Samanich K M, Belisle J T, Sonnenberg M G, Keen M A, Zolla-Pazner S, Laal S
Department of Pathology, New York University Medical Center, New York, USA.
J Infect Dis. 1998 Nov;178(5):1534-8. doi: 10.1086/314438.
This study was undertaken to define the antigens in culture filtrates of actively replicating Mycobacterium tuberculosis that are recognized by antibodies from tuberculosis (TB) patients. Two-dimensional Western blots were probed with sera from healthy controls and TB patients that were preabsorbed with Escherichia coli lysates to deplete cross-reactive antibodies. Antibodies from TB patients recognized 26 of the >100 culture filtrate proteins, and the repertoire changed with disease progression. Only 12 of 26 antigens, including 3 proteins implicated in colonization and invasion by mycobacteria (MPT51, MPT32, and 85C), and 9 (as yet undefined proteins) were reactive with sera from TB patients with early noncavitary or cavitary disease. Eight additional antigens, including 4 undefined proteins, were recognized only by sera from a subset of patients with advanced cavitary disease. Studies suggest that 3 of the antigens recognized by sera from patients with early TB (85C, MPT32, and a 88-kDa protein) have strong serodiagnostic potential.
本研究旨在确定活跃复制的结核分枝杆菌培养滤液中可被结核病(TB)患者抗体识别的抗原。二维蛋白质免疫印迹法用来自健康对照和TB患者的血清进行检测,这些血清已用大肠杆菌裂解物预吸收以去除交叉反应性抗体。TB患者的抗体识别出100多种培养滤液蛋白中的26种,且其种类随疾病进展而变化。26种抗原中只有12种,包括3种与分枝杆菌定植和侵袭有关的蛋白(MPT51、MPT32和85C),以及9种(尚未明确的蛋白)与早期非空洞性或空洞性疾病的TB患者血清发生反应。另外8种抗原,包括4种未明确的蛋白,仅被晚期空洞性疾病患者亚组的血清识别。研究表明,早期TB患者血清识别的3种抗原(85C、MPT32和一种88 kDa蛋白)具有很强的血清诊断潜力。