Hovav Avi-Hai, Panas Michael W, Rahman Shaila, Sircar Piya, Gillard Geoffrey, Cayabyab Mark J, Letvin Norman L
Division of Viral Pathogenesis, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02115, USA.
J Immunol. 2007 Nov 15;179(10):6725-33. doi: 10.4049/jimmunol.179.10.6725.
The duration of Ag expression in vivo has been reported to have a minimal impact on both the magnitude and kinetics of contraction of a pathogen-induced CD8(+) T cell response. In this study, we controlled the duration of Ag expression by excising the ear pinnae following intradermal ear pinnae DNA immunization. This resulted in decreased magnitude, accelerated contraction and differentiation, and surprisingly greater secondary CD8(+) T cell responses. Furthermore, we found delayed and prolonged Ag presentation in the immunized mice; however, this presentation was considerably decreased when the depot Ag was eliminated. These findings suggest that the magnitude and the contraction phase of the CD8(+) T cell response following intradermal DNA immunization is regulated by the duration rather than the initial exposure to Ag.
据报道,体内抗原(Ag)表达的持续时间对病原体诱导的CD8(+) T细胞反应的强度和动力学影响极小。在本研究中,我们通过在皮内耳廓DNA免疫后切除耳廓来控制抗原表达的持续时间。这导致反应强度降低、收缩和分化加速,并且令人惊讶的是,二次CD8(+) T细胞反应更强。此外,我们发现免疫小鼠体内的抗原呈递延迟且延长;然而,当储存抗原被清除时,这种呈递显著减少。这些发现表明,皮内DNA免疫后CD8(+) T细胞反应的强度和收缩阶段是由持续时间而非最初接触抗原所调节的。