Demyelination in Leprosy Demyelination in Leprosy

Leprosy is a chronic infectious disease caused by Mycobacterium leprae that has a predilection for peripheral nerves, especially Schwann cells (SCs). Leprosy medications may only eradicate the bacteria without preventing or recovering peripheral nerve damage. Early nerve damage detection is necessary. The expression of Krox-20 in Schwann cells will be examined immunohistochemically, and the level of neuron growth factor (NGF), neuregulin 1 (NRG1), protein 0 (P0), and peripheral myelin protein 22 (PMP22) will be examined in the blood plasmas. A significant decrease was noticed in Krox-20 and NGF, NRG1, P0, and PMP22 level (p < 0.05) in disability degree 1 compared to degree 0. Studies proved that markers have shown promising results; Krox-20, NGF, NRG1, P0, and PMP22 could be useful diagnostic tools for early peripheral nerve damage detection in leprosy. levels of NF protein content in the infected nerve. These results indicate the presence of hypo-phosphorylated NF subunits during leprosy infection, which are thought to lead to increasing susceptibility to proteolytic degradation of NFS. This result is consistent with the previous research, where phosphorylation was found to protect NFS against nonspecific proteolysis by calpain. Several studies by Shetty et al. found that lipoarabinomannan (LAM) M. leprae could inhibit the protein kinase C (PKC) enzyme which is responsible for the phosphorylation of the neurofilament protein. Recently, Save et al. also found that hypophosphorylation of NFS proteins by measuring the activity of enzyme kinases is responsible for NFS phosphorylation in the nerves of infected mice. The authors point out that as long as NFS loses its reactivity to specific NF-phosphate (SMI 31) antibodies, there is a decrease in KSPXK kinase activity from cyclin-dependent kinase (CDK) and MAPK in M. leprae -infected nerves. Decreases in NFS phosphorylation and NFS degradation may subsequently result in decreasing in interfilamen tary distances that affect axonal growth and result in axonal atrophy.


Leprosy is a chronic infectious disease caused by Mycobacterium leprae and has predilection for the skin and peripheral nerves, especially in Schwann cells (SCs) [1-4]. During infection, M. leprae causes peripheral nerve damage and even causes disability and deformity in patients.
Although the anti-leprosy drug treatment can already eradicate the bacteria, disability and deformity that occur cannot be restored and neither can the function of the nerve that has been lost. By understanding the mechanism of nerve damage caused by M. leprae, it is expected that nerve damage can be prevented [5].
In the central nervous system (CNS), myelin is formed by oligodendrocyte. Myelin in the CNS has a spiral structure such as peripheral nerve myelin which has an inner mesaxon and an outer mesaxon that ends in a loop or cytoplasmic junction. The cytoplasm of glia in the CNS is confined to only a portion of the myelin sheath. The glia junction continues with the oligodendrocyte plasma membrane through a layered process. One oligodendrocyte can eliminate about 40 or more axons, whereas in the peripheral nervous system (PNS), the myelin deposition of an axon can reach up to 100 layers of myelin [15].
Schwann cell differentiation is governed by the expression of certain transcription factors. After receiving signals from axons, immature Schwann cells including NRG1 will increase the expression of some transcription factors such as NFκB, Oct-6, and Brn2. These factors will stimulate initiation of the promyelination stage whereby the Schwann cell will interact with the axon and begin to express the initial myelination marker. An increase in the Krox-20 gene requires Schwann cells to initiate the myelination process and express the specific protein of myelin. In mature nerves, Schwann cells that do not express Krox-20 will remain nonmyelinated cells. In the injury condition, c-Jun and Sox-2 will increase rapidly. This will lead to a decrease in Krox-20 and Schwann cell differentiation. Cross-resistance Krox-20 and c-Jun will stimulate the switch of complex transcription. Promyelination signals from axons such as neuregulin will result in Krox-20 expression via the phosphatidylinositol-3 kinase (PI3K) pathway. The activation of the Janus kinase (JNK) pathway during the injury period will stimulate c-Jun expression. However, the signals that activate these pathways in Schwann cells are still not known [15].
The study evaluated the Krox-20 expression on Schwann cells in the skin biopsy of leprosy patients, and it was observed that there was a significant difference of Krox-20 expression among patients with degree of disability 0 and 1.
(T-tailed test shows F = 8.881 with p = 0.000 (p < 0.05)). Findings summarized a significant decline in Krox-20 expression in degree of disability 1 compared to degree of disability 0 (T-test, F = 8.881, p = 0.000 (<0.005)). Sensitivity and specificity can be 100%. It means that if the Krox-20 expression is more than 8, the degree of disability will be 0 and vice versa. ROC curve showed that area under the curve is 1.0 (100%) with p = 0.000. On the other hand, in patients with degree of disability 1, it can be seen that the expression of Krox-20 is minimal [16].
The function of Schwann cells is to synthesize the myelin sheath. When these cells are infected by M. leprae, the consequence is a demyelination resulting from neuritis. It is suspected that M. leprae infection in Schwann cells is a direct cause of Schwann cell dysfunction that can cause demyelination in leprosy patients [2].
Leprosy is one of the diseases that can cause nontraumatic nervous system disorder and is most commonly found in the world. Diagnosis of this disease can be established relatively easily because it does not require sophisticated equipment. The problem is the number of disabilities even though M. leprae has been eradicated in accordance with the applicable protocol. Early identification of the occurrence of disability is also the constraint in establishing diagnosis of disability as a sequel of leprosy. Nerve cell damage by leprosy is the result of the demyelination of peripheral nerve cells. Demyelination is caused by the entry of M. leprae into Schwann cells as the main target. The entry of these bacteria can cause the demyelination of Schwann cells suspected through the activation of the c-Jun pathway. When damage occurs in Schwann cells, automatically as a form of defense, Schwann cells will repair the damage that occurs, namely, by remyelination. The process of remyelination is influenced by NRG1 and NGF as a neurotrophic factor, as well as the availability of PMP22 and P0 as specific basic materials of myelin in peripheral nerves. Until now, based on the literature review we have read, the factors used to determine early disability in leprosy patients are unknown. Meanwhile, the use of WHO criteria to determine the degree of disability is still rough because it involves only three sensory organs: feet, hands, and eyes. This study is aimed to determine the early markers of nerve damage, namely, demyelination and remyelination in leprosy patients with degrees of damage 0 and 1 based on WHO criteria.

