Worku S, Hoft D F
Vaccine Treatment and Evaluation Unit, Department of Internal Medicine, Saint Louis University Health Sciences Center, St. Louis, MO 63110, USA.
Clin Infect Dis. 2000 Jun;30 Suppl 3:S257-61. doi: 10.1086/313887.
We investigated the ability of T cells expanded with mycobacterial antigens from healthy purified protein derivative-reactive donors and bacille Calmette-Guérin (BCG)-vaccinated volunteers to inhibit intracellular growth of BCG. Peripheral blood mononuclear cells were incubated for 7 days with mycobacterial whole lysate, live BCG, tetanus toxoid as control antigen, or medium alone. Autologous monocytes were separated by plastic adherence, allowed to mature for 6 days, and infected with BCG before serving as target cells. Expanded effector cells were cocultured with target cells for 72 h. Cocultures were then treated with 0.2% saponin to lyse infected monocytes and release intracellular BCG. Quantities of viable BCG present in these lysates were studied by colony-forming unit counting and radiometric labeling. We reproducibly found that lymphocytes expanded with mycobacterial whole lysate or live BCG significantly inhibited the intracellular growth of BCG, compared with lymphocytes expanded with tetanus toxoid or rested in medium. In addition, BCG vaccination enhanced the ability of T cells to inhibit intracellular mycobacterial growth in 3 of 5 volunteers. This assay may be useful for estimates of protective immunity induced by tuberculosis vaccines in human trials.
我们研究了从健康的纯化蛋白衍生物反应性供体和卡介苗(BCG)接种志愿者中分离出的、用分枝杆菌抗原扩增的T细胞抑制卡介苗细胞内生长的能力。外周血单个核细胞分别与分枝杆菌全菌体裂解物、活卡介苗、作为对照抗原的破伤风类毒素或仅与培养基一起孵育7天。通过塑料贴壁法分离自体单核细胞,使其成熟6天,并用卡介苗感染后作为靶细胞。将扩增的效应细胞与靶细胞共培养72小时。然后用0.2%的皂素处理共培养物,以裂解被感染的单核细胞并释放细胞内的卡介苗。通过菌落形成单位计数和放射性标记研究这些裂解物中活卡介苗的数量。我们反复发现,与用破伤风类毒素扩增或在培养基中静置的淋巴细胞相比,用分枝杆菌全菌体裂解物或活卡介苗扩增的淋巴细胞能显著抑制卡介苗的细胞内生长。此外,在5名志愿者中有3名,卡介苗接种增强了T细胞抑制细胞内分枝杆菌生长的能力。该检测方法可能有助于在人体试验中评估结核病疫苗诱导的保护性免疫。