Khan Iqbal Hassan, Sayeed M Abu, Sultana Nishat, Islam Kamrul, Amin Jakia, Faruk M Omar, Khan Umama, Khanam Farhana, Ryan Edward T, Qadri Firdausi
Incepta Pharmaceuticals Ltd., Savar, Dhaka, Bangladesh.
International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
Clin Vaccine Immunol. 2016 May 6;23(5):403-409. doi: 10.1128/CVI.00690-15. Print 2016 May.
Enteric fever is a systemic infection caused by typhoidal strains of Salmonella enterica and is a significant cause of mortality and morbidity in many parts of the world, especially in resource-limited areas. Unfortunately, currently available diagnostic tests for enteric fever lack sensitivity and/or specificity. No true clinically practical gold standard for diagnosing patients with enteric fever exists. Unfortunately, microbiologic culturing of blood is only 30 to 70% sensitive although 100% specific. Here, we report the development of a lateral-flow immunochromatographic dipstick assay based on the detection of Salmonella enterica serovar Typhi (S Typhi) lipopolysaccharide (LPS)-specific IgG in lymphocyte culture secretion. We tested the assay using samples from 142 clinically suspected enteric fever patients, 28 healthy individuals residing in a zone where enteric fever is endemic, and 35 patients with other febrile illnesses. In our analysis, the dipstick detected all blood culture-confirmed S Typhi cases (48/48) and 5 of 6 Salmonella enterica serovar Paratyphi A blood cultured-confirmed cases. The test was negative in all 35 individuals febrile with other illnesses and all 28 healthy controls from the zone of endemicity. The test was positive in 19 of 88 individuals with suspected enteric fever but with negative blood cultures. Thus, the dipstick had a sensitivity of 98% compared to blood culture results and a specificity that ranged from 78 to 100% (95% confidence interval [CI], 70 to 100%), depending on the definition of a true negative. These results suggest that this dipstick assay can be very useful for the detection of enteric fever patients especially in regions of endemicity.
肠热症是由肠道沙门氏菌伤寒菌株引起的一种全身性感染,在世界许多地区,尤其是资源有限的地区,是导致死亡和发病的重要原因。不幸的是,目前可用的肠热症诊断测试缺乏敏感性和/或特异性。目前尚无真正适用于临床实际诊断肠热症患者的金标准。不幸的是,血液微生物培养的敏感性仅为30%至70%,尽管特异性为100%。在此,我们报告了一种基于检测淋巴细胞培养分泌物中伤寒沙门氏菌(S Typhi)脂多糖(LPS)特异性IgG的侧向流动免疫色谱试纸条检测方法的开发。我们使用来自142例临床疑似肠热症患者、28例居住在肠热症流行区的健康个体以及35例其他发热性疾病患者的样本对该检测方法进行了测试。在我们的分析中,试纸条检测出了所有血培养确诊的伤寒沙门氏菌病例(48/48)以及6例血培养确诊的甲型副伤寒沙门氏菌病例中的5例。该检测在所有35例患有其他发热性疾病的个体以及来自流行区的所有28例健康对照中均为阴性。在88例疑似肠热症但血培养阴性的个体中,有19例检测呈阳性。因此,与血培养结果相比,该试纸条的敏感性为98%,特异性根据真阴性的定义在78%至100%之间(95%置信区间[CI],70%至100%)。这些结果表明,这种试纸条检测方法对于检测肠热症患者非常有用,尤其是在流行地区。