Combined measurement of soluble and cellular ICAM-1 among children with Plasmodium falciparum malaria in Uganda
© Cserti-Gazdewich et al. 2010
Received: 14 June 2010
Accepted: 16 August 2010
Published: 16 August 2010
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© Cserti-Gazdewich et al. 2010
Received: 14 June 2010
Accepted: 16 August 2010
Published: 16 August 2010
Intercellular adhesion molecule-1 (ICAM-1) is a cytoadhesion molecule implicated in the pathogenesis of Plasmodium falciparum malaria. Elevated levels of soluble ICAM-1 (sICAM-1) have previously been reported with increased malaria disease severity. However, studies have not yet examined both sICAM-1 concentrations and monocyte ICAM-1 expression in the same cohort of patients. To better understand the relationship of soluble and cellular ICAM-1 measurements in malaria, both monocyte ICAM-1 expression and sICAM-1 concentration were measured in children with P. falciparum infection exhibiting a spectrum of clinical severity.
Samples were analysed from 160 children, aged 0.5 to 10.8 years, with documented P. falciparum malaria in Kampala, Uganda. The patients belonged to one of three pre-study defined groups: uncomplicated malaria (UM), severe non-fatal malaria (SM-s), and fatal malaria (SM-f). Subset analysis was done on those with cerebral malaria (CM) or severe malaria anaemia (SMA). Monocyte ICAM-1 was measured by flow cytometry. sICAM-1 was measured by enzyme immunoassay.
Both sICAM-1 and monocyte cell-surface ICAM-1 followed a log-normal distribution. Median sICAM-1 concentrations increased with greater severity-of-illness: 279 ng/mL (UM), 462 ng/mL (SM-s), and 586 ng/mL (SM-f), p < 0.0001. sICAM-1 levels were not statistically different among children with CM compared to SMA. Monocyte ICAM-1 expression was significantly higher in cases of UM compared with SM-s or SM-f (p < 0.001) and was higher among the subset of patients with CM compared with SMA, p < 0.0014. The combination of sICAM-1 and cellular ICAM-1 identified distinct categories of patients (UM with low sICAM-1 and higher monocyte ICAM-1, CM with both sICAM-1 and monocyte ICAM-1 high, and SMA with sICAM-1 high but monocyte ICAM-1 low).
In this cohort of children with P. falciparum malaria, sICAM-1 levels were associated with severity-of-illness. Patients with UM had higher monocyte ICAM-1 expression consistent with a role for monocyte ICAM-1 in immune clearance during non-severe malaria. Among the subsets of patients with either SMA or CM, monocyte ICAM-1 levels were higher in CM, consistent with the role of ICAM-1 as a marker of cytoadhesion. Categories of disease in pediatric malaria may exhibit specific combinations of soluble and cellular ICAM-1 expression.
Intercellular adhesion molecule-1 (ICAM-1) is an important cell adhesion molecule involved in inflammation and immunity. It is the principal ligand for leukocyte function antigen-1 (LFA1) and directs localization of leukocytes to areas of inflammation. ICAM-1 is expressed on several tissues including endothelial cells, monocytes, and lymphocytes. A soluble form of ICAM-1 circulates in plasma. Soluble ICAM-1 is released from cell-surface ICAM-1 by proteolytic cleavage in response to inflammatory cytokines or endothelial damage. The plasma half-life of circulating soluble ICAM-1 is not known. ICAM-1 is one of several cell adhesion molecules important in Plasmodium falciparum malaria. Red blood cells, infected with P. falciparum, express a parasite-derived protein (Plasmodium falciparum erythrocyte membrane protein-1, PfEMP-1) associated with knob-like projections on the erythrocyte surface. Specific protein domains of PfEMP-1 bind to different target molecules of the infected host including blood group A and B antigens, platelet glycoprotein IV (CD36), chondroitin sulfate, complement receptor-1, and ICAM-1.
ICAM-1 expression can have both beneficial and deleterious consequences to the infected host. Monocyte ICAM-1 participates in the immune response to P. falciparum infection. ICAM-1 surface expression was shown to be required for the interferon-γ response of Natural Killer cells to malaria-infected red cells. Early production of interferon-γ has been shown to be protective against malaria infection in both human studies[3, 4] and animal models. In contrast, direct adhesion of parasitized erythrocytes to ICAM-1 on cerebral endothelial cells or co-localization of monocytes to areas of erythrocyte and platelet adhesion on cerebral endothelial cells may contribute to cerebral malaria[6–8].
Evidence for the role of cell-surface ICAM-1 expression in cerebral malaria comes from histologic studies. Examination of brain tissue from patients who died with cerebral malaria has demonstrated adhesion of parasitized red cells, platelets, and leukocytes to brain endothelium in association with increased endothelial expression of ICAM-1[6–8, 10–12]. When dermal microvasculature, rather than cerebral microvasculature was examined, Turner et al observed that endothelial ICAM-1 staining did not correlate with the severity of malaria. Thus, it is possible that expression of ICAM-1 on dermal endothelial cells may not reflect ICAM-1 expression on cerebral vasculature.
