Pirson Chris, Engel Regina, Jones Gareth J, Holder Thomas, Holst Otto, Vordermeier H Martin
TB Research Group, Animal Health and Veterinary Laboratories Agency, New Haw, Addlestone, Surrey, United Kingdom
Division of Structural Biochemistry, Research Centre Borstel, Leibniz Centre for Medicine and Biosciences, Borstel, Germany.
Clin Vaccine Immunol. 2015 Feb;22(2):178-84. doi: 10.1128/CVI.00638-14. Epub 2014 Dec 10.
Mycobacterial lipids play an important role in the modulation of the immune response upon contact with the host. Using novel methods, we have isolated highly purified phosphatidylinositol mannoside (PIM) molecules (phosphatidylinositol dimannoside [PIM2], acylphosphatidylinositol dimannoside [AcPIM2], diacyl-phosphatidylinositol dimannoside [Ac2PIM2], acylphosphatidylinositol hexamannoside [AcPIM6], and diacylphosphatidylinositol hexamannoside [Ac2PIM6]) from virulent Mycobacterium tuberculosis to assess their potential to stimulate peripheral blood mononuclear cell (PBMC) responses in Mycobacterium bovis-infected cattle. Of these molecules, one (AcPIM6) induced significant levels of gamma interferon (IFN-γ) in bovine PBMCs. Three PIM molecules (AcPIM6, Ac2PIM2, and Ac2PIM6) were shown to drive significant proliferation in bovine PBMCs. AcPIM6 was subsequently used to phenotype the proliferating cells by flow cytometry. This analysis demonstrated that AcPIM6 was predominantly recognized by CD3(+) CD335(+) NKT cells. In conclusion, we have identified PIM lipid molecules that interact with bovine lymphocyte populations, and these lipids may be useful as future subunit vaccines or diagnostic reagents. Further, these data demonstrate, for the first time, lipid-specific NKT activation in cattle.
分枝杆菌脂质在与宿主接触时对免疫反应的调节中起重要作用。我们采用新方法,从强毒结核分枝杆菌中分离出了高度纯化的磷脂酰肌醇甘露糖苷(PIM)分子(磷脂酰肌醇二甘露糖苷[PIM2]、酰基磷脂酰肌醇二甘露糖苷[AcPIM2]、二酰基磷脂酰肌醇二甘露糖苷[Ac2PIM2]、酰基磷脂酰肌醇六甘露糖苷[AcPIM6]和二酰基磷脂酰肌醇六甘露糖苷[Ac2PIM6]),以评估它们刺激牛分枝杆菌感染牛外周血单个核细胞(PBMC)反应的潜力。在这些分子中,有一种(AcPIM6)在牛PBMC中诱导出显著水平的γ干扰素(IFN-γ)。三种PIM分子(AcPIM6、Ac2PIM2和Ac2PIM6)在牛PBMC中显示出显著的增殖驱动作用。随后,利用AcPIM6通过流式细胞术对增殖细胞进行表型分析。该分析表明,AcPIM6主要被CD3(+) CD335(+) NKT细胞识别。总之,我们鉴定出了与牛淋巴细胞群体相互作用的PIM脂质分子,这些脂质可能作为未来的亚单位疫苗或诊断试剂。此外,这些数据首次证明了牛体内脂质特异性NKT细胞的激活。