Stem cell transfusion is widely practiced clinical regimen in a patient with impaired immune system or with an immunodeficiency disease. Immunodeficiencies lead to increased risk of infections. The goal of stem cell transfusion is to provide functionally competent myeloid and lymphoid cells, which ensure survival and regain of normal health from opportunistic infections which is the main cause of immediate morbidity.

There have been several attempts to selectively engineer stem cells, Followed by their transfusion where they regenerate more number of specific immune cells for wide spectrum bactericidal actions [1]. The attempts involve prior treatment/culture of stem cells with specific set of cytokines to induce differentiation in the required direction of progenicity. This is an expensive method and unreliable in terms of quantum of highly effective bactericidal myeloid lineages, and therefore, in the recent past this has been over looked. In this regard, strategies to enhance functional abilities intrinsically in eosinophils by iPSCs approach can be proposed.

A proof-of-concept study using mouse iPSCs has clearly shown the potential of iPSCs for therapeutic cell replacement purposes [2]. This study used the iPSCs which were derived from humanized sickle cell mice, in which the mouse a-globin genes were replaced with the human sickle globin variants [2]. Through homologous recombination, the defective gene in the autologous iPSCs was repaired, and HSCs were generated from the genetically corrected iPSCs. Transplantation of the ex vivo-generated corrected HSCs rescued the sickle cell phenotype. This was an important novel approach which can be used for cure of genetic diseases. The purpose of this review is to discuss some selected studies done by authors where differentiation of iPSCs to lineage-restricted myeloid cells (eosinophils, important effector cells releasing cytotoxic mediators such as ECP, EDN, MBP, EPO), and role of iPSCs as cell-based therapy in various immune deficient conditions. We briefly discuss the role of eosinophils implicated in the pathogenesis of numerous biological responses, opportunistic infections including helminth infections and allergic diseases. Considering the potential of induced pluripotent stem cells (iPSCs) in differentiating into any type of cell in the human system we extrapolate the application of the iPSC technology to give rise to more lineage specific cells (eosinophil) in order to enhance the cytotoxic mediators such as eosinophil cationic protein in the system to combat the infections effectively. For this concept we discuss the selected studies done by authors.

Myeloid and lymphoid cells are the caretakers of our immune system. Granules found in the eosinophil, which is a type of myeloid cell, are potent source of cytokines, basic proteins and other mediators. These substances play an important role in immune response to infections caused by bacteria [3], viruses [4], parasites [5] [6] [7] [8] and in resistance to some forms of cancer [9].

Eosinophils are derived from pluripotent hematopoietic stem cells (HSCs) in the bone marrow. Hematopoietic stem cells (HSCs), capable of self-renewal, are the precursors for all type of lineages of mature blood cells. These cells can be divided into short-term repopulating hematopoietic stem cells (ST-HSCs) and long-term repopulating hematopoietic stem cells (LT-HSCs).Short-term repopulating hematopoietic stem cells are known to differentiate into multipotent progenitor cells, which are capable of differentiation toward a subset of the hematopoietic lineage. Multipotent stem cells include the common myeloid and lymphoid precursor. Common myeloid progenitor cells,knownasthe granulocyte/erythrocyte/macrophage/megakaryocyte colony-forming unit (CFU-GEMM), can differentiate toward the erythroid, megakaryocytic, and myelomonocytic lineage. It has been demonstrated that genes specific for erythroid, myeloid, or megakaryocytic lineages are transcribed in the common myeloid progenitors before commitment to a single lineage. On commitment to a single lineage, the genes which are specific for differentiation toward other lineages are downregulated [10].

Myeloid differentiation is regulated by a variety of cytokines, including erythropoietin (EPO), granulocyte-colony-stimulating factor (G-CSF), thrombopoietin (TPO), interleukin-3 (IL-3), IL-5, granulocyte macrophage-colony-stimulating factor (GM-CSF), macrophage-colony-stimulating factor (M-CSF). IL-3 and GM-CSF are cytokines that regulate proliferation and survival during myeloid differentiation of various lineages, whereas EPO, TPO, G-CSF, M-CSF, and IL-5 are required for the final maturation of erythrocytes, megakaryocytes, platelets, neutrophils, monocytes, and eosinophils, respectively.

The myeloid lineage consists of eosinophils, mast cells, macrophages, basophils, neutrophils,and platelets.It mounts the body's first line of response, the innate immune response, when the body first encounters foreign pathogens. Pathogens that escape the first line of defense encounter the body's second line of defense, the humoral immune response, which is mounted by cells from the lymphoid lineage, including natural killer cells, T and B cells.

Eosinophils are multifunctional effector leukocytes implicated in the pathogenesis of numerous diseases and inflammatory processes. As the major effectors, eosinophils function in a variety of biological responses, opportunistic infections, allergic diseases, tumor immunity and helminth infections. The ribonucleases eosinophil-derived neurotoxin (EDN) and eosinophil cationic protein (ECP) are among the major secretory effector proteins of eosinophils in primates. The ECP and EDN are members of the RNase A superfamily, which play a crucial role in host defense against various pathogens as they are endowed with several biological activities. ECP has cytotoxic activity against gram positive and gram negative bacteria [3], viruses such as respiratory syncytial virus (RSV) [4], parasites such as trichinella spiralis, schistosoma mansoni, trypanosoma cruzi, leishmania donovani etc [5] [6] [7] [8]. Helminthic infectionresults in enhancement of eosinophil numbers, directed migration and subsequent degranulation at the parasite surface, resulting in tegumental membrane damage and eventually killing the parasite.

