Pilot study: deficiency of mannose-binding lectin-dependent lectin pathway, a novel modulator in outcome from pancreatic islet auto-transplantation.

BACKGROUND: Numerous factors influence pancreatic islet survival following auto-transplantation. Of these, the host immune response in the early peri-operative period is one of the most important. In this study we investigated the role of the mannose-binding lectin (MBL)-dependent pathway in a group of total pancreatectomy (TP) islet auto-transplantation (TPIAT) patients and classified them as competent or deficient in MBL activity. Complement pathway activities, MBL protein and inflammatory cytokine concentrations were evaluated from eleven pancreatic islet auto-transplant patients from two institutions.
METHODS: Eleven patients from two institutions were prospectively recruited. Serum was screened at different time points for 29 different cytokines and compared according to their MBL deficient or competent status. Twelve patients from previous TPIAT patients also underwent screening of MBL pathway activity.
RESULTS: A total nine of twenty three patients (39%) were MBL pathway deficient. MCP-1, IL-7 and IL-1a concentrations were significantly lower in the MBL deficient cohort compared to the normal MBL group (P=0.0237, 0.0001 and 0.0051 respectively). IL-6 and IL-8 concentrations were significantly raised in the normal MBL group. MBL functional activity was lower in insulin-independent group compared to the insulin-dependent group.
CONCLUSIONS: Complement activation is an important, possibly damaging response during intra-portal islet infusion. MBL pathway deficiency appears common in this population and the cytokine response was attenuated in MBL pathway deficient patients. Therapeutic MBL pathway blockade during and following islet auto-transplantation (IAT) may improve islet survival and function and thereby clinical outcome. 2020 Annals of Translational Medicine. All rights reserved.

Introduction

Islet auto-transplantation (IAT) is a procedure used to prevent or ameliorate postoperative diabetes in patients undergoing total pancreatectomy (TP). Although recently introduced into clinical practice, IAT is currently actively performed in the United States (1-3), United Kingdom (4), Switzerland (5) and South Korea (6), with other centres around the world developing their own islet program. Results of a recent meta-analysis confirmed the overall efficacy of IAT in the short term (7). For this reason numerous insurance companies now fund the procedure when undertaken with TP to treat intractable pain in non-diabetic patients (or C-peptide positive diabetic patients) with chronic pancreatitis (8). However, early positive results are generally counterbalanced by unpredictable long-term outcomes due to the effects of numerous and poorly understood factors. Amongst these, the inflammatory response produced during and immediately after islet infusion probably contributes to the long-term loss of graft survival and function (9).

The complement cascade is one of the major activators and amplifiers of inflammation through the stimulation of a non-specific immune response and the production of pro-inflammatory cytokines. In clinical transplantation, the activation of complement and the consequent inflammatory reaction exerts a significant influence on graft survival (10) including islet transplants (11). The complement system consists of the classical (CP), alternative (AP) and mannose-binding lectin (MBL) pathways of activation (12). Congenital deficiencies have been described for all pathways (13) but MBL deficiency is the most common (14). This condition produces recurrent infections (15) and decreased inflammatory response to ischemic-reperfusion injuries (16,17). Therefore, in the setting of clinical transplantation; MBL-deficiency could be beneficial because the attenuated immune response produced would affect autografts less than in MBL-competent patients, with a potential for better graft survival and long-term function.

The purpose of our study is to investigate the inflammatory response elicited in MBL-deficient patients and compare it to that of MBL-competent patients undergoing TP and IAT and compare this with graft survival and function post-operatively

Methods

Patients

Twelve patients who had undergone previous total pancreatectomy islet auto-transplantation (TPIAT) in Leicester were recruited to the study and a further eleven patients were prospectively recruited from the Leicester General Hospital (LGH; Leicester, United Kingdom) and the Baylor Research Institute (BRI; Dallas, United States). This study was approved by the institutional review board (IRB), and written informed consent was obtained from all patients included. The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.

Islet isolation and transplantation

In the Leicester series, islets were prepared and infused as previously described (18). Pancreas was digested with Neutral Protease NB GMP Grade in combination with purified Collagenase NB 1 GMP Grade (SERVA Electrophoresis GmbH, Heidelberg, Germany). Unpurified whole pancreatic digest was suspended in M199 transplant media containing 20% human serum albumin. Islets were prepared while the surgeons completed the enteroenterostomy and choledochojejunostomy reconstruction (19). Immediately prior to the transplant, the patients received 5,000 U heparin intravenously. Islets were infused into the portal vein via an umbilical vein (with heparin) over 20–30 minutes (20). During the islet cell infusion the portal pressures were continuously monitored to ensure that the levels reached did not exceed 20 mmHg.

