Hoheisel G, Roth M, Chan C H, Ruff P W, Tsakiris D A, Hornung M, Perruchoud A P
Department of Research, University of Basel, Switzerland.
Tuber Lung Dis. 1994 Dec;75(6):441-6. doi: 10.1016/0962-8479(94)90118-X.
Human mononuclear cells from a previously sensitized donor generate procoagulant activity (PCA) following stimulation with purified protein derivative (PPD). Lymphocytes of tuberculous pleural effusions are also highly responsive to PPD stimulation. We examined the influence of cryopreservation on lymphocytes following stimulation with PPD.
Peripheral blood lymphocytes of 5 healthy PPD skin test positive subjects were incubated with either PPD, thromboplastin, or concanavalin A (Con A) at concentrations of 0, 1, and 10 micrograms/ml. PCA was determined by measuring the recalcification time. Tests were repeated following cryopreservation for 4 weeks.
Incubation of fresh lymphocytes led to a dose dependent shortening of recalcification time: PPD (0-1-10 micrograms/ml: 100-84-65%), thromboplastin (0-1-10 micrograms/ml: 100-85-62%), and Con A (0-1-10 micrograms/ml: 100-85-42%). These results were highly reproducible when tests were repeated 6 weeks later. Cryopreservation did not significantly affect the expression of PCA following incubation with PPD and with thromboplastin. In contrast, cryopreservation significantly diminished the degree of Con A generated PCA.
Cryopreservation and storage of human lymphocytes is possible without alteration of PCA expression following their incubation with PPD or thromboplastin.
来自先前致敏供体的人单核细胞在用纯化蛋白衍生物(PPD)刺激后会产生促凝血活性(PCA)。结核性胸腔积液中的淋巴细胞对PPD刺激也高度敏感。我们研究了冷冻保存对PPD刺激后淋巴细胞的影响。
将5名PPD皮肤试验阳性的健康受试者的外周血淋巴细胞与浓度为0、1和10微克/毫升的PPD、凝血活酶或刀豆球蛋白A(Con A)一起孵育。通过测量复钙时间来测定PCA。在冷冻保存4周后重复进行测试。
新鲜淋巴细胞孵育导致复钙时间呈剂量依赖性缩短:PPD(0 - 1 - 10微克/毫升:100 - 84 - 65%)、凝血活酶(0 - 1 - 10微克/毫升:100 - 85 - 62%)和Con A(0 - 1 - 10微克/毫升:100 - 85 - 42%)。6周后重复测试时,这些结果具有高度可重复性。冷冻保存对与PPD和凝血活酶孵育后的PCA表达没有显著影响。相比之下,冷冻保存显著降低了Con A产生的PCA程度。
人淋巴细胞的冷冻保存和储存是可行的,在用PPD或凝血活酶孵育后PCA表达不会改变。