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Rajeev Kumar, S.; Sakthiswary, R.; Lokanathan, Y. Stem Cell-Derived Extracellular Vesicles in Systemic Lupus Erythematosus. Encyclopedia. Available online: https://encyclopedia.pub/entry/55811 (accessed on 16 April 2024).
Rajeev Kumar S, Sakthiswary R, Lokanathan Y. Stem Cell-Derived Extracellular Vesicles in Systemic Lupus Erythematosus. Encyclopedia. Available at: https://encyclopedia.pub/entry/55811. Accessed April 16, 2024.
Rajeev Kumar, Sushmitha, Rajalingham Sakthiswary, Yogeswaran Lokanathan. "Stem Cell-Derived Extracellular Vesicles in Systemic Lupus Erythematosus" Encyclopedia, https://encyclopedia.pub/entry/55811 (accessed April 16, 2024).
Rajeev Kumar, S., Sakthiswary, R., & Lokanathan, Y. (2024, March 04). Stem Cell-Derived Extracellular Vesicles in Systemic Lupus Erythematosus. In Encyclopedia. https://encyclopedia.pub/entry/55811
Rajeev Kumar, Sushmitha, et al. "Stem Cell-Derived Extracellular Vesicles in Systemic Lupus Erythematosus." Encyclopedia. Web. 04 March, 2024.
Stem Cell-Derived Extracellular Vesicles in Systemic Lupus Erythematosus
Edit

Systemic lupus erythematosus (SLE) is a multisystemic autoimmune disease that affects nearly 3.41 million people globally, with 90% of the cases affecting women of childbearing age. Extracellular vesicles (EVs) can reduce the pro-inflammatory cytokines and increase the anti-inflammatory cytokines. Moreover, EVs can increase the levels of regulatory T cells, thus reducing inflammation. EVs also have the potential to regulate B cells to alleviate SLE and reduce its adverse effects. 

extracellular vesicles (EVs) immunomodulation inflammation mesenchymal stromal cells systemic lupus erythematosus (SLE) autoimmune

1. Introduction

Systemic lupus erythematosus (SLE) is a multisystemic autoimmune disease with an increased risk of morbidity and mortality [1][2]. This autoimmune disease is detected in women between adolescence and climacteric ages [3]. Like most autoimmune diseases, the cause of SLE development is still undetermined. However, genetic and environmental conditions can influence the pathogenesis of SLE [4]. Importantly, diagnosing this disease at an earlier stage helps reduce the disease progression and organ damage [5]. Late diagnosis of SLE and inadequate treatment can lead to uncontrolled chronic inflammation and multisystemic complications, including maculopathy, transaminitis, allergies, cytopenia, and joint deformities [6][7][8][9]. This can lead to a poor quality of life, affecting the productivity of both work-related and nonwork-related activities [10]. This can result in a direct effect on the patient’s mental health, leading to depression and anxiety [11].
SLE involves both innate and adaptive immune responses with the overt production of immune complexes and autoantibodies. SLE can also be described as the loss of immunological resistance against self-antigens, resulting in the formation of autoantibodies involved in disease pathogenicity, causing tissue damage through various immunopathogenic pathways [2]. Dysregulation of apoptotic cell clearance affects both the innate and adaptive immune responses (Figure 1). In the innate immune response, impaired clearance of apoptotic cells dysregulates the type 1 interferon [12]. This dysregulation of the type 1 interferons increases the expression of neutrophil extracellular traps (NETs) from polymorphonuclear cells (PMN). This induces the secretion of pro-inflammatory cytokines [13]. The dysregulation of type 1 interferons also influences macrophage polarisation. Impaired clearance of apoptotic cells triggers the adaptive immune response via the overactivation of T cells and B cells [13]. The overactivation of T cells and B cells increases the stimulation of neutrophils, self-reactive lymphocytes, and monocytes [14]. The increase in immune cells increases the secretion of pro-inflammatory cytokines, thus developing an autoimmune reaction involved in the disease pathogenesis of SLE.
Figure 1. Pathogenesis of the innate and adaptive immune response in SLE.
As many organs and tissues are affected by SLE, this autoimmune disease is heterogeneous, with the clinical representations evolving with time [12]. The treatment of SLE mainly involves the use of immunosuppressants to control chronic inflammation and prevent organ damage [15][16]. However, these therapies are associated with adverse effects such as cancer, osteoporosis, diabetes induced by steroids, and avascular necrosis at joints [15]. Many patients have refractory disease despite standard therapies. Thus, there is an ongoing search for new agents and methods to achieve disease remission.

