Namhong Thitimakorn, Wangboon Chompunoot, Thanongsaksrikul Jeeraphong, Adisakwattana Poom, Thueng-In Kanyarat
Translational Medicine Program, Institute of Medicine, Suranaree University of Technology, Nakhon Ratchasima, Thailand.
School of Preclinical Science, Institute of Science, Suranaree University of Technology, Nakhon Ratchasima, Thailand.
Trop Parasitol. 2025 Jan-Jun;15(1):21-24. doi: 10.4103/tp.tp_10_24. Epub 2025 Apr 5.
Laboratory diagnosis of strongyloidiasis is most often based on the detection of antibodies against antigens in an enzyme-linked immunosorbent assay (ELISA).
The aim of the study was to validate the efficacy of the B-cell epitope peptide antigens of fatty acid and retinal binding protein in using antibodies against .
Patient samples were identified by an anonymous code and collected from volunteers at Suranaree University of Technology Hospital, Thailand.
The synthesized peptides and cell lysate of were used as antigens in an in-house ELISA format. A total of 78 serum samples were collected from patients infected with , other parasites, and healthy persons.
The receiver operating characteristic curve was used to assess the diagnostic performance of peptide antigens and analysis of variance was utilized to examine differences in peptide reactivity between groups.
The peptide-1 and cell lysate of could clearly differentiate serums among infected and noninfected groups. The peptide-1, peptide-2 of and lysate of antigen had been measured to reveal sensitivities at about 75.00%, 50.00%, and 75.00% with 75.86%, 86.21%, and 89.66% specificities, respectively.
These results could be useful for routine clinical laboratory diagnostic testing and possibly apply for surveillance investigations in the future.
类圆线虫病的实验室诊断通常基于酶联免疫吸附测定(ELISA)中针对抗原的抗体检测。
本研究的目的是验证脂肪酸和视网膜结合蛋白的B细胞表位肽抗原在检测抗体方面的有效性。
患者样本通过匿名代码识别,并从泰国苏兰拉里理工大学医院的志愿者中收集。
合成肽和[具体名称未给出]的细胞裂解物用作内部ELISA形式的抗原。共从感染[具体名称未给出]、其他寄生虫的患者以及健康人身上收集了78份血清样本。
采用受试者工作特征曲线评估肽抗原的诊断性能,并利用方差分析检查各组之间肽反应性的差异。
[具体名称未给出]的肽-1和细胞裂解物能够清晰地区分感染组和非感染组的血清。[具体名称未给出]的肽-1、肽-2以及[具体名称未给出]抗原的裂解物的敏感性分别约为75.00%、50.00%和75.00%,特异性分别为75.86%、86.21%和89.66%。
这些结果可能有助于常规临床实验室诊断检测,并可能在未来应用于监测调查。