Skip to main content
Download PDF

Release of endothelial activation markers in lungs of patients with malaria-associated acute respiratory distress syndrome

Malaria Journal volume 18, Article number: 395 (2019) Cite this article

Abstract

Background

Malaria-associated acute respiratory distress syndrome (MA-ARDS) is an understudied complication of malaria and is characterized by pulmonary inflammation and disruption of the alveolar-capillary membrane. Its pathogenesis remains poorly understood. Since endothelial activation plays an important role in other malarial complications, the expression of two endothelial activation markers, von Willebrand factor (VWF) and angiopoietin-2 (ANG-2), was investigated in the lungs of patients with MA-ARDS.

Methods

Post-mortem lung sections of Plasmodium falciparum-infected patients without alveolar oedema (NA), P. falciparum-infected patients with alveolar oedema (MA-ARDS), and uninfected people who died accidentally with no pathological changes to the lungs (CON) were immunohistochemically stained for VWF and ANG-2, and were evaluated with semi-quantitative analysis.

Results

Alveolar oedematous VWF and ANG-2 and intravascular VWF staining were significantly increased in patients with MA-ARDS versus infected and uninfected control groups. The levels of VWF in the alveolar septa and endothelial lining of large blood vessels of patients with MA-ARDS was significantly decreased compared to controls. ANG-2 expression was increased in the alveolar septa of malaria patients without alveolar oedema versus control patients, while ANG-2+ leukocytes were increased in the alveoli in both infected patient groups.

Conclusions

This study documents a high level of VWF and ANG-2, two endothelial activation markers in the oedematous alveoli of post-mortem lung sections of Thai patients with MA-ARDS. Decreased detection of VWF in the endothelial lining of blood vessels, in parallel with an increased presence of intravascular VWF staining suggests marked endothelial activation and Weibel–Palade body release in the lungs of patients with MA-ARDS.

Background

The World Health Organization (WHO) malaria report described 219 million clinical cases and 435,000 deaths in 2017 [1]. Despite the availability of efficient anti-malarial treatment, transmission and severe disease of the Plasmodium parasite still occurs in 91 countries in sub-Saharan Africa, South-East Asia and South America [1]. A malaria infection can be asymptomatic or develop into mild disease, but a significant number of patients develop lethal complications. An understudied complication is malaria-associated acute respiratory distress syndrome (MA-ARDS). MA-ARDS may occur upon a Plasmodium falciparum or Plasmodium vivax infection. MA-ARDS is also one of the most prevalent complications in Plasmodium knowlesi-infected patients [2,3,4]. This lung complication mainly occurs in adults without pre-existing semi-immunity (e.g. travellers and residents of low transmission areas). MA-ARDS has a poor prognosis and leads to a lethality rate of up to 80%, despite anti-malarial treatment. In fact, MA-ARDS has been described to emerge at hospital admission and during anti-malarial treatment [2]. MA-ARDS is characterized by disruption of the alveolar-capillary membrane, which results into alveolar oedema and leads to a decreased gas exchange and hypoxaemia. Patients also present excessive inflammation, microhemorrhages and leukocyte extravasation in the lungs. Currently, the only available remedy is mechanical ventilation.

Endothelial activation plays an important role in severe malaria. During a Plasmodium infection, the vascular endothelium becomes activated through several pathogenic factors, such as sequestration, inflammatory cytokines and parasite constituents [5,6,7]. As a result, the endothelium immediately releases the contents of its Weibel–Palade bodies and induces upregulation of inflammatory molecules, which can further aggravate the disease. Biomarkers for endothelial activation, such as von Willebrand factor (VWF) and angiopoietin-2 (ANG-2), have been associated with disease severity and mortality in Plasmodium infections [8,9,10,11].

VWF is a multimeric glycoprotein that plays an important role in haemostasis, and is synthesized in endothelial cells (ECs) and megakaryocytes [12,13,14]. In ECs, VWF multimers are stored in Weibel–Palade bodies from which they are released into the circulation upon endothelial activation. After release, VWF multimers can stay anchored onto the endothelial lining, forming platelet-decorated VWF strings. Interestingly, VWF strings have been proposed to facilitate parasite sequestration, which can induce further inflammation and endothelial activation [15]. VWF-adhering platelets can for example bind to infected red blood cells (iRBCs) and bridge iRBCs to the endothelium, which may aid the parasite to evade splenic clearance [16, 17].

Endothelial activation also induces upregulation of ANG-2 and the release of Weibel–Palade body-stored ANG-2. ANG-2 is a glycoprotein that antagonizes the binding of ANG-1 to the tyrosine kinase receptor TIE-2 on ECs [18, 19]. While ANG-1/TIE-2 interactions maintain the quiescent state of the endothelium by inducing an anti-apoptotic and anti-inflammatory response, ANG-2 binding to TIE-2 prevents ANG-1 binding and increases the endothelial sensitivity for inflammation, coagulation and vascular permeability-inducing factors. Besides its suggested use as a plasma biomarker for disease severity in P. falciparum infections [20,21,22,23,24,25], ANG-2 was found on the vascular endothelium in brain sections of Vietnamese patients with cerebral malaria (CM) [26].

VWF and ANG-2 expression has not been investigated yet in patients with MA-ARDS. Therefore, the expression of these endothelial markers was investigated by immunohistochemical (IHC) analyses on lung sections of P. falciparum-infected patients without alveolar oedema, P. falciparum-infected patients with MA-ARDS and uninfected controls who died without any damage to the lungs. These data demonstrate a vast increase of VWF and ANG-2 in the alveoli of patients with MA-ARDS. This study comprises the first observations of endothelial activation markers in lungs of patients with MA-ARDS.

