Department of Mycobacterium, Jiangsu Key Laboratory of Molecular Biology for Skin Diseases and STIs, Institute of Dermatology, Chinese Academy of Medical Sciences & Peking Union Medical College, Nanjing, China.
National Centre for STD and Leprosy Control, China CDC, Nanjing, China.
Front Cell Infect Microbiol. 2022 Apr 11;12:814413. doi: 10.3389/fcimb.2022.814413. eCollection 2022.
The diagnosis of paucibacillary (PB) leprosy often possesses a diagnostic challenge, especially for pure neuritic and lesser skin lesions with the zero bacillary load, requiring a sensitive and accurate diagnostic tool. We have included 300 clinically diagnosed new leprosy cases (comprising 98 PB cases) and analyzed the sensitivity and specificity of PB leprosy cases by nested PCR with , , , , and and Enzyme-linked Immunospot Assay test (ELISPOT) with MMPII, NDO-BSA, and LID-1 antigens by detecting interferon gamma (IFN-γ) release. The overall positivity rates of genes tested in 300 clinical specimens were identified as 55% of , 59% of , 59.3% of , 57.3% of , 61% of while 90% of nested , 92.6% of nested , and 95% of nested , and 285 (95%) of at least one gene positive cases. For PB specimens, 95% PCR positivity was achieved by three tested genes in nested PCR. The data obtained from ELISPOT for three antigens were analyzed for IFN-γ expression with 600 subjects. Among 98 PB leprosy cases, the sensitivity of MMP II, LID-1, and NDO-BSA was 90%, 87%, and 83%, respectively, and the specificity was 90%, 91%, and 86%, respectively. The total number of cases positive for at least one antigen was 90 (91.8%) in PB, which is significantly higher than that in multibacillary (MB) leprosy (56.7%). The combination of multi-targets nested PCR and ELISPOT assay provides a specific tool to early clinical laboratory diagnosis of PB leprosy cases. The two assays are complementary to each other and beneficial for screening PB patients.
少菌型(PB)麻风病的诊断常常具有挑战性,尤其是对于纯神经型和皮肤损伤较少且无细菌载量的病例,需要一种敏感和准确的诊断工具。我们纳入了 300 例临床诊断的新麻风病病例(包括 98 例 PB 病例),通过巢式 PCR 检测、、、、和 以及酶联免疫斑点试验(ELISPOT)检测 MMPII、NDO-BSA 和 LID-1 抗原检测 IFN-γ释放,分析了 PB 麻风病病例的敏感性和特异性。在 300 例临床标本中,检测基因的总阳性率分别为 、 、 、 、 的 55%, 、 、 的 59%, 、 的 59.3%, 的 57.3%, 而嵌套 的 90%,嵌套 的 92.6%,嵌套 的 95%,至少一个基因阳性的病例为 285(95%)。对于 PB 标本,通过嵌套 PCR 检测三个基因可实现 95%的 PCR 阳性。对 600 例患者进行 ELISPOT 检测,分析了三种抗原的 IFN-γ表达数据。在 98 例 PB 麻风病病例中,MMP II、LID-1 和 NDO-BSA 的敏感性分别为 90%、87%和 83%,特异性分别为 90%、91%和 86%。至少有一种抗原阳性的病例总数在 PB 中为 90(91.8%),显著高于多菌型(MB)麻风病(56.7%)。多靶点嵌套 PCR 和 ELISPOT 检测的联合为 PB 麻风病病例的早期临床实验室诊断提供了一种特异性工具。这两种检测方法相辅相成,有利于 PB 患者的筛查。