- Open Access
Augmented plasma microparticles during acute Plasmodium vivax infection
- Fernanda MF Campos†1,
- Bernardo S Franklin†1,
- Andréa Teixeira-Carvalho1,
- Agnaldo LS Filho3,
- Sálua CO de Paula3,
- Cor J Fontes2,
- Cristiana F Brito1 and
- Luzia H Carvalho1Email author
© Campos et al; licensee BioMed Central Ltd. 2010
- Received: 13 August 2010
- Accepted: 16 November 2010
- Published: 16 November 2010
In the last few years, the study of microparticles (MPs) - submicron vesicles released from cells upon activation or apoptosis - has gained growing interest in the field of inflammation and in infectious diseases. Their role in the human malaria parasite Plasmodium vivax remains unexplored. Because acute vivax malaria has been related to pro-inflammatory responses, the main hypothesis investigated in this study was that Plasmodium vivax infection is associated with elevated levels of circulating MPs, which may play a role during acute disease in non-immune patients.
Plasma MPs were analysed among thirty-seven uncomplicated P. vivax infections from an area of unstable malaria transmission in the Brazilian Amazon. The MP phenotype was analysed by flow cytometry using the classical MP marker, annexin, and fluorochrome-labeled monoclonal antibodies against specific cell surface markers. The frequencies of plasma MPs in P. vivax patients (n = 37) were further compared to malaria-unexposed controls (n = 15) and ovarian carcinoma patients (n = 12), a known MPs-inducing disease non-related to malaria.
The frequencies of plasma circulating MPs were markedly increased in P. vivax patients, as compared to healthy age-matched malaria-unexposed controls. Although platelets, erythrocytes and leukocytes were the main cellular sources of MPs during vivax malaria, platelet derived-MPs (PMPs) increased in a linear fashion with the presence of fever at the time of blood collection (β = 0.06, p < 0.0001) and length of acute symptoms (β = 0.36, p < 0.0001). Finally, the results suggest that plasma levels of PMPs diminish as patient experience more episodes of clinical malaria (β = 0.07, p < 0.003).
Abundant circulating MPs are present during acute P. vivax infection, and platelet derived-MPs may play a role on the acute inflammatory symptoms of malaria vivax.
- Falciparum Malaria
- Multiple Linear Regression Model
- Cerebral Malaria
- Vivax Malaria
Plasmodium vivax is the most widespread Plasmodium species being responsible for up to 390 million clinical cases each year [1, 2]. For long, P. vivax infection was considered a benign and self-limited disease, especially when compared to the burden of Plasmodium falciparum infection. Recent studies from Indonesia, Papua New Guinea and India have, however, highlighted the association between vivax malaria and life-threatening manifestations, such as respiratory distress, severe anaemia, and neurological manifestations with coma [3–5], placing P. vivax infection in a higher status as a global health concern.
An additional neglected effect of the "benign" P. vivax infection concerns its poorly explored pathogenesis. While a large bulk of literature on the immunological and inflammatory patterns of falciparum malaria is available, the pathogenesis of vivax malaria was not submitted to such scrutiny. It is, nevertheless, intriguing that P. vivax infection triggers fever with a lower peripheral parasitaemia [6–8]. The few studies that had addressed the pathogenesis of vivax malaria had shown that P. vivax infection induces greater host inflammatory responses compared to P. falciparum malaria [9–11] with pro-inflammatory cytokines levels being closely associated with disease severity in some studies [10–13]. Hence, the different clinical presentations of vivax malaria infection may be related to the intensity of pro-inflammatory responses. In this regard, the search for sensitive and predictive inflammatory biomarkers in vivax malaria may enhance early detection of severe cases.
