T细胞
实验性自身免疫性脑脊髓炎
离体
体内
化学
髓鞘少突胶质细胞糖蛋白
髓鞘
分子生物学
脊髓
临床前影像学
免疫学
淋巴系统
受体
细胞
细胞生物学
病理
T淋巴细胞
脑脊髓炎
中枢神经系统
少突胶质细胞
生物
抗体
髓鞘碱性蛋白
多克隆抗体
B细胞
多发性硬化
作者
Stephanie D. Scharmann,Francisca Faber,Lauren Hoorens Van Heyningen,Mirna Reljić,Brooke D. Huisman,Priscilla P M Faas,Himadri Medhi,Manpreet Meyer,Camille Le Gall,Ishani Sahay,Pavana Suresh,Floris J. van Dalen,Nanette Becht,Leif S Ludwig,Michael E. Birnbaum,Hidde L Ploegh,Novalia Pishesha
标识
DOI:10.1093/jimmun/vkag237
摘要
Through screening of a VHH phage display library constructed from an alpaca immunized with the recombinantly expressed murine myelin oligodendrocyte (MOG)-specific 2D2 T cell receptor (TCR), we identified nanobodies that reduced antigen-driven 2D2 T cell activation in vitro. Immunoblotting and staining confirmed TCRβ chain reactivity and Vβ11-associated recognition in polyclonal T cell populations. Site-specific sortase-mediated conjugation with desferrioxamine and 89Zr enabled nanobody-based immuno-PET/CT. In vivo imaging showed tracer accumulation in secondary lymphoid organs in settings enriched for Vβ11-expressing 2D2 T cells. In mice symptomatic for experimental autoimmune encephalomyelitis that had received MOG-specific 2D2 T cells, we observed a spinal cord-associated signal. This corresponded to accumulation of transferred Vβ11-expressing 2D2 T cells within inflamed spinal cord tissue. Compared with full-length immunoglobulins and multimeric peptide-MHC reagents that primarily support ex vivo detection of antigen-specific T cells, TCR-specific nanobodies show rapid clearance and improved tissue penetration that favor high-contrast immuno-PET/CT imaging of defined T cell populations in vivo.
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