Methods

Patients

Post-mortem lungs from P. falciparum-infected Thai patients and controls were fixed with formalin and embedded in paraffin. These samples were obtained by The Department of Tropical Pathology (Faculty of Tropical Medicine, Mahidol University, Thailand) over a span of 30 years [27]. The available clinical data were compiled in Table 1. Samples were classified into three groups: (1) people who died accidentally with no pathological changes to the lungs as controls (CON, n = 9), (2) P. falciparum-infected patients without alveolar oedema (NA, n = 15) and (3) P. falciparum-infected patients with alveolar oedema (MA-ARDS, n = 13). Patients with severe malaria underwent antimalarial treatment with intravenous quinine. The study protocol was reviewed and approved by the Ethics Committee of Faculty of Tropical Medicine, Mahidol University (MUTM 2016-051-01 and MUTM 2016-051-02).

Table 1 Clinical characteristics of patients
Full size table

IHC staining

Lungs were compartmentalized in smaller pieces, embedded in paraffin and cut into 4 µm thick sections. Lung sections were deparaffinized by heating and rehydrated through graded concentrations of alcohol. Sections were washed with distilled water, followed by an antigen unmasking step according to manufacturer’s instructions (Antigen unmasking solution, Vector Laboratories, CA, USA). The following steps were all executed after a washing step with Tris buffered saline (pH 7.6) unless indicated otherwise. Sections were treated with 3% H2O2 [30 min at room temperature (RT) in the dark] to inactivate the endogenous peroxidase. Then, aspecific binding was blocked with goat serum (30 min at RT). The latter step was immediately followed by incubation with the primary rabbit polyclonal antibody for VWF (1/1000, ab6994, Abcam, Cambridge, UK) or ANG-2 (1/200, ab153934, Abcam) for 1 h at 37 °C. Afterwards, secondary antibody (rabbit IgG) was added for incubation (30 min at RT) and reacted with the avidin–biotin complex conjugated with horseradish peroxidase (Vectastain ABC Kit, Vector Laboratories) according to manufacturer’s instructions. The peroxidase staining was executed with the ImmPACT® DAB peroxidase substrate Kit (Vector Laboratories). Sections were then washed with distilled water and counterstained with Mayer’s haematoxylin (Merck, Darmstadt, Germany). Finally, sections were dehydrated through graded concentrations of alcohol and mounted with a coverslip. For each patient, one lung section was IHC stained and analysed. Additionally, negative controls, i.e. serial sections that were stained without the primary antibody were analysed in parallel for each lung section (Additional files 1, 2, 3, 4).

Semi-quantitative analysis of IHC lung sections

Whole images of IHC lung sections were scanned with a Nanozoomer (Hamamatsu Photonics, Herrsching am Ammersee, Germany) and pictures were taken at 5× and 20× magnification with the NDP viewer software (Hamamatsu Photonics). Ten random pictures were taken at 20× magnification for each IHC stained lung section and examined for the following parameters: percentage of alveoli with oedema, percentage of alveoli with ANG-2+ leukocytes, percentage of blood vessels with ANG-2 and VWF staining on the endothelial lining, percentage of blood vessels with intravascular VWF staining, percentage of blood vessels with ANG-2+ leukocytes, and ANG-2 and VWF staining intensity of alveolar septa and oedema. Ten pictures for each sample were scored in a range of 0–2 for ANG-2 and VWF staining intensity of alveolar septa and oedema, where 0 is no expression, 1 is moderate staining and 2 is strong staining. The relative score for the ANG-2 and VWF staining intensity of the alveolar septa was determined by the sum of the described scores for each picture. The total relative score for the alveolar oedematous ANG-2 and VWF staining was determined by multiplying the fraction of alveoli with positively ANG-2 or VWF stained oedema, with the described intensity score for each picture, and this was summed up for the ten pictures of each sample.

Statistics

The Mann–Whitney U test was used to determine the statistical significance of differences. Statistical analysis was done using the GraphPad Prism software (GraphPad software, San Diego, USA). P-values smaller than 0.05 were considered statistically significant. P-values were defined as follows: *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001. Each dot represents the results from an individual person. Horizontal lines represent group medians. Asterisks without horizontal lines represent significant differences compared to the uninfected control group (CON). Horizontal lines with asterisk on top indicate pairwise significant differences between patient groups.

Results

Clinical data of patients

Thirty-seven patients were included in this study. The clinical characteristics of P. falciparum-infected patients are described in Table 1. There was no significant difference in age, days of hospitalization, parasitaemia, haemoglobin levels and circulating white blood cells between the NA and MA-ARDS group. A small decrease in haematocrit values was found in the MA-ARDS group compared to the NA group. Details of diagnosis are described in Table 1. Histopathological findings of these samples were previously described by Punsawad et al. [27].

Expression of VWF in lungs of patients with MA-ARDS

Since circulating VWF is correlated with disease severity in P. falciparum-infected patients, the expression of VWF in MA-ARDS was investigated [10, 11, 28, 29]. Lung sections of people that died suddenly without any lung damage (CON), P. falciparum-infected patients without alveolar oedema (NA) and P. falciparum-infected patients with alveolar oedema (MA-ARDS) were stained with IHC for the early endothelial activation marker VWF. A broad view of these lung sections demonstrated strong VWF expression on the endothelial lining of large blood vessels in control samples (Fig. 1). Strong VWF staining was also observed in alveolar oedema of patients with MA-ARDS. A more detailed view showed that the VWF immunoreactivity is present on the endothelial lining of large blood vessels, alveolar septa and alveolar oedema (Fig. 2). Several large blood vessels showed VWF staining in the lumen, suggesting thrombus-like intravascular VWF staining (Fig. 2).

