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开发一种用于评估抗结核分枝杆菌疫苗的小鼠分枝杆菌生长抑制试验。

Development of a murine mycobacterial growth inhibition assay for evaluating vaccines against Mycobacterium tuberculosis.

作者信息

Parra Marcela, Yang Amy L, Lim JaeHyun, Kolibab Kristopher, Derrick Steven, Cadieux Nathalie, Perera Liyanage P, Jacobs William R, Brennan Michael, Morris Sheldon L

机构信息

Center for Biologics Evaluation and Research, United States Food and Drug Administration, Bethesda, MD 20892, USA.

出版信息

Clin Vaccine Immunol. 2009 Jul;16(7):1025-32. doi: 10.1128/CVI.00067-09. Epub 2009 May 20.

Abstract

The development and characterization of new tuberculosis (TB) vaccines has been impeded by the lack of reproducible and reliable in vitro assays for measuring vaccine activity. In this study, we developed a murine in vitro mycobacterial growth inhibition assay for evaluating TB vaccines that directly assesses the capacity of immune splenocytes to control the growth of Mycobacterium tuberculosis within infected macrophages. Using this in vitro assay, protective immune responses induced by immunization with five different types of TB vaccine preparations (Mycobacterium bovis BCG, an attenuated M. tuberculosis mutant strain, a DNA vaccine, a modified vaccinia virus strain Ankara [MVA] construct expressing four TB antigens, and a TB fusion protein formulated in adjuvant) can be detected. Importantly, the levels of vaccine-induced mycobacterial growth-inhibitory responses seen in vitro after 1 week of coculture correlated with the protective immune responses detected in vivo at 28 days postchallenge in a mouse model of pulmonary tuberculosis. In addition, similar patterns of cytokine expression were evoked at day 7 of the in vitro culture by immune splenocytes taken from animals immunized with the different TB vaccines. Among the consistently upregulated cytokines detected in the immune cocultures are gamma interferon, growth differentiation factor 15, interleukin-21 (IL-21), IL-27, and tumor necrosis factor alpha. Overall, we have developed an in vitro functional assay that may be useful for screening and comparing new TB vaccine preparations, investigating vaccine-induced protective mechanisms, and assessing manufacturing issues, including product potency and stability.

摘要

用于测量疫苗活性的可重复且可靠的体外检测方法的缺乏,阻碍了新型结核病(TB)疫苗的研发和特性描述。在本研究中,我们开发了一种用于评估结核病疫苗的小鼠体外分枝杆菌生长抑制检测方法,该方法可直接评估免疫脾细胞控制受感染巨噬细胞内结核分枝杆菌生长的能力。使用这种体外检测方法,可以检测到用五种不同类型的结核病疫苗制剂(牛分枝杆菌卡介苗、减毒结核分枝杆菌突变株、DNA疫苗、表达四种结核抗原的改良安卡拉痘苗病毒株[MVA]构建体以及佐剂中配制的结核融合蛋白)免疫诱导的保护性免疫反应。重要的是,在共培养1周后体外观察到的疫苗诱导的分枝杆菌生长抑制反应水平与肺结核小鼠模型中攻击后28天体内检测到的保护性免疫反应相关。此外,在体外培养第7天,用不同结核病疫苗免疫的动物的免疫脾细胞诱发了相似的细胞因子表达模式。在免疫共培养中持续上调的细胞因子包括γ干扰素、生长分化因子15、白细胞介素-21(IL-21)、IL-27和肿瘤坏死因子α。总体而言,我们开发了一种体外功能检测方法,该方法可能有助于筛选和比较新型结核病疫苗制剂、研究疫苗诱导的保护机制以及评估生产问题,包括产品效力和稳定性。

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