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Stem cells bone marrow

A B lymphocyte is a specific type of white blood cell (leucocyte) derived from bone marrow stem cells. Each B lymphocyte expresses an immunoglobulin (antibody) specific for a particular antigen. Following antigenic stimulation, a B lymphocyte may differentiate and multiply into plasma cells that secrete large quantities of monoclonal antibody. [Pg.245]

An osteoblast is the cell forming new bone. Osteoblasts are derived from stromal bone marrow stem cells. [Pg.918]

Metchnikoff (1883) recognized the role of cell types (phagocytes) which were responsible for the engulfinent and digestion of microorganisms. They are a major line of defence against microbes that breach the initial barriers described above. Two types of phagocytic cells are found in the blood, both of which are derived from the totipotent bone marrow stem cell. [Pg.280]

In older adults, AML is either more likely to arise from a proximal bone marrow stem cell disorder, such as myelodys-plastic syndrome (MDS), or present as a secondary leukemia resulting from treatment with prior chemotherapy or radiation for an earlier malignancy. These forms of AML are notoriously less responsive to chemotherapy and thus have a lower CR rate and EFS.20... [Pg.1410]

Stem cells give rise to committed progenitors 504 Lessons from the hematopoietic stem cell 505 Bone marrow stem cells may not be restricted to the blood cell lineage 506... [Pg.503]

Symptoms Erythema, Blisters, Irritation of the Eyes, Cough, Dyspnea, Asymtomatic Latent Period (hours). Also, mild upper respiratory signs to marked airway damage, GI effects and bone marrow stem cell suppression possible. Mustard is a blister agent that affects the eyes, lungs, and skin. A person exposed to mustard will feel very little pain and... [Pg.255]

Marker Studies. Cells (e.g., bone marrow, stem cells) transduced with a vector expressing a marker or reporter gene used to distinguish it from other similar host tissues. [Pg.65]

Although research into stem cells is new, the use of stem cells for therapy has been with us for some time. Most of us are familiar with bone marrow transplant for patients with leukemia. This procedure involves finding a matching donor to harvest bone marrow stem cells and transfuse them into the patient with leukemia (see Exhibit 4.16 for details). [Pg.128]

Bone marrow is the spongy tissue inside the cavities of our bones. Bone marrow stem cells grow and divide into the various types of blood cells white blood cells (leukocytes) that fight infection, red blood cells (erythrocytes) that transport oxygen, and platelets that are the agents for clotting. [Pg.129]

The aim of a bone marrow transplant is to replace the abnormal bone marrow stem cells with healthy stem cells from a donor. Healthy stem cells are normally harvested using a syringe to withdraw bone marrow from the rear hip bone of the donor. They are then infused into the patient via a catheter in the chest area. Before the infusion, the patient receives chemotherapy or radiotherapy to destroy the diseased bone marrow stem cells so that the infused stem cells have a chance to grow free of complications from diseased cells. [Pg.129]

Autologous Transplant The patient donates his or her own bone marrow or stem cells before treatment, for reinfusion later. This happens when a patient is receiving radiotherapy or chemotherapy in such a high dose that the bone marrow is destroyed. The bone marrow stem cells collected previously are reinjected into the patient to reinforce the immune system. [Pg.129]

In somatic cell gene therapy, a DNA sequence is inserted into a somatic cell to correct a mutation. Cells may be removed from the patient for manipulation and subsequent reinsertion (ex vivo therapy), or they may be manipulated without removal fi om the patient (in vivo therapy). Ideally, cells with a very long life span (e.g., bone marrow stem cells) are treated, but other cells (e.g., lymphocytes) are sometimes more practical targets. [Pg.349]

In the attempt to explain the events observed, it was supposed that the reason for above has been the exhaustion of proliferative potential of hemopoietic stem cells, so called the Hayflick s limit, observed previously for the cells, proliferating in vitro (Hayflick and Moorhead, 1961 Hayflick, 1965). However, approximately at the same time it was shown, that due to successive transfers of bone marrow stem cells to lethally irradiated young recipients (mice) the proper life span of bone marrow derived stem cells exceeds at least 3 to 4 times the maximal life span of their hosts. It seems that extinction of these... [Pg.78]

