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慢性脊髓损伤会损害初始 CD8 T 细胞的抗病毒免疫,但不会影响记忆 CD8 T 细胞的产生或功能。

Chronic spinal cord injury impairs primary CD8 T cell antiviral immunity but does not affect generation or function of memory CD8 T cells.

机构信息

Biology Department, Drexel University, Philadelphia, PA 19104, United States of America.

Biology Department, Drexel University, Philadelphia, PA 19104, United States of America.

出版信息

Exp Neurol. 2019 Jul;317:298-307. doi: 10.1016/j.expneurol.2019.03.010. Epub 2019 Mar 20.

Abstract

Antiviral immunity is severely compromised following trauma to the central nervous system. In mice with chronic spinal cord injury (SCI), primary infection with influenza virus leads to high mortality rates due to impaired expansion of virus-specific CD8 T cells. One strategy to increase resistance to viral infections is to generate memory immune cells that protect from recurrent infections. However, it is unknown if chronic SCI also impairs secondary immune responses to influenza challenge as it does primary responses. Here, we used a mouse model of chronic SCI and a clinically relevant influenza A infection to investigate CD8 T cell response. As shown previously, chronic SCI mice had impaired primary antiviral responses with high mortality rates and decreased expansion of virus-specific CD8 T cells following intranasal infection. To investigate CD8 T cell memory, we used two strains of influenza A virus [PR8(H1N1) and X31(H3N2)] that share internal proteins but differ in surface antigens. Chronic SCI mice immunized with live X31 were able to generate memory CD8 T cells that secreted IFNγ upon stimulation with viral peptides ex vivo, which was comparable to immunized uninjured mice. Importantly, immunization prior to challenge with a lethal dose of PR8 resulted in no mortality and significant CD8 T cell recall responses in both uninjured and chronic SCI mice. In addition, memory CD8 T cells generated before SCI remained functional up to 8 weeks after injury. These pre-existing memory CD8 T cells provided full protection from lethal PR8 challenge given at the chronic timepoint following injury. Overall, this study shows that memory CD8 T cells generated either before or after chronic SCI still remain functional. These results highlight the need for proper immunization of SCI patients and show the potential of memory T cells to confer protection against not only influenza, but other viral infections as well.

摘要

抗病毒免疫在中枢神经系统受到创伤后严重受损。在慢性脊髓损伤 (SCI) 的小鼠中,由于病毒特异性 CD8 T 细胞的扩增受损,原发性流感病毒感染导致高死亡率。一种增加对病毒感染抵抗力的策略是产生记忆免疫细胞,以防止反复感染。然而,尚不清楚慢性 SCI 是否也会像原发性反应一样损害对流感挑战的二次免疫反应。在这里,我们使用慢性 SCI 小鼠模型和临床相关的流感 A 感染来研究 CD8 T 细胞反应。如前所述,慢性 SCI 小鼠的原发性抗病毒反应受损,死亡率高,鼻腔感染后病毒特异性 CD8 T 细胞扩增减少。为了研究 CD8 T 细胞记忆,我们使用了两种流感 A 病毒株[PR8(H1N1)和 X31(H3N2)],它们具有内部蛋白共享,但表面抗原不同。用活 X31 免疫的慢性 SCI 小鼠能够产生记忆 CD8 T 细胞,这些细胞在体外用病毒肽刺激时分泌 IFNγ,与免疫未受伤的小鼠相当。重要的是,在挑战致死剂量的 PR8 之前进行免疫接种,导致未受伤和慢性 SCI 小鼠均无死亡率和显著的 CD8 T 细胞回忆反应。此外,在 SCI 之前产生的记忆 CD8 T 细胞在受伤后 8 周内仍然保持功能。这些预先存在的记忆 CD8 T 细胞在受伤后慢性时间点给予致死性 PR8 挑战时提供了完全保护。总体而言,这项研究表明,无论是在慢性 SCI 之前还是之后产生的记忆 CD8 T 细胞仍然保持功能。这些结果强调了对 SCI 患者进行适当免疫接种的必要性,并表明记忆 T 细胞具有保护作用,不仅可以预防流感,还可以预防其他病毒感染。

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