Fig. 1
figure 1

IHC staining of VWF in lungs of P. falciparum-infected patients and control group. VWF staining was executed in lung sections of people that died suddenly without any lung damage (CON), P. falciparum-infected patients without alveolar oedema (NA) and P. falciparum-infected patients with alveolar oedema (MA-ARDS). Each panel shows a section from a different patient. Green arrowheads indicate VWF stained large blood vessels. All images were taken at ×5 magnification. Bar = 100 µM

Full size image
Fig. 2
figure 2

Expression of VWF in lungs of P. falciparum-infected patients and control group. VWF staining was executed in lung sections of people that died suddenly without any lung damage (CON), P. falciparum-infected patients without alveolar oedema (NA) and P. falciparum-infected patients with alveolar oedema (MA-ARDS). Each panel shows a section from a different patient. Green arrowheads indicate VWF staining in the alveolar septa. Red arrowheads indicate larger VWF stained blood vessel walls. Red frames demonstrate intravascular VWF staining. All images were taken at ×20 magnification. Bar = 25 µM

Full size image

Semi-quantitative analyses demonstrated a significantly higher incidence of alveolar oedema in patients with MA-ARDS compared to the CON and NA group (Fig. 3a). This was paralleled by a significant increase in VWF stained alveolar oedema in the MA-ARDS group (Fig. 3b). The alveolar oedema varied in VWF staining intensity (Figs. 1, 2), and this was taken in consideration during the scoring for the semi-quantitative analysis. Patients with MA-ARDS also showed significantly decreased VWF expression in alveolar septa and large blood vessel walls compared to uninfected controls (Fig. 3c, d). In contrast, the incidence of intravascular VWF staining was increased in the MA-ARDS group and was significantly different from the CON and NA group (Fig. 3e). No difference was observed between the NA and CON group for the mentioned parameters. Overall, these data demonstrate a vastly increased intraluminal VWF staining in alveoli and large blood vessels in lungs of patients with MA-ARDS.

Fig. 3
figure 3

Semi-quantitative analysis of VWF expression in lungs of P. falciparum-infected patients and control group. VWF staining was executed in lung sections of people that died suddenly without any lung damage (CON), P. falciparum-infected patients without alveolar oedema (NA) and P. falciparum-infected patients with alveolar oedema (MA-ARDS). a The incidence in oedema was determined. Subsequently, semi-quantitative staining was performed for the following parameters: b alveolar oedematous VWF staining, c VWF stained alveolar septa, d large blood vessels with VWF stained endothelial lining and e intravascular VWF staining. N = 9–13

Full size image

IHC analysis of ANG-2 expression in MA-ARDS

Endothelial activation in MA-ARDS was further investigated by determining the pulmonary expression of ANG-2. ANG-2 is an endothelial activation marker and has also been used as a biomarker for disease severity in P. falciparum infections [20,21,22,23,24]. Figure 4 demonstrates an extensively increased expression of ANG-2 in the alveoli of patients with MA-ARDS compared to the CON and NA group. ANG-2 expression was more specifically found in alveolar oedema, alveolar septa, endothelial lining and lumen of large blood vessels, and leukocytes in large blood vessels and alveoli (Fig. 5).

Fig. 4
figure 4

IHC staining of ANG-2 in lungs of P. falciparum-infected patients and control group. ANG-2 staining was executed in lung sections of people that died suddenly without any lung damage (CON), P. falciparum-infected patients without alveolar oedema (NA) and P. falciparum-infected patients with alveolar oedema (MA-ARDS). Each panel shows a section from a different patient. All images were taken at ×5 magnification. Bar = 100 µM

Full size image
Fig. 5
figure 5

Expression of ANG-2 in lungs of P. falciparum-infected patients and control group. ANG-2 staining was executed in lung sections of people that died suddenly without any lung damage (CON), P. falciparum-infected patients without alveolar oedema (NA) and P. falciparum-infected patients with alveolar oedema (MA-ARDS). Each panel shows a section from a different patient. Arrowheads indicate ANG-2 expression in endothelial lining of large blood vessels (blue), and ANG-2+ leukocytes in alveoli (green) and in large blood vessels (red). Red frames demonstrate intravascular ANG-2 staining. All images were taken at ×20 magnification. Bar = 25 µM

Full size image

The variability in the intensity of ANG-2 expression in alveolar oedema was taken in consideration during the scoring. The semi-quantitative analysis showed a significant increase in oedematous ANG-2 staining in patients with MA-ARDS compared to the CON and NA group (Fig. 6a). While patients with MA-ARDS had similar ANG-2 expression in the alveolar septa, P. falciparum-infected patients without alveolar oedema had a significant increase versus the CON group (Fig. 6b). A higher amount of ANG-2+ leukocytes was observed in both P. falciparum-infected patient groups (Fig. 6c). Additionally, a non-significant trend was found in P. falciparum-infected patients without alveolar oedema for increased circulating ANG-2+ leukocytes compared to CON groups (p = 0.0556) (Fig. 6d). The ANG-2 staining on the endothelial lining and in the lumen of large blood vessels did not differ in between the investigated patient groups (Fig. 6e, f).

Fig. 6
figure 6

Semi-quantitative analysis of ANG-2 expression in lungs of P. falciparum-infected patients and control group. ANG-2 staining was executed in lung sections of people that died suddenly without any lung damage (CON), P. falciparum-infected patients without alveolar oedema (NA) and P. falciparum-infected patients with alveolar oedema (MA-ARDS). Semi-quantitative staining was performed for the following parameters: a alveolar oedematous ANG-2 staining, b ANG-2 stained alveolar septa, c, d alveoli and large blood vessels with ANG-2+ leukocytes, e large blood vessels with ANG-2 stained endothelial lining and f large blood vessels with ANG-2 stained lumen. N = 8–9

Full size image

Overall, these data show that ANG-2 staining is increased in lungs of malaria patients versus controls, with a marked staining of the alveolar septa in the NA group and an extensive increase of oedematous ANG-2 staining in the alveoli of patients with MA-ARDS.

Discussion

This study documents an extensive increase of VWF and ANG-2, two endothelial activation markers in the alveoli of post-mortem lung sections of Thai patients with MA-ARDS. VWF and ANG-2 stained alveolar oedema and intravascular VWF staining were significantly increased in patients with MA-ARDS versus infected and uninfected control groups. The staining of VWF on the alveolar septa and endothelial lining of large blood vessels of patients with MA-ARDS was significantly decreased compared to controls. The staining of ANG-2 was increased on the alveolar septa in infected patients without alveolar oedema versus control patients, while ANG-2+ leukocytes were increased in the alveoli in both infected patient groups.

