The Mannose-binding lectin (MBL) pathway of complement plays a pivotal role in the pathogenesis of ischemia/reperfusion (I/R) injury after experimental ischemic stroke. As comparable data in human ischemic stroke are limited, we investigated in more detail the association of MBL deficiency with infarction volume and functional outcome in a large cohort of patients receiving intravenous thrombolysis or conservative treatment.
In a post hoc analysis of a prospective cohort study, admission MBL concentrations were determined in 353 consecutive patients with an acute ischemic stroke of whom 287 and 66 patients received conservative and thrombolytic treatment, respectively. Stroke severity, infarction volume, and functional outcome were studied in relation to MBL concentrations at presentation to the emergency department. MBL levels on admission were not influenced by the time from symptom onset to presentation (p = 0.53). In the conservative treatment group patients with mild strokes at presentation, small infarction volumes or favorable outcomes after three months demonstrated 1.5 to 2.6-fold lower median MBL levels (p = 0.025, p = 0.0027 and p = 0.046, respectively) compared to patients with more severe strokes. Moreover, MBL deficient patients (<100 ng/ml) were subject to a considerably decreased risk of an unfavorable outcome three months after ischemic stroke (adjusted odds ratio 0.38, p<0.05) and showed smaller lesion volumes (mean size 0.6 vs. 18.4 ml, p = 0.0025). In contrast, no association of MBL concentration with infarction volume or functional outcome was found in the thrombolysis group. However, the small sample size limits the significance of this observation.
MBL deficiency is associated with smaller cerebral infarcts and favorable outcome in patients receiving conservative treatment. Our data suggest an important role of the lectin pathway in the pathophysiology of cerebral I/R injury and might pave the way for new therapeutic interventions.
Citation: Osthoff M, Katan M, Fluri F, Schuetz P, Bingisser R, Kappos L, et al. (2011) Mannose-Binding Lectin Deficiency Is Associated With Smaller Infarction Size and Favorable Outcome in Ischemic Stroke Patients. PLoS ONE6(6): e21338. https://doi.org/10.1371/journal.pone.0021338
Editor: Sven G. Meuth, University of Muenster, Germany
Received: January 26, 2011; Accepted: May 26, 2011; Published: June 21, 2011
Copyright: © 2011 Osthoff et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by a SCORE fellowship form the Swiss National Science Foundation to MT (Nr. 3232B0-107248/2 and 324730-132955), a grant to young researchers from the University of Basel to MK as well as a grant of the Swiss National Science Foundation to MCC (Nr. PP00P3-12346). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: Drs. Osthoff, Fluri, Bingisser, Steck, Engelter, and Mueller report no disclosures. Dr. Schuetz received support from Brahms and BioMerieux for speaking engagements. Dr. Kappos has received payments from several companies regarding his research within the field of multiple sclerosis research unrelated to this trial. Dr. Christ-Crain received speaking honoraria from Brahms. There are no patents, products in development or marketed products to declare. This does not alter the authors' adherence to all the PLoS ONE policies on sharing data and materials, as detailed online in the guide for authors.
Complement mannose-binding lectin (MBL), a member of the collectin subfamily of C-type lectins, is a key component of innate immunity . Besides its important contribution to host defense against pathogens, MBL is also involved in the binding and removal of apoptotic cells leading to complement activation in an antibody- and complement C1q independent manner , . In humans polymorphisms within the coding and promoter regions of the MBL2 gene lead to functional MBL deficiency in up to one third of the Caucasian population characterized by reduced levels of circulating functional MBL multimers . During lifetime individual MBL serum levels remain remarkably stable highlighting the dominating influence of genetics as compared to environmental factors. Even during acute inflammation, low MBL serum concentrations are predictive for moderate to severe deficiency . However, there is considerable interindividual MBL level variability (up to ten-fold) in people with the same genotype.
Numerous studies have acknowledged the deleterious effects of complement activation in the pathogenesis of ischemia/reperfusion (I/R) injury (reviewed in ) via free-radical production, activation of the coagulation cascade and direct tissue damage. In particular, several lines of evidence from murine models, one human experimental model, and one clinical trial emphasize a central and active role for complement MBL in aggravating tissue damage after I/R injury of the heart , , , , kidney , gut , , and skeletal muscle . With respect to cerebral I/R injury results from two recent experimental studies demonstrate that MBL deficiency or inhibition leads to diminished complement C3 deposition and neutrophil influx into the affected brain region and is associated with smaller infarct volumes and better functional outcomes in mice , . In humans comparable data are scarce. Activation of the complement system has been confirmed in three clinical studies after acute ischemic stroke , , . Regarding the effect of MBL, Cervera et al. could demonstrate a significant association of genetically defined MBL deficiency with favorable outcome after three months, though in a small cohort that included a considerable number (19%) of hemorrhagic stroke patients . Moreover, the impact of MBL deficiency on the outcome after thrombolytic treatment was not analyzed. Thrombolytic agents cause a striking systemic activation of the complement system , but data on the role of MBL in cerebral I/R injury after thrombolysis is lacking. Hence, the aim of this study was to investigate the impact of functional MBL deficiency in human acute ischemic stroke in a prospective cohort of consecutive patients receiving intravenous thrombolysis or conservative treatment according to the European Guidelines .
