Disis Mary L, Salazar Lupe G, Knutson Keith L
Tumor Vaccine Group, Oncology, University of Washington, Seattle, WA 98195-6527, USA.
Breast Dis. 2004;20:3-11. doi: 10.3233/bd-2004-20102.
Human tumors are immunogenic and tumor-associated proteins that generate immunity in cancer patients have been defined. Many of these proteins are involved in the malignant transformation and play a role in either initiating or maintaining the malignant phenotype. Furthermore, due to technical advances in basic immunology over the last decade we have a better understanding of the immune effector cell phenotypes that are potentially involved in tumor eradication and have developed methods to quantitate and characterize these immune effectors. Breast cancer is an intriguing model tumor to target with active immunization. Dozens of breast cancer antigens have been defined [1]. Although many patients with breast cancer can be rendered free of disease with standard therapy such as surgery, radiation, and chemotherapy, some patients will have their disease recur. However, relapse may not occur for many months to years after definitive treatment giving an extended period of micrometastatic disease that may be amenable to immune eradication or modulation. Peptide based vaccines are one of the most commonly studied vaccine strategies targeting breast cancer.
人类肿瘤具有免疫原性,并且已经明确了在癌症患者中产生免疫的肿瘤相关蛋白。其中许多蛋白质参与恶性转化,并在启动或维持恶性表型中发挥作用。此外,由于过去十年基础免疫学的技术进步,我们对可能参与肿瘤根除的免疫效应细胞表型有了更好的理解,并开发了定量和表征这些免疫效应器的方法。乳腺癌是主动免疫治疗的一个有趣的模型肿瘤。已经确定了数十种乳腺癌抗原[1]。尽管许多乳腺癌患者可以通过手术、放疗和化疗等标准治疗摆脱疾病,但一些患者的疾病仍会复发。然而,在确定性治疗后的许多个月甚至数年都可能不会复发,从而产生一段可能适合免疫根除或调节的微转移疾病期。基于肽的疫苗是针对乳腺癌最常研究的疫苗策略之一。