Persistence of P. falciparum HRP-2 antigenaemia post treatment is not associated with gametocytes

Author:

Oulton Tate1,Mahamar Almahamoudou2,Sanogo Koualy2,Diallo Makonon2,Youssouf Ahamadou2,Niambele Sidi M2,Samaké Siaka2,Keita Sekouba2,Sinaba Youssouf2,Sacko Adama2,Traore Sekou F2,Lanke Kjerstin3,Collins Katharine3,Bradley John4,Drakeley Chris1,Stone William1,Dicko Alassane2

Affiliation:

1. London School of Hygiene & Tropical Medicine

2. University of Sciences Techniques and Technologies of Bamako

3. Radboud University Medical Center, University of Nijmegen

4. MRC International Statistics and Epidemiology Group, London School of Hygiene and Tropical Medicine

Abstract

Abstract Background In some settings, sensitive field diagnostic tools may be needed to achieve elimination of falciparum malaria. To this end, rapid diagnostic tests (RDTs) based on the detection of the Plasmodium falciparum protein HRP-2 are being developed with increasingly lower limits of detection. However, it is currently unclear how parasite stages that are unaffected by standard drug treatments may contribute to HRP-2 detectability and potentially confound RDT results even after clearance of blood stage infection. In this study, we assessed the detectability of HRP-2 in periods of post-treatment residual gametocytaemia. Methods A cohort of 100 Plasmodium falciparum infected, gametocyte positive individuals were treated with or without the gametocytocidal drug primaquine (PQ), alongside standard artemisinin-based combination therapy (ACT), in the context of a randomised clinical trial in Ouelessebougou, Mali. We used a quantitative ELISA to measure levels of HRP-2, and compared time to test negativity using a standard and ultra-sensitive RDT (uRDT) between residual gametocyte positive and negative groups. Findings Time to test negativity was longest by uRDT, followed by ELISA and then standard RDT. No significant difference in time to negativity was found between the treatment groups with and without residual gametocytes: uRDT (HR 0.79 [95% CI 0.52–1.21], p = 0.28), RDT (HR 0.77 [95% CI 0.51–1.15], p = 0.20) or ELISA (HR 0.88 [95% CI 0.59–1.32], p = 0.53). Similarly, no difference was observed when adjusting for baseline asexual parasite density. Quantified levels of HRP-2 over time were similar between groups, with differences attributable to asexual parasite densities. Furthermore, no difference in levels of HRP-2 was found between individuals who were or were not infectious to mosquitoes (OR 1.19 [95% CI 0.98–1.46], p = 0.077). Interpretation Surviving sexual stage parasites after standard ACT treatment do not contribute to the persistence of HRP-2 antigenaemia, and appear to have little impact on RDT results.

Publisher

Research Square Platform LLC

Reference27 articles.

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