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DNA免疫后体内抗原表达的持续时间会改变CD8 + T淋巴细胞的数量、收缩情况及二次反应。

Duration of antigen expression in vivo following DNA immunization modifies the magnitude, contraction, and secondary responses of CD8+ T lymphocytes.

作者信息

Hovav Avi-Hai, Panas Michael W, Rahman Shaila, Sircar Piya, Gillard Geoffrey, Cayabyab Mark J, Letvin Norman L

机构信息

Division of Viral Pathogenesis, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02115, USA.

出版信息

J Immunol. 2007 Nov 15;179(10):6725-33. doi: 10.4049/jimmunol.179.10.6725.

Abstract

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.

摘要

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。

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本文引用的文献

1
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2
Persistent antigen presentation after acute vesicular stomatitis virus infection.
J Virol. 2007 Feb;81(4):2039-46. doi: 10.1128/JVI.02167-06. Epub 2006 Dec 6.
3
Duration of the initial TCR stimulus controls the magnitude but not functionality of the CD8+ T cell response.
J Exp Med. 2006 Sep 4;203(9):2135-43. doi: 10.1084/jem.20060928. Epub 2006 Aug 14.
4
Programming, demarcating, and manipulating CD8+ T-cell memory.
Immunol Rev. 2006 Jun;211:67-80. doi: 10.1111/j.0105-2896.2006.00384.x.
5
CD4+ T cells can protect APC from CTL-mediated elimination.
J Immunol. 2006 Jun 15;176(12):7379-84. doi: 10.4049/jimmunol.176.12.7379.
7
Secondary memory CD8+ T cells are more protective but slower to acquire a central-memory phenotype.
J Exp Med. 2006 Apr 17;203(4):919-32. doi: 10.1084/jem.20052237. Epub 2006 Mar 27.
10
Unexpected prolonged presentation of influenza antigens promotes CD4 T cell memory generation.
J Exp Med. 2005 Sep 5;202(5):697-706. doi: 10.1084/jem.20050227.

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