Haddad J G, Caldwell J G
J Clin Invest. 1972 Dec;51(12):3133-41. doi: 10.1172/JCI107140.
15 patients with Paget's bone disease were treated with varying schedules of porcine (3.8-157.5 MRCU/kg per wk) and/or salmon (1.5-210 MRCU/kg per wk) calcitonins over periods ranging from 4 to 24 months. All of the subjects experienced a striking decrease in serum alkaline phosphatase during the first 4 months of treatment. In six patients, however, resistance to these peptides was suggested by a subsequent elevation of alkaline phosphatase activity in spite of continued and augmented hormone administration. These rebounds in alkaline phosphatase levels correlated with the appearance of calcitonin-binding substances and neutralizing material in serum. Incubations of calcitonins-(125)I and sera from these six subjects resulted in the association of radioactivity with material whose behavior on chromatoelectrophoresis (6/6), sucrose density ultracentrifugation and immunoelectrophoresis (one subject) was identical with that of 7S immunoglobulin. Specific, reversible in vitro binding of salmon calcitonins-(125)I was observed in sera obtained from these patients 5 to 12 months after initiation of salmon calcitonin therapy. All six of these subjects' sera acquired the capacity to neutralize salmon calcitonin's hypocalcemic effect in rat bioassay. Neutralization titers correlated with maximal binding capacities, which ranged from 0.042 to 6.6 mg/liter of serum. Competitive displacement of calcitonins-(125)I from the sera of one patient treated with both porcine and salmon calcitonin indicated separate populations of antibodies to these hormones. In spite of return of disease activity comparable to baseline levels, 3/5 resistant subjects treated with salmon calcitonin failed to develop hypocalcemia after injection of 300-1000 MRCU of salmon calcitonin, but two of these patients developed hypocalcemia in response to the porcine hormone. The disappearance of total radioactivity from the circulation after intravenous administration of salmon calcitonin-(125)I was retarded and the amount of serum radioactivity precipitable in 50% (NH(4))(2)SO(4) greater in 3/3 resistant patients compared to control subjects. These observations on the incidence of significant titers of neutralizing antibodies to salmon (40%) and porcine (66%) calcitonins during their chronic (> 4 months) administration to man clearly indicate that an appraisal of this possibility be included in studies involving protracted use of these hormones.
15例佩吉特骨病患者接受了不同疗程的猪降钙素(3.8 - 157.5 MRCU/kg每周)和/或鲑鱼降钙素(1.5 - 210 MRCU/kg每周)治疗,疗程为4至24个月。所有受试者在治疗的前4个月血清碱性磷酸酶均显著下降。然而,6例患者尽管持续增加激素给药量,碱性磷酸酶活性随后仍升高,提示对这些肽产生了抵抗。碱性磷酸酶水平的这些反弹与血清中降钙素结合物质和中和物质的出现相关。对这6例受试者的降钙素 - (125)I与血清进行孵育,结果显示放射性与在色谱电泳(6/6)、蔗糖密度超速离心和免疫电泳(1例受试者)中行为与7S免疫球蛋白相同的物质相结合。在开始鲑鱼降钙素治疗5至12个月后从这些患者获得的血清中观察到鲑鱼降钙素 - (125)I的特异性、可逆性体外结合。这6例受试者的所有血清均获得了在大鼠生物测定中中和鲑鱼降钙素降钙作用的能力。中和效价与最大结合能力相关,最大结合能力范围为0.042至6.6 mg/升血清。对同时接受猪降钙素和鲑鱼降钙素治疗的1例患者的血清进行降钙素 - (125)I的竞争性置换,表明存在针对这些激素的不同抗体群体。尽管疾病活动恢复到与基线水平相当,但3/5接受鲑鱼降钙素治疗的抵抗患者在注射300 - 1000 MRCU鲑鱼降钙素后未出现低钙血症,但其中2例患者对猪降钙素产生了低钙血症反应。与对照受试者相比,3/3抵抗患者静脉注射鲑鱼降钙素 - (125)I后循环中总放射性的消失延迟,且50%硫酸铵((NH(4))(2)SO(4))可沉淀的血清放射性量更高。这些关于在对人长期(>4个月)给药期间鲑鱼降钙素(40%)和猪降钙素(66%)中和抗体高滴度发生率的观察清楚地表明,在涉及长期使用这些激素的研究中应评估这种可能性。