, Hematol, Pisa, Italy
[2] Univ Pisa, Dept Clin & Expt Med, Hematol, I-56126 Pisa, Italy
关键词
AL amyloidosis; anselamimab; anti-amyloid directed therapy; birtamimab; CAEL001; daratumumab; AL AMYLOIDOSIS; STAGING SYSTEM; P COMPONENT; CARDIAC BIOMARKERS; PHASE; 1A/B; DEXAMETHASONE; DIAGNOSIS; 11-1F4; SAFETY;
D O I
10.1002/hon.3270
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Light chain amyloidosis is a rare disease caused by clonal plasma cells in the bone marrow generating an excessive amount of immunoglobulin light chains. These chains misfold and produce insoluble fibrils that deposit in various organs, including the heart, kidneys, liver, nervous system, and digestive tract. Life expectancy and symptoms during the course of the disease vary depending on which and how many organs are affected. Targeted plasma cell therapy has significantly advanced the clinical management of amyloidosis, with ongoing progress. However, current clinical studies are investigating innovative targets, drug combinations and treatment strategies to improve therapeutic outcomes by minimizing adverse effects and refining patient prognosis in these challenging hematological conditions. In this paper, we review the state of the art regarding the use of anti-amyloid antibodies, as a revolutionary and innovative approach in the current scenario of amyloid treatment.
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收藏
页数:6
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