2. Extracellular Vesicles (EVs)

EVs have surfaced as a therapeutic agent in immunotherapy, regenerative medicine, and tissue engineering due to their characteristics that promote immunomodulatory properties and the potential to induce tissue regeneration [17][18]. Moreover, EVs are highly biocompatible due to their low levels of immunogenicity and toxicity when used for therapeutic purposes [19]. EVs consist of exosomes, apoptotic vesicles, and microparticles that are released by cells, categorised based on the size range in diameters of (~40 nm–160 nm), (500 nm–2 µm), and (100 nm–500 nm), respectively [18][20]. EVs are usually derived from body fluids such as urine, amniotic fluid, and blood [21]. A variety of cells ranging from macrophages, dendritic cells (DCs), mesenchymal stem cells (MSCs), epithelial cells, platelets, lymphocytes, and fibroblasts secrete EVs. EVs must be isolated and characterised to understand the size, shape, density, surface charge, and porosity, which have a direct effect on biological interactions. Common characterisation methods include flow cytometry, nanoparticle tracking analysis (NTA), transmission electron microscopy (TEM), resistive pulse sensing (RPS), and atomic force microscopy (AFM) [22]. Different cells secrete EVs carrying different proteins and messages of the cells. [23].
EVs are released in various biological processes in the body that can be observed during cell motility, proliferation, apoptosis, differentiation, and immune response [24][25][26][27]. The correlation between the release of EVs during this process led to possible clinical approaches in disease pathogenesis and treatment of diseases. EVs are responsible for intercellular communications between cells [28]. The functionality of EVs depends entirely on the intercellular communication between cells and EVs [29]. This pathway can be targeted as a potential treatment mechanism in diseases such as cancer [30], neurological diseases [31] and metabolic-related diseases [32]
EV research has shown an upward trend in the last 5 years, proving the therapeutic potential of EVs in ameliorating various spectrum of diseases. In various studies, stem-cell-derived EVs have shown notable progress in the therapy of cancer. In a study by Zhu et al. [33], NK cell-derived EVs were able to suppress tumour progression and increase cytolytic levels in human cancer cell lines. A study by Bruno et al. [34] proved that EVs derived from BM-MSCs could inhibit tumour progression significantly, thus ameliorating the progression of the disease. Apart from cancer, therapeutic effects of EVs were observed in neurological disorders as well. EVs derived from MSCs of human adipose tissue have a positive effect on Alzheimer’s disease. The secreted EVs carry enzymatically active neprilysin that clears the accumulation of amyloid-β (Aβ) in Alzheimer’s disease [35]
The therapeutic effects of EVs in other complex diseases have paved the way as a potential treatment for autoimmune diseases. The therapeutic potential can be observed in many studies, such as rheumatoid arthritis and type 1 diabetes. In rheumatoid arthritis (RA), in vivo studies have reported immunosuppressive properties of EVs that inhibit the proliferation of T lymphocytes and reduction in pro-inflammatory cytokines IL-6, TNF-α, and IL-1β [36].

3. Stem Cell-Derived Extracellular Vesicles in Systemic Lupus Erythematosus 

3.1. Isolation of EVs

The isolation method of EVs is crucial to obtain the possible highest purity of EVs to further enhance the specific mechanism of action required [22]. In all the studies, EVs were isolated from the supernatant only after reaching 80–90% confluency of MSCs. The supernatant derived from the conditioned media undergoes centrifugation between 10,000× g and 125,000× g and further undergoes ultracentrifugation at 140,000× g to isolate the EVs based on the size from the precipitate obtained [37]. Apart from that, some studies have included EVs that are also isolated from supernatants using super high-speed centrifugation of 175,000× g. There are other studies that have stated the use of only ultracentrifugation between 125,000× g and 140,000× g for the isolation of EVs [1][38][39][40][41].