Definitions
Leprosy is a chronic granulomatic infection caused by M. leprae. This disease attacks the skin, nasal mucous membranes, and peripheral nerves [17].

Etiology
The cause of leprosy is M. leprae which is transmitted by droplet from nasal secretions and received by the nasal mucosa and other respiratory tracts. This bacterium mainly attacks Schwann cells in the peripheral nervous system and can cause peripheral nerve functional disabilities as well as disability [18].

Epidemiology
Multidrug therapy (MDT) program has greatly reduced the prevalence of leprosy to less than 1 case per 10,000 people in 90% of endemic countries where leprosy is considered as a public health problem. However, the leprosy case detection rate is still high [19].

Diagnosis
Based on physical examination, according to the WHO, there are three special physical signs for leprosy which can already be used to make the diagnosis. The three special signs are:

Redness or hypopigmented skin lesions with loss of sensation (especially sensation of touch and temperature)
2. Peripheral nerve involvement, such as peripheral nerve thickening with loss of sensation (especially touch and temperature)

Acid-resistant bacteria in the skin smear of the patient in a certain place
The diagnosis of the degree of disability in leprosy patients is based on the criteria published by the WHO as shown in Table 1.
The main classification according to WHO leprosy disease consists of paucibacillary (PB) and multibacillary (MB). If five hypopigmented patches can be found in the patient's skin and there is no BTA in the skin smear, it can be classified as PB type. However, if more than five leprosy hypopigmentations are spotted, and/or BTA are found in skin smear, it may be considered as MB leprosy patients [19].

Monofilament test
One of the techniques which is used to assess neuronal function in leprosy patients is monofilament test (MFT). The test is performed using five different single filaments, i.e., 200 mg, 2 g, 4 g, 10 g, and 300 g. Each site is then assessed by the perceived filament, which is the heaviest monofilament obtained and the highest value with a total value of 15 for the ulnar, median, and radial (four filaments) nerves and a total value of 12 for the foot (three filaments). The normal threshold value is 200 mg for the hand and 2 g for the foot (other than the heel) [10,11]. This test is considered positive if the MFT value is 3 for each nerve. "Fixed" or "unchanged" test result is when the test score has one-or two-point difference from the previous test score (basal value). If the value increases by three points or more, it is said to be "damaged" or "broken." If the value decreases three points or more, it is said to be "improved." If the patient's examination value improves by three points or more, and the total value of the neural examination is reduced by two points or less when compared to the current patient condition, it is said to be "cured." For the ulnar, median, and posterior tibial nerves, the same examination as the INFIR study is performed, except for the median nerve on the tip of middle finger rather than the little finger ( Figure 1).

