دانلود رایگان مقاله انگلیسی پیشرفت در ایمونوتراپی برای ملانوما - هینداوی 2017

عنوان فارسی
پیشرفت در ایمونوتراپی برای ملانوما: یک بررسی جامع
عنوان انگلیسی
Advances in Immunotherapy for Melanoma: A Comprehensive Review
صفحات مقاله فارسی
0
صفحات مقاله انگلیسی
15
سال انتشار
2017
نشریه
هینداوی - Hindawi
فرمت مقاله انگلیسی
PDF
کد محصول
E5936
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پزشکی
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ایمنی شناسی
مجله
واسطه های التهاب - Mediators of Inflammation
دانشگاه
Dermatology Service - Hospital do Meixoeiro and University of Vigo - Vigo - Spain
۰.۰ (بدون امتیاز)
امتیاز دهید
چکیده

Melanomas are tumors originating from melanocytes and tend to show early metastasis secondary to the loss of cellular adhesion in the primary tumor, resulting in high mortality rates. Cancer-specific active immunotherapy is an experimental form of treatment that stimulates the immune system to recognize antigens on the surface of cancer cells. Current experimental approaches in immunotherapy include vaccines, biochemotherapy, and the transfer of adoptive T cells and dendritic cells. Several types of vaccines, including peptide, viral, and dendritic cell vaccines, are currently under investigation for the treatment of melanoma. These treatments have the same goal as drugs that are already used to stimulate the proliferation of T lymphocytes in order to destroy tumor cells; however, immunotherapies aim to selectively attack the tumor cells of each patient. In this comprehensive review, we describe recent advancements in the development of immunotherapies for melanoma, with a specific focus on the identification of neoantigens for the prediction of their elicited immune responses. This review is expected to provide important insights into the future of immunotherapy for melanoma.

نتیجه گیری

6. Conclusion


Advances in immuno-oncology have improved our understanding of the interaction between the immune system, cancer cells, and the tumor microenvironment, and application of these discoveries has great significance for the treatment of melanoma. Treatments based on molecular inhibitors are only effective in some patients. However, rational combinations between new immunotherapy technologies and immunotherapeutic agents are currently being evaluated. In addition, tumors can create antigens and neoantigens that are very different from those of normal tissues; thus, elucidating these differences may be the key for developing customized immunological strategies with decreased side effects and increased immune responses. One important field to develop is prophylactic vaccination for the prevention of melanoma. In the foreseeable future, prophylactic vaccines will probably only be used to a limited extent. Thus, current research efforts are primarily aimed at the development of therapeutic vaccines that can reduce the tumor volume or provide protection against relapse in patients who have already had cancer. The ultimate goal is to achieve effective therapies for metastatic disease. Moreover, the presence of tumor-infiltrating mononuclear cells (TIMC) and the absence of PD-L1 are reportedly associated with a better response to treatment. Thus, TIM-3, LAG-3, and CEACAM1 are some molecules that can be blocked by monoclonal antibodies. Agents capable of inhibiting immunosuppressive metabolites, such as IDO or arginase, could also be considered for therapy.


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