Khaliq Aasia, Ravindran Resmi, Hussainy Syed Fahadulla, Krishnan Viwanathan V, Ambreen Atiqa, Yusuf Noshin Wasim, Irum Shagufta, Rashid Abdul, Jamil Muhammad, Zaffar Fareed, Chaudhry Muhammad Nawaz, Gupta Puneet K, Akhtar Muhammad Waheed, Khan Imran H
College of Earth and Environmental Sciences, University of the Punjab, Lahore, Pakistan.
Department of Pathology and Laboratory Medicine, University of California, Davis, California, United States of America.
PLoS One. 2017 Apr 5;12(4):e0173359. doi: 10.1371/journal.pone.0173359. eCollection 2017.
Over 9 million new active tuberculosis (TB) cases emerge each year from an enormous pool of 2 billion individuals latently infected with Mycobacterium tuberculosis (M. tb.) worldwide. About 3 million new TB cases per year are unaccounted for, and 1.5 million die. TB, however, is generally curable if diagnosed correctly and in a timely manner. The current diagnostic methods for TB, including state-of-the-art molecular tests, have failed in delivering the capacity needed in endemic countries to curtail this ongoing pandemic. Efficient, cost effective and scalable diagnostic approaches are critically needed. We report a multiplex TB serology panel using microbead suspension array containing a combination of 11 M.tb. antigens that demonstrated overall sensitivity of 91% in serum/plasma samples from TB patients confirmed by culture. Group wise sensitivities for sputum smear positive and negative patients were 95%, and 88%, respectively. Specificity of the test was 96% in untreated COPD patients and 91% in general healthy population. The sensitivity of this test is superior to that of the frontline sputum smear test with a comparable specificity (30-70%, and 93-99%, respectively). The multiplex serology test can be performed with scalability from 1 to 360 patients per day, and is amenable to automation for higher (1000s per day) throughput, thus enabling a scalable clinical work flow model for TB endemic countries. Taken together, the above results suggest that well defined antibody profiles in blood, analyzed by an appropriate technology platform, offer a valuable approach to TB diagnostics in endemic countries.
全球有20亿人潜伏感染结核分枝杆菌,每年从中出现900多万例新的活动性肺结核病例。每年约有300万例新的肺结核病例未得到统计,其中150万人死亡。然而,如果诊断正确及时,肺结核通常是可以治愈的。目前用于肺结核的诊断方法,包括最先进的分子检测,在结核病流行国家未能提供遏制这一持续大流行所需的能力。迫切需要高效、经济有效且可扩展的诊断方法。我们报告了一种使用微珠悬浮阵列的多重肺结核血清学检测板,该检测板包含11种结核分枝杆菌抗原的组合,在经培养确诊的肺结核患者的血清/血浆样本中显示出91%的总体敏感性。痰涂片阳性和阴性患者的组敏感性分别为95%和88%。该检测在未经治疗的慢性阻塞性肺疾病患者中的特异性为96%,在一般健康人群中的特异性为91%。该检测的敏感性优于一线痰涂片检测,特异性相当(分别为30 - 70%和93 - 99%)。多重血清学检测每天可对1至360名患者进行检测,并且适合自动化以实现更高的通量(每天数千例),从而为结核病流行国家建立一个可扩展的临床工作流程模型。综上所述,上述结果表明,通过适当的技术平台分析血液中明确的抗体谱,为结核病流行国家的结核病诊断提供了一种有价值的方法。