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      Estimation of the Total Parasite Biomass in Acute Falciparum Malaria from Plasma PfHRP2

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          Abstract

          Background

          In falciparum malaria sequestration of erythrocytes containing mature forms of Plasmodium falciparum in the microvasculature of vital organs is central to pathology, but quantitation of this hidden sequestered parasite load in vivo has not previously been possible. The peripheral blood parasite count measures only the circulating, relatively non-pathogenic parasite numbers. P. falciparum releases a specific histidine-rich protein (PfHRP2) into plasma. Quantitative measurement of plasma PfHRP2 concentrations may reflect the total parasite biomass in falciparum malaria.

          Methods and Findings

          We measured plasma concentrations of PfHRP2, using a quantitative antigen-capture enzyme-linked immunosorbent assay, in 337 adult patients with falciparum malaria of varying severity hospitalised on the Thai–Burmese border. Based on in vitro production rates, we constructed a model to link this measure to the total parasite burden in the patient. The estimated geometric mean parasite burden was 7 × 10 11 (95% confidence interval [CI] 5.8 × 10 11 to 8.5 × 10 11) parasites per body, and was over six times higher in severe malaria (geometric mean 1.7 × 10 12, 95% CI 1.3 × 10 12 to 2.3 × 10 12) than in patients hospitalised without signs of severity (geometric mean 2.8 × 10 11, 95% CI 2.3 × 10 11 to 3.5 × 10 11; p < 0.001). Parasite burden was highest in patients who died (geometric mean 3.4 × 10 12, 95% CI 1.9 × 10 12 to 6.3 × 10 12; p = 0.03). The calculated number of sequestered parasites increased with disease severity and was higher in patients with late developmental stages of P. falciparum present on peripheral blood smears. Comparing model and laboratory estimates of the time of sequestration suggested that admission to hospital with uncomplicated malaria often follows schizogony—but in severe malaria is unrelated to stage of parasite development.

          Conclusion

          Plasma PfHRP2 concentrations may be used to estimate the total body parasite biomass in acute falciparum malaria. Severe malaria results from extensive sequestration of parasitised erythrocytes.

          Abstract

          Measuring sequestered parasites using plasma PfHRP2 concentrations may provide a more accurate estimate of total parasite mass and hence severity in falciparum malaria.

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          Most cited references18

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          A quantitative analysis of the microvascular sequestration of malaria parasites in the human brain.

          Microvascular sequestration was assessed in the brains of 50 Thai and Vietnamese patients who died from severe malaria (Plasmodium falciparum, 49; P. vivax, 1). Malaria parasites were sequestered in 46 cases; in 3 intravascular malaria pigment but no parasites were evident; and in the P. vivax case there was no sequestration. Cerebrovascular endothelial expression of the putative cytoadherence receptors ICAM-1, VCAM-1, E-selectin, and chondroitin sulfate and also HLA class II was increased. The median (range) ratio of cerebral to peripheral blood parasitemia was 40 (1.8 to 1500). Within the same brain different vessels had discrete but different populations of parasites, indicating that the adhesion characteristics of cerebrovascular endothelium change asynchronously during malaria and also that significant recirculation of parasitized erythrocytes following sequestration is unlikely. The median (range) ratio of schizonts to trophozoites (0.15:1; 0.0 to 11.7) was significantly lower than predicted from the parasite life cycle (P < 0.001). Antimalarial treatment arrests development at the trophozoite stages which remain sequestered in the brain. There were significantly more ring form parasites (age < 26 hours) in the cerebral microvasculature (median range: 19%; 0-90%) than expected from free mixing of these cells in the systemic circulation (median range ring parasitemia: 1.8%; 0-36.2%). All developmental stages of P. falciparum are sequestered in the brain in severe malaria.
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            A controlled trial of artemether or quinine in Vietnamese adults with severe falciparum malaria.

            Artemisinin (qinghaosu) and its derivatives are rapidly effective antimalarial drugs derived from a Chinese plant. Preliminary studies suggest that these drugs may be more effective than quinine in the treatment of severe malaria. We studied artemether in Vietnam, where Plasmodium falciparum has reduced sensitivity to quinine. We conducted a randomized, double-blind trial in 560 adults with severe falciparum malaria. Two hundred seventy-six received intramuscular quinine dihydrochloride (20 mg per kilogram of body weight followed by 10 mg per kilogram every eight hours), and 284 received intramuscular artemether (4 mg per kilogram followed by 2 mg per kilogram every eight hours). Both drugs were given for a minimum of 72 hours. There were 36 deaths in the artemether group (13 percent) and 47 in the quinine group (17 percent; P = 0.16; relative risk of death in the patients given artemether, 0.74; 95 percent confidence interval, 0.5 to 1.11). The parasites were cleared more quickly from the blood in the artemether group (mean, 72 vs. 90 hours; P < 0.001); however, in this group fever resolved more slowly (127 vs. 90 hours, P < 0.001), the time to recovery from coma was longer (66 vs. 48 hours, P = 0.003), and the hospitalization was longer (288 vs. 240 hours, P = 0.005). Quinine treatment was associated with a higher risk of hypoglycemia (relative risk, 2.7; 95 percent confidence interval, 1.7 to 4.4; P < 0.001), but there were no other serious side effects in either group. Artemether is a satisfactory alternative to quinine for the treatment of severe malaria in adults.
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              The treatment of malaria.

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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                PLoS Med
                pmed
                PLoS Medicine
                Public Library of Science (San Francisco, USA )
                1549-1277
                1549-1676
                August 2005
                23 August 2005
                : 2
                : 8
                : e204
                Affiliations
                [1] 1Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand,
                [2] 2Centre for Clinical Vaccinology and Tropical Medicine, Churchill Hospital, Oxford, United Kingdom,
                [3] 3Wellcome Trust–Mahosot Hospital, Vientiane, Lao People's Democratic Republic,
                [4] 4Cellabs, Brookvale, New South Wales, Australia
                St. George's Hospital Medical School United Kingdom
                Author notes
                *To whom correspondence should be addressed. E-mail: nickw@ 123456tropmedres.ac

                Competing Interests: The authors have declared that no competing interests exist.

                Author Contributions: AMD and NJW designed the study. AMD and PNN enrolled the patients. VD, DS, KS, KC, PP, and AMS contributed to the laboratory studies. AMD, WP, and NPJD analyzed the data. All authors contributed to writing the paper.

                Article
                10.1371/journal.pmed.0020204
                1188247
                16104831
                9d65ef94-c165-4621-8087-ffaf701c2e31
                Copyright: © 2005 Dondorp et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
                History
                : 24 November 2004
                : 26 April 2005
                Categories
                Research Article
                Infectious Diseases
                Infectious Diseases
                Malaria
                Medicine in Developing Countries

                Medicine
                Medicine

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