Ellis J A, Morrison W I, Goddeeris B M, Emery D L
International Laboratory for Research on Animal Diseases (ILRAD), Nairobi, Kenya.
Vet Immunol Immunopathol. 1987 Dec;17(1-4):125-34. doi: 10.1016/0165-2427(87)90133-4.
Monoclonal antibodies (mAb) which react with bovine monocytes have been produced. These include three mAb (P8, IL-A22 and IL-A24) that recognize the majority of monocytes and granulocytes in peripheral blood; two of these mAb were also shown to react with 30-40% of cells in bone marrow, including both monocytic and granulocytic cells, and with variable percentages of tissue macrophages. Thus these mAb can act as markers for myeloid cells in haemopoietic tissues and for monocytes in cell populations devoid of granulocytes. A further two mAb (IL-A23 and IL-A25) recognize monocytes and/or macrophages. The reactivity of one of these mAb (IL-A25) appears to be mainly restricted to pulmonary macrophages. The other mAb reacts with a variable proportion of blood monocytes and generally with a higher percentage of tissue macrophages, suggesting that its expression may relate to activation or maturation of monocytes. In order to study the functional properties of peripheral blood monocytes, techniques were developed for obtaining populations of peripheral blood mononuclear cells (PBM) depleted of monocytes to less than 0.2% and monocyte populations of greater than 97% purity. Removal of monocytes from PBM abrogated the capacity of the cells to proliferate in response to Con A and PBS, although addition of 2-mercaptoethanol to the cultures restored proliferation. In both allogeneic and autologous mixed leukocyte cultures (MLC), monocytes were required in the stimulator cell populations for induction of the proliferative responses, and both responses could be elicited with purified monocytes. However, proliferation in the autologous MLC occurred only with responder cell populations that were depleted of monocytes. Moreover, it was shown that addition of more than 5% unirradiated monocytes to the autologous MLC suppressed proliferation. These findings indicate that monocytes play an important role in the induction and regulation of cellular immune responses in cattle. Two of the mAb that react with monocytes and granulocytes were tested for their capacity to inhibit proliferative responses of PBM to mitogens, alloantigens or the soluble antigen, KLH.(ABSTRACT TRUNCATED AT 400 WORDS)
已制备出与牛单核细胞发生反应的单克隆抗体(mAb)。其中包括三种识别外周血中大多数单核细胞和粒细胞的单克隆抗体(P8、IL - A22和IL - A24);其中两种单克隆抗体还显示与骨髓中30 - 40%的细胞发生反应,包括单核细胞和粒细胞,以及不同比例的组织巨噬细胞。因此,这些单克隆抗体可作为造血组织中髓细胞以及缺乏粒细胞的细胞群体中单核细胞的标志物。另外两种单克隆抗体(IL - A23和IL - A25)识别单核细胞和/或巨噬细胞。其中一种单克隆抗体(IL - A25)的反应性似乎主要局限于肺巨噬细胞。另一种单克隆抗体与不同比例的血液单核细胞发生反应,通常与更高比例的组织巨噬细胞发生反应,这表明其表达可能与单核细胞的激活或成熟有关。为了研究外周血单核细胞的功能特性,已开发出技术来获得外周血单核细胞(PBM)群体,其中单核细胞减少至低于0.2%,以及纯度大于97%的单核细胞群体。从PBM中去除单核细胞消除了细胞对刀豆蛋白A和磷酸盐缓冲盐水(PBS)产生增殖反应的能力,尽管向培养物中添加2 - 巯基乙醇可恢复增殖。在同种异体和自体混合淋巴细胞培养(MLC)中,刺激细胞群体中需要单核细胞来诱导增殖反应,并且两种反应都可以用纯化的单核细胞引发。然而,自体MLC中的增殖仅发生在去除单核细胞的应答细胞群体中。此外,研究表明向自体MLC中添加超过5%未照射的单核细胞会抑制增殖。这些发现表明单核细胞在牛细胞免疫反应的诱导和调节中起重要作用。测试了两种与单核细胞和粒细胞发生反应的单克隆抗体抑制PBM对有丝分裂原、同种异体抗原或可溶性抗原钥孔戚血蓝蛋白(KLH)增殖反应的能力。(摘要截短于400字)