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Clinical and Vaccine Immunology, February 2007, p. 129-133, Vol. 14, No. 2
1071-412X/07/$08.00+0     doi:10.1128/CVI.00278-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Evaluation of an Indirect Immunofluorescence Assay for Strongyloidiasis as a Tool for Diagnosis and Follow-Up{triangledown}

Marina Boscolo,1 Maria Gobbo,1 William Mantovani,2 Monica Degani,1 Mariella Anselmi,1 Geraldo Badona Monteiro,1 Stefania Marocco,1 Andrea Angheben,1 Manuela Mistretta,1 Maria Santacatterina,1 Stefano Tais,1 and Zeno Bisoffi1*

Centre for Tropical Diseases, Sacro Cuore Hospital, Negrar, Verona, Italy,1 Medicine and Public Health Department, University of Verona, Verona, Italy2

Received 12 July 2006/ Returned for modification 2 October 2006/ Accepted 16 November 2006

The diagnostic accuracy of an indirect immunofluorescence antibody test (IFAT) for Strongyloides stercoralis at different serum antibody titers was evaluated. To assess diagnostic sensitivity, sera from 156 patients with known strongyloidiasis were collected. Negative control sera were obtained from a composite group of 427 subjects (blood donors and hospitalized patients). With an area under the receiver-operating characteristic plot of 0.98, the IFAT showed a high level of diagnostic accuracy for strongyloidiasis. An antibody titer of ≥1:20, with 97% sensitivity and 98% specificity, was identified as the diagnostic threshold with the best overall performance. Cross-reactions were evaluated with 41 additional samples from patients with other known helminth infections, and the IFAT detected low-titer positivity in only one subject with filariasis. A positive IFAT result at an antibody dilution of ≥1:80 was virtually 100% specific, with 71% sensitivity. To test the usefulness of the IFAT as a monitoring tool, the changes in specific-antibody titers after treatment in a group of 155 patients were evaluated. Seroreversion or a decrease in antibody titer of twofold or more was observed in 60% of the patients. Response to treatment was directly correlated to the initial antibody titer, and a baseline titer of ≥1:80 was identified as the best predictor of response. In conclusion, a positive IFAT result at an antibody dilution of ≥1:20 is the optimal cutoff for screening. A titer of ≥1:80, with virtually no false-positive result, is a reliable cutoff for a serological assessment of treatment efficacy and for inclusion in clinical trials.


* Corresponding author. Mailing address: Centre for Tropical Diseases, Sacro Cuore Hospital, via Sempreboni 5, 37024, Negrar, Verona, Italy. Phone: (0039) 045-601-3326. Fax: (0039) 045-601-3694. E-mail: zeno.bisoffi{at}sacrocuore.it.

{triangledown} Published ahead of print on 29 November 2006.


Clinical and Vaccine Immunology, February 2007, p. 129-133, Vol. 14, No. 2
1071-412X/07/$08.00+0     doi:10.1128/CVI.00278-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.







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