Histopathological findings of these samples have been described in an earlier study [27]. Haematoxylin–eosin staining of lung sections of patients with MA-ARDS demonstrated alveolar oedema, vast infiltration of leukocytes and haemorrhages. This post-mortem study also showed presence of iRBCs in the blood vessels, suggesting parasite sequestration in the lungs [27]. Samples of patients with MA-ARDS were compared with P. falciparum-infected patients without alveolar oedema and uninfected people that died suddenly without any damage to the lungs. These three patient groups are suited to investigate the expression of endothelial activation markers in MA-ARDS.

VWF is released early into the circulation upon infection with P. falciparum infection [30]. Higher VWF antigen and VWF propeptide plasma values were found in patients infected with P. falciparum compared to healthy controls [23, 29, 31,32,33]. Moreover, a correlation between circulating VWF and disease severity was observed in P. falciparum-infected patients [10, 11, 28], but conflicting results were also published [29]. A Disintegrin and Metalloproteinase with a ThromboSpondin type 1 motif, member 13 (ADAMTS13) cleaves the ultra large-VWF multimer in smaller less reactive multimers. ADAMTS13 plasma levels and activity were decreased in Plasmodium-infected patients [28, 32, 34, 35]. This decrease in ADAMTS13 plasma levels and activity correlated with disease severity.

Patient data were validated in a mouse model for CM i.e. the infection of Plasmodium berghei (ANKA strain) in C57BL/6 mice. These mice develop experimental CM with increased VWF antigen plasma levels, ultra large-VWF multimers and VWF activity [36]. However, ADAMTS13 activity stayed unchanged. Kraisin et al. investigated VWF in the experimental MA-ARDS model, i.e. the infection of P. berghei (NK65-E strain) in C57BL/6 mice [37,38,39]. Similar to patient data, they found increased VWF levels and reduced ADAMTS13 activity levels in plasma of infected mice. Infected VWF KO developed less alveolar oedema versus WT mice upon infection. However, these infected mice still died earlier, possibly due to an increased parasite load in the circulation and the lungs [37]. Despite this difference in survival, the study does propose a pathogenic role of VWF on the integrity of the endothelial barrier.

These data showed a significant increase of VWF stained alveolar oedema and intravascular VWF staining in patients with MA-ARDS. VWF stained alveolar oedema may be the result of circulating VWF leaking into the alveoli due to the disruption of the alveolar-capillary membrane. The intravascular staining is not observed in the control group, suggesting that it is not the result of an isolation artefact. The increased incidence of intravascular VWF staining together with the decreased immunoreactivity of VWF in the endothelial lining of large blood vessels in the MA-ARDS group strongly suggest endothelial activation with a massive exocytosis of the Weibel–Palade bodies.

In lungs of healthy controls, strong VWF staining is present on the endothelial lining of larger blood vessels, however the capillary endothelium has been described to be mostly unreactive for VWF [40,41,42]. This VWF staining intensity was also described to increase with vessel size [40, 43]. These data demonstrated VWF staining in the alveolar septa (Fig. 2), which may be ascribed to the few septal capillaries that have positive VWF immunoreactivity. Additionally, pulmonary circulating megakaryocytes, which constitutively express VWF, have been found to generate 50% of the platelet reservoir in mice [44, 45]. Thrombocytopaenia is one of the most common haematological complications in malaria infections and studies have proposed dysmegakaryopoiesis to be one of the mechanisms behind this haematological disturbance in malaria [46, 47]. The decreased VWF staining in the alveolar septa of patients with MA-ARDS versus the control group may possibly be due to an even more decreased VWF staining of capillaries and/or a decreased expression of VWF in circulating megakaryocytes in the lungs.

Another commonly investigated endothelial activation marker is ANG-2. In line with the meta-analysis of De Jong et al. [48], an increased ANG-2/ANG-1 ratio and a decreased ANG-1 may be used as a biomarker for disease severity in P. falciparum infections, and seems to be prominent in cerebral complications [20,21,22,23,24]. However, ANG-2 plasma levels was also used alone as a biomarker [49,50,51]. ANG-2 plasma levels remain high after anti-malarial treatment in paediatric patients with CM, suggesting a persistent endothelial activation [51].

A protective effect of ANG-1 has been shown in the mouse model of experimental CM [24]. ANG-2, which competitively antagonizes the TIE-2 receptor for ANG-1 binding, may therefore aggravate the disease. Kim et al. showed that on 5 days post-infection (dpi), ANG-2 expression in brains of P. berghei (ANKA strain)-infected C57BL/6 mice was increased compared to uninfected mice [52]. The limited data regarding the ANG/TIE-2 pathway in experimental malaria models, illustrate the need for more studies.

A significant increase of ANG-2 staining in patients with MA-ARDS was demonstrated through increased alveolar oedematous ANG-2 staining. The presence of ANG-2 in the alveolar oedema may also be due to a vascular leakage into the alveoli. ANG-2+ leukocytes may further increase the ANG-2 levels in oedematous alveoli through secretion of ANG-2. ANG-2 expression in the alveolar septa was increased in P. falciparum-infected patients without alveolar oedema, but not in patients with MA-ARDS, suggesting a different ANG/TIE-2 pathway regulation between infected groups.

An inherent limitation of this post-mortem study is the anti-malarial treatment of these hospitalized patients. Upon admission and diagnosis, patients started a seven-day treatment scheme of intravenous quinine, but died on average 4–5 days after hospitalization. It cannot be excluded that the intravenous quinine treatment affected the development of MA-ARDS and/or endothelial activation in these patients. Nevertheless, the data clearly show increased pulmonary VWF and ANG-2 staining in post-mortem MA-ARDS samples, suggesting massive endothelial activation.

