Lanoix Jean-Philippe, Betoudji Fabrice, Nuermberger Eric
Center for Tuberculosis Research, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA INSERM U1088, Amiens, France.
Center for Tuberculosis Research, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Antimicrob Agents Chemother. 2015 Dec 7;60(2):1091-6. doi: 10.1128/AAC.02637-15. Print 2016 Feb.
Pyrazinamide (PZA) is a key sterilizing drug in first-line tuberculosis (TB) regimens and exerts its activity entirely during the first 2 months in human infections. We recently described the reduced activity of PZA in C3HeB/FeJ mice with large caseous tubercles due to neutral pH. Here, we aimed to determine the contribution of PZA to the sterilizing activity of the first-line TB regimen in C3HeB/FeJ and BALB/c mice. Three regimens were compared (in combinations: R, rifampin; H, isoniazid; E, ethambutol; Z, pyrazinamide; with numbers indicating the treatment duration, in months): 2RHEZ/4RH, 2RHE/4RH, and 2RHEZ/4RHZ. Lung CFU counts were assessed after 0 and 2 months of treatment, and relapse rates were assessed 3 months after 3, 4.5, and 6 months of treatment. The relapse rates after 3 months of treatment were 53% and 95% in C3HeB/FeJ mice receiving 2RHEZ/1RH and 2RHE/1RH, respectively, and 67%, 100%, and 80% in BALB/c receiving 2RHEZ/1RH, 2RHE/1RH, and 2RHEZ/1RHZ, respectively. The relapse rates after 4.5 months of treatment were 32%, 20%, and 0% in C3HeB/FeJ mice receiving 2RHEZ/2.5RH, 2RHE/2.5RH, and 2RHEZ/2.5RHZ, respectively, and 0% and 67% in BALB/c receiving 2RHEZ/2.5RH and 2RHE/2.5RH, respectively. The month-6 relapse rates were 0%, 13%, and 0% in C3HeB/FeJ mice given 2RHEZ/4RH, 2RHE/4RH, and 2RHEZ/4RHZ, respectively, and 7% in BALB/c mice receiving 2RHE/4RH. The addition of PZA shortens the duration of treatment needed to prevent relapse in both mouse strains. However, while its contribution is limited to the first 2 months of treatment in BALB/c mice, continuing PZA beyond the first 2 months is beneficial in C3HeB/FeJ mice by preventing relapse among those with the highest disease burden.
吡嗪酰胺(PZA)是一线抗结核治疗方案中的关键杀菌药物,其杀菌活性仅在人类感染的前2个月发挥作用。我们最近报道,由于中性pH值,PZA在患有大的干酪样结核结节的C3HeB/FeJ小鼠中的活性降低。在此,我们旨在确定PZA对一线抗结核治疗方案在C3HeB/FeJ和BALB/c小鼠中的杀菌活性的贡献。比较了三种治疗方案(联合用药:R,利福平;H,异烟肼;E,乙胺丁醇;Z,吡嗪酰胺;数字表示治疗持续时间,单位为月):2RHEZ/4RH、2RHE/4RH和2RHEZ/4RHZ。在治疗0个月和2个月后评估肺部菌落形成单位(CFU)计数,并在治疗3个月、4.5个月和6个月后3个月评估复发率。在接受2RHEZ/1RH和2RHE/1RH的C3HeB/FeJ小鼠中,治疗3个月后的复发率分别为53%和95%,在接受2RHEZ/1RH、2RHE/1RH和2RHEZ/1RHZ的BALB/c小鼠中,复发率分别为67%、100%和80%。在接受2RHEZ/2.5RH、2RHE/2.5RH和2RHEZ/2.5RHZ的C3HeB/FeJ小鼠中,治疗4.5个月后的复发率分别为32%、20%和0%,在接受2RHEZ/2.5RH和2RHE/2.5RH的BALB/c小鼠中,复发率分别为0%和67%。在给予2RHEZ/4RH、2RHE/4RH和2RHEZ/4RHZ的C3HeB/FeJ小鼠中,6个月时的复发率分别为0%、13%和0%,在接受2RHE/4RH的BALB/c小鼠中复发率为7%。添加PZA可缩短两种小鼠品系预防复发所需的治疗时间。然而,虽然其作用在BALB/c小鼠中仅限于治疗的前2个月,但在C3HeB/FeJ小鼠中,在最初2个月后继续使用PZA通过预防疾病负担最高的小鼠复发是有益的。