The study had been approved by the local ethical committee at the University Hospital of Basel and all participants or their representative gave written informed consent for the study.
We conducted a post hoc analysis of a previously published, prospective cohort study at the University Hospital Basel, Basel, Switzerland consisting of 359 patients presenting to the emergency department with an acute ischemic stroke within 72 hours after symptom onset between November 2006 and November 2007. Patients were classified as either receiving conservative treatment (including monitoring of blood pressure, oxygen saturation, serum glucose, temperature and neurological symptoms, early mobilization, prevention of complications, and treatment of hypoxia, hyperglycemia, pyrexia and dehydration) or intravenous thrombolysis according to the European Guidelines . A complete description of the study including information about clinical work-up, recorded clinical variables, blood-sampling and neuroimaging has been reported previously .
Definitions of endpoints
The primary endpoint for this analysis was favorable functional outcome (score 0 or 1) on the modified Rankin scale (mRS) within 90 days after admission. Secondary endpoints included functional status as assessed by the Barthel Index (BI) at day 90 (favorable outcome was defined as BI> = 95%), death from any cause within a 90-day follow-up, severity of stroke as assessed by the National Institutes of Health Stroke Scale (NIHSS) score on admission, and infarction volume assessed by magnetic resonance imaging (MRI) during initial work-up (categorized according to Katan and colleagues ). MRI scans were available in 157/297 and 42/66 patients receiving conservative and thrombolytic treatment, respectively.
MBL level analysis
For the MBL analysis serum samples drawn immediately on admission to our emergency department (within 0–72 hours after symptom onset) prior to any diagnostic imaging or thrombolytic treatment were available from 353 of 359 patients, of whom 287 and 66 individuals received conservative and intravenous (i.v.) thrombolytic treatment, respectively. For the i.v. treatment group we analyzed additional samples 24 and 72 hours after admission which were available from 56 patients. Quantification of functional MBL was performed by an investigator blinded to any patient data using a commercially available Sandwich-ELISA Kit (MBL Oligomer ELISA KIT 029, Lucerna Chem, Luzern, Switzerland) as described previously . Since the definition of functional MBL deficiency is likely to be dependent on the clinical setting, we first analyzed the predefined endpoints in relation to MBL levels. Only in a secondary analysis functional MBL deficiency was defined as serum levels ≤100 ng/ml, as this cut-off has been shown to discriminate reasonably well between individuals with or without homozygosity for MBL variant alleles  and to be clinical relevant in human cardiac IR injury . As our study was not powered to identify significant differences in mortality with regard to the predefined MBL cut-off, patients were stratified according to MBL level tertiles in the analysis of Kaplan-Meier survival curves.
Differences in patient characteristics and outcome measures according to treatment and MBL serostatus were analyzed using the Fisher's exact test or the Mann-Whitney-U-Test where appropriate. Due to the non-Gaussian distribution of human MBL levels two-group comparisons of MBL concentrations were performed using a Mann-Whitney-U-test, whereas for multigroup comparison a Kruskal-Wallis one-way analysis of variance or Friedman test was applied where appropriate. Dunn's post test was used to correct p-values for multiple comparisons. Mortality was analyzed by the log-rank test. Kaplan-Meier estimates were plotted over the observation period of 90 days.
Stepwise logistic regression models were used to estimate the association of MBL levels on predefined endpoints in multivariate analyses after adjustment for covariables being present prior to the ischemic event with univariate p values less than 0.1. Covariables tested in univariate analyses included patient age, sex, vital parameters and Charlson comorbidity index on admission, history of vascular risk factors, time from symptom onset to admission, and body mass index. All testing was two-tailed, and p values less than 0.05 were considered to be statistically significant.
Admission serum samples were available from 353 of 359 consecutive patients with an acute ischemic stroke and a complete follow-up, of whom 287 and 66 patients underwent conservative treatment and intravenous thrombolysis, respectively. The baseline and outcome characteristics of the whole study cohort and classified according to the therapeutic intervention are summarized in Table 1. In summary, patients in the conservative treatment group were older (median age of 76 (interquartile range (IQR) 66–83) vs. 71 (IQR 57–70), p<0.001), suffered from more comorbidities (median Charlson Index of 1 (IQR 0–2) vs. 0 (IQR 0–1), p = 0.002), and presented with a less severe stroke (median NIHSS score of 4 (IQR 2–8) vs. 12 (IQR 7–19), p<0.001), whereas unadjusted outcomes after 90 days were similar (data not shown).
