, Fernando González2 , Eduardo Lorca2 , Andrés Tapia3 , Valentina G López4 , Rocío Strodthoff1 , Francisca Fajre1 , Juan E. Carreño1 , Ricardo Valjalo2 , César Vergara1 , Manuel Lecanda1 , Jorge Bartolucci4 , Fernando E. Figueroa3,5,6 , Maroun Khoury3,4,5 Chronic kidney disease (CKD) is a growing public health concern, and available treatments are insufficient in limiting disease progression. New strategies, including regenerative cell-based therapies, have emerged as therapeutic alternatives. Results from several groups, including our own, have reported evidence of a supportive role for mesenchymal stromal cells (MSCs) in functional recovery and prevention of tissue damage in murine models of CKD. Prompted by these data, an open pilot study was conducted to assess the safety and efficacy of a single injection of autologous adipose tissue-derived MSCs (AT-MSCs) for treatment of CKD.
AT-MSCs were infused intravenously into six CKD patients at a dose of 1 million cells/kg. Patients were stabilized and followed for one year prior to MSC infusion and one year following infusion.
No patients presented with adverse effects. Statistically significant improvement in urinary protein excretion was observed in AT-MSCs transplanted patients, from a median of 0.75 g/day (range, 0.15–9.57) at baseline to 0.54 g/day (range, 0.01v2.66) at month 12 (
Findings from this pilot study demonstrate that intravenous infusion of autologous expanded AT-MSCs into CKD patients was not associated with adverse effects and could benefit patients already undergoing standard medical treatment.
Chronic kidney disease (CKD) is characterized by a progressive and permanent loss of kidney function. CKD represents a major public health problem due to its growing incidence and prevalence, the high cost of renal substitutive therapies and a marked increase of morbidity and mortality [1,2]. Available pharmacologic agents do not halt disease progression and have significant risks [3], thus prompting the search for new therapeutic strategies [4]. Mesenchymal stromal cells (MSCs) are multipotent stromal cells that reside within the vascular network of vascularized organs and have broad tissue-supporting roles throughout the body [5]. The ability of MSCs to preserve renal structure and function in experimental acute renal injury [6] and also in CKD has been demonstrated in rodent models of diabetic nephropathy [7], partial nephrectomy [8], and allograft nephropathy [9]. Beneficial effects of MSCs have included restriction of the inflammatory response [6], decreases in proteinuria, and preservation of the tubular and interstitial architecture [7]. Of note, whole bone marrow (BM) transplant does not appear to exert similar beneficial effects [10]. CKD has been linked to a loss of stem cell quantity and function, particularly as patients progress to end stage disease [11]. Evidence also suggests that the pro-inflammatory state associated with CKD and uremic toxins, such as homocysteine [12] or p-cresol [13], can hasten stem cell senescence and apoptosis [14]. Hyperparathyroidism and insufficient erythropoietin activity can also contribute to progenitor cell dysfunction [15].
A recent meta-analysis demonstrated that cell-based therapies are effective in preclinical models of CKD [16], and systemic administration of MSCs is considered safe to treat renal and cardiovascular diseases in humans [17,18]. However, clinical translation of MSC-based therapeutics for human CKD is still in an early phase, and the optimal cell source, mode of administration and expected clinical effects are still not well characterized.
MSCs derived from adipose tissue (AT-MSCs) exhibit differentiation potential, kinetics, cell senescence, gene transduction efficiency and multi-lineage differentiation capacity similar to BM-derived MSCs (BM-MSCs) [19]. Since BM samples require invasive procedures and yield fewer MSCs, AT-MSCs have been tested in different experimental and clinical scenarios. Indeed, we previously evaluated the use of AT-MSCs in a murine model of CKD and reported marked recovery in renal function and disease biomarkers [20]. We thus hypothesized that the injection of autologous
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Given the scarcity of data on the effect of AT-MSCs in CKD, we collected clinical data that might inform the design of a future trial. Therefore, CKD patients (n = 7) were enrolled for treatment with MSCs, using the following inclusion criteria.
CKD with an estimated glomerular filtration rate (eGFR) between 20 and 40 mL/min/1.73 m2 using the Modification of Diet in Kidney Disease (MDRD) formula, daily proteinuria > 150 mg, and blood pressure < 140/90 mmHg with or without antihypertensive medications, at the recruitment visit. Diabetic patients were required to have a glycated hemoglobin ≤ 7.5%.
Clinical and laboratory evidence of progressive disease in the twelve months prior to the recruitment date.
No other significant co-morbidity or condition that could affect the clinical disease course. These exclusion criteria included: active cancer or immunosuppressive treatments; women intending to be pregnant and/or not on effective contraception; and breast-feeding women. Additionally, patients could not have planned elective surgical procedures or significant allergies reported.