Orlic, D. (2003). Adult bone marrow stem cells regenerate myocardium in ischemic heart disease. Ann N Y Acad Sci. 996, 152-157. [Pg.122]

In practical veterinary the SC can be used in substitution therapy in case of different pathologies. The methods of making 3-D cell construction have been already invented and are applied for the substitution of large bone, skin, and cartilage defects. The transplantation of bone marrow stem cells is used in the case of animal oncology diseases. The methods of cell therapy with the usage of SC are approbated in the treatment of autoimmune and endocrine diseases of domestic animals. [Pg.219]

The inhibitors available for human use, azacitidine and decitabine, have been approved for the treatment of myelodysplastic syndrome (MDS) [98, 99[. MDS summarizes a set of different conditions that affect the maturation of blood cells. It is a group of bone marrow stem cell malignancies that have a pathogenetic overlap with acute myeloid leukemia, show peripheral blood cytopenias and, in more advanced subtypes, varied degrees of maturation arrest [100]. Both drugs are approved for all subtypes of MDS. Response rates are usually around 30%. The question whether the clinical benefit results more from epigenetic effects and re-activation of silenced maturation factors or more from cytotoxic effects on the immature hyperproliferative cells remains open. [Pg.175]

Bone marrow stem cells are aspirated from the patient s iliac crest under local anesthesia. The... [Pg.97]

Outside the AMI setting, stem cells have been used to treat patients with ischemic heart disease with or without systolic functional compromise and patients unsuitable for myocardial revascularization (Tables 7.3 and 7.4). Autologous bone marrow stem cells have been used to treat patients with chronic myocardial ischemia, including ischemic heart failure with or without systolic functional compromise, and patients ineligible for myocardial revascularization (Table 7.4). The preliminary clinical evidence supports the efficacy of this new therapy and, at this point, all the evidence appears to substantiate its safety. [Pg.114]

The transdifferentiation of HSCs into a mature hematopoietic fate (e.g., endothelium) in the heart is less controversial [148]. In animal models of stem cell therapy in ischemic heart disease, the evidence points toward increased neovascularization (with reduced myocardial ischemia) and consequent improvement in cardiac function [149-151]. Bone marrow stem cells may directly contribute to an increase in contractility or, more likely, may passively limit infarct expansion and remodeling. Unfortunately, the limitations of the present animal models leave this question unanswered. [Pg.118]

Another potential deleterious effect of bone marrow stem cell therapy is myocardial calcification. In a recent study, Yoon et al. [155] noted that direct transplantation of unselected bone marrow cells into acutely infarcted myocardium could induce significant intramyocardial calcification. In the same study, however, ABMMNCs did not. [Pg.121]

C, Nienaber CA, Freund M, Steinhoff G. CABG and bone marrow stem cell transplantation after myocardial infarction. Thorac Cardiovasc Surg 2QQA 52 152-158. [Pg.126]

Kudo M, Wang Y, Wani MA, Xu M, Ayub A, Ashraf M. Implantation of bone marrow stem cells reduces the infarction and fibrosis in ischemic mouse heart. J Mol Cell Cardiol 2003 35 1113-1119. [Pg.127]

Thomsen BJ, Schroder H, Kristinsson J et al. Possible carcinogenic effect of 6-mercaptopurine on bone marrow stem cells relation to thiopurine metabolism. Cancer 1999 86 1080-1086. [Pg.201]

Hirashima, K.. Bessho, M., Hayata, I., Nara, N., Kawase, Y, and Ohtani, M. (1982). Thmsformation of bone marrow stem cells and radiation induced myeloid leukemia in mice, page 85 in Proceedings of the workshop on... [Pg.140]


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See also in sourсe #XX -- [ Pg.439 ]

See also in sourсe #XX -- [ Pg.298 ]




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