Oran Alp E, Robinson Harriet L
Emory Vaccine Center and Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, Georgia 30329, USA.
J Virol. 2004 Apr;78(8):4376-80. doi: 10.1128/jvi.78.8.4376-4380.2004.
For this study, we used DNA-based immunizations to elicit gamma interferon-producing (Tc1) or interleukin 4 (IL-4)-producing (Tc2) CD8 T cells to the influenza virus nucleoprotein. We examined the response of these cells to an intranasal viral challenge. Both the Tc2- and Tc1-biased responses were present in mice with predominantly IL-4-producing (Th2) CD4 T cells. After viral challenge, Tc1 cells underwent more efficient expansion than did Tc2 cells, and only Tc1 cells were detected at the site of infection. In contrast, the CD4 response remained IL-4 biased. However, only a limited number of CD4 cells appeared in the postchallenge lung, and these were strongly enriched for the Th1 phenotype. Thus, the type of memory T-cell response induced by DNA vaccination does not determine the type of response that will predominate at the site of an infection.
在本研究中,我们使用基于DNA的免疫接种方法,诱导产生γ干扰素的(Tc1)或产生白细胞介素4(IL-4)的(Tc2)CD8 T细胞对流感病毒核蛋白产生反应。我们检测了这些细胞对鼻内病毒攻击的反应。在主要产生IL-4的(Th2)CD4 T细胞的小鼠中,同时存在Tc2偏向性反应和Tc1偏向性反应。病毒攻击后,Tc1细胞比Tc2细胞经历了更有效的扩增,并且在感染部位仅检测到Tc1细胞。相比之下,CD4反应仍偏向IL-4。然而,攻击后肺中仅出现有限数量的CD4细胞,并且这些细胞强烈富集Th1表型。因此,DNA疫苗接种诱导的记忆性T细胞反应类型并不能决定在感染部位占主导的反应类型。