All were receiving evidence based optimized stable pharmacological treatment for at least 12 months prior to recruitment, including dietary restricted salt (≤ 2 g/day of sodium) and protein (0.8 g/day) and renin angiotensin axis blockade (enalapril ≤ 40 mg/day or losartan ≤ 100 mg/day) with the addition of furosemide, nitrendipine, atenolol or doxazosin as needed to achieve blood pressure control (< 140/90 mmHg). Interventions were not changed (drugs and dosage) during the follow-up period.
Change in CKD functional parameters, including the GFR and quantitative 24-hour urinary protein excretion rate in the 12-month period following MSC infusion. Because of the pilot nature of this study and the small sample size with no control group, variables were measured during the 12 months prior to treatment (control period) and compared to measurements taken during the 12 months following MSC administration (intervention period).
Clinical or biochemical changes suggestive of treatment-associated adverse events or warnings as described below.
Adipose tissue harvest: Adipose tissue (20–25 g) was aspirated from the abdominal subcutaneous fat pad from all patients by a single plastic surgeon, using a 19-G bore needle attached to a standard plastic syringe under local anesthesia.
Each autologous adipose tissue sample was suspended in sterile phosphate-buffered saline (PBS), passed through a 70-μm Falcon cell strainer (BD Biosciences, San Jose, USA) and centrifuged at 350 ×
MSCs were immune-phenotyped by flow cytometry using a FACSCanto II cytometer (BD Biosciences) after staining with the following anti-human monoclonal antibodies: CD105, CD90, CD73, HLA-ABC, HLA-DR, CD34 and CD45 (all from BD Pharmingen, San Jose, USA). In brief, cells were harvested, washed with cytometer buffer (PBS + 0.2% bovine serum albumin + 0.01% sodium azide; all from Sigma-Aldrich, St. Louis, USA) and incubated with the fluorescently-labeled antibodies in cytometer buffer for 20 minutes at 4°C. Matched isotype antibodies were used as negative controls.
To induce adipogenic differentiation, confluent cells were cultured in medium supplemented with 1 × 10−6 M dexamethasone, 0.02 mg/mL indomethacin and 10 μg/mL insulin (Sigma-Aldrich). After 12 days, cell differentiation into lipid-laden adipocytes was confirmed by oil red O staining (Sigma-Aldrich). For chondrogenic differentiation, cells were incubated for 1 hour at 5 × 103 cells/μL in 10 μL of culture medium to achieve conditions for micromass formation. Cells were cultured in medium supplemented with 107 M dexamethasone, 50 μg/mL ascorbic acid, and 10 ng/mL of transforming growth factor-β3 (Sigma-Aldrich) for 7 days, and chondrogenic differentiation was assessed by Safranin O staining (Merck, Darmstadt, Germany). To induce osteogenic differentiation, adherent cells were grown at 3 × 104 cells/cm2 in culture medium with 10−7 M dexamethasone, 50 g/mL ascorbic acid, and 10 mM β-glycerophosphate (Sigma-Aldrich). After 21 days of culture, calcium deposits were detected by Alizarin Red staining (Sigma-Aldrich).
The criteria for MSC batch release included: > 90% of cells expressing CD105, CD73, and CD90, and < 3% of cells expressing CD34, CD45, and CD14; negative microbiology testing for mycoplasma, aerobic bacteria, anaerobic bacteria and fungi; and viability > 85% by trypan blue. Freshly harvested cells were resuspended in a 1:1 mixture of Ringer’s lactate and autologous patient serum and transported in a cooled container to the administration site.
Patients were transiently hospitalized to receive 1 million AT-MSCs per kg of body weight suspended in 120 mL Ringer’s lactate solution. Infusions were done into a peripheral vein over 30 to 40 minutes. Asymptomatic patients were discharged after 2 hours of observation. Given the ample evidence from controlled trials of the safety of MSCs administered intravenously (i.v.) at much higher doses [18], we did not screen regularly for ischemic events.
Patients were instructed to communicate with the clinician in charge in the case of an adverse event. Vital signs were measured and physical examinations were performed at monthly follow-up appointments. Additional follow-up evaluations included the assessment of serum creatinine, 24 hour urinary quantitative protein excretion rate, additional blood and urinary testing, and screening for solid organ or coagulation abnormalities, including transaminases and prothrombin or active thromboplastin times. Collection of adverse events was done in accordance with US Food and Drug Administration 21 312.32 Code of Federal regulations and International Conference of Harmonization ICH E-6 Good Clinical Practices. Given the two-yearly periods of follow-up, the adverse event type and frequency were retrieved as follows; All adverse events occurring between MSC infusion and the monthly follow-up visit (month 1). All further events that were not attributable to CKD were judged by treating physicians and were reported as adverse effects either related to the MSC treatment or not related, according to GCP rules.
