Basham T Y, Kaminski M S, Kitamura K, Levy R, Merigan T C
J Immunol. 1986 Nov 1;137(9):3019-24.
Both IFN-alpha and anti-idiotype monoclonal antibody therapy have significant antitumor activity in vivo in a murine B cell lymphoma model. Combination therapy with syngeneic anti-idiotype antibody of the IgG2a or IgG2b isotype (a single i.p. injection of 100 micrograms) and recombinant human hybrid interferon-alpha A/D (10(4) to 10(6) U three times weekly for 3 wk) synergistically increased median survival time in mice challenged with a lethal dose of tumor cells compared with the sum of the median survival times of the two individual treatments. IFN-alpha has direct antiproliferative activity against 38C13 in vitro and enhances in vitro macrophage anti-idiotype antibody-specific cytolysis for IgG2a, IgG2b, and IgG1 isotypes.
在小鼠B细胞淋巴瘤模型中,干扰素-α(IFN-α)和抗独特型单克隆抗体疗法在体内均具有显著的抗肿瘤活性。将同基因的IgG2a或IgG2b亚型抗独特型抗体(单次腹腔注射100微克)与重组人杂交干扰素-α A/D(10⁴至10⁶单位,每周三次,共3周)联合治疗,与两种单独治疗的中位生存时间之和相比,协同增加了接受致死剂量肿瘤细胞攻击的小鼠的中位生存时间。IFN-α在体外对38C13具有直接的抗增殖活性,并增强了体外巨噬细胞对IgG2a、IgG2b和IgG1亚型抗独特型抗体特异性的细胞溶解作用。