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皮肤屏障破坏对白喉毒素的局部应用交叉反应物质CRM(197)免疫反应的影响。

Effect of skin barrier disruption on immune responses to topically applied cross-reacting material, CRM(197), of diphtheria toxin.

作者信息

Godefroy S, Peyre M, Garcia N, Muller S, Sesardic D, Partidos C D

机构信息

UPR 9021, Institut de Biologie Moléculaire et Cellulaire, CNRS, 15 Rue René Descartes, F-67084, Strasbourg, France.

出版信息

Infect Immun. 2005 Aug;73(8):4803-9. doi: 10.1128/IAI.73.8.4803-4809.2005.

DOI:10.1128/IAI.73.8.4803-4809.2005
PMID:16040993
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1201251/
Abstract

The high accessibility of the skin and the presence of immunocompetent cells in the epidermis makes this surface an attractive route for needle-free administration of vaccines. However, the lining of the skin by the stratum corneum is a major obstacle to vaccine delivery. In this study we examined the effect of skin barrier disruption on the immune responses to the cross-reacting material CRM(197), a nontoxic mutant of diphtheria toxin (DTx) that is considered as a vaccine candidate. Application of CRM(197), together with cholera toxin (CT), onto the tape-stripped skin of mice elicited antibody responses that had anti-DTx neutralizing activity. Vaccine delivery onto mildly ablated skin or intact skin did not elicit any detectable anti-CRM(197) antibodies. Mice immunized with CRM(197) alone onto the tape-stripped skin mounted a vigorous antigen-specific proliferative response. In contrast, the induction of cellular immunity after CRM(197) deposition onto mildly ablated or intact skin was adjuvant dependent. Furthermore, epidermal cells were activated and underwent apoptosis that was more pronounced when the stratum corneum was removed by tape stripping. Overall, these findings highlight the potential for transcutaneous delivery of CRM(197) and establish a correlation between the degree of barrier disruption and levels of antigen-specific immune responses. Moreover, these results provide the first evidence that the development of a transcutaneous immunization strategy for diphtheria, based on simple and practical methods to disrupt the skin barrier, is feasible.

摘要

皮肤的高可及性以及表皮中免疫活性细胞的存在,使得皮肤表面成为无针接种疫苗的一个有吸引力的途径。然而,角质层对皮肤的覆盖是疫苗递送的一个主要障碍。在本研究中,我们检测了皮肤屏障破坏对交叉反应物质CRM(197)免疫反应的影响,CRM(197)是白喉毒素(DTx)的一种无毒突变体,被视为一种候选疫苗。将CRM(197)与霍乱毒素(CT)一起应用于小鼠的胶带剥离皮肤上,可引发具有抗DTx中和活性的抗体反应。将疫苗递送至轻度消融的皮肤或完整皮肤上,未引发任何可检测到的抗CRM(197)抗体。单独在胶带剥离皮肤上用CRM(197)免疫的小鼠产生了强烈的抗原特异性增殖反应。相比之下,将CRM(197)沉积在轻度消融或完整皮肤上后,细胞免疫的诱导依赖于佐剂。此外,表皮细胞被激活并发生凋亡,当通过胶带剥离去除角质层时,这种凋亡更为明显。总体而言,这些发现突出了经皮递送CRM(197)的潜力,并建立了屏障破坏程度与抗原特异性免疫反应水平之间的相关性。此外,这些结果提供了首个证据,即基于简单实用的方法破坏皮肤屏障的白喉经皮免疫策略的开发是可行的。

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J Infect Dis. 2004 Sep 15;190(6):1177-82. doi: 10.1086/423327. Epub 2004 Aug 11.
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Modulation of immune responses with transcutaneously deliverable adjuvants.经皮可递送佐剂对免疫反应的调节作用。
Vaccine. 2004 Jun 23;22(19):2385-90. doi: 10.1016/j.vaccine.2003.11.063.
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Topical delivery of imiquimod to a mouse model as a novel adjuvant for human immunodeficiency virus (HIV) DNA.咪喹莫特向小鼠模型的局部给药作为人类免疫缺陷病毒(HIV)DNA的新型佐剂。
Vaccine. 2004 Apr 16;22(13-14):1791-8. doi: 10.1016/j.vaccine.2003.10.051.
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Transcutaneous immunization induces mucosal CTLs and protective immunity by migration of primed skin dendritic cells.经皮免疫通过致敏皮肤树突状细胞的迁移诱导黏膜细胞毒性T淋巴细胞及保护性免疫。
J Clin Invest. 2004 Apr;113(7):998-1007. doi: 10.1172/JCI20261.
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J Immunol. 2004 Jan 1;172(1):302-9. doi: 10.4049/jimmunol.172.1.302.
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Physicochemical and immunochemical techniques predict the quality of diphtheria toxoid vaccines.物理化学和免疫化学技术可预测白喉类毒素疫苗的质量。
Vaccine. 2003 Dec 12;22(2):156-67. doi: 10.1016/j.vaccine.2003.08.003.
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