Autoimmunity associated with immunotherapy of cancer

被引:142
作者
Amos, Sally M. [1 ]
Duong, Connie P. M. [1 ]
Westwood, Jennifer A. [1 ]
Ritchie, David S. [2 ]
Junghans, Richard P. [3 ]
Darcy, Phillip K. [1 ,4 ,5 ]
Kershaw, Michael H. [1 ,4 ,5 ]
机构
[1] Peter MacCallum Canc Ctr, Canc Immunol Res Program, Melbourne, Vic 3002, Australia
[2] Peter MacCallum Canc Ctr, Dept Hematol & Med Oncol, Melbourne, Vic 3002, Australia
[3] Roger Williams Med Ctr, Providence, RI USA
[4] Univ Melbourne, Dept Pathol, Melbourne, Vic, Australia
[5] Monash Univ, Dept Immunol, Clayton, Vic, Australia
基金
英国医学研究理事会;
关键词
CHRONIC LYMPHOCYTIC-LEUKEMIA; ACUTE MYELOID-LEUKEMIA; TUMOR-INFILTRATING LYMPHOCYTES; CHIMERIC ANTIGEN RECEPTOR; COLONY-STIMULATING FACTOR; INTERFERON-ALPHA THERAPY; HIGH-DOSE INTERLEUKIN-2; MANTLE-CELL LYMPHOMA; VERSUS-HOST-DISEASE; RESECTED STAGE-III;
D O I
10.1182/blood-2011-01-325266
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
In this age of promise of new therapies for cancer, immunotherapy is emerging as an exciting treatment option for patients. Vaccines and cytokines are being tested extensively in clinical trials, and strategies using monoclonal antibodies and cell transfer are mediating dramatic regression of tumors in patients with certain malignancies. However, although initially advocated as being more specific for cancer and having fewer side effects than conventional therapies, it is becoming increasingly clear that many immunotherapies can lead to immune reactions against normal tissues. Immunotoxicities resulting from treatment can range from relatively minor conditions, such as skin depigmentation, to severe toxicities against crucial organ systems, such as liver, bowel, and lung. Treatment-related toxicity has correlated with better responses in some cases, and it is probable that serious adverse events from immune-mediated reactions will increase in frequency and severity as immunotherapeutic approaches become more effective. This review introduces immunotherapeutic approaches to cancer treatment, provides details of toxicities arising from therapy, and discusses future potential ways to avoid or circumvent these side effects. (Blood. 2011;118(3):499-509)
引用
收藏
页码:499 / 509
页数:11
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