Cellular microparticles (MPs) - submicron (< 1 μm) membrane vesicles released from cells into the blood stream in response to a variety of stimuli, i.e. cell activation, stress, serine proteases, pro-inflammatory cytokines and apoptosis, have emerged as potential inflammatory biomarkers as elevated levels are found in plasma during many diseases of inflammatory etiology . Consequently, this heterogeneous population of small, membrane-coated vesicles has been used as sensitive markers of diverse process, such as inflammation, coagulation, vascular function and apoptosis. In addition, MPs are important carriers of membrane components or bioactive molecules  being involved in a series of "gain of function" phenomena . As an example, MPs derived from activated platelets have been shown to play a role on the pathogenesis of P. falciparum cerebral malaria by transferring platelet antigens to the surface of iRBCs and dramatically enhancing their cytoadherence to endothelial cells within brain micro vessels [17, 18]. MPs have also been shown to contribute to inflammation during P. berghei malaria by inducing potent activation of macrophages . However, their role in vivax malaria pathogenesis has not been investigated.
The main hypothesis to be investigated here is that P. vivax infection is associated with elevated levels of circulating MPs of different cellular origins, and those MPs play a role in P. vivax induced inflammation. For this purpose, the phenotype of circulating MPs in plasma from P. vivax malaria patients in a hypoendemic area of the Brazilian Amazon was assessed. As control, the plasma MP phenotype from healthy malaria-unexposed donors and patients with ovarian carcinoma, a known MPs-inducing disease non-related to malaria, was simultaneously investigated. The results showed that platelet (PMPs), erythrocyte (EMPs) and leukocyte (LMPs) derived-MPs are significantly increased in plasma from P. vivax patients as compared to healthy donors. Interestingly, the frequencies of annexin V/CD41a double-positive MPs (PMPs) were associated with the length of acute illness and the presence of fever at the time of blood collection. The results presented here comprise the first evidence of the presence of MPs during vivax malaria and offer a new tool for the study of the pro-inflammatory patterns of P. vivax infection.
Study site and subjects
This study was conducted between January and November 2008, in the outpatient clinic of the Tropical Medicine Center of Porto Velho (CEMETRON), the capital of Rondônia State, Brazilian Amazon area. In the Amazon area, malaria is mainly an occupational disease, with population at risk largely represented by adult males. Low rates of transmission occur throughout the year with large dominance of vivax over falciparum malaria . The main vector is Anopheles darlingi and the number of infective bites associated with malaria is estimated to be between 2 to 10 per inhabitant per year .
Individuals who sought care at CEMETRON and whose thick blood smear was positive for P. vivax, were invited to participate in the study. Selected volunteers were all negative for P. falciparum and/or Plasmodium malariae infection by both microscopic examination and a nested-PCR, carried-out latter. Thirty-seven patients, aging 15 to 66 years, were enrolled in the study after the written informed consent, in accordance with guidelines for human research, as specified by the Brazilian National Council of Health (Resolution 196/96). Antimalarial and supportive therapies were given according to standard protocols.
Characteristics of the thirty seven uncomplicated Plasmodium vivax patients
Median Age, years (range)
N° of previous malaria episodes, n (%)
6 - 10
N° of days of acute illness, n (%)
3 - 5
Symptoms in the last 3 days, n (%)
Parasitaemia, parasites/μl of blood, n (%)
500 - 10,000
Body temperature ( o C)
37 - 37.8
Haemoglobin levels g/dL, median (range)
13.26 (9.7 - 16.6)
Platelet counts ×1000/mm 3 , median (range)
115 (53 - 208)
Leukocyte counts ×100/mm 3 , median (range)
52 (23 - 117)
Haematocrit %, median (range)
41 (32.2 - 50.6)
In the studied area, subjects were migrants from malaria-free areas. Consequently, their ages do not necessarily correlate with malaria exposure. Cumulative exposure to malaria was, therefore, based on self-reported number of lifetime malaria episodes. As their previous malaria experience showed a variable number of infections, extreme values and the possibility of recall bias were avoided by categorizing patients into three groups: i) five or less previous malaria episodes (PME); ii) 6 to10 PME; and ii) more than 10 PME. Venous blood was obtained from patients on admission, and in those with fever (above 37.5°C) at the time of blood collection. In five patients it was possible to take additional samples, during convalescence, on day 7 and 21 after treatment. Plasma samples from fifteen age-matched malaria-unexposed donors were used as baseline control. As MPs positive samples plasma from 12 patients, aging 45 to 65 years, diagnosed with ovarian carcinoma, as it has been shown that cancer cells from this highly lethal gynaecological malignancy can release MPs .
