Mannose binding lectin: a biomarker of systemic lupus erythematosus disease activity
© Panda et al.; licensee BioMed Central Ltd. 2012
Received: 21 February 2012
Accepted: 27 September 2012
Published: 15 October 2012
A role for mannose binding lectin (MBL) in autoimmune diseases has been demonstrated earlier and elevated level of MBL has been shown in systemic lupus erythematosus (SLE) patients. In the current study, we investigated MBL as a potential biomarker for disease activity in SLE.
In a case control study SLE patients (93 females) and 67 age, sex, ethnicity matched healthy controls were enrolled. Plasma MBL levels were quantified by enzyme linked immunosorbent assay (ELISA). Clinical, serological and other markers of disease activity (C3, C4 and anti-dsDNA) were measured by standard laboratory procedures.
Plasma MBL levels were significantly high in SLE patients compared to healthy controls (P < 0.0001). MBL levels were variable in different clinical categories of SLE. Lower levels were associated with musculoskeletal and cutaneous manifestations (P = 0.002), while higher and intermediate MBL levels were significantly associated with nephritis in combination with other systemic manifestations (P = 0.01 and P = 0.04 respectively). Plasma MBL correlated with systemic lupus erythematosus disease activity index (SLEDAI) (P = 0.0003, r = 0.36), anti-dsDNA (P < 0.0001, r = 0.54), proteinuria (P < 0.0001, r = 0.42) and negatively correlated with C3 (P = 0.007, r = -0.27) and C4 (P = 0.01, r = -0.29).
Plasma MBL is a promising marker in the assessment of SLE disease activity.
Systemic lupus erythematosus (SLE) is a multi-factorial chronic autoimmune disorder characterized by dysfunction of T and B lymphocytes and affects various vital organ systems; 70 to 90% of SLE patients are female . The etiology of the disease is still unclear, although environmental, host genetic and hormonal factors have been proposed to play major roles in pathogenesis of SLE . There are limited studies on Indian SLE patients. Although the prevalence of SLE in India is rare (3/100,000) , the survival rates of these patients (70% at 5 years, 50% at 10 years) are very low compared to Western cohorts [4, 5]. Several factors are thought to be responsible for poor survival rates, the most important being delayed diagnosis . Several serological biomarkers such as complement components C3 and C4, and anti-dsDNA have been identified, which are not always consistent [7, 8].
The innate immune system plays an important role in the pathogenesis of SLE . Mannose binding lectin (MBL) is an essential component of innate immunity that recognizes carbohydrate residues on the surface of micro-organisms, namely, bacteria, viruses, fungi, and protozoa, and activates the complement system through MBL-associated serine proteases . Upon activation, early complement factor C3 is cleaved to C3a and C3b. C3a induces inflammation and recruits phagocytes . C3b enhances opsonisation by binding to both phagocytes and pathogens . In addition, C3b binds to other proteins on the surface of pathogens, forming membrane attack complexes which clear foreign pathogens .
The role of MBL in the pathogenesis of SLE has so far not been clearly defined. Higher plasma MBL levels in SLE patients have been reported in various populations [14–16]. MBL appears to have a dual mode of action: increased MBL leads to enhanced complement activation and tissue damage, while its deficiency has been linked with defective clearance of apoptotic cells that provide a stimulus for autoantibody formation . Also, MBL deficiency is linked to susceptibility to secondary infections, which is presumed to be a contributory factor in the development of SLE .
Variants of the MBL2 gene associated with lower plasma MBL levels have been associated with susceptibility to SLE [19–23] and the development of nephritis [19, 20]. Recently, we have observed predisposition of patients with low MBL-producing genotype (LXA/LYB, LYB/LYB and LXB/LXB) to develop SLE and autoimmune hemolytic anemia (AIHA) . Literature is limited on the association of MBL with disease activity [14, 25]. The current study investigates the association between plasma MBL levels and SLE disease activity in a cohort of female patients from Eastern India.
Materials and methods
Patients and controls
Clinical characteristics of patients with systemic lupus erythematosus (SLE) and healthy controls (HC)
SLE (n= 93)
HC (n= 67)
Age, years, mean ± SD
28.80 ± 8.891
29.14 ± 6.48
Duration of disease, years, mean ± SD
1.927 ± 2.151
Disease onset, years, mean ± SD
25.78 ± 8.630
Plasma MBL measurement
MBL levels in plasma were quantified by ELISA, according to the manufacturer's instructions (R&D systems, Minneapolis, MN, USA). All samples and standards were measured in duplicate and concentrations were determined from a standard curve using mean optical density values. Serum MBL concentrations were expressed as μg/ml.
Statistical analysis was performed using Graph Pad Prism, version 5.01 (Graph Pad Software, La Jolla, CA, USA). Mean MBL levels in HCs and SLE patients and mean values among different clinical categories were analyzed by the Student's t-test. The distribution of various MBL producer phenotypes (high, low and intermediate) in different clinical groups of SLE patients was analyzed by the Fisher exact test. Correlations among various parameters were evaluated with Spearman's rank correlation test. A P-value < 0.05 was considered significant.