The increase of VWF and ANG-2 may not be specific for MA-ARDS since endothelial activation is also prominently present in non-malarial ARDS [53]. Several clinical studies have shown a prognostic value for circulating VWF and ANG-2 in these patients [54,55,56,57]. However, conflicting data have been found [55,56,57,58,59,60]. While Attia et al. did not observe a difference in ANG-2 levels in bronchoalveolar lavage fluid of patients with ARDS versus healthy controls, the research group of Ando et al. did demonstrate a significant increase of ANG-2 in patients with ARDS versus patients with idiopathic pulmonary fibrosis [57, 61]. These inconsistencies may be ascribed to multiple factors, such as variable ARDS severities and different non-malarial ARDS pathologies (e.g. direct versus indirect lung injury). Due to limited data, more studies including post-mortem analyses, are suggested to obtain a better view on the expression of endothelial activation markers in lungs of patients with non-malarial ARDS.

Conclusions

In conclusion, these data show a high level of VWF and ANG-2 in the oedematous alveoli of post-mortem lung sections of Thai patients with MA-ARDS. The decreased detection of VWF in the endothelial lining of large blood vessels and increased presence of intravascular VWF staining suggest an extensive endothelial activation and the content release of the Weibel–Palade bodies. This study demonstrates the first findings for the endothelial activation markers VWF and ANG-2 in lungs of patients with MA-ARDS. Therefore, more studies to fully understand the VWF and ANG/TIE-2 axis in MA-ARDS are warranted.

Availability of data and materials

All data generated or analysed during this study are included in this published article (and its additional information files).

Abbreviations

ADAMTS13:

A Disintegrin and Metalloproteinase with a Thrombospondin type 1 motif, member 13

ANG-1:

angiopoietin-1

ANG-2:

angiopoietin-2

CM:

cerebral malaria

CON:

control

dpi:

days post-infection

EC:

endothelial cell

IHC:

immunohistochemical

iRBC:

infected red blood cell

MA-ARDS:

malaria-associated acute respiratory distress syndrome

NA:

no alveolar oedema

RT:

room temperature

VWF:

von Willebrand factor

References

  1. WHO. World Health Organization. Geneva: World Health Organization; 2018. http://www.who.org. Accessed 20 July 2019.

  2. Van den Steen PE, Deroost K, Deckers J, Van Herck E, Struyf S, Opdenakker G. Pathogenesis of malaria-associated acute respiratory distress syndrome. Trends Parasitol. 2013;29:346–58.

    Article  PubMed  CAS  Google Scholar 

  3. William T, Menon J, Rajahram G, Chan L, Ma G, Donaldson S, et al. Severe Plasmodium knowlesi malaria in a tertiary care hospital, Sabah, Malaysia. Emerg Infect Dis. 2011;17:1248–55.

    Article  PubMed  PubMed Central  Google Scholar 

  4. Daneshvar C, Davis TME, Cox-Singh J, Zakri M, Zakaria K, Divis PCS, et al. Clinical and laboratory features of human Plasmodium knowlesi infection. Clin Infect Dis. 2009;49:852–60.

    Article  PubMed  Google Scholar 

  5. Storm J, Jespersen JS, Seydel KB, Szestak T, Mbewe M, Chisala NV, et al. Cerebral malaria is associated with differential cytoadherence to brain endothelial cells. EMBO Mol Med. 2019;11:e9164.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  6. Gillrie MR, Lee K, Gowda DC, Davis SP, Monestier M, Cui L, et al. Plasmodium falciparum histones induce endothelial proinflammatory response and barrier dysfunction. Am J Pathol. 2012;180:1028–39.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  7. Patel SN, Lu Z, Ayi K, Serghides L, Gowda DC, Kain KC. Disruption of CD36 impairs cytokine response to Plasmodium falciparum glycosylphosphatidylinositol and confers susceptibility to severe and fatal malaria in vivo. J Immunol. 2007;178:3954–61.

    Article  CAS  PubMed  Google Scholar 

  8. Graham SM, Chen J, Chung DW, Barker KR, Conroy AL, Hawkes MT, et al. Endothelial activation, haemostasis and thrombosis biomarkers in Ugandan children with severe malaria participating in a clinical trial. Malar J. 2016;15:56.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  9. Yeo TW, Lampah DA, Gitawati R, Tjitra E, Kenangalem E, Piera K, et al. Angiopoietin-2 is associated with decreased endothelial nitric oxide and poor clinical outcome in severe falciparum malaria. Proc Natl Acad Sci USA. 2008;105:17097–102.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Park GS, Ireland KF, Opoka RO, John CC. Evidence of endothelial activation in asymptomatic Plasmodium falciparum parasitemia and effect of blood group on levels of von Willebrand factor in malaria. J Pediatric Infect Dis Soc. 2012;1:16–25.

    Article  PubMed  PubMed Central  Google Scholar 

  11. Phiri HT, Bridges DJ, Glover SJ, van Mourik JA, de Laat B, M’baya B, et al. Elevated plasma von Willebrand factor and propeptide levels in Malawian children with malaria. PLoS ONE. 2011;6:e25626.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  12. McCormack JJ, Lopes da Silva M, Ferraro F, Patella F, Cutler DF. Weibel-Palade bodies at a glance. J Cell Sci. 2017;130:3611–7.

    Article  CAS  PubMed  Google Scholar 

  13. Schwameis M, Schörgenhofer C, Assinger A, Steiner MM, Jilma B. VWF excess and ADAMTS13 deficiency: a unifying pathomechanism linking inflammation to thrombosis in DIC, malaria, and TTP. Thromb Haemost. 2015;113:708–18.

    Article  PubMed  Google Scholar 

  14. De Ceunynck K, De Meyer SF, Vanhoorelbeke K. Unwinding the von Willebrand factor strings puzzle. Blood. 2013;121:270–7.

    Article  CAS  Google Scholar 

  15. Bridges DJ, Bunn J, Van Mourik JA, Grau G, Roger JS, Molyneux M, et al. Rapid activation of endothelial cells enables P. falciparum adhesion to platelet decorated von Willebrand factor strings Daniel. Blood. 2010;115:1472–4.