Purification of MPs from plasma
MPs were prepared as described elsewhere [17, 19]. Briefly, Citrated blood (0.5 mL) was centrifuged at 1,500 × g for 15 min, and plasma was then cooled to -20°C before storage at -80°C. Samples were further centrifuged at 13,000 x g for 3 min to obtain platelet-free plasma. The latter was diluted 1:3 in citrated PBS containing heparin and centrifuged at 14,000 x g for 90 min at 15°C. The resultant MP pellet was then resuspended in 1× annexin V binding buffer (BD Biosciences, California, US).
Flow cytometry assays
Quantification of plasma MPs levels
To confirm if the absolute numbers of plasma MPs were different between malaria patients and healthy donors, as well as to determinate the numbers of plasma MPs per microliter (MPs/μl), the cytometer was set to operate at a high flow rate setting for 60 seconds for each sample. The number of MPs/μl of plasma was calculated as described elsewhere : MPs/μl = (N × 400)/(60 × 100), in which N is the number of events, 400 is the total volume of in the tube before analysis, 60 is the sample volume analysed, and 100 is the original volume of MPs suspension.
Platelet, erythrocyte and leukocytes are the main sources of plasma MPs during acute P. vivax malaria
The phenotype of plasma circulating MPs during acute vivax malaria was investigated, with specific mAbs for cell markers i.e. CD41a, CD235a, CD45, CD144 and CD14 were used to discriminate the cellular sources of annexin V+ MPs. The percentages of annexin V+ MPs stained for each cell marker was compared between samples from P. vivax malaria patients, healthy donors or samples from a MPs-induced disease non-related to malaria (Figure 1C).
The frequency of platelet (PMPs) (p < 0.0001), erythrocyte (EMPs) (p = 0.0023) and leukocyte derived-microparticles (LMPs) (p = 0.0087) were significantly increased in plasma samples from malaria patients as compared to healthy donors. The increased levels of PMPs, EMPs and LMPs were confirmed when the absolute number of MPs per μl of plasma was calculated (additional file 1). As expected, the frequencies of PMPs and EMPs, but not LMPs, were also significantly increased in plasma from patients with ovarian carcinoma (p < 0.05). These results suggest that platelets, erythrocytes and leukocytes are the main source of plasma circulating MPs during acute P. vivax malaria and its presence may be associated with inflammation.
Plasma MPs associate with acute malaria symptoms
To investigate the role of MPs in the pathogenesis of vivax malaria, potential factors that could be associated with the presence of circulating MPs in acute P. vivax infection were analysed, including demographic, clinical, haematological and parasitological parameters. No association was found between levels of MPs and haematological (haemoglobin levels, haematocrit, platelet or leukocyte counts) or parasitological data. Of note, positive linear trends were observed between the presence of fever at the time of blood collection and the frequency of PMPs in plasma (β = 0.06, p < 0.0001) (Figure 2A). Significant association was also observed between higher frequencies of PMPs and prolonged malaria symptoms, estimated here by number of days with acute illness (β = 0.36, p < 0.0001) (Figure 2B). More specifically, patients reporting symptoms in the last four or more days before seeking care at CEMETRON had significant higher levels of PMPs in plasma when compared to patients reporting more immediate symptoms. Apparently, the levels of PMPs in plasma diminish as previous clinical malaria episodes increases (β = 0.07, p < 0.003) (Figure 2C). No significant association was found between PMP levels and days elapsed since last malarial episode (Figure 2D).
Although manifestation of acute malaria such as fever can be influenced by different factors including host age and immunological background - evaluated here by previous malaria experience - multiple linear regression models confirmed the independent association between fever and microparticles, as well as length of symptoms and microparticles (p < 0.001).
