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首页> 外文期刊>The Journal of Immunology: Official Journal of the American Association of Immunologists >Antigen-Specific CD8~+ T Cells Persist in the Upper Respiratiory Tract Following Influenza Virus Infection
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Antigen-Specific CD8~+ T Cells Persist in the Upper Respiratiory Tract Following Influenza Virus Infection

机译:流感病毒感染后,抗原特异性CD8〜+ T细胞持续存在于上呼吸道

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Because little is known about lymphocyte responses in the nasal mucosa,lymphocyte accumulation in the nasal mucosa,nasal-associated lymphoid tissue (NALT),and cervical lymph nodes (CLN) were determined after primary and heterosubtypic intranasal influenza challenge of mice.T cell accumulation peaked in the nasal mucosa on day 7,but peaked slightly earlier in the CLN (day 5) and later (day 10) in the NALT.Tetrameric staining of nasal mucosal cells revealed a peak accumulation of CD8 T cells specific for either the H-2C~b influenza nucleoprotein epitope 366-374 (D~BNP_366) or the H-2D~b polymerase 2 protein epitope 224-233 (D~bPA_224) at 7 days.By 13,D~bPA_(224)-specific CD8 T cells were undetectable in the mucosa,whereas D~bNP_(366)-specific CD8 T cells persisted for at least 35 days in the mucosa and spleen.After heterosubtypic virus challenge,the accumulation of CD8 T cells in the nasal mucosa was quicker,more intense,and predominantly D~bNP_(366) specific relative to the primary inoculation.The kinetics and specificity of the CD8 T cell response were similar to those in the CLN, but responses in the NALT and spleen were again slower and more protracted.These results indicate that similar to what was reported in the lung,D~bNP_(366)-specific CD8 T cells persist in the nasal mucosa after primary influenza infection and predominate in an intensified nasal mucosal response to heterosubtypic challenge.In addition,differences in the kinetics of the CD8 T cell responses in the CLN,NALT,and spleen suggest different roles of these lymphoid tissues in the mucosal response.
机译:由于对鼻粘膜的淋巴细胞反应了解甚少,因此在对小鼠进行原发性和异型鼻内流感攻击后,确定了鼻粘膜中的淋巴细胞蓄积,鼻相关淋巴样组织(NALT)和颈淋巴结(CLN).T细胞蓄积鼻粘膜在第7天达到峰值,但在CLN(第5天)稍晚达到峰值,在NALT稍晚(第10天)达到峰值。鼻粘膜细胞的四聚体染色显示了H8特异性CD8 T细胞的峰值积累7天时2C〜b流感核蛋白表位366-374(D〜BNP_366)或H-2D_b聚合酶2蛋白表位224-233(D〜bPA_224).13,D〜bPA_(224)特异性CD8 T在粘膜中未检测到细胞,而D〜bNP_(366)特异性CD8 T细胞在粘膜和脾脏中持续至少35天。异型病毒攻击后,鼻粘膜中CD8 T细胞的积累更快,更多。相对于主要接种物具有强烈的D_bNP_(366)特异性CD8 T细胞反应的动力学和特异性与CLN相似,但NALT和脾脏的反应又较慢且更持久。这些结果表明,与肺中报道的相似,D〜bNP_ (366)特异性CD8 T细胞在原发性流感感染后在鼻黏膜中持续存在,并在对异型挑战的鼻黏膜反应增强中占主导地位。此外,CLN,NALT和脾脏中CD8 T细胞反应的动力学差异提示这些淋巴组织在粘膜反应中的不同作用。

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