    Article  CAS  PubMed  Google Scholar 

  16. López JA. Malignant malaria and microangiopathies: merging mechanisms. Blood. 2010;115:1317–8.

    Article  PubMed  Google Scholar 

  17. Wassmer SC, Lépolard C, Traoré B, Pouvelle B, Gysin J, Grau GE. Platelets reorient Plasmodium falciparum-infected erythrocyte cytoadhesion to activated endothelial cells. J Infect Dis. 2004;189:180–9.

    Article  CAS  PubMed  Google Scholar 

  18. Page AV, Liles WC. Biomarkers of endothelial activation/dysfunction in infectious diseases. Virulence. 2013;4:507–16.

    Article  PubMed  PubMed Central  Google Scholar 

  19. Fiedler U, Augustin HG. Angiopoietins: a link between angiogenesis and inflammation. Trends Immunol. 2006;27:552–8.

    Article  CAS  PubMed  Google Scholar 

  20. Conroy AL, Lafferty EI, Lovegrove FE, Krudsood S, Tangpukdee N, Liles WC, et al. Whole blood angiopoietin-1 and -2 levels discriminate cerebral and severe (non-cerebral) malaria from uncomplicated malaria. Malar J. 2009;8:295.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  21. Lovegrove FE, Tangpukdee N, Opoka RO, Lafferty EI, Rajwans N, Hawkes M, et al. Serum angiopoietin-1 and -2 levels discriminate cerebral malaria from uncomplicated malaria and predict clinical outcome in African children. PLoS ONE. 2009;4:1–8.

    Article  CAS  Google Scholar 

  22. Jain V, Lucchi NW, Wilson NO, Blackstock AJ, Nagpal AC, Joel PK, et al. Plasma levels of angiopoietin-1 and -2 predict cerebral malaria outcome in Central India. Malar J. 2011;10:383.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  23. Conroy AL, Phiri H, Hawkes M, Glover S, Mallewa M, Seydel KB, et al. Endothelium-based biomarkers are associated with cerebral malaria in Malawian children: a retrospective case-control study. PLoS ONE. 2010;5:e15291.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  24. Higgins SJ, Purcell L, Silver K, Tran V, Crowley V, Hawkes M, et al. Dysregulation of angiopoietin-1 plays a critical mechanistic role in the pathogenesis of cerebral malaria. Sci Transl Med. 2016;8:358ra128.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  25. de Moura Carvalho LJ, da Silva Moreira A, Daniel-Ribeiro CT, Martins YC. Vascular dysfunction as a target for adjuvant therapy in cerebral malaria. Mem Inst Oswaldo Cruz. 2014;109:577–88.

    Article  Google Scholar 

  26. Prapansilp P, Medana IM, Mai NTH, Day NPJ, Phu NH, Yeo TW, et al. A clinicopathological correlation of the expression of the angiopoietin-Tie-2 receptor pathway in the brain of adults with Plasmodium falciparum malaria. Malar J. 2013;12:50.

    Article  PubMed  PubMed Central  Google Scholar 

  27. Punsawad C, Viriyavejakul P, Setthapramote C, Palipoch S. Enhanced expression of Fas and FasL modulates apoptosis in the lungs of severe P. falciparum malaria patients with pulmonary edema. Int J Clin Exp Pathol. 2015;8:10002–13.

    CAS  PubMed  PubMed Central  Google Scholar 

  28. Löwenberg EC, Charunwatthana P, Cohen S, Van Den Born BJ, Meijers JCM, Yunus EB, et al. Severe malaria is associated with a deficiency of von Willebrand factor cleaving protease, ADAMTS13. Thromb Haemost. 2010;103:181–7.

    Article  PubMed  CAS  Google Scholar 

  29. Erdman LK, Dhabangi A, Musoke C, Conroy AL, Hawkes M, Higgins S, et al. Combinations of host biomarkers predict mortality among Ugandan children with severe malaria: a retrospective case-control study. PLoS ONE. 2011;6:e17440.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  30. de Mast Q, Groot E, Lenting PJ, de Groot PG, McCall M, Sauerwein RW, et al. Thrombocytopenia and release of activated von Willebrand Factor during early Plasmodium falciparum malaria. J Infect Dis. 2007;196:622–8.

    Article  PubMed  CAS  Google Scholar 

  31. O’Regan N, Moxon CA, Gegenbauer K, O’Sullivan JM, Chion A, Smith OP, et al. Marked elevation in plasma osteoprotegerin constitutes an early and consistent feature of cerebral malaria. Thromb Haemost. 2016;115:773–80.

    Article  PubMed  PubMed Central  Google Scholar 

  32. Barber BE, William T, Grigg MJ, Parameswaran U, Piera KA, Price RN, et al. Parasite biomass-related inflammation, endothelial activation, microvascular dysfunction and disease severity in vivax malaria. PLoS Pathog. 2015;11:e1004558.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  33. De Mast Q, Groot E, Asih PB, Syafruddin D, Oosting M, Sebastian S, et al. ADAMTS13 deficiency with elevated levels of ultra-large and active von willebrand factor in P. falciparum and P. vivax malaria. Am J Trop Med Hyg. 2009;80:492–8.

    Article  PubMed  Google Scholar 

  34. Larkin D, De Laat B, Jenkins PV, Bunn J, Craig AG, Terraube V, et al. Severe Plasmodium falciparum malaria is associated with circulating ultra-large von willebrand multimers and ADAMTS13 inhibition. PLoS Pathog. 2009;5:e1000349.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  35. Riedl J, Mordmüller B, Koder S, Pabinger I, Kremsner PG, Hoffman SL, et al. Alterations of blood coagulation in controlled human malaria infection. Malar J. 2016;15:15.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  36. O’Regan N, Gegenbauer K, O’Sullivan JM, Maleki S, Brophy TM, Dalton N, et al. A novel role for von Willebrand factor in the pathogenesis of experimental cerebral malaria. Blood. 2015;127:1192–201.