Therapy
Patients with PB type can be given two types of drugs which are already available in the package. The first is for 6 months, i.e. In PB case, in patients over 15 years old, the drug is given in multidrug treatment (MDT) form with rifampicin 600 mg and dapsone 100 mg on the first day, the second day, and until the 28th day and so on for up to 6 months. The second is for 1 year, i.e., MB case. In patients over 15 years, rifampicin 600 mg, clofazimine 300 mg, and dapsone 100 mg on the first day of the first month can be given. In the second and subsequent days, they are given dapsone 100 mg and clofazimine 50 mg [19].

Prognosis
In general, the prognosis of leprosy after getting the correct treatment is good. Healing in complications of neurological disorders is very limited, which means they are difficult to heal. Lesions on the skin can usually be healed in the first year of treatment, while color disorder of the skin and skin damage usually persist. Physical therapy, reconstructive surgery, nerve and tendon transplantation, and surgical operations to correct contractures can improve the patient's quality of life [20].

Complications
Good care and attention to the possibility of reversal reactions due to leprosy treatment will minimize long-term neurological sequelae. Here are some possible leprosy complications:

Reaction type 1:
Slow hypersensitivity reaction occurs when BL leprosy shifts into LL leprosy during treatment. This reaction is a description of good immune response and formation of IFN-γ and TNF-α locally. This reaction is characterized by edema and erythema in skin lesions, the formation of skin lesions, neuritis, and loss of sensation and motor. The incidence of type 1 reactions in leprosy patients with BL is about 30%. Nonsteroidal anti-inflammatory drugs (NSAIDs) and high-dose steroids can be given in the treatment of type 1 reactions.

Reaction type 2:
It is often referred to as erythema nodosum leprosum (ENL), which is the complication of LL type. This reaction is characterized by the formation of subcutaneous inflammatory nodules with fever, lymphadenopathy, and arthralgia. High levels of TNF-α and deposition of the immune complex are suspected to be closely related to ENL.
In addition, a complication that may also occur is Lucio phenomenon, which is a severe complication in MB-type leprosy characterized by bluish bleeding plaque and necrotic ulceration. In this phenomenon, leprosy bacteria may have spread to endothelial cells along with the appearance of necrotic and vasculitic epidermis with thrombus formation and endothelial proliferation [6, 20].

Immunoprophylaxis and chemoprophylaxis
Bacille Calmette-Guerin (BCG) vaccine has been widely used in leprosy endemic countries to provide protection against leprosy. The first dose of BCG provides protection between 14 and 80% against leprosy, while the second dose provides protection between 0 and 50%. Single dose of rifampicin administered to close contacts from newly diagnosed leprosy patients shows an efficacy of 57% in reducing new cases of leprosy [22]. Other studies show the protective effect of immunoprophylaxis and chemoprophylaxis in controlling leprosy. This is done by giving BCG vaccine at infancy in combination with rifampicin given to leprosy contacts. However, the effect of this combination is more useful for PB form contacts rather than MB form [23].

The peripheral nerve as a target of M. leprae
The Schwann cell (SC) of the peripheral nervous system (PNS) is essential for the survival and function of neurons, that is, to enclose axons. SCs were discovered by Theodore Schwann who investigated peripheral nerves. The function of this SC is to assist the myelination of axons and to direct the neurons. SC develops after birth from immature cells to become myelin or without myelin. The first immature cells go through the myelination path at birth and then go through the non-myelin path later in its development [24].  [25]. MBP in the PNS has four polypeptide bands ranging from 14 to 21 kD. This structure has various posttranslational modifications such as phosphorylation and methylation, and this is one of the major autoantigens in multiple sclerosis disease. Myelin P2 or fatty acid-binding protein 8 is a small protein (14 kD) with a high positive charge and is concentrated mainly in thick myelin sheaths. This structure is a member of the family of fatty acid-binding proteins with a high affinity for oleic acid, retinoic acid, and retinol. This structure function is to assemble and maintain myelin lipids. P2 is also an autoantigen in autoimmune peripheral neuropathy, Guillain-Barre syndrome (GBS). Its function is related to stabilizing the dynamics of myelin membranes and transport to and from lipid membranes [26,27].