Laboratory studies also support a role for adhesion of parasitized erythrocytes to ICAM-1 in malaria pathogenesis. Newbold et al found that in-vitro binding of parasitized red cells to ICAM-1 was more common among patients with cerebral malaria compared with controls. Tripathi et al demonstrated in-vitro that exposure of human brain microvascular endothelial cell cultures to either parasitized red cells or the supernatant of cultured parasitized red cells resulted in increased expression of ICAM-1 on brain microvascular endothelial cells, and suggested that ICAM-1 expression was driven by P. falciparum proteins rather than host cytokines. Favre et al infected wild type and ICAM-1 knock out mice with Plasmodium berghei and found that despite similar levels of parasitaemia, wild type mice had decreased survival, greater accumulation of macrophages in brain venules and greater sequestration of parasitized red cells in alveolar capillaries.
Soluble plasma levels of ICAM-1 have been measured in several studies of P. falciparum malaria. Initial small studies identified increased levels of soluble ICAM-1 in patients with severe malaria[17–21]. In a larger case-control study conducted in the Gambia, McGuire et al measured soluble ICAM-1 levels in 157 children with cerebral malaria, 89 with acute non-cerebral malaria, and 156 non-malarial controls. Soluble ICAM-1 levels were significantly higher (p < 0.001) among those with malaria (735 ng/mL) compared with controls (440 ng/mL), but did not discriminate those with cerebral malaria. sICAM levels also correlated with disease severity in the large study reported by Turner et al . More recently, Tchinda et al reported plasma levels of soluble ICAM-1, soluble vascular adhesion molecule-1, soluble endothelial cell leukocyte adhesion molecule and TNF in children with malaria in Cameroon. Among 114 children with severe malaria, 55 children with uncomplicated malaria, and 43 non-malaria controls, soluble ICAM-1 levels were significantly higher among those with severe disease compared with either uncomplicated malaria or controls. However, among those with severe malaria syndromes, soluble ICAM-1 levels did not distinguish cerebral malaria or severe malaria anaemia from other malaria syndromes. Taken together, the published literature suggests that plasma ICAM-1 concentrations are higher in patients with more severe disease, but that levels cannot be used to distinguish children with cerebral malaria.
Few clinical studies have examined ICAM-1 expression on circulating monocytes among subjects with malaria. Using flow cytometry, Jenkins et al examined monocyte ICAM-1 expression among 117 children with severe malaria and 239 with uncomplicated malaria. Among those with both severe and non-severe malaria, they observed higher monocyte ICAM-1 expression at onset of disease compared with convalescence. Monocyte ICAM-1 fluorescence was not different among those with cerebral malaria versus those without cerebral malaria.
To further explore the relationship between cell-surface and soluble ICAM-1 among patients with severe malaria syndromes, both peripheral blood monocyte ICAM-1 expression and plasma soluble ICAM-1 concentrations were measured in a cohort of children with acute P. falciparum infection in Kampala, Uganda. To better understand both potentially beneficial and detrimental effects of ICAM-1 in malaria, soluble and cellular ICAM-1 measurements were obtained at presentation of illness among children with different categories of disease severity including those with uncomplicated malaria, severe malaria anaemia, and cerebral malaria.
Patients were selected for testing from those enrolled in a larger observational case-control clinical study (enrollment dates Oct 2007-Oct 2009) of children aged 6 months to 12 years with P. falciparum malaria treated at Mulago Hospital in Kampala, Uganda. Prior to any testing, patients were categorized into three groups: uncomplicated malaria under treatment as outpatients (UM), severe malaria survivors treated as inpatients (SM-s), and fatal severe malaria treated as inpatients (SM-f). In addition, patients were sub-categorized according to WHO classifications of malaria syndromes as either cerebral malaria (CM) or severe malaria anaemia (SMA). Patient samples from the above 3 categories were selected from a larger study sample archive based on availability of an adequate volume of previously unthawed plasma. All patients had confirmed P. falciparum infection based on independent review of anonymized and clinically blinded peripheral blood smears by two experts at a university malaria confirmatory laboratory (Makerere-UCSF Molecular Laboratory, Dr Samuel Nsobya, Director). The number of parasitized red cells was determined relative to leukocyte counts. No threshold level of parasitaemia was required and assessment of quantitative parasitaemia by independent reviewers agreed within < 2%. The median concentration of parasitized red cells was 39,200/μL (range 64/μL-2,033,920/μL). Peripheral blood samples were obtained from each patient on one occasion at the time of presentation to hospital for care. Citrated plasma was separated from whole blood by centrifugation, transferred to screw-cap cryovials, and promptly frozen at -20°C shortly after phlebotomy for later testing of soluble ICAM-1 concentration. At the same phlebotomy, a peripheral whole blood sample collected in EDTA was tested for ICAM-1 expression on monocytes by flow cytometry (see below). Patients were treated in the Acute Care Unit of Mulago Hospital (a university teaching hospital setting) by Study Clinicians skilled in the management of paediatric malaria. Anti-malarial treatment was administered according to Ugandan national guidelines. Parents of enrolled children gave written informed consent to participate in the study and to test stored samples. The study was approved by the Research Ethics Board of the University of Toronto, Makerere University College of Health Sciences, and the Uganda National Council for Science and Technology.
