Redhuan Nur Eliyana Mohd, Chin Kai Ling, Adnan Azreen Syazril, Ismail Asma, Balaram Prabha, Phua Kia Kien
PhD Student, School of Veterinary Medicine, Universiti Malaysia Kelantan, Kelantan, Malaysia.
PhD Student, Institute for Research in Molecular Medicine, Universiti Sains Malaysia, Penang, Malaysia.
J Clin Diagn Res. 2017 Jun;11(6):DC10-DC13. doi: 10.7860/JCDR/2017/21928.10055. Epub 2017 Jun 1.
Typhoid fever remains a scourge of humanity, especially in developing and under-developed countries due to poor sanitation and food hygiene. Diagnostic methods available for detection of this disease are not satisfactory due to a lack of sensitive, specific, rapid and convenient diagnostic test kits available in the market.
To evaluate the feasibility of a Dot-EIA method for Ig-class specific salivary antibody detection for diagnosis of typhoid fever.
Paired saliva and serum samples were collected in the year 2010 from patients and normal volunteers in Hospital Universiti Sains Malaysia, Kelantan, Malaysia, which is endemic for typhoid fever. A total of 11 culture-confirmed typhoid fever patients, 43 non-typhoid fever patients and 53 normal human control subjects were evaluated for antibodies against a 50 kDa antigen specific for Typhi using Dot-EIA.
Ig class-specific screening of the test samples showed a higher sensitivity for IgA (90.9%) compared to either IgG (72.7%) or IgM (72.7%) antibodies in saliva, but for serum, IgG (90.9%) had a higher degree of sensitivity compared to IgA (36.4%) and IgM (63.6%). Combining all isotypes (IgA, IgG or IgM), serum showed a higher sensitivity (100.0%) compared to saliva (90.9%). Also, the specificity for serum (100.0%) was much higher than saliva (85.4%).
Salivary IgA anti-50kDa antibody was found to be more suitable biomarker for routine screening, whereas serum IgG was more suitable for confirmatory test as it has higher specificity. Nevertheless, salivary IgA Dot-EIA is a convenient method for rapid testing, such as for Point-of-Care Diagnostics (POCD) and field epidemiological studies, due to its non-invasive nature and ease of use.
伤寒热仍然是人类的一大祸害,尤其是在发展中国家和欠发达国家,因为卫生条件差和食品卫生状况不佳。由于市场上缺乏灵敏、特异、快速且便捷的诊断试剂盒,现有的用于检测该疾病的诊断方法并不令人满意。
评估斑点酶免疫测定法(Dot-EIA)检测伤寒热特异性Ig类唾液抗体用于诊断伤寒热的可行性。
2010年从马来西亚吉兰丹州马来西亚理科大学医院的患者和正常志愿者中收集配对的唾液和血清样本,该地区为伤寒热流行区。使用Dot-EIA对总共11例培养确诊的伤寒热患者、43例非伤寒热患者和53名正常对照受试者进行针对伤寒杆菌特异性50 kDa抗原的抗体检测。
对检测样本进行Ig类特异性筛查发现,唾液中IgA抗体的敏感性(90.9%)高于IgG(72.7%)或IgM(72.7%)抗体,但在血清中,IgG(90.9%)的敏感性高于IgA(36.4%)和IgM(63.6%)。综合所有同种型(IgA、IgG或IgM),血清的敏感性(100.0%)高于唾液(90.9%)。此外,血清的特异性(100.0%)远高于唾液(85.4%)。
唾液IgA抗50 kDa抗体被发现是更适合常规筛查的生物标志物,而血清IgG因其更高的特异性更适合用于确证试验。然而,由于其非侵入性和易用性,唾液IgA Dot-EIA是一种用于快速检测的便捷方法,如即时诊断(POCD)和现场流行病学研究。