Mannose-binding lectin serum levels
On admission the median MBL serum level of all patients included in this study was 1482 ng/ml (IQR 411–2675 ng/ml), and 37 of 353 (10%) individuals showed levels below 100 ng/ml, thereby closely resembling frequency distributions observed in the general population , . Furthermore, initial MBL levels were similar in patients presenting to our emergency department within 0–3 (median 1502 ng/ml), 3–12 (median 1388 ng/ml), 12–24 (median 1768 ng/ml) and 24–72 hours (median 1607 ng/ml) after symptom onset (p = 0.53), as was the case in the two treatment groups. Sequential analysis of MBL serum levels in the thrombolysis group revealed stable MBL levels during the first 24 hours after administration of thrombolytic agents (admission: median 1500 (IQR 490–2250) ng/ml; after 24 hours: median 1610 (IQR 459–2259) ng/ml). However, a significant increase in MBL levels occurred after five days (median 2167 (IQR 548–3281) ng/ml, p<0.001 for the comparison of admission vs. day 5), reflecting a mild acute phase reaction. As expected from previous studies, this increase was only observed in MBL sufficient patients, whereas MBL levels remained constant in MBL deficient patients .
Conservative treatment group
Association with functional outcome and death after ischemic stroke.
Uni- and multivariate analysis of the primary endpoint showed that MBL levels were significantly associated with functional outcome after three months in this treatment group: Patients with a complete recovery (i.e., a mRS of 0 or 1) had lower MBL levels than individuals with an unfavorable outcome (median MBL level 1116 (IQR 370–2524) vs. 1713 (IQR 420–3018) ng/ml, p = 0.046, Figure 1). After adjusting for potential confounders being present prior to the ischemic event MBL levels remained independently associated with an unfavorable outcome three months after ischemic stroke (OR 1.23, 95% CI 1.02–1.48, for every 1000 ng/ml increase, p = 0.036) in addition to age (Table 2).
Conservative treatment group: differences in MBL serum concentrations according to the functional outcome as assessed by the modified Rankin Scale 90 days after presentation. Horizontal lines represent medians.
To confirm the influence of MBL levels on functional recovery after ischemic stroke a second outcome measure (Barthel Index) was analyzed. A strong trend towards higher MBL levels in patients with an unfavorable recovery within 90 days after admission (defined as a BI score of > = 95%) could be observed as compared to individuals with a favorable outcome (median MBL levels 1754 vs. 1270 ng/ml, p = 0⋅06), which was significant in the multivariate analysis (OR 1.26, 95% CI 1.04–1.54, for every 1000 ng/ml increase, p = 0.02).
The conservative treatment group consisted of 28/287 (9.8%) patients with MBL levels below 100 ng/ml, a cut-off generally accepted for the definition of functional MBL deficiency. Baseline characteristics were similar in MBL deficient patients as compared to patients with MBL levels ≥100 ng/ml with the exception of a history of hypertension (15/28 vs. 205/259, p = 0.004). In this MBL deficient group there were 19 patients (68%) with a favorable recovery (i.e., a mRS score of 0 or 1) three months after admission, five (18%) with an unfavorable outcome (mRS score of 2–5) and four (14%) individuals who died (mRS score of 6), as compared to 116 (45%), 115 (44%) and 28 (11%) corresponding patients with MBL levels above 100 ng/ml (p = 0.025, Figure 2A). In a multivariate analysis (including history of hypertension as a cofactor) MBL deficient patients were subject to an almost 3-fold decreased risk to suffer from significant disabilities or to die within three months after ischemic stroke (OR 0.38, 95% CI 0.14–0.98, p = 0.046). Besides absence of MBL deficiency, only older age (OR 1.05, 95% CI 1.02–1.07, for every year increase, p<0.0001) and more comorbidities (OR 1.22, 95% CI 1.02–1.46, for every unit increase in the Charlson Comorbidity index, p = 0.03) were independent predictors of an unfavorable outcome after three months. Analysis of the secondary outcome measure, the Barthel Index further underscored the beneficial effect of MBL deficiency in ischemic stroke (p = 0.028, Figure 2B).
Conservative treatment group: association of functional MBL deficiency (MBL<100 ng/ml) with functional recovery three months after ischemic stroke as assessed by (A) the modified Rankin Scale and (B) the Barthel Index.
For the association with mortality alone Kaplan-Meier survival curves were calculated stratified by MBL tertiles. The risk for death within three months after admission was lowest in patients in the first tertile (MBL<542 ng/ml; survival rate 92±2.8%), intermediate in the second (MBL 542–2288 ng/ml; survival rate 89±3.1%) and highest in the third tertile (MBL>2288 ng/ml, survival rate 86±3.5%). However, these differences did not reach statistical significance (p = 0.26 for the comparison of the first vs. third tertile; data not shown).
Association with severity and size of stroke.
Patients with a mild stroke at presentation (defined as a NIHSS score of ≤7 , ) showed significantly lower MBL levels than individuals with intermediate or high (8–14 and >14, respectively) NIHSS scores (median MBL level 1176 (IQR 386–2640) vs. 1893 (IQR 555–3536) ng/ml, p = 0.025, Figure 3). Analysis of a subgroup of patients (n = 157 in whom MRI as part of the initial work-up was available revealed a striking association between lesion size and MBL serum levels. Median MBL levels were lowest in patients with a small (<10 ml) lesion (685 (IQR 255–2577) ng/ml) as compared to patients with medium (10–100 ml) and large (>100 ml) infarction volumes (1653 (IQR 497–2877) ng/ml and 3826 (IQR 1356–4433) ng/ml, respectively. p = 0.0027, Figure 4).
