健康成人口服卡介苗接种牛分枝杆菌里约热内卢莫罗卡介苗(RDJ)的体液免疫应答调节

Renata Monteiro-Maia, Maria B Ortigão-de-Sampaio, Rosa T Pinho, Luiz R R Castello-Branco
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引用次数: 18

摘要

背景:卡卡苗口服给药最初是卡尔梅特和古姆格林使用的途径,但在吕贝克事故后,几乎所有国家都被皮内给药所取代。然而,巴西继续使用口服卡介苗Moreau RDJ,直到20世纪70年代中期才被皮内途径所取代。虽然自1921年以来,卡介苗疫苗已用于人类,但人们对其诱导的免疫反应知之甚少。本研究的目的是分析口服牛分枝杆菌卡介苗RDJ后的免疫反应。方法:本研究在巴西里约热内卢的健康志愿者中测量了口服牛分枝杆菌卡介苗RDJ免疫反应的细胞和体液方面。描述了t细胞运输和Th1和Th2细胞因子反应,以及使用新技术产生的同型特异性抗体。结果:口服免疫无不良反应。我们已经证明,口服免疫后存在细胞和体液免疫反应。在应答者中,口服再接种不会诱导皮肤试验阳性,而在先前接种过的受试者中,口服多种增强剂能够诱导体液免疫反应的调节(从IgG转变为IgA),并且不能诱导耐受性。相反,细胞免疫反应在皮肤试验阳性和阴性的接种个体之间没有差异。结论:所有受试者,包括那些在研究开始时对皮肤试验没有反应的受试者,都能够对测试的抗原产生体液和细胞免疫反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Modulation of humoral immune response to oral BCG vaccination by Mycobacterium bovis BCG Moreau Rio de Janeiro (RDJ) in healthy adults.

Modulation of humoral immune response to oral BCG vaccination by Mycobacterium bovis BCG Moreau Rio de Janeiro (RDJ) in healthy adults.

Modulation of humoral immune response to oral BCG vaccination by Mycobacterium bovis BCG Moreau Rio de Janeiro (RDJ) in healthy adults.

Modulation of humoral immune response to oral BCG vaccination by Mycobacterium bovis BCG Moreau Rio de Janeiro (RDJ) in healthy adults.

Background: Oral administration of BCG was the route initially used by Calmette and Guérin, but was replaced by intradermal administration in virtually all countries after the Lubeck accident. However, Brazil continued to administer oral BCG Moreau RDJ, which was maintained until the mid-1970s when it was substituted by the intradermal route. Although BCG vaccination has been used in humans since 1921, little is known of the induced immune response. The aim of this study was to analyse immunological responses after oral vaccination with M. bovis BCG Moreau RDJ.

Methods: This study in healthy volunteers has measured cellular and humoral aspects of the immunological response to oral M. bovis BCG Moreau RDJ in Rio de Janeiro, Brazil. T-cell trafficking and Th1 and Th2 cytokine responses are described, as well as isotype-specific antibody production using novel techniques.

Results: Oral immunisation has no adverse effects. We have shown that there are cellular and humoral immunological responses after oral immunisation. Oral revaccination does not induce a positive skin test in responsive individuals and multiple booster orally was able to induce modulation in humoral immunological responses (switch from IgG to IgA) in previously immunised subjects and incapable of inducing tolerance. In contrast, the cellular immune response does not differ between vaccinated individuals with positive and negative skin test reactions.

Conclusion: All subjects, including those who did not respond to the skin test at study commencement, were capable of mounting humoral and cellular immune response to the antigens tested.

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