    Article  PubMed  CAS  Google Scholar 

  37. Kraisin S, Verhenne S, Pham T-T, Martinod K, Tersteeg C, Vandeputte N, et al. von Willebrand factor in experimental malaria-associated acute respiratory distress syndrome. J Thromb Haemost. 2019;17:1372–83.

    Article  CAS  PubMed  Google Scholar 

  38. Van den Steen PE, Geurts N, Deroost K, Van Aelst I, Verhenne S, Heremans H, et al. Immunopathology and dexamethasone therapy in a new model for malaria-associated acute respiratory distress syndrome. Am J Respir Crit Care Med. 2010;181:957–68.

    Article  PubMed  CAS  Google Scholar 

  39. Vandermosten L, Pham T-T, Possemiers H, Knoops S, Van Herck E, Deckers J, et al. Experimental malaria-associated acute respiratory distress syndrome is dependent on the parasite-host combination and coincides with normocyte invasion. Malar J. 2018;17:102.

    Article  PubMed  PubMed Central  Google Scholar 

  40. Pusztaszeri MP, Seelentag W, Bosman FT. Immunohistochemical expression of endothelial markers CD31, CD34, von Willebrand factor, and Fli-1 in normal human tissues. J Histochem Cytochem. 2006;54:385–95.

    Article  CAS  PubMed  Google Scholar 

  41. Kawanami O, Enjing J, Ghazizadeh M, Fujiwara M, Jiang L, Nagashima M, et al. heterogeneous distribution of thrombomodulin and von Willebrand factor in endothelial cells in the human pulmonary microvessels. J Nippon Med Sch. 2000;67:118–25.

    Article  CAS  PubMed  Google Scholar 

  42. Müller AM, Skrzynski C, Skipka G, Müller KM. Expression of von Willebrand factor by human pulmonary endothelial cells in vivo. Respiration. 2002;69:526–33.

    Article  PubMed  Google Scholar 

  43. Kawanami O, Enjing J, Ghazizadeh M, Fujiwara M, Jiang L, Ohaki Y, et al. Mosaic-like distribution of endothelial cell antigens in capillaries and juxta-alveolar microvessels in the normal human lung. Pathol Int. 2000;50:136–41.

    Article  CAS  PubMed  Google Scholar 

  44. Tomer A. Human marrow megakaryocyte differentiation: multiparameter correlative analysis identifies von Willebrand factor as a sensitive and distinctive marker for early (2 N and 4 N) megakaryocytes. Blood. 2004;104:2722–7.

    Article  CAS  PubMed  Google Scholar 

  45. Lefrançais E, Ortiz-Muñoz G, Caudrillier A, Mallavia B, Liu F, Sayah DM, et al. The lung is a site of platelet biogenesis and a reservoir for haematopoietic progenitors. Nature. 2017;544:105–9.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  46. Lacerda MVG, Mourão MPG, Coelho HC, Santos JB. Thrombocytopenia in malaria: who cares? Mem Inst Oswaldo Cruz. 2011;106:52–63.

    Article  PubMed  Google Scholar 

  47. Menendez C, Fleming AF, Alonso PL. Malaria-related anaemia. Parasitol Today. 2000;16:469–76.

    Article  CAS  PubMed  Google Scholar 

  48. de Jong GM, Slager JJ, Verbon A, van Hellemond JJ, van Genderen PJJ. Systematic review of the role of angiopoietin-1 and angiopoietin-2 in Plasmodium species infections: biomarkers or therapeutic targets? Malar J. 2016;15:581.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  49. Weinberg JB, Volkheimer AD, Rubach MP, Florence SM, Mukemba JP, Kalingonji AR, et al. Monocyte polarization in children with falciparum malaria: relationship to nitric oxide insufficiency and disease severity. Sci Rep. 2016;6:29151.

    Article  PubMed  PubMed Central  Google Scholar 

  50. Hanson J, Lee SJ, Hossain MA, Anstey NM, Charunwatthana P, Maude RJ, et al. Microvascular obstruction and endothelial activation are independently associated with the clinical manifestations of severe falciparum malaria in adults: an observational study. BMC Med. 2015;13:122.

    Article  PubMed  PubMed Central  Google Scholar 

  51. Moxon CA, Chisala NV, Wassmer SC, Taylor TE, Seydel KB, Molyneux ME, et al. Persistent endothelial activation and inflammation after Plasmodium falciparum infection in Malawian children. J Infect Dis. 2014;209:610–5.

    Article  CAS  PubMed  Google Scholar 

  52. Kim H, Erdman LK, Lu Z, Serghides L, Zhong K, Dhabangi A, et al. Functional roles for C5a and C5aR but not C5L2 in the pathogenesis of human and experimental cerebral malaria. Infect Immun. 2014;82:371–9.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  53. Hendrickson CM, Matthay MA. Endothelial biomarkers in human sepsis: pathogenesis and prognosis for ARDS. Pulm Circ. 2018;8:1–12.

    Article  CAS  Google Scholar 

  54. Rubin DB, Wiener-Kronish JP, Murray JF, Green DR, Turner J, Luce JM, et al. Elevated von Willebrand factor antigen is an early plasma predictor of acute lung injury in nonpulmonary sepsis syndrome. J Clin Invest. 1990;86:474–80.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  55. Calfee CS, Gallagher D, Abbott J, Thompson BT, Matthay MA. Plasma angiopoietin-2 in clinical acute lung injury: prognostic and pathogenetic significance. Crit Care Med. 2012;40:1731–7.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  56. Zinter MS, Spicer A, Orwoll BO, Alkhouli M, Dvorak CC, Calfee CS, et al. Plasma angiopoietin-2 outperforms other markers of endothelial injury in prognosticating pediatric ARDS mortality. Am J Physiol Lung Cell Mol Physiol. 2016;310:L224–31.

