Talbot P J, Buchmeier M J
Immunology. 1987 Apr;60(4):485-9.
Two neutralizing monoclonal hybridoma antibodies to the surface spike glycoprotein E2 of the JHM strain of murine hepatitis virus were injected into homologous BALB/c mice, and their biological half-lives were determined by sequential titration of plasma samples in a virus-specific enzyme immunoassay. Intravascular half-lives of monomeric immunoglobulins were estimated at 8.0 +/- 1.5 days for antibody 5B19.3, an IgG1, and 12.7 +/- 2.4 days for antibody 4B11.6, an IgG2a. These catabolic rates are statistically different from each other (P less than 0.001) and significantly higher than previously reported values, which were all obtained with radiolabelled polyclonal or myeloma immunoglobulins of unknown specificities. Failure to remove aggregated 4B11.6 antibodies by high-speed centrifugation yielded a statistically significant acceleration of biological turnover (half-life 9.9 +/- 1.6 days; P less than 0.01).
将两种针对鼠肝炎病毒JHM株表面刺突糖蛋白E2的中和性单克隆杂交瘤抗体注射到同源的BALB/c小鼠体内,并通过在病毒特异性酶免疫测定中对血浆样本进行连续滴定来确定它们的生物半衰期。对于IgG1抗体5B19.3,单体免疫球蛋白的血管内半衰期估计为8.0±1.5天,对于IgG2a抗体4B11.6,血管内半衰期估计为12.7±2.4天。这些分解代谢率在统计学上彼此不同(P小于0.001),并且显著高于先前报道的值,先前的值均通过放射性标记的、特异性未知的多克隆或骨髓瘤免疫球蛋白获得。通过高速离心未能去除聚集的4B11.6抗体,导致生物周转率在统计学上显著加快(半衰期9.9±1.6天;P小于0.01)。