Chen Qing, Evans Sharon S
Department of Immunology, Roswell Park Cancer Institute, Buffalo, NY 14263-0001, USA.
Int J Hyperthermia. 2005 Dec;21(8):723-9. doi: 10.1080/02656730500271734.
Lymphocytes use extensive vascular networks to traffic to various destinations in the body, including lymphoid organs and extra-lymphoid tissues. This discussion will focus on the emerging evidence that thermal stress regulates the traffic signals that direct the exit of lymphocytes from the vascular freeway. This issue is particularly relevant to T cell-based cancer immunotherapy where delivery of immune effector lymphocytes to neoplastic lesions depends on their extravasation across tumour micro-vessels. Although tumours are frequently highly vascularized by vessels that are competent to support blood flow, the tumour micro-environment has been characterized as non-permissive to lymphocyte extravasation. This may lead to a scenario where limited leukocyte infiltration at tumour sites correlates with a poor prognosis. These observations support the thesis that adjuvant strategies that promote trafficking of tumour-reactive cytolytic leukocytes to tumour sites have the potential to improve the efficacy of immune-based cancer therapy.
淋巴细胞利用广泛的血管网络在体内运输到各个目的地,包括淋巴器官和非淋巴组织。本讨论将聚焦于新出现的证据,即热应激调节引导淋巴细胞离开血管通道的运输信号。这个问题与基于T细胞的癌症免疫疗法特别相关,在这种疗法中,免疫效应淋巴细胞输送到肿瘤病变部位取决于它们穿过肿瘤微血管的渗出。尽管肿瘤通常由能够支持血流的血管高度血管化,但肿瘤微环境的特征是不允许淋巴细胞渗出。这可能导致一种情况,即肿瘤部位白细胞浸润有限与预后不良相关。这些观察结果支持这样一个论点,即促进肿瘤反应性溶细胞白细胞向肿瘤部位运输的辅助策略有可能提高基于免疫的癌症治疗的疗效。