In the Baylor series, islets were prepared and infused as previously described (21). Pancreas was digested with either LiberaseTM MTF with ThermolysinTM (Roche, Indianapolis, United States) or Collagenase NB 1 GMP Grade (SERVA Electrophoresis GmbH, Heidelberg, Germany). Isolated islets were infused into the portal vein via the mesenteric vein with heparin (70 U/kg body weight) over 30 to 60 minutes while the patients were under general anaesthesia. During islet infusion, portal vein pressure was monitored intermittently. If portal vein pressure exceeded 20 mmHg, the infusion of islets was stopped until portal vein pressure decreased.

The islet yield was converted into a standard number of islet equivalents (IEQ), with the diameter standardized to 150 µm. Islet viability in the final product was evaluated with fluorescein diacetate/propidium iodide staining.

Serum tests

Serum samples were obtained retrospectively at follow up baseline levels were obtained at preoperatively, prior to islet infusion, during islet infusion, at the completion of islet infusion. Subsequently, serum samples were obtained at 1 hour, 3 hours, 6 hours, 24 hours, 3 days, 5 days, and 7 days post islet infusion. Serum samples were stored at –80 °C until assayed.

The Wieslab® Complement system Screen (Euro-Diagnostica, Malmö, Sweden) was used according to the manufacturer instructions. The following kits were used for MBL protein evaluation: Human MBL ELISA kit HK3223 (Hycult Biotech, Uden, The Netherlands), and as controls for assay: MBL standard serum SER101 and MBL oligomer deficient serum, B/B genotype SER102, from Antibodyshop (BioPorto Diagnostics A/S, Gentofte, Denmark).

Concentrations of cytokines and chemokines were determined by measuring serum samples in a Luminex 200 (Millipore, Billerca, Massachusetts, USA) using xMAP technology. The bead assay was performed according to the manufacturer’s instructions. Markers were: interferon alpha (IFN-α), interferon gamma (IFN-γ), interleukin-10 (IL-10), interleukin-12p40 (IL-12p40), interleukin-12p70 (IL-12p70), interleukin-13 (IL-13), interleukin-15 (IL-15), interleukin-17 (IL-17), interleukin-1ra (IL-1ra), interleukin-1 alpha (IL-1α), interleukin-1 beta (IL-1β), interleukin-2 (IL-2), interleukin-3 (IL-3), interleukin-4 (IL-4), interleukin-5 (IL-5), interleukin-6 (IL-6), interleukin-7 (IL-7), interleukin-8 (IL-8), Epidermal growth factor (EGF), Eotaxin, Granulocyte colony-stimulating factor (G-CSF), Granulocyte-macrophage colony-stimulating factor (GM-CSF), Vascular endothelial growth factor (VEGF), Monocyte Chemotactic Protein-1 (MCP-1), macrophage inflammatory protein 1 alpha (MIP-1α), macrophage inflammatory protein 1 beta (MIP-1β), Tumor necrosis factor-alpha (TNF-α) and Tumor necrosis factor-beta (TNF-β).

Statistical analysis

All data were initially entered into an Excel database (Microsoft, Redmond, Washington, United States) and the analysis was performed using the Statistical Package for the Social Sciences Windows, version 13.0 (SPSS, Chicago, Illinois, USA). Descriptive statistics consisted of the mean and standard deviation for parametric distributions and median and range for non-parametric distributions after confirmation with the Kolmogorov-Smirnov test and histograms.

Comparisons over time were performed with the ANOVA for repeated measures for parametric variables or Friedman for non-parametric variables. Comparison among MBL competent and MBL deficient patients was performed with ANOVA for repeated measures for parametric variables and the Mann-Whitney test for non-parametric variables. P values of <0.05 were considered statistically significant.

Results

In the LGH group, the whole pancreatic digest was used without purifying the islets, in the BRI group islets were purified in 5 cases and not purified in 3 cases (). The amount of transplanted IEQ was not different between the LGH and BRI. Four patients (40%) were identified with MBL pathway activity deficiency and one patient had very low MBL activity (; ). Two MBL pathway deficiency patients were associated with MBL protein deficiency (). Retrospectively, twelve patients from Leicester series were recruited from previous TPIAT. Five/twelve (41.7%) were MBL pathway deficiency (; ). There were 5/9 (55.6%) insulin free in MBL deficient patients compared to 4/14 (28.6%) insulin free in MBL competent patients ().

