Primer on tumor immunology and cancer immunotherapy

Journal for ImmunoTherapy of Cancer

Charles G Drake¹  Timothy J Harris² 

[1] Department of Oncology and Brady Urological Institute, Johns Hopkins University School of Medicine and Sidney Kimmel Comprehensive Cancer Center, 1650 Orleans St., CRB I #410, Baltimore, MD 21231, USA;Department of Radiation Oncology & Molecular Radiation Sciences, Johns Hopkins University School of Medicine and Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD, USA

关键词: Adoptive T cell therapy;    Immune checkpoint;    Cancer vaccine;    Immunotherapy;   

Others  :  815008
DOI  :  10.1186/2051-1426-1-12

 received in 2013-04-04, accepted in 2013-07-10,  发布年份 2013

【 摘 要 】

Individualized cancer therapy is a central goal of cancer biologists. Immunotherapy is a rational means to this end—because the immune system can recognize a virtually limitless number of antigens secondary to the biology of genetic recombination in B and T lymphocytes. The immune system is exquisitely structured to distinguish self from non-self, as demonstrated by anti-microbial immune responses. Moreover the immune system has the potential to recognize self from “altered-self”, which is the case for cancer. However, the immune system has mechanisms in place to inhibit self-reactive responses, many of which are usurped by evolving tumors. Understanding the interaction of cancer with the immune system provides insights into mechanisms that can be exploited to disinhibit anti-tumor immune responses. Here, we summarize the 2012 SITC Primer, reviewing past, present, and emerging immunotherapeutic approaches for the treatment of cancer—including targeting innate versus adaptive immune components; targeting and/or utilizing dendritic cells and T cells; the role of the tumor microenvironment; and immune checkpoint blockade.

【 授权许可】

   
2013 Harris and Drake; licensee BioMed Central Ltd.

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