School of Life and Environmental Sciences, The University of Sydney, Sydney, New South Wales 2006, Australia.
Marie Bashir Institute for Infectious Diseases and Biosecurity, The University of Sydney, Sydney, New South Wales 2006, Australia.
J Immunol. 2018 Oct 1;201(7):2176-2186. doi: 10.4049/jimmunol.1800339. Epub 2018 Aug 24.
Anti-CD4 or anti-CD8α Ab-mediated depletion strategies are widely used to determine the role of T cell subsets. However, surface expression of CD4 and CD8α is not limited to T cells and occurs on other leukocyte populations as well. Using both unbiased -distributed stochastic neighbor embedding of flow cytometry data and conventional gating strategies, we assessed the impact of anti-CD4 and anti-CD8α Ab-mediated depletion on non-T cell populations in mice. Our results show that anti-CD4 and anti-CD8α Ab injections not only resulted in depletion of T cells but also led to depletion of specific dendritic cell subsets in a dose-dependent manner. Importantly, the extent of this effect varied between mock- and virus-infected mice. We also demonstrate the importance of using a second, noncompeting Ab (clone CT-CD8α) to detect CD8α cells following depletion with anti-CD8α Ab clone 2.43. Our study provides a necessary caution to carefully consider the effects on nontarget cells when using Ab injections for leukocyte depletion in all experimental conditions.
抗 CD4 或抗 CD8α Ab 耗竭策略被广泛用于确定 T 细胞亚群的作用。然而,CD4 和 CD8α 的表面表达不仅局限于 T 细胞,也发生在其他白细胞群体上。我们使用无偏分布随机邻域嵌入流式细胞术数据和传统门控策略,评估了抗 CD4 和抗 CD8α Ab 耗竭对小鼠中非 T 细胞群体的影响。我们的结果表明,抗 CD4 和抗 CD8α Ab 注射不仅导致 T 细胞耗竭,而且还以剂量依赖的方式导致特定树突状细胞亚群耗竭。重要的是,这种效应的程度在 mock 和病毒感染的小鼠之间有所不同。我们还证明了在使用抗 CD8α Ab 克隆 2.43 耗尽 CD8α 细胞后,使用第二种非竞争 Ab(克隆 CT-CD8α)检测 CD8α 细胞的重要性。我们的研究提供了一个必要的警示,即在所有实验条件下使用 Ab 注射进行白细胞耗竭时,要仔细考虑对非靶细胞的影响。