Conservative treatment group: differences in MBL serum concentrations according to stroke severity as assessed by the NIHSS at presentation. Horizontal lines represent medians.
Conservative treatment group: differences in MBL serum concentrations according to infarction volume on MRI scan (subgroup analysis). Horizontal lines represent medians. Horizontal dashed line corresponds to the cut-off of <100 ng/ml representing MBL deficient patients. Abbreviation: DWI = Diffusion-weighted imaging.
Furthermore, MBL deficient patients (<100 ng/ml) showed significantly smaller infarctions as compared to MBL sufficient patients (mean size 0.6 (SD 0.8) vs. 18.4 (SD 43.6) ml, p = 0.0025). Notably, none of the MBL deficient patients experienced a medium or large cerebral lesion (volume of >10 ml) as compared to 39 of 140 (28%) patients with MBL levels above 100 ng/ml (p = 0.0073).
After adjustment for covariables being present prior to the ischemic event only MBL levels remained independently associated with lesion size on MRI: The average infarction volume increased by 7.3 ml for every 1000 ng/ml increase in MBL serum levels (standard error 2.32, 95% CI 2.9–12.2, p = 0.002).
Thrombolysis treatment group
In contrast to the conservatively treated group MBL levels did not influence any of the above mentioned outcome measures in patients receiving thrombolytic agents after admission. Notably, median MBL levels were similar in patients with a less severe (NIHSS score <7) vs. a severe stroke (NIHSS score >7) at presentation (1508 vs. 1488 ng/ml, p = 0.96), in patients with small vs. medium/large stroke lesions on MRI (1315 vs. 1482 ng/ml, p = 0.66), in patients with a complete recovery vs. an unfavorable outcome (1325 vs. 1680, p = 0.24) and in patients surviving vs. dying during a 90-day follow-up (1620 vs. 1341 ng/ml, p = 0.5). This holds also true for the cut-off of <100 ng/ml, representing MBL deficient patients.
If all study participants (thrombolysis and conservative treatment group) were analyzed together, MBL levels were still independently associated with an unfavorable outcome three months after ischemic stroke (OR 1.23, 95% CI 1.03–1.46, for every 1000 ng/ml increase, p = 0.019) in addition to only age (OR 1.03, 95% CI 1.02–1.05, for every year increase, p<0.0001). Furthermore, the association of low MBL levels with smaller infarction size persisted in the pooled analysis (data not shown).
Several lines of evidence have emphasized the pivotal role of the complement system in general and the MBL pathway in particular in the pathogenesis of I/R injury, including ischemic stroke , , , , . In the present study, we demonstrate that functional MBL deficiency is associated with smaller cerebral lesion volumes and favorable outcomes in patients with conservative treatment after acute ischemic stroke but not in patients receiving i.v. thrombolysis.
These results are in line with data from Cervera et al. who demonstrated a significant association of genetically defined MBL deficiency with favorable outcome albeit in a smaller mixed hemorrhagic and ischemic stroke cohort . By analyzing infarction size on MRI and comparing outcome measures in a conservative vs. thrombolytic treatment cohort we highlight in more detail the potential pathogenetic relevance of the MBL pathway after human ischemic stroke. In the conservative treatment group MBL deficiency seems to considerably restrict propagation of damage after ischemic stroke. Patients with MBL levels <100 ng/ml were almost three times more likely to recover without significant disabilities within three months after admission when compared to MBL sufficient patients. This protective effect was even more pronounced when analyzing the association of MBL levels with infarction volumes on MRI in a subgroup of patients. Compared to patients with a small cerebral lesion median MBL serum concentration was more than two-fold and five-fold higher in patients with medium and large infarction volumes, respectively. In particular, functionally MBL deficient patients invariably experienced small cerebral lesions. This is well in line with experimental data using either MBL-deficient mice or an inhibitor of the MBL pathway , .
Notably, the magnitude of association was more evident in the analysis of early infarction volumes than of functional outcome. Hence, the role of MBL seems to be most prominent in the early phase of ischemic stroke, whereas functional recovery might not only be influenced by lesion size and stroke severity (as assessed by the NIHSS) but several other factors such as age, localization of infarct, secondary complications, and early initiation of rehabilitation services . Alternatively, data from Rahpeyma Y et al. suggest that complement activation in the brain may not only exacerbate tissue damage in the acute setting (lesion size) but on the other hand also promote neurogenesis and regeneration after ischemia in the long-term (functional outcome) .
A significant influence of MBL deficiency on mortality after ischemic stroke was not evident in our study. Considering that there were only 32 events in the conservatively treated group (11%), the study was not powered to analyze smaller differences between MBL sufficient and deficient patients. Furthermore, mortality after stroke might be more affected by preexisting comorbidities and infections than MBL status.
