Moreau J F, Bonneville M, Peyrat M A, Godard A, Jacques Y, Desgranges C, Soulillou J P
J Clin Invest. 1986 Oct;78(4):874-9. doi: 10.1172/JCI112674.
Mechanically harvested lymphocytes invading an irreversibly rejected human kidney allograft were seeded at limiting dilution to calculate the frequency of growing precursors. Optimal growth frequency (1/13) was obtained when Epstein-Barr virus (EBV)-transformed donor B lymphocytes were used as stimulators (D-BLCL) in the presence of interleukin 2 (IL-2). The 55 clones analyzed were all T11+ and T3+, and all expressed DR antigens (45% were T8+ and 55% T4+). Only one clone had a double-labeled (T4+ T8+) surface. All cells proliferated significantly against D-BLCL, although T4+ clones had a significantly shorter average doubling time than T8+ clones. Nearly all T8+ clones were specifically cytotoxic for D-BLCL, while both T4 and T8 did not react against K562, autologous EBV-BLCL, and third-party EBV-BLCL. Detectable IL-2 was found in the culture supernatants of only a minority of clones (all T4+).
将机械收获的侵入不可逆排斥的人肾移植器官的淋巴细胞以有限稀释度接种,以计算生长前体细胞的频率。当在白细胞介素2(IL-2)存在下,使用爱泼斯坦-巴尔病毒(EBV)转化的供体B淋巴细胞作为刺激物(D-BLCL)时,可获得最佳生长频率(1/13)。分析的55个克隆均为T11+和T3+,且均表达DR抗原(45%为T8+,55%为T4+)。只有一个克隆具有双标记(T4+T8+)表面。所有细胞对D-BLCL均有显著增殖,尽管T4+克隆的平均倍增时间明显短于T8+克隆。几乎所有T8+克隆对D-BLCL具有特异性细胞毒性,而T4和T8均不与K562、自体EBV-BLCL和第三方EBV-BLCL反应。仅在少数克隆(均为T4+)的培养上清液中检测到可检测的IL-2。