Parsons Sven D C, Morar-Leather Darshana, Buss Peter, Hofmeyr Jennifer, McFadyen Ross, Rutten Victor P M G, van Helden Paul D, Miller Michele A, Michel Anita Luise
DST/NRF Centre of Excellence for Biomedical Tuberculosis Research, Cape Town, South Africa.
SAMRC Centre for TB Research, Cape Town, South Africa.
Front Immunol. 2017 Dec 22;8:1831. doi: 10.3389/fimmu.2017.01831. eCollection 2017.
is the cause of tuberculosis (TB) in a wide range of species, including white rhinoceroses (). Control of the disease relies on the indirect detection of infection by measuring pathogen-specific responses of the host. These are poorly described in the white rhinoceros and this study aimed to characterize the kinetics of immune responses to infection in this species. Three white rhinoceroses were infected with and their immune sensitization to this pathogen was measured monthly for 20 months. Cell-mediated immunity was characterized in whole blood samples as the differential release of interferon-gamma in response to bovine purified protein derivative (PPDb) and avian PPD (PPDa) as well as the release of this cytokine in response to the proteins 6 kDa early secretory antigenic target (ESAT-6)/10 kDa culture filtrate protein (CFP-10). Humoral immunity was quantified as the occurrence or the magnitude of antibody responses to the proteins ESAT-6/CFP-10, MPB83, MPB83/MPB70, and PPDb. The magnitude and duration of immune reactivity varied between individuals; however, peak responses to these antigens were detected in all animals circa 5-9 months postinfection. Hereafter, they gradually declined to low or undetectable levels. This pattern was associated with limited TB-like pathology at postmortem examination and appeared to reflect the control of infection following the development of the adaptive immune response. Measurement of these markers could prove useful for assessing the disease status or treatment of naturally infected animals. Moreover, immune responses identified in this study might be used to detect infection; however, further studies are required to confirm their diagnostic utility.
是多种物种结核病(TB)的病因,包括白犀牛()。该疾病的控制依赖于通过测量宿主病原体特异性反应来间接检测感染。白犀牛中对这些反应的描述很少,本研究旨在描述该物种对感染的免疫反应动力学。三只白犀牛感染了,在20个月内每月测量它们对这种病原体的免疫致敏情况。在全血样本中,细胞介导的免疫表现为对牛纯化蛋白衍生物(PPDb)和禽PPD(PPDa)的γ干扰素差异释放,以及对6 kDa早期分泌抗原靶标(ESAT-6)/10 kDa培养滤液蛋白(CFP-10)的细胞因子释放。体液免疫通过对ESAT-6/CFP-10、MPB83、MPB83/MPB70和PPDb蛋白的抗体反应的发生情况或强度进行量化。免疫反应的强度和持续时间因个体而异;然而,在所有动物感染后约5-9个月检测到对这些抗原的峰值反应。此后,它们逐渐下降到低水平或无法检测到的水平。这种模式与死后检查中有限的类结核病理相关,似乎反映了适应性免疫反应发展后感染的控制情况。测量这些标志物可能对评估自然感染动物的疾病状态或治疗有用。此外,本研究中确定的免疫反应可能用于检测感染;然而,需要进一步研究来证实它们的诊断效用。