Interestingly, we did not observe a similar protective effect of MBL deficiency in patients receiving i.v. thrombolysis, which in theory should more closely mimic experimental I/R injury than conservative treatment. Several reasons might account for this important difference. First, our thrombolysis group was rather small and only powered to detect substantial differences in outcome, yet results were consistent over all endpoints analyzed. Second, animal as well as human data assessing the effect of MBL deficiency on ischemic stroke outcome after systemic thrombolysis are lacking. Therefore, we a priori chose to separately analyze patients receiving systemic thrombolysis vs. conservative treatment. In theory, massive systemic complement activation occurring after thrombolysis might have masked or offset any favorable effect of MBL deficiency that is usually evident after experimental cerebral I/R injury . On the other hand, the benefit of a successful thrombolysis might have significantly outweighed any effect of the MBL pathway, e.g. by attenuating inflammatory reaction after ischemic stroke which is only partly mediated by the MBL pathway. Audebert et al. found that successful thrombolysis was associated with subsequently lower C-reactive protein (CRP) and white blood count levels . Moreover, CRP levels were not predictive of functional outcome in a study of patients receiving thrombolysis  in contrast to several studies involving exclusively or mainly conservatively treated patients , , , , thereby further underscoring the influence of thrombolysis on inflammation after stroke. In conclusion, additional prospective trials are warranted to further investigate the effect of the MBL pathway in patients undergoing thrombolysis.
Recently, recombinant human C1-Inhibitor has been shown to function as a powerful inhibitor of MBL and its detrimental cerebral effects in a mouse model of cerebral I/R injury . By demonstrating smaller lesion volume and improved functional outcome in MBL deficient patients the present study draws further attention to MBL as a promising target for reducing cerebral I/R injury and supports the investigation of functional MBL inhibition in human ischemic stroke, especially in patients who do not qualify for thrombolytic treatment.
Despite the precisely characterized cohort the present prospective observation study has limitations including the post hoc analysis of MBL serum levels. Furthermore, MRI testing was not available for all patients in both groups, which may have biased results. Yet, analysis of functional outcome in patients with MRI data revealed similar effect of MBL deficiency as compared to the whole cohort (data not shown). Regarding the thrombolysis group the small sample size limits the significance of the observed data. At first sight the fact that MBL2 genotypes were not determined could appear as a limitation. However, MBL serum levels show little variation throughout life. In particular, MBL levels have never been shown to strongly fluctuate during acute diseases, and MBL levels in our patients were not influenced by the interval from symptom onset to presentation and blood sampling in our emergency department. Therefore, measurement of MBL serum levels by ELISA allows reliable quantification of the functional activity of the MBL pathway in vivo in this setting . When evaluating associations with diseases measurement of MBL serum levels might in fact represent a more sensitive approach than determination of genotypes as individuals with the same genotype may vary up to tenfold in MBL serum levels , , . Moreover, MBL2 genotyping cannot account for the significant changes of MBL serum levels induced by thyroid dysfunction .
In conclusion, functional MBL deficiency was associated with smaller infarction volume and favorable functional outcome in patients receiving conservative treatment after acute ischemic stroke. These findings support the concept of a significant contribution of the MBL pathway to cerebral tissue injury in human ischemic stroke. Thus, transient and early blockade of MBL or inhibition of the lectin complement pathway may represent a therapeutically promising strategy for reducing I/R associated cerebral damage.
Conceived and designed the experiments: MO MK MT. Performed the experiments: MO. Analyzed the data: MO MK PS. Contributed reagents/materials/analysis tools: FF RB LK AJS STE BM MC-C. Wrote the paper: MO MK. Critically revised the article for important intellectual content: FF RB LK AJS STE BM MCC MT.
- 1. Bouwman LH, Roep BO, Roos A (2006) Mannose-binding lectin: clinical implications for infection, transplantation, and autoimmunity. Hum Immunol 67: 247–256.LH BouwmanBO RoepA. Roos2006Mannose-binding lectin: clinical implications for infection, transplantation, and autoimmunity.Hum Immunol67247256
