کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5675596 1594326 2017 18 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
The current state of therapeutic and T cell-based vaccines against human papillomaviruses
موضوعات مرتبط
علوم زیستی و بیوفناوری ایمنی شناسی و میکروب شناسی ویروس شناسی
پیش نمایش صفحه اول مقاله
The current state of therapeutic and T cell-based vaccines against human papillomaviruses
چکیده انگلیسی


- HPV is a causal factor for multiple cancers and diseases.
- Preventative HPV vaccine is not effective at clearing preexisting infections.
- Therapeutic and T cell based HPV vaccines typically target oncoproteins E6 and E7.
- Several clinical trials have been performed to assess the efficacy of the vaccines.
- More trials are expected as new strategies to enhance vaccine potency are developed.

Human papillomavirus (HPV) is known to be a necessary factor for many gynecologic malignancies and is also associated with a subset of head and neck malignancies. This knowledge has created the opportunity to control these HPV-associated cancers through vaccination. However, despite the availability of prophylactic HPV vaccines, HPV infections remain extremely common worldwide. In addition, while prophylactic HPV vaccines have been effective in preventing infection, they are ineffective at clearing pre-existing HPV infections. Thus, there is an urgent need for therapeutic and T cell-based vaccines to treat existing HPV infections and HPV-associated lesions and cancers. Unlike prophylactic vaccines, which generate neutralizing antibodies, therapeutic, and T cell-based vaccines enhance cell-mediated immunity against HPV antigens. Our review will cover various therapeutic and T cell-based vaccines in development for the treatment of HPV-associated diseases. Furthermore, we review the strategies to enhance the efficacy of therapeutic vaccines and the latest clinical trials on therapeutic and T cell-based HPV vaccines.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Virus Research - Volume 231, 2 March 2017, Pages 148-165
نویسندگان
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