The values for blood ICAM-1 and plasma ICAM-1 are listed in Additional file 1.
ICAM-1 expression on monocytes was measured by flow cytometry using a FACSCalibur™ (BD Biosciences; San Jose, CA) with CellQuest™ (BD Biosciences, version 3.3) acquisition software and Flowjo™ (Tree Star, Ashland, OR) for analysis. Instrument setup and calibration were performed daily with CaliBRITE™ beads according to the manufacturer's recommendations. Peripheral blood, collected in EDTA, was tested within 48 hours of collection. Previous work demonstrated that monocyte ICAM-1 cell-surface levels were stable for 72 hours after sample collection and were unaffected by the platelet concentration in the sample. Prior to beginning the study, serial testing of samples stored as anticoagulated whole blood in EDTA without continuous mixing at local temperatures demonstrated no statistical difference between monocyte ICAM-1 measurements at day 0 (day of phlebotomy) and day 3 of storage. During the study, 61% of patients were tested on the same day as phlebotomy or the next day, 21% on day 2, and 14% on day 3. Thus > 95% of samples were tested within three days of collection. There was furthermore no difference in monocyte ICAM-1 expression distributions as a function of the days of storage before cytometry testing (p = 0.245, ANOVA). Whole blood (100 μL) was incubated for 15 minutes at room temperature with the following monoclonal antibodies obtained from BD Biosciences: anti-CD61-FITC (clone RUU-PL7F12); anti-CD54-APC (clone HA58); and anti-CD14-PerCP (clone MΦ-P9). Following incubation, the cell suspension was lysed, washed, fixed and acquired within 24 hours. Gating strategy was based on forward scatter vs side scatter vs CD14 and CD14 vs CD61. Monocyte-platelet aggregates, identified as events double-positive for both CD14 and CD61, were eliminated from the final analysis. CD54 expression on the resulting monocyte singlets (CD14+ CD61-) was displayed as a histogram of at least 4,000 CD14 positive events and the geometric mean fluorescence intensity (MFI) channel recorded for each sample.
Cumulative probability plots were used to characterize the distribution of plasma soluble ICAM-1, whole blood sICAM, and monocyte MFI. Comparison between multiple groups was done by the Kruskal-Wallis test. Comparison between two groups was done using the Wilcoxon sum test. Correlations were tested for best fit using an automated curve fitting programme .
Clinical characteristics of the patients.
n = 160
n = 53
Severe malaria survivors
n = 80
Fatal malaria (SM-f),* n = 27
Age (years) median (IQR)
2.2 (1.2 - 4.4)
4.4 (2.2 - 8)
1.6 (1 - 3.1)
# of days ill prior to presentation median (IQR)
Haemoglobin (g/dL) median (IQR)
10.1 (9.4 - 11.3)
4.4 (3.4 - 5.6)
5.9 (4.6 - 8.5)
10,200 (6,800 - 14,300)
7,500 (5,200 - 9,000)
12,150 (9,375 - 16,000)
13,000 (8,500 - 25,125)
66 (39 - 114)
48 (33 - 63)
94 (50 - 137)
83 (51 - 125)
Parasitized red cells/μL
# with cerebral malaria
# with severe malaria anaemia
# with both cerebral malaria and severe malaria anaemia
ICAM-1 is a major cytoadhesion ligand for PfEMP-1, which is expressed by parasitized erythrocytes. Previous histologic studies in cerebral malaria have demonstrated that ICAM-1 expression may directly contribute to cytoadhesion of malaria infected red cells or may serve to recruit leukocytes to sites of endothelial activation[6, 9–12]. Studies measuring soluble ICAM-1 alone have found increased levels with greater disease severity, but no association with specific cytoadhesive syndromes[13, 17, 18, 20–23]. Studies of ICAM-1 expression on circulating monocytes found higher levels in acute illness compared with convalescence. Previous studies have not measured both soluble ICAM-1 and peripheral blood monocyte ICAM-1 expression in the same cohort of patients. This study examined the association between measurements of both soluble and cellular ICAM-1 with categories of clinical severity and with specific malaria syndromes in 160 children with documented P. falciparum infection.
