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Comparative Study
. 2018 Mar 28;12(3):e0006386.
doi: 10.1371/journal.pntd.0006386. eCollection 2018 Mar.

Prospective evaluation of a rapid diagnostic test for Trypanosoma brucei gambiense infection developed using recombinant antigens

Affiliations
Comparative Study

Prospective evaluation of a rapid diagnostic test for Trypanosoma brucei gambiense infection developed using recombinant antigens

Crispin Lumbala et al. PLoS Negl Trop Dis. .

Abstract

Background: Diagnosis and treatment are central elements of strategies to control Trypanosoma brucei gambiense human African trypanosomiasis (HAT). Serological screening is a key entry point in diagnostic algorithms. The Card Agglutination Test for Trypanosomiasis (CATT) has been the most widely used screening test for decades, despite a number of practical limitations that were partially addressed by the introduction of rapid diagnostic tests (RDTs). However, current RDTs are manufactured using native antigens, which are challenging to produce.

Methodology/principal findings: The objective of this study was to evaluate the accuracy of a new RDT developed using recombinant antigens (SD BIOLINE HAT 2.0), in comparison with an RDT produced using native antigens (SD BIOLINE HAT) and CATT. A total of 57,632 individuals were screened in the Democratic Republic of the Congo, either passively at 10 health centres, or actively by 5 mobile teams, and 260 HAT cases were confirmed by parasitology. The highest sensitivity was achieved with the SD BIOLINE HAT 2.0 (71.2%), followed by CATT (62.5%) and the SD BIOLINE HAT (59.0%). The most specific test was CATT (99.2%), while the specificity of the SD BIOLINE HAT and SD BIOLINE HAT 2.0 were 98.9% and 98.1%, respectively. Sensitivity of the tests was lower than previously reported, as they identified cases from partially overlapping sub-populations. All three tests were significantly more sensitive in passive than in active screening. Combining two or three tests resulted in a markedly increased sensitivity: When the SD BIOLINE HAT was combined with the SD BIOLINE HAT 2.0, sensitivity reached 98.4% in passive and 83.0% in active screening.

Conclusions/significance: The recombinant antigen-based RDT was more sensitive than, and as specific as, the SD BIOLINE HAT. It was as sensitive as, but slightly less specific than CATT. While the practicality and cost-effectiveness of algorithms including several screening tests would need to be investigated, using two or more tests appears to enhance sensitivity of diagnostic algorithms, although some decrease in specificity is observed as well.

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Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Fig 1
Fig 1. STARD diagram describing the flow of participants through the study.
Fig 2
Fig 2. Sensitivity (A), specificity (B) and accuracy (C) of the RDT2, RDT1 and CATT tests, by screening method.
RDT1: SD BIOLINE HAT rapid diagnostic test; RDT2: SD BIOLINE HAT 2.0 rapid diagnostic test; CATT: card agglutination test for trypanosomiasis.
Fig 3
Fig 3. Sensitivity (A) and specificity (B) of all possible combinations of two or three screening tests, by screening method and by disease stage.
Test combinations are shown in descending order of sensitivity. RDT1: SD BIOLINE HAT rapid diagnostic test; RDT2: SD BIOLINE HAT 2.0 rapid diagnostic test; CATT: card agglutination test for trypanosomiasis. The result of the combination of tests is positive if at least one of the tests is positive, while the result is negative if all the tests of the combination are negative.
Fig 4
Fig 4. Venn diagrams showing the number of true positive results obtained with the RDT2, RDT1 and CATT tests.
(A) Results from active and passive screening combined (N = 258 true positives); (B) results from active screening (N = 136 true positives); (C) results from passive screening (N = 122 true positives). For the sake of simplicity, only results obtained by the first reader are shown. The total number of true positives does not equal the total number of cases enrolled in the study (N = 260), as the first reader missed two cases in active screening.
Fig 5
Fig 5. Venn diagrams showing the number of false positive results obtained with the RDT2, RDT1 and CATT tests.
(A) Results from active and passive screening combined (N = 1,768 false positives); (B) results from active screening (N = 769 false positives); (C) results from passive screening (N = 999 false positives). For the sake of simplicity, only results obtained by the first reader are shown.

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