E25Bio, Cambridge, Massachusetts, United States of America.
Institute for Medical Engineering & Science, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.
PLoS Negl Trop Dis. 2020 Jun 24;14(6):e0008203. doi: 10.1371/journal.pntd.0008203. eCollection 2020 Jun.
Dengue virus (DENV) infections pose one of the largest global barriers to human health. The four serotypes (DENV 1-4) present different symptoms and influence immune response to subsequent DENV infections, rendering surveillance, risk assessments, and disease control particularly challenging. Early diagnosis and appropriate clinical management is critical and can be achieved by detecting DENV nonstructural protein 1 (NS1) in serum during the acute phase. However, few NS1-based tests have been developed that are capable of differentiating DENV serotypes and none are currently commercially available.
METHODOLOGY/PRINCIPLE FINDINGS: We developed an enzyme-linked immunosorbent assay (ELISA) to distinguish DENV-1-4 NS1 using serotype-specific pairs of monoclonal antibodies. A total of 1,046 antibodies were harvested from DENV-immunized mice and screened for antigen binding affinity. ELISA clinical performance was evaluated using 408 polymerase chain reaction-confirmed dengue samples obtained from patients in Brazil, Honduras, and India. The overall sensitivity of the test for pan-DENV was 79.66% (325/408), and the sensitivities for DENV-1-4 serotyping were 79.1% (38/48), 80.41% (78/97), 100% (45/45), and 79.6% (98/123), respectively. Specificity reached 94.07-100%.
Our study demonstrates a robust antibody screening strategy that enabled the development of a serotype NS1-based ELISA with maximized specific and sensitive antigen binding. This sensitive and specific assay also utilized the most expansive cohort to date, and of which about half are from Latin America, a geographic region severely underrepresented in previous similar studies. This ELISA test offers potential enhanced diagnostics during the acute phase of infection to help guide patient care and disease control. These results indicate that this ELISA is a promising aid in early DENV-1-4 diagnosis and surveillance in regions of endemicity in addition to offer convenient monitoring for future vaccine interventions.
登革热病毒(DENV)感染是全球人类健康面临的最大挑战之一。四种血清型(DENV1-4)表现出不同的症状,并影响对后续 DENV 感染的免疫反应,这使得监测、风险评估和疾病控制变得特别具有挑战性。早期诊断和适当的临床管理至关重要,可通过在急性期中检测血清中的 DENV 非结构蛋白 1(NS1)来实现。然而,目前开发的能够区分 DENV 血清型的 NS1 检测方法很少,并且没有商业化的产品。
方法/原理发现:我们开发了一种酶联免疫吸附试验(ELISA),使用血清型特异性的单克隆抗体对 DENV-1-4 NS1 进行区分。从 DENV 免疫的小鼠中总共收获了 1046 种抗体,并对其抗原结合亲和力进行了筛选。使用从巴西、洪都拉斯和印度的患者中获得的 408 个经聚合酶链反应(PCR)确认的登革热样本评估了该检测的临床性能。该检测对 pan-DENV 的总体敏感性为 79.66%(325/408),DENV-1-4 血清型的敏感性分别为 79.1%(38/48)、80.41%(78/97)、100%(45/45)和 79.6%(98/123)。特异性达到 94.07-100%。
我们的研究展示了一种强大的抗体筛选策略,该策略可用于开发基于血清型 NS1 的 ELISA,从而实现最大化的特异性和灵敏性的抗原结合。该灵敏且特异性的检测还使用了迄今为止最广泛的队列,其中约一半来自拉丁美洲,这是之前类似研究中严重代表性不足的地区。这种 ELISA 检测在感染的急性期具有潜在的增强诊断能力,有助于指导患者护理和疾病控制。这些结果表明,该 ELISA 是在流行地区进行早期 DENV-1-4 诊断和监测的有前途的辅助手段,并为未来的疫苗干预提供了方便的监测。