Department of Pathology, University of Massachusetts Chan Medical School, Worcester, MA.
Division of Immunity and Pathogenesis, Burnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando, FL.
J Immunol. 2023 Jun 15;210(12):1950-1961. doi: 10.4049/jimmunol.2200337.
Initial TCR affinity for peptide Ag is known to impact the generation of memory; however, its contributions later, when effectors must again recognize Ag at 5-8 d postinfection to become memory, is unclear. We examined whether the effector TCR affinity for peptide at this "effector checkpoint" dictates the extent of memory and degree of protection against rechallenge. We made an influenza A virus nucleoprotein (NP)-specific TCR transgenic mouse strain, FluNP, and generated NP-peptide variants that are presented by MHC class II to bind to the FluNP TCR over a broad range of avidity. To evaluate the impact of avidity in vivo, we primed naive donor FluNP in influenza A virus-infected host mice, purified donor effectors at the checkpoint, and cotransferred them with the range of peptides pulsed on activated APCs into second uninfected hosts. Higher-avidity peptides yielded higher numbers of FluNP memory cells in spleen and most dramatically in lung and draining lymph nodes and induced better protection against lethal influenza infection. Avidity determined memory cell number, not cytokine profile, and already impacted donor cell number within several days of transfer. We previously found that autocrine IL-2 production at the checkpoint prevents default effector apoptosis and supports memory formation. Here, we find that peptide avidity determines the level of IL-2 produced by these effectors and that IL-2Rα expression by the APCs enhances memory formation, suggesting that transpresentation of IL-2 by APCs further amplifies IL-2 availability. Secondary memory generation was also avidity dependent. We propose that this regulatory pathway selects CD4 effectors of highest affinity to progress to memory.
初始 TCR 对肽 Ag 的亲和力已知会影响记忆的产生;然而,在效应器必须在感染后 5-8 天再次识别 Ag 以成为记忆时,其贡献尚不清楚。我们研究了在这个“效应器检查点”时,效应 TCR 对肽的亲和力是否决定了记忆的程度和对再挑战的保护程度。我们构建了一种流感 A 病毒核蛋白(NP)特异性 TCR 转基因小鼠品系 FluNP,并生成了 NP 肽变体,这些变体由 MHC Ⅱ类呈递,以广泛的亲和力结合 FluNP TCR。为了评估亲和力在体内的影响,我们在感染流感 A 病毒的宿主小鼠中对幼稚供体 FluNP 进行了免疫,在检查点纯化供体效应器,并将其与在激活的 APC 上呈递的肽范围一起转输给第二个未感染的宿主。更高亲和力的肽在脾脏中产生更多数量的 FluNP 记忆细胞,在肺部和引流淋巴结中最为显著,并诱导更好的抗致死性流感感染保护。亲和力决定了记忆细胞的数量,而不是细胞因子谱,并且在转移后的几天内就已经影响了供体细胞的数量。我们之前发现,检查点处的自分泌 IL-2 产生可防止默认效应细胞凋亡并支持记忆形成。在这里,我们发现肽亲和力决定了这些效应物产生的 IL-2 水平,并且 APCs 上的 IL-2Rα 表达增强了记忆形成,表明 APCs 通过转呈 IL-2 进一步放大了 IL-2 的可用性。二级记忆的产生也依赖于亲和力。我们提出,这种调节途径选择具有最高亲和力的 CD4 效应物来进展为记忆。