3.2. Characterisation of EVs

The isolated EVs are required to be characterised based on their size and specific EV markers to identify the protein expressed by the EVs [37]. From the studies, the common characterisation method of EVs is the Western blot assay. The Western blot assay is used to determine specific protein markers related to EVs, which are commonly identified as CD9, CD36, and endoplasmic reticulum-oriented calnexin [37]. Other protein markers found in the selected studies that were used to identify and characterise EVs include CD63, Alix, CD81, CD63, GAPDH, and TSG101 [37][38][39][40][41][42][43][44][45]. Characterisation of EVs based on morphology was conducted using a transmission electron microscope and was recorded in a few of the studies. The morphology of EVs that were reported in the studies includes EVs shaped like a saucer, round, or sphere-shaped vesicles that include an entire capsule, bilayer-membrane structure, and a hollow globular vesicle [1][37][38][39][43][45]. Apart from that, most studies included the characterisation of EVs by size, using either a nanoparticle tracking analyser or a particle tracking assay [1][37][38][39][44]. However, some studies included a different characterisation method to understand the uptake of EVs using the ExoGlow-Protein EV labelling kit-(Green, System Bioscience, Palo Alto, CA, USA) that dyes EVs fluorescent green [45]. The study involving SHED-EVs reported a unique characterisation method based on the Ag expression on the surface of the EVs that were analysed using ExoAB Ab kit (System Bioscience, Palo Alto, CA) and R-PE-conjugated anti-rabbit IgG Ab (Cell Signalling Technology, Dancers, MA) using flow cytometry (BD Biosciences) [44].

3.3. Range of Dose of EVs Administered

To investigate the efficacy of EV treatment for SLE in in vivo models, the dose of EVs required is an important factor that can determine the immunomodulation effects in SLE. In the study of Chen et al. [37] and Chen et al. [40], the mice were injected with 100 μL of 0.2 mg/mL EVs derived from hUC-MSCs via intravenous injection through the tail vein every 2 days for 14 days. Instead of 2 days, the study carried out by Wei et al. [42] reported 2 × 105 cells per 10 g animal weight of ADSC/miR-20a per 150 μL PBS solution weekly for 14 days. Instead of multiple injections of EVs, a study by Sun et al. [41] recorded single doses of EVs of 200 μg based on the protein concentration that were administered.

3.4. Mechanism of Action (EVs)

3.4.1. Effects of EVs on Pro-Inflammatory Cytokines

The immunomodulatory characteristics of EVs have championed the role of EVs in downregulating disease progression of SLE through various pathways and mechanisms. In terms of macrophage polarisation, in the study by Chen et al. [37], EVs derived from hUC-MSCs are involved in decreasing the levels of NOTCH1, IL-1β, and iNOS which are markers indicating activation of the M1 phenotype (pro-inflammatory). Specifically, the iNOS marker was also downregulated when BM-MSC EVs were used [45]. The effect of EVs on macrophage polarisation is also proven in the study by Dou et al. [43], where EVs derived from human bone marrow mesenchymal stem cells (BM-MSCs) decreased the polarisation of macrophage into the M1 phenotype. The expression of CD80, NOS2, and MCP-1, which are protein expression markers in M1 macrophages, was significantly decreased.

3.4.2. Effects of EVs on Anti-Inflammatory Cytokines

Moreover, the EVs played a pivotal role in increasing the CD206, CD86+, CD116+, Arginase-1, and IL-10, which are part of markers indicating M2 macrophage polarisation leading to anti-inflammatory effects [37][40]. CD206+ and CD163+ markers can also be seen to be upregulated in the study carried out by Sun et al. [41] using UC-MSCs to inhibit lupus via M2 macrophage polarisation. The upregulation of Arg-1 markers is also recorded in the study carried out by Zhang et al. [45] involving EVs derived from BM-MSCs. The study by Dou et al. [43] also recorded an upregulation of CD206, MRC-2, and ARG-1, which are M2 macrophage markers indicating an anti-inflammatory response. Different markers of M2 macrophage, such as CD14+ and CD163+, were alleviated and recorded in the study by Sun et al. [41].

3.4.3. Effects of EVs on T Cell Lineage

Apart from the secretion of anti-inflammatory and pro-inflammatory cytokines, EVs have proven to be involved in the regulation of Treg and T helper cells to suppress the disease progression of SLE. In the study by Tu et al. [38], Th17 subsets were significantly downregulated, showing a reduction in pro-inflammation effects. The cytokine level IL-17 co-relates to the production of Th17 cells. Lower levels of IL-17 indicate lower production of Th17 cells, as IL-17 acts as a biomarker to examine the disease activity in SLE patients [46].

