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Immunogenicity of DNA vaccines expressing tuberculosis proteins fused to tissue plasminogen activator signal sequences.表达与组织型纤溶酶原激活剂信号序列融合的结核蛋白的DNA疫苗的免疫原性。
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针对结核分枝杆菌的早期分泌性抗原靶蛋白6亚单位疫苗接种

ESAT-6 subunit vaccination against Mycobacterium tuberculosis.

作者信息

Brandt L, Elhay M, Rosenkrands I, Lindblad E B, Andersen P

机构信息

Department of TB Immunology, Statens Serum Institut, Copenhagen, Denmark.

出版信息

Infect Immun. 2000 Feb;68(2):791-5. doi: 10.1128/IAI.68.2.791-795.2000.

DOI:10.1128/IAI.68.2.791-795.2000
PMID:10639447
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC97206/
Abstract

The ESAT-6 antigen from Mycobacterium tuberculosis is a dominant target for cell-mediated immunity in the early phase of tuberculosis (TB) in TB patients as well as in various animal models. The purpose of our study was to evaluate the potential of ESAT-6 in an experimental TB vaccine. We started out using dimethyl dioctadecylammonium bromide (DDA), an adjuvant which has been demonstrated to be efficient for the induction of cellular immune responses and has been used successfully before as a delivery system for TB vaccines. Here we demonstrate that, whereas immune responses to both short-term-culture filtrate and Ag85B are efficiently induced with DDA, this adjuvant was inefficient for the induction of immune responses to ESAT-6. Therefore, we investigated the modulatory effect of monophosphoryl lipid A (MPL), an immunomodulator which in different combinations has demonstrated strong adjuvant activity for both cellular and humoral immune responses. We show in the present study that vaccination with ESAT-6 delivered in a combination of MPL and DDA elicited a strong ESAT-6-specific T-cell response and protective immunity comparable to that achieved with Mycobacterium bovis BCG.

摘要

结核分枝杆菌的早期分泌性抗原靶6(ESAT-6)抗原是结核病(TB)患者以及各种动物模型中结核病早期细胞介导免疫的主要靶点。我们研究的目的是评估ESAT-6在实验性结核病疫苗中的潜力。我们最初使用的是二甲基二十八烷基溴化铵(DDA),一种已被证明能有效诱导细胞免疫反应且此前已成功用作结核病疫苗递送系统的佐剂。在此我们证明,虽然DDA能有效诱导对短期培养滤液和Ag85B的免疫反应,但该佐剂对诱导ESAT-6的免疫反应效率低下。因此,我们研究了单磷酰脂质A(MPL)的调节作用,MPL是一种免疫调节剂,在不同组合中已证明对细胞免疫和体液免疫反应均具有强大的佐剂活性。我们在本研究中表明,用MPL和DDA组合递送的ESAT-6进行疫苗接种可引发强烈的ESAT-6特异性T细胞反应和与牛分枝杆菌卡介苗相当的保护性免疫。