Both SCs which are myelin and without myelin produce an extracellular matrix that forms basal lamina containing collagen around axons. These neurons consist of units of axon cells-
Myelin is only produced if the cell is in contact with several types of axons. Axons send signals that are important to identify the SC. Examples of axon signals are beta-neuregulin-1 (NRG1) and glial growth factor (GGF). SC can be activated to enter proliferation via axonal signaling NRG1 to bind and activate the ErbB2/ErbB3 receptor complex on SC to activate MAPK for cell proliferation. The factors governing myelination of SC include transcriptional factors Krox-20, Oct-6, and Sox-10; they also inhibit cell death and proliferation. Special myelin protein, P0 for diminished myelinated SC if immature cells are not associated with axons. If SC loses interaction with an axon, there can be dedifferentiation into an immature SC. If the cells associate with their axon again, they will become myelinated or nonmyelinated depending on the stimulating signal. SC has the ability to block apoptosis through the effects of growth factors such as insulin-like growth factors (IGFs), platelet-derived growth factor-BB (PDGF-BB), and neurotrophin-3 (NT-3) on autocrine circuit [24].
One of the events associated with SC pathogenesis is nerve injury and demyelination. This can be due to axonal damage and axon-SC signal interference. Another cause is the immune stimulation (autoimmunity) that targets myelin as in multiple sclerosis and Guillain-Barre syndrome (GBS). As with autoimmune disorders, M. leprae causes peripheral nerve demyelination that begins with damage to the myelin sheath and decreases the speed of the actionpotential conduction [28].

Nerve damage in leprosy
Nerve damage is a major characteristic of leprosy pathogenesis. The first stage of nerve damage in leprosy is the localization of M. leprae in peripheral nerves. A recent research about leprosy in experimental animal armadillos successfully revealed that after M. leprae successfully penetrate the skin barrier, these bacteria gather in epineurial lymph and blood vessels around the nerve and then go into the endoneurium compartment through the blood supply. However, if M. leprae can enter SC freely through the only way through the Schwann cells exposed to the dermis; the only way to prevent transmission of leprosy is to prevent the attachment of leprosy to Schwann cells [2].

The role of cellular immunity
SC can take, process, and present the specific antigen of M. leprae to T cells resulting in the production of Th1 modulatory immune cytokines such as TNF-α and INF-γ [32]. SC can present mycobacterial antigen to MHC class I, CD8+ cytotoxic T cell, and also can present mycobacterial antigen to class II MHC, CD4+ CTLs. SC was found to express co-stimulatory molecules and adhesions to T cells. As a result of this stimulation, SC will be killed by cytotoxic granules (granulysin, granzyme, and perforins) produced by CTLs [33]. SC can express TLRs (TLR1 and TLR2) which are activated by LAM M. leprae, a lipoprotein such as 19 and 33 kD. SC activation will lead to cytokine production (TNF-α, IL-12) and apoptosis [34]. TLR expression was found to be greater in TT patients than LL patients [35]. The large amount of cytokines released by Th1 cells, especially IL-12, IL-2, and TNF-α, will cause apoptosis of infected cells and decrease in bacterial load and increase granuloma formation such as lesions in TT type [36].

Macrophages also play role in the stimulation of immunity in leprosy. Infected macrophages by M. leprae can present its antigens to T and B cells and release cytokines including TNF-α [1]. Both of these cells can produce reactive oxygen intermediate (ROI) which results in fur-
ther nerve damage at the site of granuloma [26]. M. leprae stimulates macrophages to produce TGF-β which is responsible for decreased nerve regeneration [26]. Other cells may also present antigens which are dendritic cells, also found to effectively present the M. leprae antigen and stimulate CD4+ and CD8+ cytotoxic T cells. Th1 cells are thought to be involved in CMI-DTH reactions (cell-mediated immunity-delayed-type hypersensitivity) and are important in response to intracellular pathogens. In contrast, Th2 cytokines stimulate the production of antibodies. C-type lectin DC-SIGN shows binding to LAM and triggers the production of IL-10 and TGF-β and inhibits the production of IL-12 and TNF-α [37].

