卡介苗接种儿童抗r32kDaBCG体外干扰素γ水平的年龄相关性减弱

B Anuradha, C M Santosh, V Hari Sai Priya, G Suman Latha, K J R Murthy, Valluri Vijaya Lakshmi
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引用次数: 17

摘要

背景:在不同地理区域进行的不同试验中,牛分枝杆菌卡介苗显示出不一致的疗效。然而,它大大降低了严重儿童结核病的风险,并在许多国家继续用于预防结核病。许多研究表明,疫苗的效力随着年龄的增长而减弱。大多数研究都是基于体内和体外对结核菌素的反应。随着诸如体外干扰素- γ测定和强效免疫原性分枝杆菌蛋白鉴定等新试验的出现,有必要证实这些观察结果。本研究旨在通过体外释放ifn - γ来确定老年患者是否需要增强剂,同时评估Ag85A作为抗原的作用。方法:90例无临床证据的健康儿童,45例有bcg瘢痕,45例无瘢痕,25例有结核。分析了1996-2005年期间在DOTS诊所就诊的216名儿童的结核病发病率。流式细胞术检测CD3+、CD4+、CD8+细胞计数。采用r32kDaBCG (Ag85A-BCG)蛋白刺激T细胞体外T细胞应答,ELISA法检测上清液中干扰素γ (ifn - γ)细胞因子水平。结果:13-14岁儿童结核病发病率最高,10-12岁儿童次之(χ 2平方数242.22;P < 0.000)。所有受试者的T细胞亚群均在正常范围内。79%接种疫苗的儿童增殖反应呈阳性,平均SI值为4.98 +/- 1.99,而未接种疫苗的儿童增殖反应呈阳性,平均SI值为2.9 +/- 1.6 (p < 0.001), 58%接种疫苗的儿童增殖反应呈阳性,平均SI值为2.9 +/- 1.6 (p < 0.001), 2.9 +/- 1.7(p < 0.057)。接种疫苗儿童的刺激指数在年龄较大的儿童中下降,同时结核病发病率增加。结论:本研究显示,接种卡介苗的儿童体外ifn - γ水平显著升高,证实了卡介苗对儿童有效,但作用可能随着年龄的增长而减弱。改良后的卡介苗r32kDa (Ag85A)可增强免疫。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Age-related waning of in vitro Interferon-gamma levels against r32kDaBCG in BCG vaccinated children.

Age-related waning of in vitro Interferon-gamma levels against r32kDaBCG in BCG vaccinated children.

Age-related waning of in vitro Interferon-gamma levels against r32kDaBCG in BCG vaccinated children.

Age-related waning of in vitro Interferon-gamma levels against r32kDaBCG in BCG vaccinated children.

Background: Mycobacterium bovis BCG vaccine has displayed inconsistent efficacy in different trials conducted in various geographical regions. Nevertheless, it significantly reduces the risk of severe childhood tuberculosis and continues to be used to prevent tuberculosis in many countries. Many studies revealed that efficacy of vaccine wanes with age. Most of the studies were based on in vivo and in vitro responses to tuberculin. With the advent of newer tests such as in vitro interferon-gamma assays and identification of potent immunogenic mycobacterial proteins there is a need to corroborate the observations. This study aims at ascertaining the need for a booster at a later age as indicated by in vitro release of IFN-gamma while evaluating Ag85A as an antigen.

Methods: Ninety healthy children who were without any clinical evidence of the disease, 45 with a BCG-scar and the remaining 45 without scar and 25 with tuberculosis were included in the study. The incidence of TB was analyzed in 216 children attending a DOTS clinic during 1996-2005. CD3+, CD4+ and CD8+ cell counts were measured by Flow cytometry. r32kDaBCG (Ag85A-BCG) protein was used to stimulate T cells in in vitro T cell responses and interferon-gamma (IFN-gamma) cytokine levels in the supernatants were measured by ELISA.

Results: High incidence of TB was observed in age group 13-14 years followed by children in the age group 10-12 years (Chi-square 242.22; p < 0.000). T cell subsets were within the normal range in all subjects. 79% of vaccinated children showed positive proliferative responses with a mean SI value of 4.98 +/- 1.99 while only 39% of the unvaccinated and 58% of the tuberculosis children showed positive responses with mean values of 2.9 +/- 1.6 (p < 0.001) and 2.9 +/- 1.7(p < 0.057), respectively. The stimulation indices in vaccinated children decreased in the older children concurring with an increase in the incidence of TB.

Conclusion: Significantly high levels of in vitro IFN-gamma demonstrated in BCG vaccinated children in our study substantiate the observation that BCG is effective in children, but the effect may wane with age. The immunity could be boosted using modified r32kDa (Ag85A) of BCG.

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