Department of Radioimmunology, Institute of Radiopharmaceutical Cancer Research, Helmholtz-Zentrum Dresden-Rossendorf (HZDR), 03128 Dresden, Germany.
University Cancer Center (UCC), Tumor Immunology, University Hospital Carl Gustav Carus Dresden, Technical University Dresden, 01307 Dresden, Germany.
Int J Mol Sci. 2021 Jan 26;22(3):1198. doi: 10.3390/ijms22031198.
Since the first description of nuclear autoantigens in the late 1960s and early 1970s, researchers, including ourselves, have found it difficult to establish monoclonal antibodies (mabs) against nuclear antigens, including the La/SS-B (Sjögrens' syndrome associated antigen B) autoantigen. To date, only a few anti-La mabs have been derived by conventional hybridoma technology; however, those anti-La mabs were not bona fide autoantibodies as they recognize either human La specific, cryptic, or post-translationally modified epitopes which are not accessible on native mouse La protein. Herein, we present a series of novel murine anti-La mabs including truly autoreactive ones. These mabs were elicited from a human La transgenic animal through adoptive transfer of T cells from non-transgenic mice immunized with human La antigen. Detailed epitope and paratope analyses experimentally confirm the hypothesis that somatic hypermutations that occur during T cell dependent maturation can lead to autoreactivity to the nuclear La/SS-B autoantigen.
自 20 世纪 60 年代末和 70 年代初首次描述核自身抗原以来,包括我们在内的研究人员发现很难针对核抗原(包括 La/SS-B [干燥综合征相关抗原 B] 自身抗原)建立单克隆抗体(mab)。迄今为止,仅通过常规杂交瘤技术获得了少数抗-La mab;然而,那些抗-La mab 并不是真正的自身抗体,因为它们识别的是人 La 特定的、隐蔽的或翻译后修饰的表位,而这些表位在天然的鼠 La 蛋白上是无法获得的。在此,我们提出了一系列新的鼠抗-La mab,包括真正的自身反应性 mab。这些 mab 是通过从用人 La 抗原免疫的非转基因小鼠中过继转移 T 细胞,从小鼠中获得的。详细的表位和位分析实验证实了这样一个假设,即 T 细胞依赖性成熟过程中发生的体细胞超突变可导致对核 La/SS-B 自身抗原的自身反应性。