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Journal of Clinical Microbiology, March 2001, p. 1025-1031, Vol. 39, No. 3
0095-1137/01/$04.00+0   DOI: 10.1128/JCM.39.3.1025-1031.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.

Persistent ICT Malaria P.f/P.v Panmalarial and HRP2 Antigen Reactivity after Treatment of Plasmodium falciparum Malaria Is Associated with Gametocytemia and Results in False-Positive Diagnoses of Plasmodium vivax in Convalescence

Emiliana Tjitra,1,2 Sri Suprianto,3 James McBroom,2 Bart J. Currie,2 and Nicholas M. Anstey2,*

Communicable Diseases Research Centre, National Institute of Health Research and Development,1 and Directorate General of Communicable Disease Control and Environmental Health,3 Jakarta, Indonesia, and Tropical Medicine and International Health Unit, Menzies School of Health Research and Royal Darwin Hospital Clinical School, Darwin, Northern Territory, Australia2

Received 28 July 2000/Returned for modification 23 October 2000/Accepted 20 December 2000

A problem with rapid Plasmodium falciparum-specific antigen histidine-rich protein 2 (HRP2) detection tests for malaria is the persistence of antigen in blood after the disappearance of asexual-stage parasitemia and clinical symptoms, resulting in false-positive (FP) test results following treatment. The ICT P.f/P.v immunochromatographic test detects both HRP2 and a panmalarial antigen (PMA) found in both P. falciparum and Plasmodium vivax. To examine posttreatment antigen persistence with this test and whether persistent sexual-stage forms (gametocytes) are a cause of FP tests after treatment, we compared serial antigen test results with microscopy results from patients symptomatic with P. falciparum malaria in Indonesia for 28 days following treatment with chloroquine (CQ; n = 66), sulfadoxine-pyrimethamine (SP; n = 36), and artesunate plus sulfadoxine-pyrimethamine (ART + SP; n = 15). Persistent FP antigenemia following SP treatment occurred in 29% (HRP2) and 42% (PMA) of the patients on day 7 and in 10% (HRP2) and 23% (PMA) on day 14. The high rates of persistent HRP2 and PMA antigenemia following CQ and SP treatment were strongly associated with the presence of gametocytemia, with the proportion with gametocytes on day 7 posttreatment being significantly greater in those with FP results than in those with true-negative PMA and HRP2 results. Gametocyte frequency on day 14 post-SP treatment was also greater in those with FP PMA results. Following SP treatment, PMA persisted longer than HRP2, giving an FP diagnosis of P. vivax in up to 16% of patients on day 14, with all FP P. vivax diagnoses having gametocytemia. In contrast, PMA was rapidly cleared following ART + SP treatment in association with rapid clearance of gametocytemia. Gametocytes appear to be an important cause of persistent posttreatment panmalarial antigenemia in areas of endemicity and may also contribute in part to persistent HRP2 antigenemia following treatment.


* Corresponding author. Mailing address: Tropical Medicine and International Health Unit, Menzies School of Health Research and Royal Darwin Hospital Clinical School, P.O. Box 41096, Casuarina, Darwin, Northern Territory 0811, Australia. Phone: 61-8-8922 8932. Fax: 61-8-8927 5187. E-mail: anstey{at}menzies.edu.au.


Journal of Clinical Microbiology, March 2001, p. 1025-1031, Vol. 39, No. 3
0095-1137/01/$04.00+0   DOI: 10.1128/JCM.39.3.1025-1031.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.



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