Table 1

Prospectively, patients recruited from two institutions

Patient	Age (years)	Etiology	BMI (kg/m2)	MBL status	Total IEQ	IEQ/kg	Tissue volume	Cleavage/purity	Viability	Outcomes	HBA1c (%)
Pt 1	56	Idiopathic	24	Competent	645,066	10,523	24	67%	99%	Insulin dependent	5.2
Pt 2	46	Pancreas divisum	25.39	Deficient	292,866	3,854	23	36%	97%	Insulin free	5.1
Pt 3	38	Idiopathic	20	Competent	369,177	6,616	31	67%	95%	Insulin dependent	5.9
Pt 4	54	Alcoholic	19.2	Competent	209,818	3,568	10	40%	96.8%	Insulin dependent	5.5
Pt 5	40	Idiopathic	29	Competent	507,664	6,418	9.5	50%	97.4%	Insulin free	5.5
Pt 6	41	Idiopathic	19.7	Deficient (no MBL protein)	363,938	6,972	10	60%	94.3%	Insulin free	4.9
Pt 7	26	Autoimmune	21.8	Competent	168,263	3,319	9	50%	95.5%	Insulin dependent	8
Pt 8	48	Idiopathic	27.1	Deficient	1,010,127	13,669	18	53%	96.1%	Insulin dependent	5.5
Pt 9	54	idiopathic	28.4	Deficient (no MBL protein)	331,800	4,628	9.5	20%	94.4%	Insulin dependent	6.6
Pt 10	44	Divisum	30	Competent	375,417	4,995	0.8	45%	96.8%	Insulin dependent	6.1
Pt 11	35	Idiopathic	40.4	Competent	500,351	4,284	10	20%	95.5%	Insulin dependent	6

MBL, mannose-binding lectin; IEQ, islet equivalent.

Figure 1

Shows pre-operative MBL functional activity and protein level. (A) MBL pathway activity assay. Pt 1–3 (Leicester General Hospital), Pt 4–11 (Baylor Research Institute) and Pt12–Pt23 (LGH series). (B) MBL protein ELISA assay in islet auto transplant patients. Pt 1–3 (Leiceter General Hospital), Pt 4–11 (Baylor Research Institute). MBL, mannose-binding lectin.

Table 2

Retrospectively recruited from previous TPIAT Leicester series

Patient	Age (years)	Etiology	BMI (kg/m2)	MBL status	Total IEQ	IEQ/kg	Cleavage/purity	Outcomes (1 year)
Pt 12	53	ERCP-pancreatitis	28.58	Competent	24,687	329.16	77%	Insulin free
Pt 13	43	Idiopathic	22.86	Competent	57,296	954.93	18%	Insulin free
Pt 14	38	alcohol	20.45	Deficient	139,420	2,359	12%	Insulin free
Pt 15	43	Idiopathic	29.65	Deficient	607,822	8,008.19	68%	Insulin free
Pt 16	42	Idiopathic	18.59	Deficient	192,850	3,506.36	25%	Insulin (17 units)
Pt 17	54	Idiopathic	23.95	Competent	645,066	10,523.1	67%	Insulin (12 units)
Pt 18	45	Pancreas divisum	25.39	Competent	290,000	3,853.5	36%	Insulin free
Pt 19	43	Idiopathic	20.23	Competent	217,500	5,330	18%	Insulin (10 units)
Pt 20	34	Idiopathic	24.15	Deficient	369,177	6,616.08	67%	Insulin (18 units)
Pt 21	45	Gallstones	20.23	Competent	222,000	4,230.8		Insulin (15 units)
Pt 22	34	Idiopathic	24.15	Competent	491,260	7,038.11	65%	Insulin (6 units)
Pt 23	41	alcohol	26.05	Deficient	284,592	3,298	40%	Insulin free

TPIAT, total pancreatectomy islet auto-transplantation; IEQ, islet equivalent.

Complement activity

No significant differences were present in the CP and AP activities between MBL deficient vs. competent patients (P=0.167 and P=0.053 respectively). There was a significant difference MBL pathway activity between MBL deficient vs. competent patients (P<0.001). The CP activity was reduced, compared to baseline levels, from the completion of islets infusion (P<0.001) to the 3rd postoperative day when it recovered to preoperative values (). The MBL activity was reduced, compared to baseline levels, before the islets infusion (P<0.05) to the 4th postoperative day when it recovered to preoperative values (). The AP activity was reduced, compared to baseline levels, before the islets infusion (P<0.05) to the 3rd postoperative day when it recovered to preoperative values ().

Figure 2

Complement activities over time (A,B,C). Patients with no MBL pathway activity have been removed. MBL, mannose-binding lectin.

