Hilchey Shannon P, Kobie James J, Cochran Mathew R, Secor-Socha Shelley, Wang Jyh-Chiang E, Hyrien Ollivier, Burack W Richard, Mosmann Tim R, Quataert Sally A, Bernstein Steven H
James P. Wilmot Cancer Center, University of Rochester Medical Center, Rochester, NY 14642, USA.
J Immunol. 2009 Nov 15;183(10):6157-66. doi: 10.4049/jimmunol.0900475. Epub 2009 Oct 28.
Our previous work has demonstrated that human follicular lymphoma (FL) infiltrating T cells are anergic, in part due to suppression by regulatory T cells. In this study, we identify pericellular adenosine, interacting with T cell-associated G protein-coupled A(2A/B) adenosine receptors (AR), as contributing to FL T cell hyporesponsiveness. In a subset of FL patient samples, treatment of lymph node mononuclear cells (LNMC) with specific A(2A/B) AR antagonists results in an increase in IFN-gamma or IL-2 secretion upon anti-CD3/CD28 Ab stimulation, as compared with that seen without inhibitors. In contrast, treatment with an A(1) AR antagonist had no effect on cytokine secretion. As the rate limiting step for adenosine generation from pericellular ATP is the ecto-ATPase CD39, we next show that inhibition of CD39 activity using the inhibitor ARL 67156 partially overcomes T cell hyporesponsiveness in a subset of patient samples. Phenotypic characterization of LNMC demonstrates populations of CD39-expressing CD4(+) and CD8(+) T cells, which are overrepresented in FL as compared with that seen in normal or reactive nodes, or normal peripheral blood. Thirty percent of the FL CD4(+)CD39(+) T cells coexpress CD25(high) and FOXP3 (consistent with regulatory T cells). Finally, FL or normal LNMC hydrolyze ATP in vitro, in a dose- and time-dependent fashion, with the rate of ATP consumption being associated with the degree of CD39(+) T cell infiltration. Together, these results support the finding that the ATP-ectonucleotidase-adenosine system mediates T cell anergy in a human tumor. In addition, these studies suggest that the A(2A/B) AR as well as CD39 are novel pharmacological targets for augmenting cancer immunotherapy.
我们之前的研究表明,人类滤泡性淋巴瘤(FL)浸润性T细胞处于无反应状态,部分原因是受到调节性T细胞的抑制。在本研究中,我们确定细胞周围腺苷与T细胞相关的G蛋白偶联A(2A/B)腺苷受体(AR)相互作用,是导致FL T细胞反应性降低的原因之一。在一部分FL患者样本中,用特异性A(2A/B) AR拮抗剂处理淋巴结单核细胞(LNMC)后,与未使用抑制剂时相比,抗CD3/CD28抗体刺激后IFN-γ或IL-2的分泌增加。相比之下,用A(1) AR拮抗剂处理对细胞因子分泌没有影响。由于细胞周围ATP生成腺苷的限速步骤是胞外ATP酶CD39,我们接下来表明,使用抑制剂ARL 67156抑制CD39活性可部分克服一部分患者样本中T细胞的低反应性。LNMC的表型特征显示,表达CD39的CD4(+)和CD8(+) T细胞群体在FL中比在正常或反应性淋巴结或正常外周血中更为常见。30%的FL CD4(+)CD39(+) T细胞共表达CD25(高)和FOXP3(与调节性T细胞一致)。最后,FL或正常LNMC在体外以剂量和时间依赖性方式水解ATP,ATP消耗速率与CD39(+) T细胞浸润程度相关。总之,这些结果支持了ATP-胞外核苷酸酶-腺苷系统在人类肿瘤中介导T细胞无反应性这一发现。此外,这些研究表明A(2A/B) AR以及CD39是增强癌症免疫治疗的新型药理学靶点。