Based on the limited sample size and unknown distribution, we employed non-parametric analyses and Wilcoxon or Mann–Whitney tests. We also computed the slopes of the linear regression equations for the change in eGFRs of each individual patient, spanning the four quarterly measurements from the 12 months prior to treatment and the 12 monthly measurements taken after the MSC infusion. The percent change was calculated as difference for each variable from pre- to post-treatment divided by pre-treatment level multiplied by 100. The
Seven patients with stage III–IV CKD and no prior dialysis therapy were recruited between January 2013 and August 2014. Specific diagnoses were 1) focal and segmental glomerulosclerosis (FSGS), 2) immunoglobulin A (IgA) nephropathy, 3) diabetic nephropathy, 4) post-acute kidney (AKI) injury RIFLE stage L, 5) Tubulo-interstitial chronic nephritis due to Sjögren’s disease, 6) renal dysplasia, and 7) hypertensive nephrosclerosis. Patient clinical characteristics are shown in Table 1. One patient with diabetic nephropathy was excluded from the study due to poor proliferation and a resulting low number of AT-MSCs in culture.
All patients were on stable renin angiotensin blockade during the study period, as described in the inclusion criteria. While this achieved blood pressures < 140/90 mmHg in four cases, two patients required the addition of 40 mg/day nitrendipine to reach goal blood pressure. Patients reported not fully adhering to dietary protein restriction; nevertheless, four patients decreased (1–4 kg) and two increased in body weight (2–4 kg) in the year following AT-MSC infusion. Only the nephrotic patient with FSGS had low serum albumin (< 3.5 g/dL).
The AT-MSCs isolated from 6 patients that completed study procedures proliferated normally and exhibited typical tri-lineage differentiation into adipocyte, chondrocyte and osteoblast lineages (Fig. 1A–F). As described, AT-MSCs expressed CD105, CD73, and CD90 (Fig. 1G) and were negative for CD45, CD34, CD14, and HLA-DR (data not shown). There was no difference in the expression of these markers between CKD and control AT-MSCs derived from a healthy individual (Fig. 1G).
All infusions were well-tolerated, and no treatment-related adverse events were reported. To assess disease progression, patients were stabilized with optimization and stabilization of therapy 12 months prior to study entry and then followed for one year. Individual clinical courses are summarized in Supplementary Table 1 (available online).
Over the 12 months prior to treatment, 4 of 6 patients demonstrated increased protein excretion (ranging from 20% to 205% increase). In contrast, in the 12 months after MSC infusion, a reduction of proteinuria occurred in all cases, with the exception of patient 4 with renal dysplasia, falling from a baseline median of 0.75 g/day (range, 0.15–9.57) to 0.54 (range, 0.01–2.66 g/day) at month 12 after infusion (
Overall, renal function as assessed by plasma creatinine levels and MDRD eGFR was decreased at 12 months following MSC infusion, although this decrease was not statistically significant (
The laboratory measurements regarding patient safety and measurements including coagulation (prothrombin and thromboplastin clotting times and platelet number), liver function (aspartate aminotransferase, alanine aminotransferase, alkaline phosphatases, gama glutamil transpeptidase, total bilirubin, direct bilirubin, and serum albumin) and metabolic tests (glycaemia, uric acid, total cholesterol, high-density lipoprotein and low density lipoprotein cholesterol, and triglycerides) did not change between pre- and post-infusion periods (data not shown).
Although not all six patients responded equally, these results indicate that autologous AT-MSC infusion reduced 24-hour proteinuria without recognizable adverse effects in six patients. However, this small and heterogeneous sample precludes wider generalization of these findings.
There is increasing evidence regarding the possible mechanisms of cell therapy in CKD. MSCs are capable of self-renewal, proliferation and migration to damaged areas, where they can differentiate into mature and functional cells [16]. Because low levels of persistent tissue engraftment can occur after i.v. MSC infusion [21], it is believed that therapeutic benefits are explained mainly by trophic and/or immune mediated effects [6,8]. Immunoactivity of MSCs is mediated by both secreted molecules and cell-cell contact and can involve dendritic cells, B cells, natural killer cells, and a variety of T helper cells [22]. Significant paracrine and trophic effects are mediated by the secretion of angiogenic and antiapoptotic factors such as vascular endothelial growth factor, insulin growth factor, and hepatocyte growth factor [23,24]. The broad repertoire of secreted and immunomodulatory factors produced by MSCs has potential to contribute to kidney regeneration, as MSC-conditioned culture media can confer renoprotective benefits comparable to those of direct cells [25]. Additional effects are mediated partially through microvesicles containing different protein and RNA cargo [26], and more recent data have suggested that stromal cell administration can rescue damaged cells even in the absence of MSC persistence in tissues and improve tissue regeneration through the transfer of active mitochondria [27]. In animal CKD models, such as 5/6 nephrectomy remnant kidney [28], diabetic nephropathy [7], and unilateral ureteral obstruction [29], MSC infusion has been associated with reduction in pro-fibrotic markers as well as with a decrease in inflammation, as evidenced by a decrease in interleukin (IL)-6 and tumor necrosis factor-α levels and heightened levels of the anti-inflammatory cytokines IL-4 and IL-10 [28,24,30]. Conditioned media from MSC cultures can also induce the migration and proliferation of kidney-derived epithelial cells [26].