Cytokines with changes between MBL competent vs. deficient patients

IL-6 concentrations were raised in the normal MBL group but not statistically significant compared to MBL deficient group (P=0.0828) (). However, IL-6 level rose significantly in the normal group from its baseline before the islet infusion until the 1st postoperative day (P<0.001). MCP-1 concentrations were raised significantly on the 1st day (P<0.001) and MCP-1 levels were significantly lower in MBL deficient vs. competent patients (P=0.0237) (). Lower concentrations in the MBL deficient patients, compared with MBL competent ones, were found for IL-1α (P=0.0051) (). IL-8 increased significantly compared to baseline levels before the islet infusion (P<0.001) until the 3rd postoperative day where it recovered to preoperative values, but there were not statistically different between both groups (P=0.11) (). IL-7 concentrations were raised significantly in the normal MBL group compared to MBL deficient group (P=0.0001) ().

Figure 3

Comparison of IL-6 (A), MCP-1 (B), IL-1a (C), IL-8 (D) and IL-7 (E) cytokine levels between MBL deficient and intact groups and over time. *, P<0.05. IL-6, interleukin-6; MCP-1, monocyte chemotactic protein-1; IL-8, interleukin-8; IL-7, interleukin-7; MBL, mannose-binding lectin.

Cytokines with/without changes over time and between MBL competent vs. deficient patients (Table 3)

IL-15 concentrations were significantly raised from the 1st postoperative hour to the 3rd postoperative day (P<0.001). GM-CSF concentrations were significantly elevated compared to baseline levels only at the 3rd postoperative hour (P<0.05). Compared to values before islet infusion, EGF concentrations significantly decreased during the infusion until the 3rd postoperative day included in the MBL competent patients (P<0.001). IL-6, IL-15, EGF, GM-CSF and MCP-1 concentrations were significantly lower in MBL deficient vs. competent patients (P<0.001). Lower concentrations in the MBL deficient patients, compared with MBL competent ones, were found for Eotaxin (P<0.001), IL-1α (P<0.001), IL-2 (P<0.001), IL-3 (P<0.001), IL-5 (P<0.05), TNF-β (P<0.001). Higher concentrations were present only for IL-17 (P<0.001). G-CSF increased significantly compared to baseline levels before the islet infusion (P<0.001) until the 3rd postoperative day where it recovered to preoperative values. Similar results were achieved for IL-8 (P<0.001). For IL-10 the significant increase compared to baseline levels was present only at the completion of the islet infusion (P=0.001) and 15 minutes after (P=0.005). At one hour from the end of the operation, the difference was not significant (P=0.293). For TNF-α the increase compared to baseline was significant from the 3rd postoperative hour (P=0.018) onwards until the 7th postoperative day (P=0.001). IL-1β concentration was not significantly different among groups (P=0.299) and over time compared to baseline levels (P=0.865). Similar results were found for IL-4 (groups P=0.414; time P=0.532), IL-5 (groups P=0.268; time P=0.181), IL-10 (groups P=0.589; time P=0.067), IL-12p40 (groups P=0.505; time P=0.673), IL-12p70 (groups P=0.171; time P=0.967), IL-13 (groups P=0.059; time P=0.515), IFN-α (groups P=0.520; time P=0.992), IFN-γ (groups P=0.08; time P=0.595), MIP-1α (groups P=0.288; time P=0.937), MIP-1β (groups P=0.571; time P=0.105), VEGF (groups P=0.218; time P=0.128).

Correlations with insulin-free or insulin-dependent outcome after IAT with MBL deficient patients

A total of 9/23 (39%) TPIAT patients were MBL deficiency. When comparing outcomes after IAT, no statistically significant differences in MBL functional activity deficiency compared to normal were seen between the two groups (nonparametric Fisher test P=0.089). MBL functional activity was seven-fold lower in the insulin free group compared to insulin dependent group (). MBL protein level was nearly half 0.167±0.049 µg in the insulin free group compared to 0.265±0.099 µg in the insulin dependent group ().

Figure 4

Differences observed between the deficiency of MBL activity and MBL protein groups in achieving insulin-independence following pancreatic islet auto-transplantation. (A) MBL functional activity in insulin-dependent and insulin-free groups. (B) MBL protein level in insulin-dependent and insulin-free groups. MBL, mannose-binding lectin.

Discussion

Complement plays an important role in islet transplantation. It is a part of the instant blood-mediated inflammatory reaction (IBMIR) at the time of intra-portal transplantation which involves the coagulation and complement cascades. Here we have studied complement activation and deficiency in a cohort of islet auto-transplanted patients and the relationship with inflammation.

