Sundsmo J S
J Immunol. 1983 Aug;131(2):886-91.
The results presented here show that Fab' antibody fragments directed to complement proteins C5, C6, and C7 inhibit lymphocyte stimulation in mixed lymphocyte culture (MLC) by up to 65%, as determined by decreased incorporation of 3H-thymidine. Lymphocyte stimulation induced by PHA-mitogen was also inhibited up to 100% by anti-C5 Fab'. Specificity of these reactions was established by the findings that goat anti-C5 or murine hybridoma anti-C5 both inhibited MLC; the inhibitory activity of anti-C5 Fab' was absorbed with highly purified C5 (but not with C3), and antibody directed to C3 did not inhibit lymphocyte stimulation by MLC or PHA. The effects of anti-C5 were exerted in a nontoxic manner. Cleavage of lymphocyte associated C5 with factor B (Bb) or with trypsin resulted in stimulation of lymphocyte thymidine incorporation. Purified C5a was found to induce lymphocyte stimulation in serum-free medium in pulse-chase types of experiments. Anti-C6 and C7 Fab' also inhibited lymphocyte stimulation induced in one-way MLC. These results suggest that C5, C5a, and/or C6 and C7 may play a role in triggering of lymphocyte blastogenesis.
此处呈现的结果表明,针对补体蛋白C5、C6和C7的Fab'抗体片段在混合淋巴细胞培养(MLC)中可将淋巴细胞刺激抑制高达65%,这是通过3H-胸腺嘧啶核苷掺入量的减少来确定的。抗C5 Fab'对PHA-丝裂原诱导的淋巴细胞刺激也可抑制高达100%。这些反应的特异性通过以下发现得以确立:山羊抗C5或鼠杂交瘤抗C5均能抑制MLC;抗C5 Fab'的抑制活性可被高度纯化的C5(而非C3)吸收,且针对C3的抗体不会抑制MLC或PHA诱导的淋巴细胞刺激。抗C5的作用以无毒方式发挥。用B因子(Bb)或胰蛋白酶切割淋巴细胞相关的C5会导致淋巴细胞胸腺嘧啶核苷掺入增加。在脉冲追踪类型的实验中发现,纯化的C5a可在无血清培养基中诱导淋巴细胞刺激。抗C6和C7 Fab'也抑制单向MLC中诱导的淋巴细胞刺激。这些结果表明,C5、C5a和/或C6及C7可能在触发淋巴细胞增殖方面发挥作用。