Department of Veterinary Immunology, LMU Munich, Lena-Christ-Straße 48, 82152 Planegg-Martinsried, Germany.
Department of Veterinary Immunology, LMU Munich, Lena-Christ-Straße 48, 82152 Planegg-Martinsried, Germany.
Dev Comp Immunol. 2024 Dec;161:105250. doi: 10.1016/j.dci.2024.105250. Epub 2024 Aug 17.
Chickens are a species with a high number of γδ T cells in various tissues. Despite their abundance, γδ T cells are poorly characterized in chickens, partially due to a lack of specific reagents to characterize these cells. Up until now, the TCR1 clone has been the only γδ T cell-specific monoclonal antibody (mAb) in chickens and additional reagents for γδ T cell subsets are needed. In order to address this issue, new mAb were generated in our laboratory by immunizing mice with in vitro cultured γδ T cells. In an initial flow cytometric screen a new mAb, clone "8D2", displayed an interesting staining pattern that mirrored γδ TCR up- and downregulation in the γδ T cell line D4 over time, prompting us to characterize this antibody further. We compared the expression of the unknown 8D2 epitope in combination with TCR1 staining across various primary cells. In splenocytes, peripheral blood lymphocytes and intestinal epithelial cells, 8D2 consistently labeled a subset of TCR1 cells. To determine, whether specific γδ T cell receptors were recognized by 8D2, we sorted γδ T cells according to their 8D2 and TCR1 expression and analyzed their TCR V(D)J gene usage by TCR profiling. Strikingly, sorted 8D2 cells preferentially expressed Vγ3 genes, whereas the TCR Vγ genes used by TCR1 8D2 cells were more variable. γδ TCR in 8D2 cells were most frequently comprised of gamma chain VJ genes TRGV3-8 and TRGJ3, and delta chain VDJ genes TRDV1-2, TRDD2, TRDJ1. To confirm binding of 8D2 to specific γδ TCR, the preferentially utilized combination of TRG and TRD was expressed in HEK293 cells in combination with CD3, demonstrating surface binding of the 8D2 mAb to this Vγ3 γδ TCR-expressing cell line. Conversely, HEK293 cells expressing either Vγ1 or Vγ2 TCR did not react with 8D2. In conclusion, 8D2 is a novel tool for identifying specific Vγ3 bearing γδ T cells.
鸡是一类在各种组织中具有大量γδ T 细胞的物种。尽管它们数量众多,但鸡的γδ T 细胞特征描述并不完善,部分原因是缺乏用于这些细胞特征描述的特定试剂。到目前为止,TCR1 克隆一直是鸡中唯一的γδ T 细胞特异性单克隆抗体(mAb),需要更多用于γδ T 细胞亚群的试剂。为了解决这个问题,我们实验室通过用体外培养的γδ T 细胞免疫小鼠,生成了新的 mAb。在最初的流式细胞术筛选中,一种新的 mAb,克隆“8D2”,显示出一种有趣的染色模式,随着时间的推移,该模式反映了γδ T 细胞系 D4 中 γδ TCR 的上调和下调,促使我们进一步表征这种抗体。我们比较了在各种原代细胞中与 TCR1 染色相结合的未知 8D2 表位的表达。在脾细胞、外周血淋巴细胞和肠上皮细胞中,8D2 始终标记 TCR1 细胞的一个亚群。为了确定 8D2 是否识别特定的 γδ T 细胞受体,我们根据 8D2 和 TCR1 的表达对 γδ T 细胞进行分选,并通过 TCR 谱分析分析它们的 TCR V(D)J 基因使用情况。令人惊讶的是,分选的 8D2 细胞优先表达 Vγ3 基因,而 TCR1 8D2 细胞使用的 TCR Vγ 基因则更为多样化。8D2 细胞中的 γδ TCR 最常由 γ 链 VJ 基因 TRGV3-8 和 TRGJ3 以及 δ 链 VDJ 基因 TRDV1-2、TRDD2 和 TRDJ1 组成。为了确认 8D2 与特定 γδ TCR 的结合,将优先使用的 TRG 和 TRD 组合在 HEK293 细胞中与 CD3 一起表达,证明 8D2 mAb 表面结合到表达这种 Vγ3 γδ TCR 的细胞系。相反,表达 Vγ1 或 Vγ2 TCR 的 HEK293 细胞不与 8D2 反应。总之,8D2 是鉴定特定 Vγ3 携带 γδ T 细胞的新型工具。