Hwang C, Sanda M G
Department of Surgery/Urology, University of Michigan School of Medicine, Ann Arbor 48109, USA.
Curr Opin Mol Ther. 1999 Aug;1(4):471-9.
Prostate cancer is a disease that may be amenable to immunotherapy approaches, as evidenced by the ability to induce human cytotoxic immune responses against prostate cancer cells. Recent interest in recombinant poxvirus vaccines coupled with the need for new prostate cancer therapies has led to the development of several recombinant poxvirus agents designed for prostate cancer treatment. Whether these agents will be effective in treating prostate cancer is under investigation in several ongoing and upcoming clinical trials. In the meantime, data from preclinical tumor models have provided information that may aid in improving recombinant poxviruses for clinical use. While animal studies have shown the ability of recombinant poxvirus vaccination to induce an immune response that protects against lethal tumor, these antitumor effects are variable and depend on a number of factors. Co-expression of immunomodulating gene products, such as cytokines and costimulatory molecules, have been shown to influence antitumor immunity; in fact, cytokine delivery alone can be enough to protect against tumor-related death. Patterns and levels of recombinant antigen expression also affect the immune response to that antigen, as seen by studies of various poxvirus promoters and cell compartment-targeting sequences. In addition, vaccine strategies targeting self-antigens have shown that immunological tolerance can negatively impact the induction of antitumor and antigen-specific immunity. Although vaccinia virus has been most intensely studied thus far, other poxviruses, including fowlpox and canarypox, are also promising vaccine candidates. These alternative vectors may circumvent some of the disadvantages associated with vaccinia virus, such as pre-existing vaccinia immunity. A deeper understanding of these factors and others that impact the development of antitumor immunity will be necessary to guide the development of recombinant poxviruses for prostate cancer therapy.
前列腺癌是一种可能适合免疫治疗方法的疾病,这一点可通过诱导针对前列腺癌细胞的人细胞毒性免疫反应的能力得到证明。最近对重组痘病毒疫苗的兴趣,再加上对新的前列腺癌治疗方法的需求,导致了几种设计用于前列腺癌治疗的重组痘病毒制剂的开发。这些制剂是否能有效治疗前列腺癌正在几项正在进行和即将开展的临床试验中进行研究。与此同时,临床前肿瘤模型的数据提供了可能有助于改进用于临床的重组痘病毒的信息。虽然动物研究表明重组痘病毒疫苗接种能够诱导免疫反应以预防致死性肿瘤,但这些抗肿瘤作用是可变的,并且取决于许多因素。免疫调节基因产物(如细胞因子和共刺激分子)的共表达已被证明会影响抗肿瘤免疫;事实上,仅细胞因子递送就足以预防肿瘤相关死亡。重组抗原表达的模式和水平也会影响对该抗原的免疫反应,各种痘病毒启动子和细胞区室靶向序列研究即表明了这一点。此外,针对自身抗原的疫苗策略表明,免疫耐受会对抗肿瘤和抗原特异性免疫的诱导产生负面影响。虽然迄今为止对痘苗病毒的研究最为深入,但其他痘病毒,包括禽痘病毒和金丝雀痘病毒,也是很有前景的疫苗候选物。这些替代载体可能会规避与痘苗病毒相关的一些缺点,例如预先存在的痘苗免疫力。为了指导用于前列腺癌治疗的重组痘病毒的开发,有必要更深入地了解这些因素以及其他影响抗肿瘤免疫发展的因素。