Stamm Ivonne, Wuhrer M, Geyer R, Baljer G, Menge Ch
Institut für Hygiene und Infektionskrankheiten der Tiere der Justus-Liebig-Universität, Giessen, Germany.
Microb Pathog. 2002 Dec;33(6):251-64. doi: 10.1006/mpat.2002.0527.
Interactions of Shiga toxins (Stxs) and immune cells contribute to the pathogenesis of diseases due to Stx-producing Escherichia coli (STEC) infections in humans and facilitate the persistence of infection in asymptomatically infected cattle. Our recent findings that bovine B and T lymphocytes express Gb(3)/CD77, the human Stx-receptor, prompted us to determine whether the bovine homologue also mediates binding and internalization of Stx1. In fact, Stx1 holotoxin and recombinant B subunit (rStxB1) bound to stimulated bovine peripheral blood mononuclear cells, especially to those subpopulations (B cells, BoCD8(+) T cells) that are highly sensitive to Stx1. Competition and HPTLC-binding studies confirmed that Stx1 binds to bovine Gb(3), but different receptor isoforms with varying affinities for rStxB1 were expressed during the course of lymphocyte activation. At least one of these isoforms mediated toxin uptake. An anti-StxB1 mouse monoclonal antibody, used as a model for bovine serum antibodies specific for Stx1, modulated rather than generally prevented rStxB1 binding to and internalization by the receptors. The presence of functional Stx1-receptors on bovine lymphocytes explains the immunomodulatory effect of Stx1 observed in cattle at a molecular level. Furthermore, expression of such receptors by bovine but not human T cells enlightens the background for the differential outcome of STEC infections in cattle and man, i.e., persistent infection and development of disease, respectively.
志贺毒素(Stxs)与免疫细胞的相互作用,在人类因产志贺毒素大肠杆菌(STEC)感染而引发的疾病发病机制中发挥作用,并促使无症状感染牛的感染持续存在。我们最近发现牛B淋巴细胞和T淋巴细胞表达人志贺毒素受体Gb(3)/CD77,这促使我们去确定牛同源物是否也介导志贺毒素1(Stx1)的结合与内化。事实上,Stx1全毒素和重组B亚基(rStxB1)与受刺激的牛外周血单个核细胞结合,尤其是与那些对Stx1高度敏感的亚群(B细胞、牛CD8(+) T细胞)结合。竞争和高效薄层层析结合研究证实Stx1与牛Gb(3)结合,但在淋巴细胞激活过程中表达了对rStxB1具有不同亲和力的不同受体亚型。这些亚型中至少有一种介导毒素摄取。一种抗StxB1小鼠单克隆抗体,用作牛血清中对Stx1特异抗体的模型,调节而非普遍阻止rStxB1与受体的结合及内化。牛淋巴细胞上功能性Stx1受体的存在,在分子水平上解释了在牛身上观察到的Stx1的免疫调节作用。此外,牛T细胞而非人T细胞表达此类受体,揭示了STEC感染在牛和人身上产生不同结果的背景,即分别为持续感染和疾病发展。