Targeting CD22 for the Treatment of B-Cell Malignancies

被引:33
作者
Shah, Nikesh N. [1 ]
Sokol, Lubomir [2 ]
机构
[1] Univ S Florida, Morsani Coll Med, Dept Internal Med, Tampa, FL 33620 USA
[2] H Lee Moffitt Canc Ctr & Res Inst, Dept Malignant Hematol, 12902 USF Magnolia Dr, Tampa, FL 33612 USA
关键词
CD22; epratuzumab; inotuzumab ozogamicin; bispecific antibody; chimeric antigen receptor; lymphoma; acute lymphoblastic leukemia; ACUTE LYMPHOBLASTIC-LEUKEMIA; HUMANIZED ANTI-CD22 ANTIBODY; PHASE-II TRIAL; IMMUNOTOXIN RFB4(DSFV)-PE38 BL22; NON-HODGKINS-LYMPHOMA; INOTUZUMAB-OZOGAMICIN; ONCOLOGY-GROUP; FRACTIONATED RADIOIMMUNOTHERAPY; PREDNISONE CHEMOTHERAPY; CLINICAL ACTIVITY;
D O I
10.2147/ITT.S288546
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Immunotherapeutic agents play an increasingly important role in the treatment of B-cell malignancies. CD19 and CD20 are common targets for lymphoid malignancies, though patients who relapse have few therapeutic options remaining. CD22 is a cell surface sialoglycoprotein uniquely present on B-cells and regulates B-cell function and proliferation. Thus, it is an appealing therapeutic target for autoimmune disorders and B-cell malignancies. A variety of therapies targeting CD22 have been developed, including monoclonal antibodies, antibody-drug conjugates, radioimmunoconjugates, chimeric antigen receptor T cells, and bispecific antibodies. Here, we review the biology of CD22 and key therapies targeting CD22 in lymphoid malignancies.
引用
收藏
页码:225 / 236
页数:12
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