Autor: |
Francesca Tamarozzi, Tamara Ursini, Pytsje T. Hoekstra, Ronaldo Silva, Cecilia Costa, Federico Gobbi, Gerardo B. Monteiro, Leonardo Motta, Govert J. van Dam, Paul L. Corstjens, Lisette van Lieshout, Dora Buonfrate |
Jazyk: |
angličtina |
Rok vydání: |
2021 |
Předmět: |
|
Zdroj: |
Parasites & Vectors, Vol 14, Iss 1, Pp 1-11 (2021) |
Druh dokumentu: |
article |
ISSN: |
1756-3305 |
DOI: |
10.1186/s13071-021-04655-z |
Popis: |
Abstract Background An accurate test for the diagnosis and post-treatment follow-up of patients with schistosomiasis is needed. We assessed the performance of different laboratory parameters, including the up-converting reporter particle technology lateral flow assay to detect circulating anodic antigen (UCP-LF CAA), for the post-treatment follow-up of schistosomiasis in migrants attending a dedicated outpatient clinic in a non-endemic country. Methods Routine anti-Schistosoma serology results and eosinophil counts were obtained of patients with positive urine/stool microscopy and/or PCR (confirmed cases) or only positive serology (possible cases), and at least one follow-up visit at 6 (T6) or 12 (T12) months after praziquantel treatment. All sera samples were tested with the UCP-LF CAA assay. Results Forty-eight patients were included, 23 confirmed and 25 possible cases. The percentage seropositivity and median antibody titers did not change significantly during follow-up. UCP-LF CAA was positive in 86.9% of confirmed and 20% of possible cases. The percentage positivity and median CAA levels decreased significantly post-treatment, with only two patients having positive CAA levels at T12. Conclusions The UCP-LF CAA assay proved useful for the diagnosis of active infection with Schistosoma spp. and highly valuable for post-treatment monitoring in migrants, encouraging the development of a commercial test. |
Databáze: |
Directory of Open Access Journals |
Externí odkaz: |
|