Scollard proposes that M. leprae interacts with the vascular endothelial cells and perineurium before successfully infecting the SC. This leads to the possibility that M. leprae infects the peripheral nerve tissue through the bloodstream [2]
. This mechanism is thought to play an important role in SC immunopathogenesis and peripheral nerve damage to leprosy.

High levels of antibodies (IgM and IgG) are usually found in LL-type leprosy patients. Th2 (IL-4, IL-5, and IL-10) cytokines found in LL patients decrease TLR2 expression and stimulate activation of B cells. Activated B cells can make IgM, IgA, and IgG antibodies ineffective in killing intracellular bacteria. Therefore, M. leprae is able to survive and spread, causing various nerve damages [38]. After chemotherapy, there is usually a decrease in antibody levels.
There is a strong correlation between bacterial load and humoral immune response. Analysis of antibody response has also been proposed as a tool for leprosy classification [39].
The antibodies produced against M. leprae play a role in the uptake of M. leprae by phagocyte cells and initiate the pathogenesis of the disease. For example, the discovered antibodies are binding to complement, which then binds PGL-I and binds C3 complement to M. leprae. The binding of this complement will mediate the uptake of bacilli through complement receptors in phagocytes [40]. In addition, secreted antibodies can form immune complexes with M. leprae antigen or with cross-reactive host molecules. This complex can then be recognized by antigen-presenting cells through specific receptors and delivered to T cells. In LL patients an excess of immune complex antibodies is found. However, if the antibodies are taken by APC cells (macrophages), they fail to activate T cells. Specific mature B-cell markers (CD20, CD79, CD138) that produce antibodies are found to be higher in skin lesions of BL/LL patients than BT patients [41]. In addition, when compared to gene expression of leprosy skin lesions of LL and TT types, it showed upregulation of B-cell-specific gene. Immunohistology of LL and TT skin lesions showed that IgM and IgA are more common in LL-type leprosy lesions, correlated with Th2 immunity and increased IL-5. LL is associated with an increase in systemic humoral response [42].

Guillain-Barre syndrome (GBS), and rheumatoid arthritis. The formation of antigen-antibody complexes and complement stimulation as well as the recruitment of PMN cells can cause tissue damage and injury to the vessel wall as seen in autoimmune and leprosy diseases [42].
T cells in leprosy lesions may be produced either against specific antigens of M. leprae or autoantigens such as HSP-66. This may cause other mechanisms of nerve damage caused by autoimmune damage such as from tissue (neuropathy). In LL-type leprosy patients, there was a decrease in the specific antigen level of T cells against M. leprae antigen 65 kD, but at the same time, there was an increase in anti-antibody levels of 65 kD IgG. The similarity between bacterial proteins and host components or the presence of molecular mimicry is an important aspect for host-pathogen interactions. By using this mechanism, pathogen can avoid detection by the immune system or may cause autoimmunity. The monoclonal antibodies that arise against M. leprae antigens such as 65 kD antigen react with host antigens such as peripheral axons found in the skin.
In addition, the protein sequence of myelin PNS P0 is compared to the M. leprae protein sequence (leproma) and also other genomic databases for protein sequences and structural equations in other pathogens involved in neurodegeneration. This resulted in 11 hits with the right pair ranging from six to seven P0 myelin residues in the M. leprae genome, but not in other genomes of mycobacteria. Among these, two suitable on M. leprae are special proteins including ferredoxin NADP reductase (62%) and conserved membrane protein (36%) (ML2453, ML1504).

