Bielefeldt-Ohmann H, Sabara M, Lawman M J, Griebel P, Babiuk L A
Department of Veterinary Virology and Immunology, Royal Veterinary and Agricultural University, Copenhagen, Denmark.
J Immunol. 1988 Apr 1;140(7):2201-9.
A mAb EBM11, raised against human macrophages [M phi] was found to detect a bovine M phi diameter-subpopulation. The Ag was strictly intracellular and was expressed in M phi only at a certain state of maturation. Its expression was regulated independently of the activation state of the cells, as revealed by treating M phi in vitro with bovine rIFN-alpha I1, IFN-gamma, or TNF-alpha, all potent M luminal diameter activators. Such treatment had no apparent effect on Ag expression. The Ag was present in 1 to 5% of peripheral blood leukocytes, i.e., up to 20% of circulating blood monocytes, in both normal noninfected cattle and in cattle persistently infected with bovine viral diarrhoea virus. Blood monocytes of the latter group were activated in vivo, but apparently did not reach a more mature state than found in noninfected animals. After an acute infection with bovine herpes virus type 1, the frequency and total number of EBM11+ cells decreased dramatically in inverse relationship to an equally significant increase in frequency and total number of circulating monocytes. In cryostat sections of normal tissues, the EBM11 mAb reacted with sinus M phi and M phi in germinal centers of lymphoid tissues, with alveolar M phi and liver Kupffer cells. In skin it reacted with few scattered M phi in the dermis, but not with epidermal Langerhans cells. This latter feature distinguishes the bovine system from the human. In virus-induced inflammatory processes in skin and keratinized epithelia EBM11+ cells constituted a subpopulation of the infiltrating M phi. The data obtained suggest that EBM11 mAb could be useful both for the elucidation of differentiation/maturation pathways of cells of the monocyte-macrophage lineage as well as for studies of M phi-virus interactions in virus infections. In either aspect cattle could provide a useful comparative model.
一种针对人巨噬细胞产生的单克隆抗体EBM11,被发现可检测牛巨噬细胞直径亚群。该抗原严格位于细胞内,仅在巨噬细胞特定的成熟状态下表达。如用牛重组干扰素αI1、干扰素γ或肿瘤坏死因子α(均为有效的巨噬细胞激活剂)在体外处理巨噬细胞所显示的那样,其表达独立于细胞的激活状态进行调节。这种处理对抗原表达没有明显影响。在正常未感染的牛以及持续感染牛病毒性腹泻病毒的牛中,该抗原存在于1%至5%的外周血白细胞中,即高达20%的循环血液单核细胞中。后一组的血液单核细胞在体内被激活,但显然没有达到比未感染动物中更成熟的状态。在感染牛疱疹病毒1型后,EBM11+细胞的频率和总数急剧下降,与循环单核细胞频率和总数同样显著的增加呈反比关系。在正常组织的冷冻切片中,EBM11单克隆抗体与淋巴组织生发中心的窦巨噬细胞和巨噬细胞、肺泡巨噬细胞和肝库普弗细胞发生反应。在皮肤中,它与真皮中少数散在的巨噬细胞发生反应,但不与表皮朗格汉斯细胞发生反应。后一特征将牛的系统与人类的系统区分开来。在皮肤和角化上皮的病毒诱导炎症过程中,EBM11+细胞构成浸润巨噬细胞的一个亚群。所获得的数据表明,EBM单克隆抗体对于阐明单核细胞 - 巨噬细胞谱系细胞的分化/成熟途径以及研究病毒感染中巨噬细胞 - 病毒相互作用可能是有用的。在这两个方面,牛都可以提供一个有用的比较模型。