Guirado Evelyn, Gil Olga, Cáceres Neus, Singh Mahavir, Vilaplana Cristina, Cardona Pere-Joan
Unitat de Tuberculosi Experimental, Department of Microbiology, Fundació Institut per a la Investigació en Ciències de la Salut Germans Trias i Pujol, Universitat Autònoma de Barcelona, Badalona, Catalonia, Spain.
Clin Vaccine Immunol. 2008 Aug;15(8):1229-37. doi: 10.1128/CVI.00094-08. Epub 2008 Jun 4.
RUTI is a therapeutic vaccine that is generated from detoxified and liposomed Mycobacterium tuberculosis cell fragments that has demonstrated its efficacy in the control of bacillus reactivation after short-term chemotherapy. The aim of this study was to characterize the cellular immune response generated after the therapeutic administration of RUTI and to corroborate the lack of toxicity of the vaccine. Mouse and guinea pig experimental models were infected with a low-dose M. tuberculosis aerosol. RUTI-treated animals showed the lowest bacillary load in both experimental models. RUTI also decreased the percentage of pulmonary granulomatous infiltration in the mouse and guinea pig models. This was not the case after Mycobacterium bovis BCG treatment. Cellular immunity was studied through the characterization of the intracellular gamma interferon (IFN-gamma)-producing cells after the splenocytes' stimulation with M. tuberculosis-specific structural and growth-related antigens. Our data show that the difference between the therapeutic administration of BCG and RUTI resides mainly in the stronger activation of IFN-gamma(+) CD4(+) cells and CD8(+) cells against tuberculin purified protein derivative, ESAT-6, and Ag85B that RUTI generates. Both vaccines also triggered a specific immune response against the M. tuberculosis structural antigens Ag16kDa and Ag38kDa and a marked mRNA expression of IFN-gamma, tumor necrosis factor, interleukin-12, inducible nitric oxide synthase, and RANTES in the lung. The results show that RUTI's therapeutic effect is linked not only to the induction of a Th1 response but also to the stimulation of a quicker and stronger specific immunity against structural and growth-related antigens that reduces both the bacillary load and the pulmonary pathology.
RUTI是一种治疗性疫苗,由经解毒和脂质体包裹的结核分枝杆菌细胞片段制成,已证明其在短期化疗后控制杆菌再激活方面的疗效。本研究的目的是表征RUTI治疗性给药后产生的细胞免疫反应,并证实该疫苗无毒性。小鼠和豚鼠实验模型用低剂量结核分枝杆菌气溶胶感染。在两个实验模型中,接受RUTI治疗的动物的细菌载量最低。RUTI还降低了小鼠和豚鼠模型中肺部肉芽肿浸润的百分比。牛分枝杆菌卡介苗治疗后则并非如此。通过用结核分枝杆菌特异性结构和生长相关抗原刺激脾细胞后对产生细胞内γ干扰素(IFN-γ)的细胞进行表征来研究细胞免疫。我们的数据表明,卡介苗和RUTI治疗性给药之间的差异主要在于RUTI产生的针对结核菌素纯化蛋白衍生物、早期分泌性抗原靶6(ESAT-6)和Ag85B的IFN-γ(+) CD4(+)细胞和CD8(+)细胞的更强激活。两种疫苗还引发了针对结核分枝杆菌结构抗原Ag16kDa和Ag38kDa的特异性免疫反应,以及肺部中IFN-γ、肿瘤坏死因子、白细胞介素-12、诱导型一氧化氮合酶和调节激活正常T细胞表达和分泌的趋化因子(RANTES)的显著mRNA表达。结果表明,RUTI的治疗效果不仅与Th1反应的诱导有关,还与对结构和生长相关抗原的更快更强的特异性免疫刺激有关,从而降低了细菌载量和肺部病理状况。