Comparisons to other pathogen databases show that P0 has similar sequences with polio virus
receptors (23.4%) and herpes virus (4%). In addition, searching for the myelin P0 sequence on the whole genomic database revealed that it has similar sequence to the immunoglobulin superfamily. This family plays an important role in the interactions of proteins-proteins and protein-ligands. The similarity between bacteria and host is that they can cause autoimmunity and neurodegeneration (demyelination) as can be seen in leprosy transmission. For example, anti-neural antibodies from serum of leprosy patients were found to bind the myelin protein P0.
Since leprosy is one of the differential diagnoses of rheumatic diseases, some autoantibodies can be examined in leprosy serum using ELISA techniques and correlated with joint involvement. For example, in Brazil, most leprosy patients have no active reaction. Therefore, the frequency of IgM-rheumatoid factor (RF), anti-cyclic citrullinated peptide (anti-CCP) antibody, antinuclear antibody (ANA), and antineutrophil cytoplasmic antibody (ANCA) is low in leprosy patients. However, the prevalence of anticardiolipin (aCL) antibodies and anti-β2 glycoprotein I (β2GPI) antibodies is significantly higher in leprosy patients than in the control group.
Glycolipids and glycosphingolipids expressed as determinants of myelin surfaces in SST are important for the function and stability of myelin itself. The resistance to these molecules (glycolipids) by autoantibodies can cause demyelination and nerve damage as found in leprosy patients. Therefore, many scientists study the autoantibody and its relationship to nerve damage found in leprosy. Glycolipid or glycosphingolipid neural antibodies such as ceramide have been studied in leprosy patients in India. The anti-ceramide antibody IgM titers were found to be significantly higher in MB-type leprosy patients than both control and PB leprosy patients (96% of MB-type and 60% of PB-type patients). Groups in Brazil found elevated levels of anticardiolipin (aCL) and anti-β2-glycoprotein I (anti-β2-GPI) in leprosy patients, especially in LL-type patients with IgM-isotype dominant. The percentage of antiphospholipids in leprosy can be due to exposure to phospholipid antigen by tissue damage during the infection process. Another explanation is that the homology between PL bacteria and host results in the production of antibodies against cross-reactive heterological sequences.
Other anti-glycolipid antibodies are anti-sulfatide (cerebroside) which has also been reported in various cases of demyelinated peripheral polyneuropathy. Sulfatide, a glycolipid with single sulfate saccharide, is associated with the myelin membrane of nerve cells. Antibodies inhibit sulfatide synthesis expressed on myelin as a surface determinant, resulting in demyelination. IgM-subtype antibodies against sulfatide were increase in MB-or LL-type leprosy compared to PB and control. IgM anti-sulfatide is positively correlated with the patient's bacterial index. The similarity between mycobacterial sulfolipid with trehalose sulfate and host tissue (sulfatide) can stimulate autoantibodies against host sulfatide with galactose sulfate.

Variations in the number of autoantibodies found in leprosy patients can be attributed to the genetic background of the study population, the presence of infectious diseases, and the techniques used to detect autoantibodies. The hypothesis proposed for the development of such antibodies during infection is due to adaptive immune responses and activation of polyclonal B cells. Bacterial or viral antigens, with homologous sequences to tissue hosts, will be presented to T lymphocytes that stimulate B lymphocytes to produce antibodies against heterologous sequences.
In addition, autoantibodies to the antigenic epitope of myelin protein are reported in various chronic demyelinating diseases. For example, in chronic inflammatory polyradiculoneuropathy (CIPD), in which both humoral and cellular immunities are involved, there are antibodies to the myelin protein. The major antigenic components of myelin are myelin P0, P2 myelin, and peripheral myelin protein 22 (PMP22). These proteins are also associated with induced experimental autoimmune neuritis (EAN). Such autoantibodies may be produced during tissue damage and then continue to exacerbate further tissue damage during the disease process.

Demyelination without immunological process
Beside inflammatory process, axon demyelination can be caused by the presence of M. leprae. leprae succeeds in inducing SC proliferation and demyelination [5]. Rambukkana stated that the mechanism of nerve damage in the absence of an immunological process played a role in the early stages of the disease. However, it is an immune system-mediated element that eventually causes nerve damage. When the M. leprae antigen is presented by myelinated and unmyelinated SC, both types of cells are subjected to attack by macrophages, T cells, and cytokines that are released as a result of the cell's inflammatory response. This inflammatory process will produce two SC phenotypes and sensoric-motoric damage subsequently [5].

