Vaccination against Her-2/neu, with focus on peptide-based vaccines

被引:27
|
作者
Tobias, J. [1 ]
Garner-Spitzer, E. [1 ]
Drinic, M. [1 ]
Wiedermann, U. [1 ]
机构
[1] Med Univ Vienna, Ctr Pathophysiol Infectiol & Immunol, Inst Specif Prophylaxis & Trop Med, Kinderspitalgasse 15, A-1090 Vienna, Austria
关键词
cancer; Her-2/neu; vaccination; T-cell peptide vaccine; B-cell peptide vaccine/mimotopes; HER2-POSITIVE BREAST-CANCER; CELL-ELICITING VACCINE; CLINICAL-TRIAL; MONOCLONAL-ANTIBODIES; TYROSINE KINASES; NELIPEPIMUT-S; IN-VIVO; TRASTUZUMAB; GROWTH; PERTUZUMAB;
D O I
10.1016/j.esmoop.2021.100361
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Immunotherapy has been a milestone in combatting cancer, by complementing or even replacing classic treatments like surgery, chemotherapy, radiation, and anti-hormonal therapy. In 15%-30% of breast cancers, overexpression of the human epidermal growth factor receptor 2 (Her-2/neu) is associated with more aggressive tumor development. Passive immunization/immunotherapy with the recombinantly produced Her-2/neu-targeting monoclonal antibodies (mAbs) pertuzumab and trastuzumab has been shown to effectively treat breast cancer and lead to a significantly better prognosis. However, allergic and hypersensitivity reactions, cardiotoxicity, development of resistance, lack of immunological memory which results in continuous application over a long period, and cost-intensiveness are among the drawbacks associated with this treatment. Furthermore, intrinsic or acquired resistance is associated with the application of therapeutic mAbs, leading to the disease recurrence. Conversely, these drawbacks could be potentially overcome by vaccination, i.e. an active immunization/immunotherapy approach by activating the patient's own immune system to target cancer, along with inducing immunological memory. This review aims to summarize the main approaches investigated and undertaken for the production of Her-2/neu vaccine candidates, with the main focus on peptide-based vaccines and their evaluation in clinical settings.
引用
收藏
页数:12
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