3.4.4. Effects of EVs on B Cells

Having said that, EVs also have the potential to regulate B cells, which was recorded in the study carried out by Zhao et al. [39], which further confirms immunomodulation effects via B cells. EVs have been shown to increase the levels of B cell apoptosis while inhibiting the excessive proliferation of B cells. Cytokine levels further confirmed that the hyperactivation of B cells reduced significantly after the treatment with EVs.

3.4.5. Effects of EVs on Lupus Nephritis (c-Complements)

Furthermore, SLE can also lead to complications such as lupus nephritis, which is caused by kidney inflammation. EVs were also reported in various studies, proving to have positive effects by alleviating inflammation and its effects on the kidneys. In the study by Wei et al. [42] and Zhang et al. [45], levels of IgG and C3, which are immune complexes, were significantly downregulated in the glomerular mesangial and endocapillary of the kidney after the treatment with EVs.

3.5. Role of miRNAs and tsRNAs in Extracellular Vesicles in Ameliorating the Disease Progression of SLE

To further improve or understand the immunomodulatory effects of EVs, the effectiveness of inhibition and overexpression of miRNAs related to EVs are included in the studies and shown in Figure 2. The study by Chen et al. [37] indicated that the inhibition of miR-146a-5p resulted in adverse effects on lung injuries. NOTCH1, IL-1β, and iNOS were overexpressed while IL-10 and TGF-β levels were downregulated. The inhibition produced a negative effect, thus proving that expression of miR-146a-5p in EVs can upregulate IL-10, CD206, Arg-1, and TGF-β and decrease the expression of NOTCH1, IL-1β, and iNOS in patients diagnosed with SLE.
Figure 2. EVs and miRNAs that are related in ameliorating the disease progression of SLE. BMMSCS, bone marrow mesenchymal stromal cells; SHED, stem cells from human exfoliated deciduous teeth; hucMSCs, human umbilical cord mesenchymal stromal cells; AD-MSCS, adipose-derived mesenchymal stromal cells; UC-MSCs, umbilical cord mesenchymal stromal cells [1][37][38][39][40][41][42][43][44][45][47].
Another study by Tu et al. [38] investigated the expression of miR-19b in EVs derived from UCB-MSCs to further express miR-19b in T cells. The results indicated that miR-19b expressed in T cells via EVs lowered TNF, IL-6, and IL-17 expression levels and increased IL-10 and TGF-beta levels. The miR-19b also inhibited the expression of KLF13 in T cells. The study also indicated that EVs could promote the T cells to express more mir-19b, which can inhibit the levels of KLF3 that regulate the balance of Th17/Treg cells. The miR-19b also increases the production of anti-inflammatory cytokines IL-10 and TGF-beta while downregulating levels of IL-16, IL-17, and TNF-alpha.
With regard to miRNA, another study by Wei et al. [42] recorded the isolation of miR-20a from EVs derived from ADSCs and the overexpression of miR-20a. The overexpression of miR-20a has recorded a positive effect on lupus nephritis models where anti-dsDNA antibody, urine protein, and serum creatinine levels were significantly lowered. It also triggered higher autophagy markers of Beclin 1, LC3-II/LC3-I, and p62 that indicated higher levels of autophagosomes. The autophagy mechanism stimulated the reduction in podocyte damage and reduced histopathologic abnormalities in the kidney.

3.6. EVs and Signalling Pathways

It is important to understand the effects of EVs and their specific miRNA and tsRNA on the pathway that is involved in the disease progression of SLE. This is to ensure further understanding of the mechanism of action of EVs in immunomodulation. In the study by Chen et al. [37], the NOTCH 1 pathway was identified to play a crucial role in macrophage polarisation into the M1 phenotype.
Apart from the NOTCH 1 pathway, inhibition of the MAPK/ERK signalling pathway plays an essential role in regulating B cells and inhibiting B cell overactivation in SLE patients. The SHIP-1 protein levels have a direct effect on the ERK signalling pathway. To prove the mechanism of action of EVs through this pathway, miR-155 was inhibited in B cells through EVs. The inhibition of miR-155 increased the expression of SHIP-1 proteins. Increased levels of SHIP-1 protein inhibit the ERK signalling pathway, thus reducing B cell proliferation and activation while increasing B cell apoptosis [39]
Other inflammatory-related pathways that were included in the studies include the T cell receptor signalling pathway. The TCR pathway is involved in the regulation of cytokines, survival of T cells, proliferation, and differentiation of T cells. Dysregulation of this pathway can increase the chances of developing SLE [48]

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