- 2. Ogden CA, deCathelineau A, Hoffmann PR, Bratton D, Ghebrehiwet B, et al. (2001) C1q and mannose binding lectin engagement of cell surface calreticulin and CD91 initiates macropinocytosis and uptake of apoptotic cells. J Exp Med 194: 781–795.CA OgdenA. deCathelineauPR HoffmannD. BrattonB. Ghebrehiwet2001C1q and mannose binding lectin engagement of cell surface calreticulin and CD91 initiates macropinocytosis and uptake of apoptotic cells.J Exp Med194781795
- 3. Lu JH, Thiel S, Wiedemann H, Timpl R, Reid KB (1990) Binding of the pentamer/hexamer forms of mannan-binding protein to zymosan activates the proenzyme C1r2C1s2 complex, of the classical pathway of complement, without involvement of C1q. J Immunol 144: 2287–2294.JH LuS. ThielH. WiedemannR. TimplKB Reid1990Binding of the pentamer/hexamer forms of mannan-binding protein to zymosan activates the proenzyme C1r2C1s2 complex, of the classical pathway of complement, without involvement of C1q.J Immunol14422872294
- 4. Garred P, Larsen F, Seyfarth J, Fujita R, Madsen HO (2006) Mannose-binding lectin and its genetic variants. Genes Immun 7: 85–94.P. GarredF. LarsenJ. SeyfarthR. FujitaHO Madsen2006Mannose-binding lectin and its genetic variants.Genes Immun78594
- 5. Herpers BL, Endeman H, de Jong BA, de Jongh BM, Grutters JC, et al. (2009) Acute-phase responsiveness of mannose-binding lectin in community-acquired pneumonia is highly dependent upon MBL2 genotypes. Clin Exp Immunol 156: 488–494.BL HerpersH. EndemanBA de JongBM de JonghJC Grutters2009Acute-phase responsiveness of mannose-binding lectin in community-acquired pneumonia is highly dependent upon MBL2 genotypes.Clin Exp Immunol156488494
- 6. Arumugam TV, Shiels IA, Woodruff TM, Granger DN, Taylor SM (2004) The role of the complement system in ischemia-reperfusion injury. Shock 21: 401–409.TV ArumugamIA ShielsTM WoodruffDN GrangerSM Taylor2004The role of the complement system in ischemia-reperfusion injury.Shock21401409
- 7. Walsh MC, Bourcier T, Takahashi K, Shi L, Busche MN, et al. (2005) Mannose-binding lectin is a regulator of inflammation that accompanies myocardial ischemia and reperfusion injury. J Immunol 175: 541–546.MC WalshT. BourcierK. TakahashiL. ShiMN Busche2005Mannose-binding lectin is a regulator of inflammation that accompanies myocardial ischemia and reperfusion injury.J Immunol175541546
- 8. Trendelenburg M, Theroux P, Stebbins A, Granger C, Armstrong P, et al. (2010) Influence of functional deficiency of complement mannose-binding lectin on outcome of patients with acute ST-elevation myocardial infarction undergoing primary percutaneous coronary intervention. Eur Heart J 31: 1181–1187.M. TrendelenburgP. TherouxA. StebbinsC. GrangerP. Armstrong2010Influence of functional deficiency of complement mannose-binding lectin on outcome of patients with acute ST-elevation myocardial infarction undergoing primary percutaneous coronary intervention.Eur Heart J3111811187
- 9. Busche MN, Pavlov V, Takahashi K, Stahl GL (2009) Myocardial ischemia and reperfusion injury is dependent on both IgM and mannose-binding lectin. Am J Physiol Heart Circ Physiol 297: H1853–1859.MN BuscheV. PavlovK. TakahashiGL Stahl2009Myocardial ischemia and reperfusion injury is dependent on both IgM and mannose-binding lectin.Am J Physiol Heart Circ Physiol297H18531859
- 10. Jordan JE, Montalto MC, Stahl GL (2001) Inhibition of mannose-binding lectin reduces postischemic myocardial reperfusion injury. Circulation 104: 1413–1418.JE JordanMC MontaltoGL Stahl2001Inhibition of mannose-binding lectin reduces postischemic myocardial reperfusion injury.Circulation10414131418
- 11. de Vries B, Walter SJ, Peutz-Kootstra CJ, Wolfs TG, van Heurn LW, et al. (2004) The mannose-binding lectin-pathway is involved in complement activation in the course of renal ischemia-reperfusion injury. Am J Pathol 165: 1677–1688.B. de VriesSJ WalterCJ Peutz-KootstraTG WolfsLW van Heurn2004The mannose-binding lectin-pathway is involved in complement activation in the course of renal ischemia-reperfusion injury.Am J Pathol16516771688
- 12. Hart ML, Ceonzo KA, Shaffer LA, Takahashi K, Rother RP, et al. (2005) Gastrointestinal ischemia-reperfusion injury is lectin complement pathway dependent without involving C1q. J Immunol 174: 6373–6380.ML HartKA CeonzoLA ShafferK. TakahashiRP Rother2005Gastrointestinal ischemia-reperfusion injury is lectin complement pathway dependent without involving C1q.J Immunol17463736380
- 13. Matthijsen RA, Derikx JP, Steffensen R, van Dam RM, Dejong CH, et al. (2009) Mannose-binding lectin null alleles are associated with preserved epithelial cell integrity following intestinal ischemia reperfusion in man. Mol Immunol 46: 2244–2248.RA MatthijsenJP DerikxR. SteffensenRM van DamCH Dejong2009Mannose-binding lectin null alleles are associated with preserved epithelial cell integrity following intestinal ischemia reperfusion in man.Mol Immunol4622442248
