Varadhachary Atul, Wolf Jeffrey S, Petrak Karel, O'Malley Bert W, Spadaro Michela, Curcio Claudia, Forni Guido, Pericle Federica
Agennix, Inc., Houston, TX 77046, USA.
Int J Cancer. 2004 Sep 1;111(3):398-403. doi: 10.1002/ijc.20271.
In this work, we investigated the anticancer activity of orally administered recombinant human lactoferrin (rhLF) alone and in combination with chemotherapy in tumor-bearing mice. rhLF inhibited the growth of squamous cell carcinoma (O12) tumors in T cell-immunocompromised nu/nu mice by 80% when administered at 1,000 mg/kg (2.9 g/m2) by oral gavage twice daily for 8 days (p < 0.001). Similar activity was observed in syngeneic, immunocompetent BALB/c mice, where orally administered rhLF (1,000 mg/kg, 2.9 g/m2 once daily) halted the growth of mammary adenocarcinoma TUBO. Oral rhLF (200 mg/kg, 0.57 g/m2) was also used alone and in combination with cis-platinum (5 mg/kg) to treat head-and-neck squamous cell carcinoma in a syngeneic murine model. Monotherapy with oral rhLF or cis-platinum caused 61% or 66% tumor growth inhibition over placebo, respectively. Mice receiving both therapies showed 79% growth inhibition, a statistically significant improvement over each drug alone. We then demonstrated that administration of oral rhLF (300 mg/kg, 0.86 g/m2) to tumor-bearing or naive mice resulted in (i) significantly increased production of IL-18 in the intestinal tract, (ii) systemic NK cell activation and (iii) circulating CD8+ T-cell expansion. These data suggest that oral rhLF is an immunomodulatory agent active against cancer as a single agent and in combination chemotherapy, exerting its systemic effect through stimulation of IL-18 and other cytokines in the gut enterocytes. rhLF has been administered orally to 211 people without a single serious drug-related adverse event. Thus, rhLF shows promise as a safe and well-tolerated novel immunomodulatory anticancer agent.
在本研究中,我们调查了口服重组人乳铁蛋白(rhLF)单独及与化疗联合应用对荷瘤小鼠的抗癌活性。当以1000mg/kg(2.9g/m²)的剂量通过口服灌胃,每天两次,连续8天给药时,rhLF可使T细胞免疫缺陷的裸鼠(nu/nu)体内的鳞状细胞癌(O12)肿瘤生长抑制80%(p<0.001)。在同基因、具有免疫活性的BALB/c小鼠中也观察到了类似的活性,口服rhLF(1000mg/kg,2.9g/m²,每天一次)可使乳腺腺癌TUBO的生长停止。口服rhLF(200mg/kg,0.57g/m²)也单独或与顺铂(5mg/kg)联合用于同基因小鼠模型中治疗头颈部鳞状细胞癌。口服rhLF或顺铂单药治疗相对于安慰剂分别导致61%或66%的肿瘤生长抑制。接受两种治疗的小鼠显示出79%的生长抑制,相对于每种药物单独使用有统计学上的显著改善。然后我们证明,给荷瘤或未荷瘤小鼠口服rhLF(300mg/kg,0.86g/m²)会导致:(i)肠道中IL-18的产生显著增加;(ii)全身自然杀伤细胞活化;(iii)循环CD8⁺T细胞扩增。这些数据表明,口服rhLF作为单一药物和联合化疗时都是一种对癌症有效的免疫调节剂,通过刺激肠道肠细胞中的IL-18和其他细胞因子发挥其全身作用。rhLF已口服给药于211人,未发生一例严重的药物相关不良事件。因此,rhLF有望成为一种安全且耐受性良好的新型免疫调节抗癌药物。