Complement system in Anti-CD20 mAb therapy for cancer: A mini-review

被引:4
作者
Gao, Yiwen [1 ]
机构
[1] Xinjiang Prod & Construct Corps Hosp, 5 Div Hosp 84 Regiment Branch, 5 Div Hosp 84 Regiment Branch Liguo Rd, Shuanghe 833408, Peoples R China
关键词
Innate immunity; complement system; anti-CD20; anti-cancer; monoclonal antibody therapy; CHRONIC LYMPHOCYTIC-LEUKEMIA; DECAY-ACCELERATING FACTOR; IN-VITRO; MONOCLONAL-ANTIBODIES; CLASSICAL PATHWAY; HUMAN CD20; RITUXIMAB; MECHANISMS; ACTIVATION; INHIBITOR;
D O I
10.1177/03946320231181464
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The complement system is an important part of innate immunity. Through complement-dependent cytotoxicity (CDC), it plays an important role in the clearance of invading pathogens but also cancerous host cells. Therapy with anti-CD20 monoclonal antibodies (mAbs), for example, rituximab and ofatumumab, is a well-established treatment for lymphoid malignancies, and CDC is one of the main mechanisms underlying their anti-cancer activity. However, there are still some issues with the clinical application of anti-CD20 antibodies. On the one hand, anti-CD20 can cause some clinical side effects; on the other hand, anti-CD20 has low potency in some patients, and increasing the dosage does not enhance its effectiveness in these patients. Previous studies have reported that a gain-of-function in a certain complement component can boost the cytolytic activity of anti-CD20 mAbs. Through reviewing the literature on complement system control and anti-CD20 mAbs, this article aims to provide a thorough understanding of the potential of targeting complement components in lymphoma therapy.
引用
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页数:12
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