Plasma MPs levels decrease after anti-malarial chemotherapy
Despite increasing evidence of multidrug-resistant P. vivax associated with severe and fatal disease, little is known about its pathogenesis. This study provides the first evidence that microparticles (MPs) from leukocytes, platelets, and erythrocytes are significantly increased in plasma from acute P. vivax malaria patients. These results are consistent with the observation that active, non-cytokine, factors are present in paroxysm plasma from non-immune patients with acute P. vivax infections [23, 24]. As some of the active components in paroxysm plasma are lipids, of unknown nature, and, importantly, are present in particulate form , MPs could contribute to P. vivax paroxysms. However, at this time, it is not possible to conclude on the role of MPs during paroxysm, because it remains as undefined complex phenomenon, which involves several components, including host-derived cytokines .
As virtually all cell types can release MPs, the presence of MPs of different origins circulating during acute P. vivax malaria is not unexpected. It rather suggests that different cell types are activated and participate in the myriad of inflammatory processes induced by P. vivax parasites/infection. In fact, these data are in concordance with a recently published study reporting that children infected with P. falciparum presents high levels of circulating MPs, including those from platelet, erythrocytes, endothelial cells and leukocytes . In these infected Cameroonian's children, MPs levels returned to normal when the patients were cured. This results are in line with the observations described here with P. vivax, and by others with P. falciparum, which shown that the levels of MPs significantly decrease after 19 - 21 days post treatment.
In the present study, elevated levels of platelet-derived microparticles (PMPs) were associated with clinical manifestation of disease, such as fever and prolonged time with malaria symptoms. At this time, the significance of this finding in P. vivax infection is not clear, but they are of particular interests as both platelets  and PMPs  have been shown to play a role in the pathogenesis of malaria caused by P. falciparum. Moreover, MPs have been shown to be mediators of the inflammatory process that occur during infection with Plasmodium berghei in mice . Recently, Boilard and colleagues  provides strong evidence for the pathogenic role of PMPs, confirming their contribution as "incendiary devices" in the conflagration of a hot, swollen, and painful rheumatoid joint.
Although evidence for a role of microparticles in human malaria diseases at present is still only limited, new evidence is accumulating rapidly to support this theory. In Cerebral Malaria, the most severe complications of P. falciparum infection, PMPs levels significantly correlated with coma depth and thrombocytopenia . Consequently, these authors have been proposed cell-specific MPs as biological marker for cerebral dysfunctions in severe falciparum malaria, and intervention to block MP production as a new therapeutic target against cerebral malaria.
As in P. falciparum PMPs facilitate cytoadherence of iRBCs to brain endothelial , it is reasonable to speculate that, similarly, they might be involved in the underlying mechanisms driving pulmonary vascular sequestration in P. vivax malaria as suggested by Anstey et al. However, as cytoadherence is not a common feature of vivax-infected RBCs and evidences for their microvascular accumulation is, at best, modest , it is conceivable that PMPs may be merely an epiphenomenon of the pro-inflammatory response previously observed in vivax malaria [12, 29–31]. Further studies will be required to investigate if circulating PMPs from P. vivax patients may act either as biomarker or mediator of inflammation/disease (or both).
A potential limitation of the statistics analysis performed here was that multiple comparison were realized, aiming to find possible associations between MPs and clinical/biological parameters; however, it should be take in consideration that these significant findings were hypothesis-generating, and, consequently, its represent a realistic interpretation of the facts. In addition, multiple linear regression models confirmed the independent association between fever and length of symptoms with platelets-derived microparticles.
An interesting finding was the presence of leukocyte and erythrocyte derived-MPs during acute P. vivax malaria. The role of leukocytes in malaria pathogenesis is still not fully understood; nevertheless, it has been shown that these cells are the main source of pro-inflammatory cytokines, especially TNFα which is highly pyrogenic . The presence of MPs derived from these cells provides evidence for their activation in acute vivax malaria. Perhaps, an attractive field of study is to investigate whether or not EMPs might contribute to the distinct erythrocyte destruction commonly observed in vivax malaria . Although severe anemia can be produced by both P. vivax and P. falciparum infections, malariotherapy studies have shown greater destruction of non-infected RBCs per infected erythrocyte in P. vivax as compared to P. falciparum malaria . Accordingly, in the present study, the frequency of erythrocyte derived MPs in plasma was not associated with parasitaemia. Actually, the absence of correlation between MPs and parasitaemia is not unexpected, because in the Brazilian Amazon area the wide range of parasitaemia found in P. vivax infection does not enable to conclude on the value of this variable as determinant of severity .
