Wang X, Luo W, Ferrone S
Department of Immunology, Roswell Park Cancer Institute, Elm & Carlton Streets, Buffalo, NY 14263, USA.
Medicina (B Aires). 2000;60 Suppl 2:48-50.
The realization that tumor cells utilize multiple mechanisms to escape from immune recognition and destruction has stimulated interest in developing and applying immunotherapeutic strategies which target both humoral and cellular immunity to malignant cells. As a result, the tumor-associated antigens (TAA) used as targets have to be expressed on the cell surface membrane of malignant cells. Furthermore, since most of the TAA used for active specific immunotherapy are self-antigens, a challenge facing tumor immunologists is to develop strategies which are effective in breaking tolerance to self-antigens. This chapter describes one strategy which relies on the use of peptide mimics of the human high molecular weight-melanoma associated antigen (HMW-MAA) as immunogens to implement active specific immunotherapy in patients with malignant melanoma. These mimics, which are isolated from phage display peptide libraries by panning with anti-HMW-MAA monoclonal antibodies, are expected to induce both humoral and cellular anti-HMW-MAA immunity.
肿瘤细胞利用多种机制逃避免疫识别和破坏这一认识,激发了人们对开发和应用针对恶性细胞的体液免疫和细胞免疫的免疫治疗策略的兴趣。因此,用作靶点的肿瘤相关抗原(TAA)必须在恶性细胞的细胞膜表面表达。此外,由于用于主动特异性免疫治疗的大多数TAA都是自身抗原,肿瘤免疫学家面临的一个挑战是制定有效打破对自身抗原耐受性的策略。本章描述了一种策略,该策略依赖于使用人类高分子量黑色素瘤相关抗原(HMW-MAA)的肽模拟物作为免疫原,对恶性黑色素瘤患者实施主动特异性免疫治疗。这些模拟物是通过用抗HMW-MAA单克隆抗体淘选从噬菌体展示肽库中分离出来的,有望诱导体液和细胞抗HMW-MAA免疫。