Foley Maria Hottelet, Forcier Talitha, McAndrew Elizabeth, Gonzalez Michael, Chen Huabiao, Juelg Boris, Walker Bruce D, Irvine Darrell J
Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America ; Ragon Institute of Massachusetts General Hospital, Massachusetts Institute of Technology, and Harvard University, Cambridge, Massachusetts, United States of America ; Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.
Ragon Institute of Massachusetts General Hospital, Massachusetts Institute of Technology, and Harvard University, Cambridge, Massachusetts, United States of America ; Department of Material Science and Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.
PLoS One. 2014 Feb 13;9(2):e87873. doi: 10.1371/journal.pone.0087873. eCollection 2014.
The dissemination of HIV from an initial site of infection is facilitated by motile HIV-infected CD4(+) T-cells. However, the impact of infected target cell migration on antigen recognition by HIV-specific CD8(+) T-cells is unclear. Using a 3D in vitro model of tissue, we visualized dynamic interactions between HIV-infected or peptide-pulsed CD4(+) T-cells and HIV-specific CD8(+) T-cells. CTLs engaged motile HIV-infected targets, but ∼ 50% of targets broke contact and escaped. In contrast, immobilized target cells were readily killed, indicating target motility directly inhibits CD8(+) T-cell function. Strong calcium signals occurred in CTLs killing a motile target but calcium signaling was weak or absent in CTLs which permitted target escape. Neutralization of adhesion receptors LFA-1 and CD58 inhibited CD8(+) T-cell function within the 3D matrix, demonstrating that efficient motile target lysis as dependent on adhesive engagement of targets. Antigen sensitivity (a convolution of antigen density, TCR avidity and CD8 coreceptor binding) is also critical for target recognition. We modulated this parameter (known as functional avidity but referred to here as "avidity" for the sake of simplicity) by exploiting common HIV escape mutations and measured their impact on CTL function at the single-cell level. Targets pulsed with low avidity mutant antigens frequently escaped while CTLs killed targets bearing high avidity antigen with near-perfect efficiency. CTLs engaged, arrested, and killed an initial target bearing high avidity antigen within minutes, but serial killing was surprisingly rare. CD8 cells remained committed to their initial dead target for hours, accumulating TCR signals that sustained secretion of soluble antiviral factors. These data indicate that high-avidity CD8(+) T-cells execute an antiviral program in the precise location where antigen has been sensed: CTL effector functions are spatiotemporally coordinated with an early lytic phase followed by a sustained stationary secretory phase to control local viral infection.
运动性的HIV感染的CD4(+) T细胞促进了HIV从初始感染部位的传播。然而,受感染靶细胞迁移对HIV特异性CD8(+) T细胞抗原识别的影响尚不清楚。利用组织的三维体外模型,我们观察了HIV感染或肽脉冲的CD4(+) T细胞与HIV特异性CD8(+) T细胞之间的动态相互作用。细胞毒性T淋巴细胞(CTL)与运动性的HIV感染靶细胞结合,但约50%的靶细胞脱离接触并逃脱。相比之下,固定的靶细胞很容易被杀死,这表明靶细胞的运动性直接抑制CD8(+) T细胞功能。在杀伤运动性靶细胞的CTL中出现强烈的钙信号,但在允许靶细胞逃脱的CTL中钙信号微弱或不存在。粘附受体LFA-1和CD58的中和抑制了三维基质内的CD8(+) T细胞功能,表明有效的运动性靶细胞裂解依赖于靶细胞的粘附结合。抗原敏感性(抗原密度、TCR亲和力和CD8共受体结合的卷积)对于靶细胞识别也至关重要。我们通过利用常见的HIV逃逸突变来调节这个参数(称为功能亲和力,但为简单起见这里称为“亲和力”),并在单细胞水平上测量它们对CTL功能的影响。用低亲和力突变抗原脉冲的靶细胞经常逃脱,而CTL以近乎完美的效率杀死携带高亲和力抗原的靶细胞。CTL在几分钟内与携带高亲和力抗原的初始靶细胞结合、捕获并杀死,但连续杀伤出奇地罕见。CD8细胞在数小时内仍专注于其最初的死亡靶细胞,积累TCR信号,持续分泌可溶性抗病毒因子。这些数据表明,高亲和力的CD8(+) T细胞在感知到抗原的精确位置执行抗病毒程序:CTL效应功能在时空上与早期裂解阶段协调,随后是持续的静止分泌阶段,以控制局部病毒感染。