Scheerlinck J P, Burssens G, Brys L, Michel A, Hauser P, De Baetselier P
Institute of Molecular Biology, Vrije Universiteit Brussel, St-Geneius-Rode, Belgium.
Immunology. 1991 May;73(1):88-94.
Different cell types, including dendritic cells, macrophages and Ia+ B cells, have been described to present soluble antigen (Ag) to T-cell hybridomas. However, it is still not clear whether these different cell types can act as antigen-presenting cells (APC) for complex and insoluble Ag such as viral particles. Using yeast recombinant hepatitis B S-preS(2)-containing particles, T-cell hybridomas were generated and used as a tool to study processing and presentation of antigen. Different types of APC were compared in regard to their capacity to process and present the protein-lipid composed S-preS(2) particles and the thereof derived T-cell epitope containing peptides by different types of APC. While a S-preS(2)-derived T-cell epitope containing peptide, which does not require processing, could be presented both by macrophage and B-cell like APC, the presentation of S-preS(2) particles required the presence of macrophages. The fact that B-cell like APC and macrophages behave differently with regard to the presentation of S-preS(2) particles suggest that the uptake and/or processing of this type of Ag by B-cell like APC and macrophages is different.
包括树突状细胞、巨噬细胞和Ia⁺ B细胞在内的不同细胞类型,已被描述为可将可溶性抗原(Ag)呈递给T细胞杂交瘤。然而,这些不同的细胞类型是否能作为针对诸如病毒颗粒等复杂和不溶性抗原的抗原呈递细胞(APC),目前仍不清楚。利用含酵母重组乙肝S-preS(2)的颗粒,制备了T细胞杂交瘤,并将其用作研究抗原加工和呈递的工具。比较了不同类型的APC处理和呈递由蛋白质-脂质组成的S-preS(2)颗粒及其衍生的含T细胞表位肽段的能力。虽然一种不需要加工的含S-preS(2)衍生T细胞表位的肽段可由巨噬细胞和类B细胞APC呈递,但S-preS(2)颗粒的呈递需要巨噬细胞的存在。类B细胞APC和巨噬细胞在S-preS(2)颗粒呈递方面表现不同,这一事实表明类B细胞APC和巨噬细胞对这类抗原的摄取和/或加工是不同的。