Department of Pathology, University of Massachusetts Medical School, 55 Lake Avenue North, Worcester, MA, 01583, USA,
Arch Immunol Ther Exp (Warsz). 2013 Oct;61(5):341-53. doi: 10.1007/s00005-013-0236-z. Epub 2013 May 25.
Recent observations have uncovered multiple pathways whereby CD4 T cells can contribute to protective immune responses against microbial threats. Incorporating the generation of memory CD4 T cells into vaccine strategies thus presents an attractive approach toward improving immunity against several important human pathogens, especially those against which antibody responses alone are inadequate to confer long-term immunity. Here, we review how memory CD4 T cells provide protection against influenza viruses. We discuss the complexities of protective memory CD4 T cell responses observed in animal models and the potential challenges of translating these observations into the clinic. Specifically, we concentrate on how better understanding of organ-specific heterogeneity of responding cells and defining multiple correlates of protection might improve vaccine-generated memory CD4 T cells to better protect against seasonal, and more importantly, pandemic influenza.
最近的观察结果揭示了 CD4 T 细胞可以通过多种途径对针对微生物威胁的保护性免疫反应做出贡献。因此,将记忆 CD4 T 细胞的产生纳入疫苗策略是一种很有吸引力的方法,可以提高对几种重要人类病原体的免疫力,尤其是那些仅靠抗体反应不足以提供长期免疫力的病原体。在这里,我们回顾了记忆 CD4 T 细胞如何提供对流感病毒的保护。我们讨论了在动物模型中观察到的保护性记忆 CD4 T 细胞反应的复杂性,以及将这些观察结果转化为临床实践所面临的潜在挑战。具体来说,我们集中讨论了更好地理解反应细胞的器官特异性异质性和定义多种保护相关性如何改善疫苗产生的记忆 CD4 T 细胞,以更好地预防季节性流感,更重要的是,预防大流行流感。