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. 2022 Jul 25;107(3):636-639.
doi: 10.4269/ajtmh.22-0076. Online ahead of print.

Comparison of Two Serological Assays in Detecting Strongyloides Infection in Immunocompromised Patients

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Comparison of Two Serological Assays in Detecting Strongyloides Infection in Immunocompromised Patients

Emelia Osman et al. Am J Trop Med Hyg. .

Abstract

Strongyloides infection may develop into fatal hyperinfection and dissemination syndrome in immunocompromised hosts. Despite suboptimal specificity issues, the detection of IgG antibodies by ELISA has been central in the serodiagnosis of Strongyloides infection. Recently, an IgG4-based lateral-flow test (SsRapid) using recombinant NIE (rNIE) protein with good diagnostic performance has been reported. This study assessed the result concordance between a commercial IgG-ELISA and the SsRapid. Additionally, we determined the Strongyloides seroprevalence and its association with clinical manifestations. Immunocompromised patients (N = 200) were from Hospital Canselor Tuanku Muhriz, Kuala Lumpur, Malaysia, and were diagnosed with HIV/AIDS, hematological malignancy, and solid organ cancers. Their plasma samples were tested using a commercial IgG-ELISA and SsRapid. A fair concordance (κ = 0.27-0.33; P < 0.05) among the tests was demonstrated. The SsRapid exhibited a significantly higher (P < 0.05) seroprevalence (10.5% [21/200]) compared with IgG-ELISA (7.5% [15/200]). After adsorption with rNIE, all SsRapid-positive samples tested negative with the rapid test, thus showing binding specificity. There was no significant association with clinical manifestations. This study revealed that SsRapid is a useful diagnostic tool for Strongyloides infection, and there is a notable seroprevalence among the immunocompromised patients.

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Figures

Figure 1.
Figure 1.
Images of some dipsticks tested with serum samples pre- and post-adsorbtion with rNIE. Arrows show the positions of the test lines of different intensities. Above the test line is the control line (goat anti-mouse IgG). Dipsticks with various test line intensities became negative after serum adsorption.

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