de la Barrera S S, Sasiain M C, Geffner J, Isturiz M A, Segal-Eiras A, de Bracco M M
Int J Lepr Other Mycobact Dis. 1985 Jun;53(2):218-24.
Antibody-dependent cellular cytotoxicity (ADCC) and total and alternative pathway complement (C) activity were found to be normal in lepromatous leprosy (LL) patients in the presence of elevated circulating immune complexes (CIC) measured by the 125I-Clq binding assay. Heat inactivation (56 degrees C, 30 min) uncovered the ADCC inhibitory activity of LL sera. The effect of C was exerted both by interfering with the blocking action of CIC and by recovering ADCC activity of CIC-blocked effector cells. Heat inactivation allowed the expression of total and alternative C pathway fixing ability of the LL sera. Thus, immune complexes potentially able to block Fc receptor-dependent functions or capable of fixing C can be detected in LL sera. We postulate that compensatory mechanisms such as those described in vitro may contribute to maintain intact ADCC activity in vivo.
在通过¹²⁵I-Clq结合试验检测到循环免疫复合物(CIC)升高的瘤型麻风(LL)患者中,发现抗体依赖性细胞毒性(ADCC)以及总补体和替代途径补体(C)活性均正常。热灭活(56℃,30分钟)揭示了LL血清的ADCC抑制活性。C的作用通过干扰CIC的阻断作用以及恢复被CIC阻断的效应细胞的ADCC活性来发挥。热灭活使LL血清的总补体和替代补体途径固定能力得以表达。因此,在LL血清中可检测到潜在能够阻断Fc受体依赖性功能或能够固定补体的免疫复合物。我们推测,诸如体外所描述的那些代偿机制可能有助于在体内维持完整的ADCC活性。