    Article  PubMed  Google Scholar 

  57. Ando M, Miyazaki E, Abe T, Ehara C, Goto A, Masuda T, et al. Angiopoietin-2 expression in patients with an acute exacerbation of idiopathic interstitial pneumonias. Respir Med. 2016;117:27–32.

    Article  PubMed  Google Scholar 

  58. Agrawal A, Matthay MA, Kangelaris KN, Stein J, Chu JC, Imp BM, et al. Plasma angiopoietin-2 predicts the onset of acute lung injury in critically ill patients. Am J Respir Crit Care Med. 2013;187:736–42.

    Article  PubMed  PubMed Central  Google Scholar 

  59. Ware LB, Eisner MD, Thompson BT, Parsons PE, Matthay MA. Significance of Von Willebrand factor in septic and nonseptic patients with acute lung injury. Am J Respir Crit Care Med. 2004;170:766–72.

    Article  PubMed  Google Scholar 

  60. Ware LB, Koyama T, Zhao Z, Janz DR, Wickersham N, Bernard GR, et al. Biomarkers of lung epithelial injury and inflammation distinguish severe sepsis patients with acute respiratory distress syndrome. Crit Care. 2013;17:R253.

    Article  PubMed  PubMed Central  Google Scholar 

  61. Attia EF, Jolley SE, Crothers K, Schnapp LM, Liles WC. Soluble vascular cell adhesion molecule-1 (sVCAM-1) is elevated in bronchoalveolar lavage fluid of patients with acute respiratory distress syndrome. PLoS ONE. 2016;11:1–10.

    Google Scholar 

Download references

Acknowledgements

The authors thank Prof. Bart Vanaudenaerde and Arno Vanstapel for their expert advice.

Funding

This work has been supported by the Research Foundation-Flanders (F.W.O.-Vlaanderen) (Grant No G086215N) and the Research Fund (Geconcerteerde Onderzoeksacties GOA 2013/014 and C1 project C16/17/010) of the KU Leuven. TP holds an aspirant PhD fellowship of the F.W.O.-Vlaanderen and PEVdS is a Research Professor at the KU Leuven. TP also received a travel grant for a short stay abroad (K215417N) of the F.W.O.-Vlaanderen.

Author information

Authors and Affiliations

  1. Laboratory of Immunoparasitology, Department of Microbiology and Immunology, Rega Institute for Medical Research, KU Leuven, University of Leuven, Leuven, Belgium

    Thao-Thy Pham & Philippe E. Van den Steen

  2. School of Medicine, Walailak University, Nakhon Si Thammarat, Thailand

    Chuchard Punsawad

  3. Department of Tropical Pathology, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand

    Supattra Glaharn & Parnpen Viriyavejakul

  4. Laboratory for Thrombosis Research, KU Leuven Campus Kulak Kortrijk, Kortrijk, Belgium

    Simon F. De Meyer

Authors
  1. Thao-Thy Pham
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Chuchard Punsawad
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Supattra Glaharn
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Simon F. De Meyer
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Parnpen Viriyavejakul
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Philippe E. Van den Steen
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

TTP performed the experiments. CP and SG assisted with the experiments. TTP, SFDM and PEVdS analysed the data. PV and PEVdS conceived the study. TTP and PEVdS wrote the first drafts of the manuscript. All authors critically read and edited the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Philippe E. Van den Steen.

Ethics declarations

Ethics approval and consent to participate

All experiments were reviewed and approved by the Ethics Committee of Faculty of Tropical Medicine, Mahidol University (MUTM 2016-051-01 and MUTM 2016-051-02).

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Additional file 1.

Negative controls of IHC staining of VWF in lungs of P. falciparum-infected patients and control group. Serial lung sections of people that died suddenly without any lung damage (CON), P. falciparum-infected patients without alveolar oedema (NA) and P. falciparum-infected patients with alveolar oedema (MA-ARDS) were stained in parallel without the primary antibody for VWF. Each panel demonstrates the complementary negative control for the sections in Fig. 1. All images were taken at 5x magnification. Bar = 100 µM.

Additional file 2.

Negative controls of IHC lung sections for VWF in lungs of P. falciparum-infected patients and control group. Serial lung sections of people that died suddenly without any lung damage (CON), P. falciparum-infected patients without alveolar oedema (NA) and P. falciparum-infected patients with alveolar oedema (MA-ARDS) were stained in parallel without the primary antibody for VWF. Each panel demonstrates the complementary negative control for the sections in Fig. 2. All images were taken at 20x magnification. Bar = 25 µM.

Additional file 3.

Negative controls of IHC staining of ANG-2 in lungs of P. falciparum-infected patients and control group. Serial lung sections of people that died suddenly without any lung damage (CON), P. falciparum-infected patients without alveolar oedema (NA) and P. falciparum-infected patients with alveolar oedema (MA-ARDS) were stained in parallel without the primary antibody for ANG-2. Each panel demonstrates the complementary negative control for the sections in Fig. 4. All images were taken at 5x magnification. Bar = 100 µM.

Additional file 4.

Negative controls of IHC lung sections for ANG-2 in lungs of P. falciparum-infected patients and control group. Serial lung sections of people that died suddenly without any lung damage (CON), P. falciparum-infected patients without alveolar oedema (NA) and P. falciparum-infected patients with alveolar oedema (MA-ARDS) were stained in parallel without the primary antibody for ANG-2. Each panel demonstrates the complementary negative control for the sections in Fig. 5. All images were taken at 20x magnification. Bar = 25 µM.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Pham, TT., Punsawad, C., Glaharn, S. et al. Release of endothelial activation markers in lungs of patients with malaria-associated acute respiratory distress syndrome. Malar J 18, 395 (2019). https://0-doi-org.brum.beds.ac.uk/10.1186/s12936-019-3040-3

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://0-doi-org.brum.beds.ac.uk/10.1186/s12936-019-3040-3

Keywords

Malaria Journal

ISSN: 1475-2875

Contact us