The effect of haemopoietic stem cell proliferation on the humoral immune response in mice.

V A Kozlov, I A Orlovskaya, I G Tsyrlova
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引用次数: 1

Abstract

A study was made of the effect of humoral factors, isolated from bone marrow cell (BMC) supernatant fluid and capable of modifying CFU-S proliferation, on the generation of IgM plaque-forming cells (PFC) against sheep red blood cells (SRBC) in mice after adoptive transfer. Adoptive transfer of BMC, preincubated with the humoral factor RBME-III, which stimulates CFU-S proliferation, was shown to suppress the splenic PFC generation in recipients; treatment of BMC with a further factor NBME-IV, which inhibits CFU-S proliferation, was followed by augmentation of PFC generation. Similar effects were obtained while studying the IgM PFC generation in the bone marrow of mice after secondary immunization when relevant factors were injected, in vivo, 24 hr following primary immunization. The results of adoptive transfer experiments indicate that populations of T- and B-cells are not the targets for the action of CFU-S proliferation regulatory factors. These factors are shown to modulate the erythroid differentiation of CFU-S. The possibility of quantitative modification of immune response parameters with the help of bone marrow factors that influence the proliferation and differentiation of CFU-S is discussed.

造血干细胞增殖对小鼠体液免疫反应的影响。
研究了从骨髓细胞(BMC)上清液中分离出的能够修饰CFU-S增殖的体液因子对过继移植后小鼠抗羊红细胞(SRBC)的IgM斑块形成细胞(PFC)产生的影响。BMC的过继转移,与体液因子RBME-III预孵育,刺激CFU-S增殖,被证明可以抑制受体脾PFC的产生;用抑制CFU-S增殖的NBME-IV因子进一步治疗BMC后,增加PFC的生成。在一次免疫后24小时,在体内注射相关因子,研究二次免疫后小鼠骨髓中IgM PFC的生成,也得到了类似的效果。过继性转移实验结果表明,T细胞和b细胞群体不是CFU-S增殖调节因子作用的靶点。这些因素均可调节CFU-S的红系分化。探讨了利用影响CFU-S增殖分化的骨髓因子定量修饰免疫应答参数的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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