Plasma MBL levels in SLE patients and healthy controls
Distribution of different mannose binding lectin (MBL) phenotypes in clinical categories of systemic lupus erythematosus (SLE)
P-value; odds ratio
Nephritis and carditis, or NPSLE, or serositis
0.04; 5.00 2
Musculoskeletal and cutaneous only
MBL levels positively correlated with SLEDAI scores
Correlation of MBL with anti-dsDNA, C3 and C4
Plasma MBL level is associated with proteinuria
MBL is a key molecule of the innate immune system that opsonises microbes through carbohydrate moieties and eliminates them through complement activation. Although the precise role of MBL in SLE pathogenesis is largely unknown, MBL plays a dual role in autoimmune disorders. Low levels of MBL impair the clearance of apoptotic bodies leading to production of antibody against self antigens, while increased MBL enhance activation of the complement system leading to the tissue damage observed in severe disease in SLE . The present study demonstrates plasma MBL as a potential biomarker of SLE disease activity. Genetic aspects of MBL in SLE have been well investigated [19, 29, 30]. The variability in levels of serum MBL in lupus patients could be attributed to variants in the MBL 2 gene [31, 32]. However, the reason for high MBL levels in SLE compared to healthy controls is not known. Some attribute it to an acute phase reactant consequent to ongoing inflammation . However, literature is limited on the association of plasma MBL and disease activity. A study on Taiwanese pediatric SLE patients showed a positive correlation. In addition, plasma MBL also correlated positively with anti-dsDNA but not with complement factors (C3 and C4) . A Japanese study of 147 adult patients did not conclusively demonstrate an association between MBL levels and disease activity, although serum MBL concentration did show significant association with serum C3 or CH50 levels . Our study of 93 patients with lupus and 67 controls showed elevated plasma MBL in SLE compared to healthy controls corroborating the observations made in previous studies [14–16]. Interestingly, SLE patients also displayed higher plasma MBL levels compared to healthy controls with similar MBL2 genetic background . Earlier reports have shown association of low-producer MBL genotypes with susceptibility to SLE [20, 32, 34–36]. The discordance in observation has not been satisfactorily explained, and further highlights the complexity associated with the pathogenesis of SLE. The level of serum MBL in SLE patients can be variable depending upon the equilibrium between production and consumption . It stands to reason that the serum MBL values will vary depending on the time of sample collection. In our study, samples were collected from treatment-naive patients at the time of assessment. The distribution of plasma MBL in SLE patients (Figure 1A) was found to be variable with a mean level as low as 0.33ug/ml to a high 2.04 ug/ml. The levels correlated with specific clinical categories. Those with arbitrarily defined high and intermediate levels had major organ involvement, such as nephritis, in combination with carditis or serositis, and/or NPSLE. Most patients with musculoskeletal and cutaneous manifestations had low MBL.
Identification of a sensitive disease activity biomarker is essential in SLE management. Currently available biomarkers for disease activity are yet to be validated . However, markers like anti-dsDNA, C3 and C4 are being widely used in clinical practice [38–41]. In the present study, plasma MBL levels correlated significantly with disease activity scores (SLEDAI). In addition, it correlated positively with anti-dsDNA and inversely with complement factors (C3 and C4). Complements play a pivotal role in the pathogenesis of SLE. They help opsonize and transport the immune complex, and maintain immune complex solubility by preventing formation of large insoluble aggregates . Their role is further highlighted by increased predisposition to develop SLE in persons with deficiency of early complement components. The failure to clear apoptotic bodies containing nuclear components leads to a break in self tolerance and the development of SLE . On the contrary, increased activation of complements mediates tissue damage. Low levels of C3 and C4 often correlate with disease flare . MBL is intimately associated with complement activation through the lectin pathway, resulting in low complement levels in patients with high MBL.
Anti-dsDNA antibodies are found in 60% of patients with SLE. They strongly correlate with renal involvement but are of limited value for other manifestations of disease. Interestingly, the levels may fall at the peak of disease activity, probably due to deposition of antibodies in tissue . In the current study we observed a positive correlation between MBL and anti-dsDNA antibodies. Tissue damage resulting from high levels of anti-dsDNA antibodies and MBL are distinct. Anti-ds DNA containing immune complex are deposited in tissue, resulting in tissue damage through the classical complement pathway , while MBL activates the lectin pathway of complement and causes tissue damage. Both appear to be independent variables of disease activity.
Lupus nephritis, a severe manifestation of SLE, affects nearly 50% of patients in the course of the disease , and 56% of the SLE patients in our series had nephritis. There are multiple mechanisms involved in the development of lupus nephritis. In the current study, proteinuria correlated positively with MBL levels (P < 0.0001). Patients with nephritis and other systemic involvement showed significantly higher levels of MBL (Table 2). Tissue damage in lupus nephritis is mediated by immune complexes or by binding of antibody to in vivo antigen, resulting in activation of the complement system and release of inflammatory cytokines. Previous studies have demonstrated deposition of MBL on glomerular tissue in SLE patients . The possible ligand for MBL in the kidney is G0 glycoprotein of IgG . Additionally, a significant galactose deficiency of IgG is also seen in lupus , which facilitates binding to MBL. Results from the current and previous studies indicate that nephritis may not directly correlate with plasma, but with tissue MBL levels.
Plasma MBL levels are elevated in SLE patients and significantly correlate with various parameters of disease activity. Furthermore, they also correlate with increased proteinuria, indicating a possible role for MBL in lupus nephritis. MBL appears to be a promising biomarker in assessing SLE disease activity.
American College of Rheumatology
autoimmune hemolytic anemia
complement component 3
complement component 4
enzyme-linked immunosorbent assay
mannose binding lectin
neuropsychiatric systemic lupus erythematosus
systemic lupus erythematosus
systemic lupus erythematosus disease activity index.
The work was supported by intra-mural grants from the Department of Biotechnology, Govt. of India to the Institute of Life Sciences, Bhubaneswar. We would like to thank all patients and controls included in this study. We also thank to Mr Subrat K Mohanty for collection of blood from patients and healthy controls.
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