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口腔癌患者对 Toll 样受体配体的功能反应降低。

Decreased functional response to Toll like receptor ligands in patients with oral cancer.

机构信息

Chiplunkar Lab, Advanced Centre for Treatment, Research and Education in Cancer (ACTREC), Tata Memorial Centre, Navi Mumbai, India.

出版信息

Hum Immunol. 2013 Aug;74(8):927-36. doi: 10.1016/j.humimm.2013.04.018. Epub 2013 Apr 27.

Abstract

Patients with oral cancer (OC) show dysregulation of variety of anti tumor immune responses. To assess the role of Toll like receptor (TLR) signaling in peripheral blood lymphocytes (PBL) from OC patients, we analyzed the expression of TLR2, TLR3, TLR4 and TLR9 on various lymphocyte subsets. Results revealed an increased expression of TLRs on unconventional T cells (like γδ T cells, NKT cells and CD4(+)CD8(+) T cells) as compared to conventional αβ T cells. Functional studies using TLR ligands (CpG, Poly I:C, LPS and Pam3CSK4) showed defects in the TLR mediated signaling in PBLs of OC patients. Proliferation of OC PBLs in response to stimulation with TLR ligands was significantly decreased. TLR ligand induced IFN-γ production by PBLs from OC patients were low as compared to HI. Stimulation with TLR ligands upregulated the levels of activation markers (CD25 and CD69) on PBLs from HI but not from OC patients. TLR ligands CpG, Poly I:C, LPS and Pam3CSK4 significantly augmented the tumor directed cytotoxic response of PBLs from HI but not from OC patients. Our data suggests that impairment of TLR function on PBLs may be another strategy adopted by tumor cells to dampen tumor directed immune responses.

摘要

口腔癌(OC)患者表现出多种抗肿瘤免疫反应的失调。为了评估 Toll 样受体(TLR)信号在 OC 患者外周血淋巴细胞(PBL)中的作用,我们分析了各种淋巴细胞亚群中 TLR2、TLR3、TLR4 和 TLR9 的表达。结果显示,与传统的αβ T 细胞相比,非常规 T 细胞(如γδ T 细胞、NKT 细胞和 CD4+CD8+T 细胞)上 TLR 的表达增加。使用 TLR 配体(CpG、Poly I:C、LPS 和 Pam3CSK4)进行的功能研究表明,OC 患者 PBL 中 TLR 介导的信号转导存在缺陷。OC PBL 对 TLR 配体刺激的增殖反应明显降低。与 HI 相比,OC 患者 PBL 对 TLR 配体诱导的 IFN-γ产生较低。与 OC 患者相比,TLR 配体刺激可上调 HI PBL 上的激活标志物(CD25 和 CD69)的水平。TLR 配体 CpG、Poly I:C、LPS 和 Pam3CSK4 显著增强了 HI PBL 的肿瘤定向细胞毒性反应,但对 OC 患者的 PBL 则没有。我们的数据表明,PBL 上 TLR 功能的损害可能是肿瘤细胞采用的另一种策略,以抑制肿瘤定向免疫反应。

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