While it is not possible at this time to characterize the mechanism by which MPs might be involved in the pathogenesis of P. vivax malaria, the data shown here raise important questions on the role of cell derived MPs in malaria pathogenesis revealing a fruitful area for investigation. Thus, the potential of circulating cell derived-MPs as non-invasive inflammatory marker of P. vivax morbidity is likely.
This paper describes the initial attempts made at characterization of the MP phenotype in vivax malaria. It is shown here that the plasma levels of platelet, erythrocyte and leukocyte-derived MPs are increased during acute uncomplicated vivax malaria. In P. vivax patients platelets derived-MPs were significantly correlated with fever and length of symptoms. Elucidation of the microparticles composition and the mechanisms involved in exertion of their effects could contribute to additional intervention strategies against malaria.
The authors would like to thank Dr. Marcus Lacerda for his critical suggestions, and Danubia L. Gomes for helping statistical analysis. The authors also thank the Program for Technological Development in Tools for Health - PDTIS - FIOCRUZ for use of its facilities. This work was supported by the Research Foundation of Minas Gerais State (FAPEMIG, PPM II), The Brazilian National Research Council (CNPq), and Oswaldo Cruz Foundation (FIOCRUZ, PAPES V), Pronex Malaria, DECIT/MS, scholarships from FAPEMIG (FMFC), CNPq-FIOCRUZ (BSF), and CNPq (LHC, ATC, and CFAB) are also acknowledged.
- Hay S, Guerra C, Tatem A, Noor A, Snow R: The global distribution and population at risk of malaria: past, present, and future. Lancet Infect Dis. 2004, 4: 327-336.PubMed CentralView ArticlePubMedGoogle Scholar
- Price R, Tjitra E, Guerra C, Yeung S, White N, Anstey N: Vivax malaria: neglected and not benign. Am J Trop Med Hyg. 2007, 77: 79-87.PubMed CentralPubMedGoogle Scholar
- Price R, Douglas N, Anstey N: New developments in Plasmodium vivax malaria: severe disease and the rise of chloroquine resistance. Curr Opin Infect Dis. 2009, 22: 430-435.View ArticlePubMedGoogle Scholar
- Genton B, D'Acremont V, Rare L, Baea K, Reeder J, Alpers M, Müller I: Plasmodium vivax and mixed infections are associated with severe malaria in children: a prospective cohort study from Papua New Guinea. PLoS Med. 2008, 5: e127.PubMed CentralView ArticlePubMedGoogle Scholar
- Tjitra E, Anstey N, Sugiarto P, Warikar N, Kenangalem E, Karyana M, Lampah D, Price R: Multidrug-resistant Plasmodium vivax associated with severe and fatal malaria: a prospective study in Papua, Indonesia. PLoS Med. 2008, 5: e128.PubMed CentralView ArticlePubMedGoogle Scholar
- Karyana M, Burdarm L, Yeung S, Kenangalem E, Wariker N, Maristela R, Umana KG, Vemuri R, Okoseray MJ, Penttinen PM, Ebsworth P, Sugiarto P, Anstey NM, Tjitra E, Price RN: Malaria morbidity in Papua Indonesia, an area with multidrug resistant Plasmodium vivax and Plasmodium falciparum. Malar J. 2008, 7: 148.PubMed CentralView ArticlePubMedGoogle Scholar
- Anstey N, Handojo T, Pain M, Kenangalem E, Tjitra E, Price R, Maguire G: Lung injury in vivax malaria: pathophysiological evidence for pulmonary vascular sequestration and posttreatment alveolar-capillary inflammation. J Infect Dis. 2007, 195: 589-596.PubMed CentralView ArticlePubMedGoogle Scholar
