Foss Francine M, Waldmann Thomas A
Tufts New England Medical Center, 750 Washington Street, Boston, MA 02111, USA.
Hematol Oncol Clin North Am. 2003 Dec;17(6):1449-58. doi: 10.1016/s0889-8588(03)00110-2.
Our emerging understanding of the IL-2/IL-2R system opens the possibility for more specific immunotherapy of CTCL. This understanding, taken in conjunction with the ability to produce humanized antibodies to the IL-2R subunit by genetic engineering; to arm these antibodies, as well as IL-2 itself with toxins or with alpha- and beta-emitting radionuclides; and to modulate IL-2R subunits to optimize targeting of these agents provides a rational therapeutic strategy for the treatment of IL-2R-expressing CTCL. Although most of these studies were conducted in HTLV-1-associated T-cell lymphomas or CTCL, it is likely that these agents may be applicable to other T-cell lymphomas, including the anaplastic large cell lymphomas, peripheral T-cell lymphomas, and the natural killer lymphomas, because these cells express the IL-2 receptor.
我们对白细胞介素-2/白细胞介素-2受体(IL-2/IL-2R)系统的新认识为蕈样肉芽肿(CTCL)的更特异性免疫治疗开辟了可能性。这种认识,结合通过基因工程生产针对IL-2R亚基的人源化抗体的能力;用毒素或发射α和β射线的放射性核素武装这些抗体以及IL-2本身;以及调节IL-2R亚基以优化这些药物的靶向性,为治疗表达IL-2R的CTCL提供了一种合理的治疗策略。尽管这些研究大多是在与人类T淋巴细胞白血病病毒1型(HTLV-1)相关的T细胞淋巴瘤或CTCL中进行的,但这些药物很可能适用于其他T细胞淋巴瘤,包括间变性大细胞淋巴瘤、外周T细胞淋巴瘤和自然杀伤细胞淋巴瘤,因为这些细胞表达IL-2受体。