Soluble ICAM-1 has been suggested by other authors to result principally from proteolytic cleavage (shedding) of membrane ICAM-1 expressed on endothelial cells and monocytes. In this study, plasma and whole blood levels of soluble ICAM-1 followed a log-normal distribution in children with malaria. Consistent with previously published work [13, 23], soluble ICAM-1 levels were found to be significantly higher among children with severe malaria syndromes or fatal malaria compared to those with uncomplicated malaria. These higher soluble ICAM-1 concentrations may reflect a combination of greater inflammatory response, increased endothelial cell activation with ICAM-1 shedding, or reduced soluble ICAM-1 clearance. Also consistent with previous work[22, 23], soluble ICAM-1 levels did not distinguish patients with cerebral malaria from those with severe malaria anaemia. This was true even when plasma soluble ICAM-1 levels were corrected for the degree of anaemia in each patient.
Increased ICAM-1 expression on monocytes may be beneficial for the host with uncomplicated P. falciparum infection. For example, ICAM-1 expression on monocytes is required for interferon-γ release by NK cells in response to parasitized red cells. In this study children with uncomplicated malaria, treated as outpatients, had significantly higher monocyte ICAM-1 expression than those with severe or fatal disease. Whether the higher observed monocyte ICAM-1 levels among outpatients were the result of higher baseline expression, increased activation in response to inflammatory cytokines, or reduced shedding due to a milder clinical course could not be determined.
In contrast, high expression of ICAM-1 on cerebral endothelial cells may contribute to cytoadhesion of parasitized red cells and cerebral malaria[11, 12]. In the subset of patients with severe disease, inflammatory cytokines result in increased expression of cell-surface ICAM-1. In contrast to those with uncomplicated infection, ICAM-1 expression measured on circulating monocytes in patients with severe inflammatory malaria syndromes may reflect levels found on endothelial cells and the subset of patients with severe a cytoadhesive syndrome such as cerebral malaria might be expected to have higher levels of ICAM-1 expression compared with those with severe malaria anaemia. In addition, among such patients with severe disease, those with monocytes exhibiting high ICAM-1 expression may co-localize monocytes to parasitized red cells adherent to brain endothelium contributing further to the lesion of cerebral malaria, while in contrast, patients with low monocyte ICAM-1 may have less co-localization and reduced risk of cerebral malaria. Consistent with either of these hypotheses, this study observed that patients with cerebral malaria had significantly higher monocyte ICAM-1 levels compared with those with severe malaria anaemia alone.
This study had several limitations. As an observational study, only associations may be drawn between ICAM-1 measurements and clinical outcomes. Such associations may be confounded by factors not included in the analysis. Secondly, although the study subjects were from the same region (urban Kampala, Uganda) and studied over a limited time frame (24 months), it is possible that different strains of parasites with different adhesive properties to ICAM-1 were distributed unequally among the different clinical groups. ICAM-1 was only measured at clinical presentation and it is not known if serial measurements would lead to different conclusions. Because monocytes are readily accessible, they are an appealing surrogate for endothelial cell expression. However, both regulation of ICAM-1 expression and membrane shedding from proteolytic cleavage may differ for endothelial cells and monocytes. Because the endothelium represents the largest organ in the body, direct assessment of endothelial ICAM-1 in specific organ beds affected by malaria may be a more important but more challenging source to study. Finally, soluble and monocyte ICAM-1 levels in patients with asymptomatic parasitaemia or healthy controls were not measured nor was testing done in individuals with genetic variants of ICAM-1[29–31].
Improved understanding of the role of ICAM-1 in the molecular pathology of malaria remains important. In the future, proteomics technology may allow investigators to distinguish between ICAM-1 shed from the vascular endothelium versus that shed from monocytes[32, 33]. The former may provide the least invasive surrogate of endothelial expression relevant in cytoadhesion, while the latter may reveal the proportion engaged in an immune response. Further examination of cases stratified by severity and by syndrome may indeed clarify the predictive dualities of the physiology of ICAM-1 in malaria. In the meantime, to clarify further the role of ICAM-1 in malaria, measurement of both cell-surface and soluble ICAM-1 are recommended for clinical and laboratory studies of ICAM-1 and malaria.
Financial support: This work was supported in part by grants from the National Blood Foundation (CMC), the International Society of Blood Transfusion Foundation (CMC), a University of Toronto Dean's Fund grant (CMC), a CIHR MD/PhD training grant (LE), a CIHR Team Grant in Malaria (KCK), operating grant MT-13721 (KCK), Genome Canada through the Ontario Genomics Institute (KCK), and CIHR Canada Research Chair (KCK). Funding agencies had no role in study design, data collection, analysis or interpretation, the writing of the manuscript, or the decision to submit the work for publication.
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