Department of Immunology, Center for Integrative Immunology and Vaccine Research, University of Connecticut Health Center, Farmington, Connecticut, USA.
J Virol. 2013 Apr;87(8):4496-506. doi: 10.1128/JVI.03413-12. Epub 2013 Feb 6.
In healthy individuals, influenza virus (IAV) infection generally remains localized to the epithelial cells of the respiratory tract. Previously, IAV-specific effector CD8 T cells found systemically during the course of IAV infection were thought to have been primed in lung-draining lymph nodes with subsequent migration to other tissues. However, little is known about whether other lymphoid sites participate in the generation of virus-specific CD8 T cells during localized IAV infection. Here, we present evidence of early CD8 T cell priming in the spleen following respiratory IAV infection independent of lung-draining lymph node priming of T cells. Although we found early indications of CD8 T cell activation in the lymph nodes draining the respiratory tract, we also saw evidence of virus-specific CD8 T cell activation in the spleen. Furthermore, CD8 T cells primed in the spleen differentiated into memory cells of equivalent longevity and with similar recall capacity as CD8 T cells primed in the draining lymph nodes. These data showed that the spleen contributes to the virus-specific effector and memory CD8 T cell populations that are generated in response to respiratory infection.
在健康个体中,流感病毒 (IAV) 感染通常局限于呼吸道的上皮细胞。此前,人们认为在 IAV 感染过程中全身性出现的 IAV 特异性效应 CD8 T 细胞是在肺部引流淋巴结中被激活的,随后迁移到其他组织。然而,对于其他淋巴组织部位是否参与局部 IAV 感染中病毒特异性 CD8 T 细胞的产生,人们知之甚少。在这里,我们提出了在呼吸道 IAV 感染后,脾脏中 CD8 T 细胞早期被激活的证据,而与肺部引流淋巴结中的 T 细胞激活无关。尽管我们在引流呼吸道的淋巴结中发现了 CD8 T 细胞激活的早期迹象,但我们也在脾脏中观察到了病毒特异性 CD8 T 细胞激活的证据。此外,在脾脏中被激活的 CD8 T 细胞分化为具有同等寿命和类似回忆能力的记忆细胞,与在引流淋巴结中被激活的 CD8 T 细胞相当。这些数据表明,脾脏有助于产生针对呼吸道感染的病毒特异性效应和记忆 CD8 T 细胞群体。