- 14. Chan RK, Ibrahim SI, Takahashi K, Kwon E, McCormack M, et al. (2006) The differing roles of the classical and mannose-binding lectin complement pathways in the events following skeletal muscle ischemia-reperfusion. J Immunol 177: 8080–8085.RK ChanSI IbrahimK. TakahashiE. KwonM. McCormack2006The differing roles of the classical and mannose-binding lectin complement pathways in the events following skeletal muscle ischemia-reperfusion.J Immunol17780808085
- 15. Cervera A, Planas AM, Justicia C, Urra X, Jensenius JC, et al. (2010) Genetically-defined deficiency of mannose-binding lectin is associated with protection after experimental stroke in mice and outcome in human stroke. PLoS One 5: e8433.A. CerveraAM PlanasC. JusticiaX. UrraJC Jensenius2010Genetically-defined deficiency of mannose-binding lectin is associated with protection after experimental stroke in mice and outcome in human stroke.PLoS One5e8433
- 16. Gesuete R, Storini C, Fantin A, Stravalaci M, Zanier ER, et al. (2009) Recombinant C1 inhibitor in brain ischemic injury. Ann Neurol 66: 332–342.R. GesueteC. StoriniA. FantinM. StravalaciER Zanier2009Recombinant C1 inhibitor in brain ischemic injury.Ann Neurol66332342
- 17. Pedersen ED, Waje-Andreassen U, Vedeler CA, Aamodt G, Mollnes TE (2004) Systemic complement activation following human acute ischaemic stroke. Clin Exp Immunol 137: 117–122.ED PedersenU. Waje-AndreassenCA VedelerG. AamodtTE Mollnes2004Systemic complement activation following human acute ischaemic stroke.Clin Exp Immunol137117122
- 18. Mocco J, Wilson DA, Komotar RJ, Sughrue ME, Coates K, et al. (2006) Alterations in plasma complement levels after human ischemic stroke. Neurosurgery 59: 28–33; discussion 28–33.J. MoccoDA WilsonRJ KomotarME SughrueK. Coates2006Alterations in plasma complement levels after human ischemic stroke.Neurosurgery592833; discussion 28–33
- 19. Szeplaki G, Szegedi R, Hirschberg K, Gombos T, Varga L, et al. (2009) Strong complement activation after acute ischemic stroke is associated with unfavorable outcomes. Atherosclerosis 204: 315–320.G. SzeplakiR. SzegediK. HirschbergT. GombosL. Varga2009Strong complement activation after acute ischemic stroke is associated with unfavorable outcomes.Atherosclerosis204315320
- 20. Agostoni A, Gardinali M, Frangi D, Cafaro C, Conciato L, et al. (1994) Activation of complement and kinin systems after thrombolytic therapy in patients with acute myocardial infarction. A comparison between streptokinase and recombinant tissue-type plasminogen activator. Circulation 90: 2666–2670.A. AgostoniM. GardinaliD. FrangiC. CafaroL. Conciato1994Activation of complement and kinin systems after thrombolytic therapy in patients with acute myocardial infarction. A comparison between streptokinase and recombinant tissue-type plasminogen activator.Circulation9026662670
- 21. (2008) Guidelines for management of ischaemic stroke and transient ischaemic attack 2008. Cerebrovasc Dis 25: 457–507.2008Guidelines for management of ischaemic stroke and transient ischaemic attack 2008.Cerebrovasc Dis25457507
- 22. Katan M, Fluri F, Morgenthaler NG, Schuetz P, Zweifel C, et al. (2009) Copeptin: a novel, independent prognostic marker in patients with ischemic stroke. Ann Neurol 66: 799–808.M. KatanF. FluriNG MorgenthalerP. SchuetzC. Zweifel2009Copeptin: a novel, independent prognostic marker in patients with ischemic stroke.Ann Neurol66799808
- 23. Manuel O, Pascual M, Trendelenburg M, Meylan PR (2007) Association between mannose-binding lectin deficiency and cytomegalovirus infection after kidney transplantation. Transplantation 83: 359–362.O. ManuelM. PascualM. TrendelenburgPR Meylan2007Association between mannose-binding lectin deficiency and cytomegalovirus infection after kidney transplantation.Transplantation83359362
- 24. Gadjeva M, Takahashi K, Thiel S (2004) Mannan-binding lectin–a soluble pattern recognition molecule. Mol Immunol 41: 113–121.M. GadjevaK. TakahashiS. Thiel2004Mannan-binding lectin–a soluble pattern recognition molecule.Mol Immunol41113121
- 25. DeGraba TJ, Hallenbeck JM, Pettigrew KD, Dutka AJ, Kelly BJ (1999) Progression in acute stroke: value of the initial NIH stroke scale score on patient stratification in future trials. Stroke 30: 1208–1212.TJ DeGrabaJM HallenbeckKD PettigrewAJ DutkaBJ Kelly1999Progression in acute stroke: value of the initial NIH stroke scale score on patient stratification in future trials.Stroke3012081212
- 26. Wahlgren N, Ahmed N, Davalos A, Ford GA, Grond M, et al. (2007) Thrombolysis with alteplase for acute ischaemic stroke in the Safe Implementation of Thrombolysis in Stroke-Monitoring Study (SITS-MOST): an observational study. Lancet 369: 275–282.N. WahlgrenN. AhmedA. DavalosGA FordM. Grond2007Thrombolysis with alteplase for acute ischaemic stroke in the Safe Implementation of Thrombolysis in Stroke-Monitoring Study (SITS-MOST): an observational study.Lancet369275282
