Durrant L G, Spendlove I
Academic Unit of Clinical Oncology, City Hospital, Nottingham, UK.
Curr Opin Investig Drugs. 2001 Jul;2(7):959-66.
Complement is an enzymatic cascade that results in the release of pro-inflammatory anaphylatoxins, C3b deposition and the assembly of the membrane attack complex (MAC), which results in cell lysis. Cells express complement regulatory proteins or inhibitors to protect themselves from bystander attack by complement. Expression of the complement-regulatory proteins CD55, CD46 and CD59 are deregulated in cancer with tumors showing loss of one or more inhibitors and strong overexpression of others. This results in tumors that are resistant to attack by complement and is a major limitation in the use of monoclonal antibodies as monotherapies. However, tumor sensitivity to complement can be restored by co-administration of antibodies that bind to the functional domains of complement-regulatory proteins. Overexpression of complement-regulatory proteins on tumors also makes them potential targets for cancer vaccines. However, these vaccines have to be carefully designed to induce immune responses that recognize inhibitors overexpressed on tumors and that do not detect the levels expressed by normal cells. A human anti-idiotypic antibody that mimics CD55 has been used successfully in over 200 colorectal cancer and osteosarcoma patients. 70% Of patients show CD55-specific immune responses with no associated toxicity. Similar vaccines targeting CD46 and CD59 would eliminate any cell overexpressing a complement inhibitor. Any remaining tumor cell or any tumor cell that loses complement-regulatory proteins in response to therapy would become highly susceptible to in situ complement deposition. In summary, targeting complement-regulatory proteins is a very attractive approach to tumor therapy, although great care must be taken in preventing normal tissue recognition as this could lead to uncontrolled complement deposition and massive cell lysis.
补体是一种酶促级联反应,可导致促炎性过敏毒素的释放、C3b沉积以及膜攻击复合物(MAC)的组装,从而导致细胞裂解。细胞表达补体调节蛋白或抑制剂以保护自身免受补体的旁观者攻击。补体调节蛋白CD55、CD46和CD59的表达在癌症中失调,肿瘤表现出一种或多种抑制剂的缺失以及其他抑制剂的强烈过表达。这导致肿瘤对补体攻击具有抗性,这是单克隆抗体作为单一疗法使用的主要限制。然而,通过共同施用与补体调节蛋白功能域结合的抗体,可以恢复肿瘤对补体的敏感性。肿瘤上补体调节蛋白的过表达也使它们成为癌症疫苗的潜在靶点。然而,这些疫苗必须经过精心设计,以诱导识别肿瘤上过表达的抑制剂且不检测正常细胞表达水平的免疫反应。一种模拟CD55的人抗独特型抗体已在200多名结直肠癌和骨肉瘤患者中成功使用。70%的患者表现出CD55特异性免疫反应且无相关毒性。针对CD46和CD59的类似疫苗将消除任何过表达补体抑制剂的细胞。任何剩余的肿瘤细胞或任何因治疗而失去补体调节蛋白的肿瘤细胞将变得极易受到原位补体沉积的影响。总之,靶向补体调节蛋白是一种非常有吸引力的肿瘤治疗方法,尽管在预防正常组织识别方面必须格外小心,因为这可能导致不受控制的补体沉积和大量细胞裂解。