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Combining rapid diagnostic tests to estimate primary and post-primary dengue immune status at the point of care.
Biggs, Joseph R; Sy, Ava Kristy; Ashall, James; Santoso, Marsha S; Brady, Oliver J; Reyes, Mary Anne Joy; Quinones, Mary Ann; Jones-Warner, William; Tandoc, Amadou O; Sucaldito, Nemia L; Mai, Huynh Kim; Lien, Le Thuy; Thai, Hung Do; Nguyen, Hien Anh Thi; Anh, Dang Duc; Iwasaki, Chihiro; Kitamura, Noriko; Van Loock, Marnix; Herrera-Taracena, Guillermo; Menten, Joris; Rasschaert, Freya; Van Wesenbeeck, Liesbeth; Masyeni, Sri; Haryanto, Sotianingsih; Yohan, Benediktus; Cutiongco-de la Paz, Eva; Yoshida, Lay-Myint; Hue, Stephane; Rosario Z Capeding, Maria; Padilla, Carmencita D; Sasmono, R Tedjo; Hafalla, Julius Clemence R; Hibberd, Martin L.
Afiliación
  • Biggs JR; Department of Infection Biology, Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom.
  • Sy AK; Department of Virology, Research Institute for Tropical Medicine, Manila, Philippines.
  • Ashall J; Dengue Study Group, Research Institute for Tropical Medicine, Manila, Philippines.
  • Santoso MS; Department of Infection Biology, Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom.
  • Brady OJ; Dengue Research Unit, Eijkman Institute for Molecular Biology, National Agency for Research and Innovation of the Republic of Indonesia, Jakarta, Indonesia.
  • Reyes MAJ; Department of Infectious Disease Epidemiology, Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London, United Kingdom.
  • Quinones MA; Centre for the Mathematical Modelling of Infectious Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom.
  • Jones-Warner W; Department of Virology, Research Institute for Tropical Medicine, Manila, Philippines.
  • Tandoc AO; Dengue Study Group, Research Institute for Tropical Medicine, Manila, Philippines.
  • Sucaldito NL; Department of Virology, Research Institute for Tropical Medicine, Manila, Philippines.
  • Mai HK; Dengue Study Group, Research Institute for Tropical Medicine, Manila, Philippines.
  • Lien LT; Department of Infection Biology, Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom.
  • Thai HD; Department of Virology, Research Institute for Tropical Medicine, Manila, Philippines.
  • Nguyen HAT; Philippine Epidemiology Bureau, Department of Health, Manila, Philippines.
  • Anh DD; Pasteur Institute of Nha Trang, Nha Trang, Vietnam.
  • Iwasaki C; Pasteur Institute of Nha Trang, Nha Trang, Vietnam.
  • Kitamura N; Pasteur Institute of Nha Trang, Nha Trang, Vietnam.
  • Van Loock M; National Institute of Hygiene and Epidemiology, Hanoi, Vietnam.
  • Herrera-Taracena G; National Institute of Hygiene and Epidemiology, Hanoi, Vietnam.
  • Menten J; Paediatric Infectious Diseases Department, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan.
  • Rasschaert F; Paediatric Infectious Diseases Department, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan.
  • Van Wesenbeeck L; Janssen Global Public Health, Janssen Pharmaceutica NV, Beerse, Belgium.
  • Masyeni S; Janssen Global Public Health, Janssen Research & Development, Horsham, Pennsylvania, United States of America.
  • Haryanto S; Quantitative Sciences, Janssen Pharmaceutica NV, Beerse, Belgium.
  • Yohan B; Janssen Global Public Health, Janssen Pharmaceutica NV, Beerse, Belgium.
  • Cutiongco-de la Paz E; Janssen Global Public Health, Janssen Pharmaceutica NV, Beerse, Belgium.
  • Yoshida LM; Department of Internal Medicine, Faculty of Medicine and Health Sciences, Universitas Warmadewa, Denpasar, Bali, Indonesia.
  • Hue S; Raden Mattaher Hospital, Jambi, Indonesia.
  • Rosario Z Capeding M; Dengue Research Unit, Eijkman Institute for Molecular Biology, National Agency for Research and Innovation of the Republic of Indonesia, Jakarta, Indonesia.
  • Padilla CD; Institute of Human Genetics, University of the Philippines, Manila, Philippines.
  • Sasmono RT; Philippine Genome Centre, University of the Philippines, Manila, Philippines.
  • Hafalla JCR; Paediatric Infectious Diseases Department, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan.
  • Hibberd ML; Department of Infectious Disease Epidemiology, Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London, United Kingdom.
PLoS Negl Trop Dis ; 16(5): e0010365, 2022 05.
Article en En | MEDLINE | ID: mdl-35507552
BACKGROUND: Characterising dengue virus (DENV) infection history at the point of care is challenging as it relies on intensive laboratory techniques. We investigated how combining different rapid diagnostic tests (RDTs) can be used to accurately determine the primary and post-primary DENV immune status of reporting patients during diagnosis. METHODS AND FINDINGS: Serum from cross-sectional surveys of acute suspected dengue patients in Indonesia (N:200) and Vietnam (N: 1,217) were assayed using dengue laboratory assays and RDTs. Using logistic regression modelling, we determined the probability of being DENV NS1, IgM and IgG RDT positive according to corresponding laboratory viremia, IgM and IgG ELISA metrics. Laboratory test thresholds for RDT positivity/negativity were calculated using Youden's J index and were utilized to estimate the RDT outcomes in patients from the Philippines, where only data for viremia, IgM and IgG were available (N:28,326). Lastly, the probabilities of being primary or post-primary according to every outcome using all RDTs, by day of fever, were calculated. Combining NS1, IgM and IgG RDTs captured 94.6% (52/55) and 95.4% (104/109) of laboratory-confirmed primary and post-primary DENV cases, respectively, during the first 5 days of fever. Laboratory test predicted, and actual, RDT outcomes had high agreement (79.5% (159/200)). Among patients from the Philippines, different combinations of estimated RDT outcomes were indicative of post-primary and primary immune status. Overall, IgG RDT positive results were confirmatory of post-primary infections. In contrast, IgG RDT negative results were suggestive of both primary and post-primary infections on days 1-2 of fever, yet were confirmatory of primary infections on days 3-5 of fever. CONCLUSION: We demonstrate how the primary and post-primary DENV immune status of reporting patients can be estimated at the point of care by combining NS1, IgM and IgG RDTs and considering the days since symptoms onset. This framework has the potential to strengthen surveillance operations and dengue prognosis, particularly in low resource settings.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Dengue / Virus del Dengue Tipo de estudio: Diagnostic_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: PLoS Negl Trop Dis Asunto de la revista: MEDICINA TROPICAL Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Dengue / Virus del Dengue Tipo de estudio: Diagnostic_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: PLoS Negl Trop Dis Asunto de la revista: MEDICINA TROPICAL Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Estados Unidos