- Anstey N, Russell B, Yeo T, Price R: The pathophysiology of vivax malaria. Trends Parasitol. 2009, 25: 220-227.View ArticlePubMedGoogle Scholar
- Yeo T, Lampah D, Tjitra E, Piera K, Gitawati R, Kenangalem E, Price R, Anstey N: Greater endothelial activation, Weibel-Palade body release and host inflammatory response to Plasmodium vivax, compared with Plasmodium falciparum: a prospective study in Papua, Indonesia. J Infect Dis. 2010, 202: 109-112.PubMed CentralView ArticlePubMedGoogle Scholar
- Hemmer C, Holst F, Kern P, Chiwakata C, Dietrich M, Reisinger E: Stronger host response per parasitized erythrocyte in Plasmodium vivax or ovale than in Plasmodium falciparum malaria. Trop Med Int Health. 2006, 11: 817-823.View ArticlePubMedGoogle Scholar
- Karunaweera N, Grau G, Gamage P, Carter R, Mendis K: Dynamics of fever and serum levels of tumor necrosis factor are closely associated during clinical paroxysms in Plasmodium vivax malaria. Proc Natl Acad Sci USA. 1992, 89: 3200-3203.PubMed CentralView ArticlePubMedGoogle Scholar
- Andrade B, Reis-Filho A, Souza-Neto S, Clarencio J, Camargo L, Barral A, Barral-Netto M: Severe Plasmodium vivax malaria exhibits marked inflammatory imbalance. Malar J. 2010, 9: 13.PubMed CentralView ArticlePubMedGoogle Scholar
- Brown A, Teja-Isavadharm P, Webster H: Macrophage activation in vivax malaria: fever is associated with increased levels of neopterin and interferon-gamma. Parasite Immunol. 1991, 13: 673-679.View ArticlePubMedGoogle Scholar
- Doeuvre L, Plawinski L, Toti F, Anglés-Cano E: Cell-derived microparticles: a new challenge in neuroscience. J Neurochem. 2009, 110: 457-468.View ArticlePubMedGoogle Scholar
- Morel O, Toti F, Hugel B, Freyssinet J: Cellular microparticles: a disseminated storage pool of bioactive vascular effectors. Curr Opin Hematol. 2004, 11: 156-164.View ArticlePubMedGoogle Scholar
- Théry C, Ostrowski M, Segura E: Membrane vesicles as conveyors of immune responses. Nat Rev Immunol. 2009, 9: 581-593.View ArticlePubMedGoogle Scholar
- Combes V, Taylor T, Juhan-Vague I, Mège J, Mwenechanya J, Tembo M, Grau G, Molyneux M: Circulating endothelial microparticles in malawian children with severe falciparum malaria complicated with coma. JAMA. 2004, 291: 2542-2544.PubMedGoogle Scholar
- Faille D, Combes V, Mitchell A, Fontaine A, Juhan-Vague I, Alessi M, Chimini G, Fusaï T, Grau G: Platelet microparticles: a new player in malaria parasite cytoadherence to human brain endothelium. FASEB J. 2009, 23: 3449-3458.View ArticlePubMedGoogle Scholar
- Couper K, Barnes T, Hafalla J, Combes V, Ryffel B, Secher T, Grau G, Riley E, de Souza J: Parasite-derived plasma microparticles contribute significantly to malaria infection-induced inflammation through potent macrophage stimulation. PLoS Pathog. 2010, 6: e1000744.PubMed CentralView ArticlePubMedGoogle Scholar
- Katsuragawa T, Gil L, Tada M, de Almeida e Silva A, Costa J, Araújo MS, Escobar A, da Silva L: The dynamics of transmission and spatial distribution of malaria in riverside areas of Porto Velho, Rondônia, in the Amazon region of Brazil. PLoS One. 2010, 5: e9245.PubMed CentralView ArticlePubMedGoogle Scholar