Rambukkana et al. have proved this both in vitro (in schwannn cell coculture) and in vivo (in
Another mechanism that is suspected to cause nerve damage can be grouped in the form of nonimmune mediated, and it is the biochemical and metabolic changes in the nerve compartment. The examples of these mechanisms are axonal atrophy due to hypophosphorylation of myelin proteins and axonal neurofilament. Many proteins in PNS are phosphorylated such as myelin P0, MAP, and neurofilament proteins. An experiment which studied the phosphorylation of PNS proteins in leprosy nerves compared to normal nerves found that decrease in protein phosphorylation protein levels of 25 kD in leprosy patients' nerves. The phosphorylated (25 kD) protein is thought to be the myelin glycoprotein P0 [43]. Later studies by the same group also found that M. leprae could bind these myelin P0 (25 kD) glycoproteins and inhibit phosphorylation in vitro. The outer binding of the myelin can help M. leprae to reach the SCs target for invasion [43]. In leprosy patients, a decrease in axonal diameter was found to be associated with the loss of sensoric and motoric function. Therefore, the relationship between neuropathy and phosphorylation of NF protein was then investigated.  In this stage, the presence of autoantibodies against nerve components is reported in leprosy as another mechanism of nerve damage. The presence of common antigenic determinant between M. leprae, the skin, and nerves such as heat-shock proteins leads to the production of autoantibodies [26].
The presence of M. leprae in the nerves can also cause leprosy neuritis which has no skin manifestation, but nerve damage can be detected. Nerve damage can be caused by a full inflammatory inflammation of macrophages that produce foam cells in granulomas. This inflammatory process causes the stimulation of cytotoxic T-cell activity, axonal degeneration after SC death, and demyelination. Using different SC and axonal markers on the immunohistochemical slide of leprosy neuritic nerve, there was a decrease in immunoreactivity of NF200 as a result of the loss of myelinated fibers. In addition, the S-100 protein staining of the myelinated fibers was reduced due to loss fiber after the onset of demyelination. NGFr staining of the neuritic nerve is also reduced in SC and/or small fiber axons. A decrease in myelinated fibers results in a decrease in MBP [44].

Nerve growth factor (NGF)
Nerve growth factor (NGF) is firstly discovered in neurotrophin family. NGF is essential in the development and maintenance of phenotypic peripheral nerve cells and for the functional integrity of the cholinergic nerves in the central nervous system. The mature form of NGF (from ProNGF precursors) has an important role in development and in adult life and also has proapoptotic and neurotropic properties.

Neuregulin 1 (NRG1)
In early life, Schwann cells are made of cells in neural plates and undergo massive migration, proliferation, and maturation before finally undergoing differentiation. During this period, Schwann cells are constantly in contact with axons and axonal signals, particularly neuregulin-1 (NRG1). In fact, NRG is a signaling protein that mediates the interactions of cells in the nervous system, heart, breast, and other organ systems. Neuregulin is also ligand for the ErbB family of tyrosine kinase receptors. Neuregulin itself has four families, namely, NRG1, NRG2, NRG3, and NRG4. However, until now, the biological functions of NRG2, NRG3, and NRG4 are still not widely known [45]. NRG1 is a growth factor that is very influential on the development of cells in the neural plate during the early stages of embryonic development. NRG1 is also involved in migration, axon growth, and synapse formation [46,47]. In addition, NRG1 is a strength for Schwann cells to differentiate. This is proven in cell cultures where many aspects of Schwann cells are administered by NRG1, which are: 1. NRG1 serves to suppress the neuronal differentiation of the neural stem cell plate but to stimulate the differentiation of glial cells.

NRG1 is required for Schwann cell progenitor survival.
3. NRG1 also serves to stimulate proliferation and migration of Schwann cell precursors.

NRG1 gives an important signal to myelinate.
In vivo, the early stages of Schwann cell development depend on NRG1/ErbB signaling, as in mouse-fed animals without Schwann cell progenitors in peripheral neuronal development such as ErbB2, ErbB3, or NRG1.

Protein 0 (P0)
P0 or MPZ is one of the major protein components of myelin nervous system. P0 protein is transmembrane glycoprotein belonging to the immunoglobulin superfamily. It is the largest part of protein in SST myelin and is thought to be responsible for the adhesion of the outer surface of the cell and the myelin plasma membrane [48].

Peripheral myelin protein 22 (PMP22)
Peripheral myelin protein 22 (PMP22) is a major component of myelin (Snipes et al., 1992). This is evidenced by the discovery of PMP22 mRNA in Schwann cells and the PMP22 protein in the solid part of the myelin sheath. Assessment of the presence of PMP22 as a peripheral nerve myelin protein is also supported by the finding that the regulation of PMP22 expression during neural development and after neuronal trauma is identical [16].