- 27. Rahpeymai Y, Hietala MA, Wilhelmsson U, Fotheringham A, Davies I, et al. (2006) Complement: a novel factor in basal and ischemia-induced neurogenesis. Embo J 25: 1364–1374.Y. RahpeymaiMA HietalaU. WilhelmssonA. FotheringhamI. Davies2006Complement: a novel factor in basal and ischemia-induced neurogenesis.Embo J2513641374
- 28. Appelros P, Nydevik I, Viitanen M (2003) Poor outcome after first-ever stroke: predictors for death, dependency, and recurrent stroke within the first year. Stroke 34: 122–126.P. AppelrosI. NydevikM. Viitanen2003Poor outcome after first-ever stroke: predictors for death, dependency, and recurrent stroke within the first year.Stroke34122126
- 29. Audebert HJ, Rott MM, Eck T, Haberl RL (2004) Systemic inflammatory response depends on initial stroke severity but is attenuated by successful thrombolysis. Stroke 35: 2128–2133.HJ AudebertMM RottT. EckRL Haberl2004Systemic inflammatory response depends on initial stroke severity but is attenuated by successful thrombolysis.Stroke3521282133
- 30. Topakian R, Strasak AM, Nussbaumer K, Haring HP, Aichner FT (2008) Prognostic value of admission C-reactive protein in stroke patients undergoing iv thrombolysis. J Neurol 255: 1190–1196.R. TopakianAM StrasakK. NussbaumerHP HaringFT Aichner2008Prognostic value of admission C-reactive protein in stroke patients undergoing iv thrombolysis.J Neurol25511901196
- 31. den Hertog HM, van Rossum JA, van der Worp HB, van Gemert HM, de Jonge R, et al. (2009) C-reactive protein in the very early phase of acute ischemic stroke: association with poor outcome and death. J Neurol. HM den HertogJA van RossumHB van der WorpHM van GemertR. de Jonge2009C-reactive protein in the very early phase of acute ischemic stroke: association with poor outcome and death.J Neurol
- 32. Idicula TT, Brogger J, Naess H, Waje-Andreassen U, Thomassen L (2009) Admission C-reactive protein after acute ischemic stroke is associated with stroke severity and mortality: the ‘Bergen stroke study’. BMC Neurol 9: 18.TT IdiculaJ. BroggerH. NaessU. Waje-AndreassenL. Thomassen2009Admission C-reactive protein after acute ischemic stroke is associated with stroke severity and mortality: the ‘Bergen stroke study’.BMC Neurol918
- 33. Elkind MS, Tai W, Coates K, Paik MC, Sacco RL (2006) High-sensitivity C-reactive protein, lipoprotein-associated phospholipase A2, and outcome after ischemic stroke. Arch Intern Med 166: 2073–2080.MS ElkindW. TaiK. CoatesMC PaikRL Sacco2006High-sensitivity C-reactive protein, lipoprotein-associated phospholipase A2, and outcome after ischemic stroke.Arch Intern Med16620732080
- 34. Whiteley W, Jackson C, Lewis S, Lowe G, Rumley A, et al. (2009) Inflammatory markers and poor outcome after stroke: a prospective cohort study and systematic review of interleukin-6. PLoS Med 6: e1000145.W. WhiteleyC. JacksonS. LewisG. LoweA. Rumley2009Inflammatory markers and poor outcome after stroke: a prospective cohort study and systematic review of interleukin-6.PLoS Med6e1000145
- 35. Petersen SV, Thiel S, Jensen L, Steffensen R, Jensenius JC (2001) An assay for the mannan-binding lectin pathway of complement activation. J Immunol Methods 257: 107–116.SV PetersenS. ThielL. JensenR. SteffensenJC Jensenius2001An assay for the mannan-binding lectin pathway of complement activation.J Immunol Methods257107116
- 36. Fidler KJ, Wilson P, Davies JC, Turner MW, Peters MJ, et al. (2004) Increased incidence and severity of the systemic inflammatory response syndrome in patients deficient in mannose-binding lectin. Intensive Care Med 30: 1438–1445.KJ FidlerP. WilsonJC DaviesMW TurnerMJ Peters2004Increased incidence and severity of the systemic inflammatory response syndrome in patients deficient in mannose-binding lectin.Intensive Care Med3014381445
- 37. Garred P, Larsen F, Madsen HO, Koch C (2003) Mannose-binding lectin deficiency–revisited. Mol Immunol 40: 73–84.P. GarredF. LarsenHO MadsenC. Koch2003Mannose-binding lectin deficiency–revisited.Mol Immunol407384
- 38. Potlukova E, Jiskra J, Freiberger T, Limanova Z, Zivorova D, et al. (2010) The production of mannan-binding lectin is dependent upon thyroid hormones regardless of the genotype: a cohort study of 95 patients with autoimmune thyroid disorders. Clin Immunol 136: 123–129.E. PotlukovaJ. JiskraT. FreibergerZ. LimanovaD. Zivorova2010The production of mannan-binding lectin is dependent upon thyroid hormones regardless of the genotype: a cohort study of 95 patients with autoimmune thyroid disorders.Clin Immunol136123129
- 39. Adams HP Jr, Bendixen BH, Kappelle LJ, Biller J, Love BB, et al. (1993) Classification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial. TOAST. Trial of Org 10172 in Acute Stroke Treatment. Stroke 24: 35–41.HP Adams JrBH BendixenLJ KappelleJ. BillerBB Love1993Classification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial. TOAST. Trial of Org 10172 in Acute Stroke Treatment.Stroke243541