Reilly R M, Domingo R, Sandhu J
Division of Nuclear Medicine, Toronto Hospital, Ontario, Canada.
Clin Pharmacokinet. 1997 Apr;32(4):313-23. doi: 10.2165/00003088-199732040-00004.
Antibodies have been investigated as specific targeting agents for cancer diagnosis and therapy, to inactivate toxic substances including drugs and also as passive immunotherapy for neoplastic or infectious diseases. In most cases the antibodies were administered systemically by the intravenous route. More recently, however, there has been increasing interest in the oral administration of antibodies for localised treatment of infections or other conditions in the gastrointestinal tract. The normal physiological handling of ingested proteins is degradation by proteases in the stomach and intestine into small peptides or amino acids which are subsequently absorbed. Proteolytic enzymes involved in the degradation of orally administered immunoglobulins include pepsin, trypsin, chymotrypsin, carboxypeptidase and elastase. These enzymes initially degrade the antibodies to F(ab')2. Fab and Fc fragments. The F(ab')2 and Fab fragments, however, retain some of their neutralising activity locally in the gastrointestinal tract. Various approaches are possible to increase the stability of orally administered antibodies against proteolysis, including formulation in liposomes, coating with polymers and genetic engineering of resistant forms. The clinical application of orally administered antibodies includes the treatment and prevention of gastrointestinal infections caused by enteric pathogens such as rotavirus, Escherichia coli or Vibrio cholerae in susceptible individuals including those with immunodeficiency diseases and patients with bone marrow transplants. There is also a suggestion that such agents may be useful in preventing chemotherapy-induced gastrointestinal mucositis. Future opportunities for research include the design of oral dosage forms of antibodies which resist proteolysis and can deliver a greater fraction of immunoreactive antibody locally in the gastrointestinal tract for the treatment of infections or perhaps even to allow the absorption of antibodies for the treatment or prevention of systemic conditions.
抗体已被作为癌症诊断和治疗的特异性靶向剂进行研究,用于使包括药物在内的有毒物质失活,也作为肿瘤或传染病的被动免疫疗法。在大多数情况下,抗体通过静脉途径全身给药。然而,最近人们对口服抗体用于胃肠道感染或其他病症的局部治疗越来越感兴趣。摄入蛋白质的正常生理处理过程是在胃和肠道中被蛋白酶降解为小肽或氨基酸,随后被吸收。参与口服免疫球蛋白降解的蛋白水解酶包括胃蛋白酶、胰蛋白酶、糜蛋白酶、羧肽酶和弹性蛋白酶。这些酶最初将抗体降解为F(ab')2、Fab和Fc片段。然而,F(ab')2和Fab片段在胃肠道局部仍保留一些中和活性。有多种方法可以提高口服抗体对蛋白水解的稳定性,包括脂质体包封、聚合物包衣以及抗性形式的基因工程。口服抗体的临床应用包括治疗和预防由肠道病原体如轮状病毒、大肠杆菌或霍乱弧菌引起的胃肠道感染,易感人群包括免疫缺陷疾病患者和骨髓移植患者。也有迹象表明,此类药物可能有助于预防化疗引起的胃肠道粘膜炎。未来的研究机会包括设计抗蛋白水解的口服抗体剂型,使其能在胃肠道局部递送更大比例的免疫反应性抗体以治疗感染,甚至可能使抗体被吸收用于治疗或预防全身性疾病。