Stevenson H C, Lacerna L V, Sugarbaker P H
Biological Response Modifiers Program, NCI-Frederick Cancer Research Facility, MD 21701.
J Clin Apher. 1988;4(2-3):118-21. doi: 10.1002/jca.2920040216.
Human blood monocytes activated by gamma interferon have been shown to be highly tumoricidal against colon cancer cells in vitro. Monocytes from patients with peritoneal colorectal carcinomatosis (PCC) were purified by a combination of cytapheresis and elutriation procedures, followed by in vitro incubation with gamma interferon for 18 hours. After debulking surgery, activated killer monocytes (AKM) were reinfused into patients' peritoneal cavities weekly for 16 weeks. To date, six patients have completed the entire protocol and three have completed maintenance therapy. All have tolerated the therapy well with acceptable toxicity. Midway through the protocol, we analyzed the trafficking pattern of the AKM by prelabeling them with 111In. Distribution was relatively homogeneous throughout the peritoneum; at the second staging celiotomy, three of the seven PCC patients were found to have very small amounts of recurrent disease in places to which the AKM were felt to have had limited access (other areas remained disease-free); these areas of recurrent disease were surgically resectable. AKM have also been infused systemically into five cancer patients. First, the patients were infused with unactivated 111In-labeled monocytes; 1 month later each patient received 111In-labeled gamma interferon-activated AKM. Trafficking studies indicated that both forms of monocytes migrated to sites in the reticuloendothelial system. We have seen virtually no complications from intravenous infusions of either unactivated or gamma interferon-activated AKM.(ABSTRACT TRUNCATED AT 250 WORDS)
γ干扰素激活的人血单核细胞已被证明在体外对结肠癌细胞具有高度的杀瘤活性。通过血细胞分离术和淘析法相结合的方法纯化来自腹膜结直肠癌(PCC)患者的单核细胞,然后在体外与γ干扰素孵育18小时。在减瘤手术后,每周将活化的杀伤单核细胞(AKM)回输到患者的腹腔中,持续16周。迄今为止,6名患者已完成整个方案,3名患者已完成维持治疗。所有患者对该治疗耐受性良好,毒性可接受。在方案进行到一半时,我们通过用111In预标记AKM来分析其迁移模式。分布在整个腹膜中相对均匀;在第二次分期剖腹探查时,7名PCC患者中有3名在AKM被认为难以到达的部位发现有非常少量的复发性疾病(其他部位无疾病);这些复发性疾病区域可通过手术切除。AKM也已全身注入5名癌症患者体内。首先,给患者注入未活化的111In标记的单核细胞;1个月后,每位患者接受111In标记的γ干扰素激活的AKM。迁移研究表明,两种形式的单核细胞都迁移到了网状内皮系统中的部位。我们几乎没有观察到静脉输注未活化或γ干扰素激活的AKM引起的并发症。(摘要截短至250字)