- Gil L, Tada M, Katsuragawa T, Ribolla P, da Silva L: Urban and suburban malaria in Rondônia (Brazilian Western Amazon) II. Perennial transmissions with high anopheline densities are associated with human environmental changes. Mem Inst Oswaldo Cruz. 2007, 102: 271-276.View ArticlePubMedGoogle Scholar
- Yokota N, Koizume S, Miyagi E, Hirahara F, Nakamura Y, Kikuchi K, Ruf W, Sakuma Y, Tsuchiya E, Miyagi Y: Self-production of tissue factor-coagulation factor VII complex by ovarian cancer cells. Br J Cancer. 2009, 101: 2023-2029.PubMed CentralView ArticlePubMedGoogle Scholar
- Wijesekera S, Carter R, Rathnayaka L, Mendis K: A malaria parasite toxin associated with Plasmodium vivax paroxysms. Clin Exp Immunol. 1996, 104: 221-227.PubMed CentralView ArticlePubMedGoogle Scholar
- Karunaweera N, Wanasekara D, Chandrasekharan V, Mendis K, Carter R: Plasmodium vivax: paroxysm-associated lipids mediate leukocyte aggregation. Malar J. 2007, 6: 62.PubMed CentralView ArticlePubMedGoogle Scholar
- Pankoui Mfonkeu J, Gouado I, Fotso Kuaté H, Zambou O, Amvam Zollo P, Grau G, Combes V: Elevated cell-specific microparticles are a biological marker for cerebral dysfunctions in human severe malaria. PLoS One. 2010, 5: e13415.PubMed CentralView ArticlePubMedGoogle Scholar
- Cox D, McConkey S: The role of platelets in the pathogenesis of cerebral malaria. Cell Mol Life Sci. 2010, 67: 557-568.View ArticlePubMedGoogle Scholar
- Boilard E, Nigrovic P, Larabee K, Watts G, Coblyn J, Weinblatt M, Massarotti E, Remold-O'Donnell E, Farndale R, Ware J, Lee DM: Ware J et al: Platelets amplify inflammation in arthritis via collagen-dependent microparticle production. Science. 2010, 327: 580-583.PubMed CentralView ArticlePubMedGoogle Scholar
- Carvalho B, Lopes S, Nogueira P, Orlandi P, Bargieri D, Blanco Y, Mamoni R, Leite J, Rodrigues M, Soares IS, Oliveira TR, Wunderlich G, Lacerda MV, del Portillo HA, Araújo MO, Russell B, Suwanarusk R, Snounou G, Rénia L, Costa FT: On the Cytoadhesion of Plasmodium vivax-Infected Erythrocytes. J Infect Dis. 2010, 202: 638-47.View ArticlePubMedGoogle Scholar
- Francischetti I, Seydel K, Monteiro R, Whitten R, Erexson C, Noronha A, Ostera G, Kamiza S, Molyneux M, Ward JM, Taylor TE: Plasmodium falciparum-infected erythrocytes induce tissue factor expression in endothelial cells and support the assembly of multimolecular coagulation complexes. J Thromb Haemost. 2007, 5: 155-165.PubMed CentralView ArticlePubMedGoogle Scholar
- Miller L, Baruch D, Marsh K, Doumbo O: The pathogenic basis of malaria. Nature. 2002, 415: 673-679.View ArticlePubMedGoogle Scholar
- Newton C, Taylor T, Whitten R: Pathophysiology of fatal falciparum malaria in African children. Am J Trop Med Hyg. 1998, 58: 673-683.PubMedGoogle Scholar
- Nyangoto E: Cell-mediated effector molecules and complicated malaria. Int Arch Allergy Immunol. 2005, 137: 326-342.View ArticlePubMedGoogle Scholar
- Collins W, Jeffery G, Roberts J: A retrospective examination of anemia during infection of humans with Plasmodium vivax. Am J Trop Med Hyg. 2003, 68: 410-412.PubMedGoogle Scholar
- Alexandre M, Ferreira C, Siqueira A, Magalhães B, Mourão M, Lacerda M, Alecrim M: Severe Plasmodium vivax malaria, Brazilian Amazon. Emerg Infect Dis. 2010, 16: 1611-1614.PubMed CentralView ArticlePubMedGoogle Scholar
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