Damage to a tissue or an organ due to an injury or infection, is an irreversible process and in such conditions the role of regenerative medicine is important. Generation of cells and tissues that could be used for cell-based therapies is the most important application of human stem cells. The present approach of using donated organs and tissues to replace destroyed and degenerated tissues is limited by the availability of donors. Human stem cells, which can be directed to differentiate into any type of cells, provide the possibility of a renewable source of replaceable cells and tissues to treat a spectrum of infectious diseases.

Induced pluripotent stem cellsare generated by the genetic reprogramming of somatic cells by certain factors which are important in producing an embryonic stem cell-like state with similar features such as their morphology, gene expression, epigenetic modifications and differentiation potential [11]. Though some recent reports show that iPSC have more profound differences compared to embryonic stem cells (ESCs) than originally assumed [12]. Findings of genetic instability of iPSCs have also raised concerns about their potential use in the clinical setting. The iPSCs have been established to be useful tools for drug development and modelling of diseases with more advanced applications to be used in regenerative medicine. Breakthrough discovery of iPSC technology has created a powerful and innovative way to "de-differentiate" cells whose developmental fates had been assumed to be predetermined. An important point is that since the cells/tissues derived from iPSCs are patient-specific, they are nearly identical match to the cell donor and therefore, avoid rejection by the immune system. The iPSC and other types of pluripotent stem cells are important in building up strategies for reprogramming cells to repair damaged tissues and for immune boosting therapies, in the human body.

Main cause of morbidity in multiple scenarios is due to infections. It is important to combat infections in order to protect life by diminishing the chances of infections or secondary infections. Eosinophils secrete many cytotoxic granule proteins that have been identified as effector molecules responsible for many of the eosinophil actions in human system. The four major eosinophil granule proteins, major basic protein (MBP), eosinophil cationic protein (ECP), eosinophil derived neurotoxin (EDN) and eosinophil peroxidase have been shown to be involved in a number of eosinophil associated functions [13]. EDN possess antiviral activity against single stranded RNA viruses like respiratory syncytial virus, Hepatitis and HIV, whereas ECP and MBP exhibit antibacterial, antiparasitic and antiviral activities. ECP has also been shown to possess antiviral activity against single stranded RNA viruses like respiratory syncytial virus.

The induced pluripotent stem cells can have an important application in such opportunistic infections by

• Their enforced differentiation leading to myeloid (eosinophil) lineage thereby increasing the eosinophils to combat infections
• Genetic engineering approach to potentiate the functional abilities of eosinophils by enhancing its infection fighting mediators (increased expression of antimicrobials such as eosinophil cationic protein).

The primary challenge is to understand as to how the undifferentiated stem cells turn into differentiated cells that ultimately regenerate the tissues and organs. Turning genes on and off is central to this process. Predictably controlling cell proliferation and differentiation requires additional basic research on the molecular and genetic signals that regulate cell division and specialization. Studies to explore early genesis of eosinophils, especially in uncovering the mechanisms controlling the development of the initial innate immune system of human being in normal and diseased individuals is important.

There are several different strategies to direct ESC and iPSC towards the blood lineage [12]. Three different methods have been employed to induce pluripotent stem cells to become mesodermal cells: (1) the formation of embryoid bodies (EB), (2) the co-culturing of pluripotent stem cells with stromal layers, and (3) the culturing of pluripotent stem cells on extracellular matrix proteins. The former two methods are mainly utilized to differentiate iPSCs into hematopoietic progenitors. Erythrocyte, platelets and neutrophils have also been successfully differentiated from hESCs or iPSCs. However, generation of other blood cells has been more limited [12].

A study reported an efficient method for producing eosinophils from human embryonic and induced pluripotent stem cells (hESC/iPSCs). By a two-step induction, the authors first generated multipotential hematopoietic progenitors by co-culturing hESC/iPSCs with mouse AGM-derived stromal cells for two weeks. Then, total co-culture cells were transferred into suspension culture favoring eosinophil development with addition of IL-3 and other factors (SCF, IL-6, TPO, Flt-3 ligand). The maturation of hESC/iPSC -derived eosinophils was shown in a time-dependent manner, first co-expressing eosinophil-and basophil-specific markers [eosinophil peroxidase (EPO), and 2D7, respectively], then the portion of eosinophil markers gradually increased while that of basophil markers decreased typically mimicking the development of eosinophils from human adult hematopoietic progenitors. By flow cytometric analysis, an eosinophil-specific surface marker, Siglec-8, was also expressed on these hESC/iPSC-derived eosinophils in a time-dependent manner paralleling to those with EPO. The expression of eosinophil-specific granule cationic proteins (EPO, MBP, ECP, EDN) and IL-5 receptor mRNA was also detected by RT-PCR. Furthermore, transmission electron microscopy (TEM) observation confirmed the eosinophil property. Eosinophils derived from hiPSCs hold similar characteristics as those from hESCs [14].

It is only a decade since the concept of induced pluripotent stem cells came into existence. Initial efforts to culture iPSCs and further carrying out preclinical studies on murine and primates gave promising insights into their potential applications. The application of iPSCs in regenerative medicine gave hope to victims who are immunodeficient and those whose organs are damaged irreversibly. Most of the injuries and an immunodeficiency state cause morbidity due to opportunistic infections. Eosinophils are important effector cells as they contain plethora of cytotoxic mediators such as ECP, EDN, MBP, EPO and many more cytokines. Among them eosinophil cationic protein play important role in immune response to infections caused by bacteria, viruses, parasites and cytotoxicity to many human cell lines. Strategies to enhance the functional abilities of eosinophils by lineage specific differentiation of iPSC and enhanced expression of cytotoxic mediators by advanced genetic engineering approach provide important future application in such opportunistic infections.

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