Dengue Research Unit, Eijkman Institute for Molecular Biology, Ministry of Research and Technology/National Agency for Research and Innovation of the Republic Indonesia, Jl. Diponegoro 69, Jakarta, 10430, Indonesia.
Department of Internal Medicine, Faculty of Medicine and Health Sciences, Universitas Warmadewa, Denpasar, Bali, 80235, Indonesia.
Virol J. 2021 Mar 11;18(1):54. doi: 10.1186/s12985-021-01522-2.
The coronavirus disease 2019 (COVID-19) pandemic remains ongoing around the world, including in areas where dengue is endemic. Dengue and COVID-19, to some extent, have similar clinical and laboratory features, which can lead to misdiagnosis, delayed treatment and patient's isolation. The use of rapid diagnostic tests (RDT) is easy and convenient for fast diagnosis, however there may be issues with cross-reactivity with antibodies for other pathogens.
We assessed the possibility of cross-reactivity between SARS-CoV-2 and dengue antibodies by: (1) testing five brands of COVID-19 IgG / IgM RDTs on 60 RT-PCR-confirmed dengue samples; (2) testing 95 RT-PCR-confirmed COVID-19 samples on dengue RDT; and (3) testing samples positive for COVID-19 IgG and/or IgM on dengue RDT.
We observed a high specificity across all five brands of COVID-19 RDTs, ranging from 98.3 to 100%. Out of the confirmed COVID-19 samples, one patient tested positive for dengue IgM only, another tested positive for dengue IgG only. One patient tested positive for dengue IgG, IgM, and NS1, suggesting a co-infection. In COVID-19 IgG and/or IgM samples, 6.3% of COVID-19 IgG-positive samples also tested positive for dengue IgG, while 21.1% of COVID-19 IgM-positive samples also tested positive for dengue IgG.
Despite the high specificity of the COVID-19 RDT, we observed cross-reactions and false-positive results between dengue and COVID-19. Dengue and COVID-19 co-infection was also found. Health practitioners in dengue endemic areas should be careful when using antibody RDT for the diagnosis of dengue during the COVID-19 pandemic to avoid misdiagnosis.
新型冠状病毒病 2019(COVID-19)大流行仍在全球范围内持续,包括登革热流行地区。登革热和 COVID-19 在某种程度上具有相似的临床和实验室特征,这可能导致误诊、治疗延误和患者隔离。快速诊断测试(RDT)易于使用且方便快速诊断,但可能存在与其他病原体抗体交叉反应的问题。
我们通过以下方法评估 SARS-CoV-2 和登革热抗体之间交叉反应的可能性:(1)用 60 份 RT-PCR 确诊的登革热样本检测五种品牌的 COVID-19 IgG/IgM RDT;(2)用 95 份 RT-PCR 确诊的 COVID-19 样本检测登革热 RDT;(3)用登革热 RDT 检测 COVID-19 IgG 和/或 IgM 阳性样本。
我们观察到五种 COVID-19 RDT 的特异性均很高,范围为 98.3%至 100%。在确诊的 COVID-19 样本中,一名患者仅检测出登革热 IgM 阳性,另一名患者仅检测出登革热 IgG 阳性。一名患者同时检测出登革热 IgG、IgM 和 NS1 阳性,提示合并感染。在 COVID-19 IgG 和/或 IgM 样本中,6.3%的 COVID-19 IgG 阳性样本也检测出登革热 IgG 阳性,而 21.1%的 COVID-19 IgM 阳性样本也检测出登革热 IgG 阳性。
尽管 COVID-19 RDT 的特异性很高,但我们观察到登革热和 COVID-19 之间存在交叉反应和假阳性结果。还发现了登革热和 COVID-19 的合并感染。在 COVID-19 大流行期间,登革热流行地区的卫生保健工作者在使用抗体 RDT 诊断登革热时应谨慎,以避免误诊。