Complement activation is a feature in ischemic reperfusion injury during organ transplantation (22,23). In liver transplantation, significantly elevated C3a and SC5b-9 levels in the absence of elevated levels for C4d suggested a predominant engagement of the alternative pathway of complement activation (22). This reinforced the finding in our cohort of a MBL pathway activity deficiency rate of 9/23 (approx. 40%). MBL deficiency occurs in 5–30% of the general population (14). MBL pathway deficiency is the most common complement pathway deficiency. Many reports have shown the different components deficient in the MBL pathway of which MBL protein deficiency is one of the most common. Deficiency is linked to recurrent infections in children (24). The MBL gene has single nucleotide polymorphisms (SNPs) (25). Therefore, the level of MBL in the blood varies according to whether the individual is heterozygous or homozygous (26,27). Two patients with presence of MBL protein and MBL pathway activity deficiency could indicate non functionality of the oligomerisation of MBL or other MBL pathway component deficiencies. Mannan-binding lectin-associated serine portease-2 (MASP-2) and L-ficolin (ficolin-2) are among the other components sometimes found deficient in MBL pathway activity (28,29).

In this study, we demonstrated that complement activation occurred immediately after surgery. Complement activation has previously been considered to be a short-lived transient innate immune response (22), but our data shows that it can, in fact, persist for several days postoperatively. Complement activation increases C3a and C5a which in turn triggers the pro-inflammatory response potentially causing additional damage to the islet graft (29).

There are many reports on the expression of a great variety of inflammatory mediators in islet transplantation, but this is the first report on the relationship between complement deficiency and its effect on inflammatory mediators. As previously described, MBL pathway deficiency is the commonest complement pathway deficiency. We examined 29 inflammatory markers of which 5 demonstrated reduced concentration in the MBL pathway deficient patients. MCP-1 was significantly reduced in the MBL deficient group (P=0.0237). In vitro, MCP-1 concentration was elevated when monocytes were exposed to MBL. MCP-1 is a potent chemokine, which attracts monocytes and T cells into the site of infection or immune activation (30). Previous studies have also shown that patients undergoing islet allo-transplantation with low concentrations of MCP-1 have better outcomes such as increased freedom from long-term insulin dependence (31). IL-6 and IL-8 are systemic proinflammatory cytokines which are also reduced in MBL deficient patients. Eotaxin, a small molecular cytokine, was slightly raised in normal compared to MBL deficient groups. Another study has suggested this elevation positively correlates with High-Mobility Group Box 1 (HMGB1), which is linked to poor clinical outcomes in IAT (23).

Conclusions

Complement activation is a sensitive intra-operative measurement of inflammation during intra-portal islet infusion and generally normalises by day 7. MBL pathway deficiency is common in recipient patients. Further investigation is merited to explore the detail of complement pathway activity in affected individuals. Therapeutic MBL pathway blockade during and following IAT may improve islet survival and function and thereby clinical outcomes.

Finally, we analysed the correlation between transplant outcomes and MBL functional activity and protein levels. Interestingly, MBL functional activity and MBL protein levels were low in the insulin free group. These results suggest that deficiency of MBL pathway results in a better clinical outcome in IAT. More patients are needed to confirm this finding.

Table 3

Schematic summary of cytokine modifications

Differences over time	Differences among groups
	No	Yes
No	IL-1β, IL-4, IL-5, IL-10, IL-12p40, IL-12p70, IL-13, IFN-α, IFN-γ, MIP-1α, MIP-1β, VEGF	Eotaxin, IL-1α, IL-2, IL-3, IL-5, TNF-β, IL-17
Yes	G-CSF, IL-8, IL-10, TNF-α	IL-6, MCP-1, IL-15, GM-CSF, EGF

IL-2, interleukin-2; IL-3, interleukin-3; IL-4, interleukin-4; IL-5, interleukin-5; IL-6, interleukin-6; IL-8, interleukin-8; IL-10, interleukin-10; IL-13, interleukin-13; IL-15, interleukin-15; IL-17, interleukin-17; IFN-α, interferon alpha; IFN-γ, interferon gamma; MIP-1α, macrophage inflammatory protein 1 alpha; MIP-1β, macrophage inflammatory protein 1 beta; VEGF, Vascular endothelial growth factor; G-CSF, granulocyte colony-stimulating factor; TNF-α, tumor necrosis factor-alpha; TNF-β, tumor necrosis factor-beta; MCP-1, monocyte chemotactic protein-1; GM-CSF, granulocyte-macrophage colony-stimulating factor; EGF, epidermal growth factor.