Clinical trials recently demonstrated no safety signals in CKD patients treated with BM-MSCs [31–33]. In a single-arm phase I study of 6 patients with autosomal dominant polycystic kidney disease treated intravenously with autologous BM-MSCs (2 × 106/kg), there were no changes in eGFR or reductions in serum creatinine at 12 months compared to baseline [32]. This might be explained by evidence that suggests autologous BM-MSCs are defective in CKD individuals [13,15]. In contrast, Packham et al [31] published a report of a placebo controlled dose escalation study of allogeneic immunoselected BM-MSCs in a population of 35 diabetic kidney disease patients, randomized (2:1) with 150 × 106 MSCs, 300 × 106 MSCs, or placebo [31]. No adverse events or alloantibodies were detected. Additionally, they reported that median levels of IL-6 decreased, and there was a suggestion of a more pronounced treatment effect within the subgroup with higher baseline eGFR that received 150 × 106 cells. Urinary protein and albumin excretion remained unchanged [31].
Although AT-MSCs also have a favorable safety profile overall [34], adverse events have been reported, and renal deterioration has occurred with i.v. administration of extremely high doses [35]. The data we report here suggest that systemic AT-MSC infusion is feasible, safe, and reduces protein excretion in CKD patients. The observed reduction in proteinuria after AT-MSC infusion, which occurred in 5 of the 6 patients studied, is promising and contrasts with prior clinical reports [31,32]. In most nephropathies, proteinuria is a validated surrogate marker for progression of disease. Indeed, protective renin-angiotensin axis blockers that decrease proteinuria are titrated until protein excretion reaches less than 300 mg daily or adverse effects become intolerable [36].
It remains unclear at what level of GFR an individual may benefit most from cell therapy aimed at slowing CKD progression. Such a “therapeutic window” has been explored in clinical nephrology trials, including the RENAAL study of diabetic nephropathy [37] and fish oil for IgA nephropathy [38]. A well-controlled trial in diabetic kidney disease suggests individuals with major deterioration of their eGFR could be less responsive [31]. We chose to study patients with an eGFR ranging from 20 to 40 mL/minute to avoid including individuals with end stage disease while still including patients at risk for deterioration. There are several evident limitations of our study. First, it is not a placebo-controlled trial, but rather an exploratory study comparing prolonged (12 month) pre- and post-treatment periods in CKD patients that underwent AT-MSC treatment. We utilized autologous AT-MSCs mainly for security reasons, but as suggested by trial results reported by Packham et al [31] and the increasing use of umbilical cord-derived MSCs [39], allogeneic cells could be explored. The main strength of this study is that it informs the safety and feasibility of a future controlled trial, which could assess additional serum and urinary biomarkers and morphological measurements on kidney biopsy samples that we were unable to assess.
In conclusion, we report an initial pilot study providing evidence that it is possible to generate autologous AT-MSCs for cell therapy in CKD patients and that the infusion treatments did not cause adverse events in the year following treatment. AT-MSCs demonstrated the potential to modify the progression of CKD, as the treatment reduced urinary protein excretion, which is a well-known surrogate marker of kidney disease progression. Such promising preliminary results justify designing and conducting future clinical trials that further evaluate the clinical response and molecular mechanisms of AT-MSC-based treatment of CKD and assess characteristics of responder patients to inform the best future candidates for treatment.
Valentina López G and Jorge Bartolucci received stipends from Cells for Cells. M. Khoury is the CSO of Cells for Cells and Consorcio Regenero. The other authors have no conflicts to report.
This work was supported by Cells for Cells (C4C).
Sandra Villanueva, Fernando González, Juan E. Carreño, Jorge Bartolucci, Fernando E. Figueroa, and Maroun Khoury participated in the study design. Fernando González performed the statistical analysis. Maroun Khoury, Fernando E. Figueroa, Eduardo Lorca, and Ricardo Valjalo participated in the conception, analysis, and interpretation of data. Valentina López, Manuel Lecanda, Rocío Strodthoff, and Francisca Fajre provided intellectual content of critical importance to the work and technical support. Andrés Tapia and César Vergar participated in the study coordination. Fernando González, Eduardo Lorca, and Ricardo Valjalo participated in patient selection and care. All authors read and approved the final manuscript.
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