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1. Full Text Human Leukocyte Antigen‐G5 Secretion by Human Mesenchymal Stem Cells Is Required to Suppress T Lymphocyte and Natural Killer Function and to Induce CD4+CD25highFOXP3+ Regulatory T Cells
by Selmani, Zohair and Naji, Abderrahim and Zidi, Ines and Favier, Benoit and Gaiffe, Emilie and Obert, Laurent and Borg, Christophe and Saas, Philippe and Tiberghien, Pierre and Rouas‐Freiss, Nathalie and Carosella, Edgardo D and Deschaseaux, Frederic
STEM CELLS, ISSN 1066-5099, 01/2008, Volume 26, Issue 1, pp. 212 - 222
Adult bone marrow‐derived mesenchymal stem cells (MSCs) are multipotent cells that are the subject of intense investigation in regenerative medicine. In... 
Immunosuppression | Regulatory T cells | Human leukocyte antigen‐G | Mesenchymal stem cells | Interleukin‐10 | Interleukin-10 | Human leukocyte antigen-G | T-Lymphocyte Subsets - immunology | T-Lymphocytes, Regulatory - metabolism | Humans | Adult Stem Cells - immunology | Lymphocyte Culture Test, Mixed | Mesenchymal Stromal Cells - immunology | T-Lymphocytes, Regulatory - immunology | Histocompatibility Antigens Class I - metabolism | Mesenchymal Stromal Cells - cytology | Flow Cytometry | Forkhead Transcription Factors - metabolism | Bone Marrow Cells - immunology | Killer Cells, Natural - immunology | T-Lymphocytes, Cytotoxic - immunology | Interferon-gamma | Adult Stem Cells - cytology | Enzyme-Linked Immunosorbent Assay | Bone Marrow Cells - cytology | Cell Communication | Mesenchymal Stromal Cells - metabolism | HLA-G Antigens | HLA Antigens - metabolism | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Microscopy, Confocal | Adult Stem Cells - metabolism | Interleukin-2 Receptor alpha Subunit - metabolism | T-Lymphocytes, Cytotoxic - metabolism | T-Lymphocyte Subsets - metabolism | Killer Cells, Natural - metabolism | Bone Marrow Cells - metabolism | CD4 Antigens - metabolism | T-Lymphocyte Subsets | Adult Stem Cells | Interleukin-2 Receptor alpha Subunit | Killer Cells, Natural | Antigens, CD4 | Histocompatibility Antigens Class I | T-Lymphocytes, Cytotoxic | Mesenchymal Stem Cells | Life Sciences | Bone Marrow Cells | Immunology | T-Lymphocytes, Regulatory | HLA Antigens | Forkhead Transcription Factors
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2. Full Text Mesenchymal Stem Cells Inhibit Generation and Function of Both CD34+-Derived and Monocyte-Derived Dendritic Cells
by Nauta, Alma J and Kruisselbrink, Alwine B and Lurvink, Ellie and Willemze, Roel and Fibbe, Willem E
The Journal of Immunology, ISSN 0022-1767, 08/2006, Volume 177, Issue 4, pp. 2080 - 2087
Mesenchymal stem cells (MSCs) are not only able to evade the immune system, but they have also been demonstrated to exert profound immunosuppressive properties... 
COLONY-STIMULATING-FACTOR | CORD-BLOOD DIFFERENTIATE | RESPONSES | CD34(+) HEMATOPOIETIC PROGENITORS | MACROPHAGES | BONE-MARROW | NECROSIS-FACTOR-ALPHA | PROLIFERATION | IMMUNOLOGY | MARROW STROMAL CELLS | T-CELLS | Mesenchymal Stem Cells - immunology | Cell Proliferation | Monocytes - cytology | Antigens, CD34 - biosynthesis | Dendritic Cells - immunology | Humans | Cells, Cultured | Immunophenotyping | Monocytes - immunology | Cell Differentiation - immunology | T-Lymphocytes - cytology | Adult | Fetus | T-Lymphocytes - immunology | Dendritic Cells - cytology | Dendritic Cells - metabolism
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3. Full Text Serial Transfer of Single-Cell-Derived Immunocompetence Reveals Stemness of CD8+ Central Memory T Cells
by Graef, Patricia and Buchholz, Veit R and Stemberger, Christian and Flossdorf, Michael and Henkel, Lynette and Schiemann, Matthias and Drexler, Ingo and Höfer, Thomas and Riddell, Stanley R and Busch, Dirk H
Immunity, ISSN 1074-7613, 07/2014, Volume 41, Issue 1, pp. 116 - 126
Maintenance of immunological memory has been proposed to rely on stem-cell-like lymphocytes. However, data supporting this hypothesis are focused on the... 
LISTERIA-MONOCYTOGENES | EFFECTOR | ADOPTIVE TRANSFER | SELF-RENEWAL | DIFFERENTIATION | IMMUNOLOGY | NAIVE | CYTOMEGALOVIRUS | RECONSTITUTION | CD8-ALPHA(+) DENDRITIC CELLS | COLONY-FORMING CELLS | T-Lymphocyte Subsets - immunology | Immunotherapy, Adoptive | CD8-Positive T-Lymphocytes - transplantation | Mice, Inbred C57BL | Immunocompetence - immunology | Multipotent Stem Cells - immunology | Listeria monocytogenes - immunology | Adult Stem Cells - immunology | Mice, Knockout | Cell Differentiation - immunology | L-Selectin - immunology | Lymphocyte Activation - immunology | Animals | Listeriosis - immunology | Mice | CD8-Positive T-Lymphocytes - immunology | Immunologic Memory - immunology | Cell Lineage - immunology | Studies | Statistical analysis | Listeria | Lymphocytes | Stem cells | Bone marrow | T cell receptors | Infections | Experiments | Blood
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4. Full Text Feeder-Free Derivation of Induced Pluripotent Stem Cells from Adult Human Adipose Stem Cells
by Ning Sun and Nicholas J. Panetta and Deepak M. Gupta and Kitchener D. Wilson and Andrew Lee and Fangjun Jia and Shijun Hu and Athena M. Cherry and Robert C. Robbins and Michael T. Longaker and Joseph C. Wu and Mark M. Davis
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 9/2009, Volume 106, Issue 37, pp. 15720 - 15725
Ectopic expression of transcription factors can reprogram somatic cells to a pluripotent state. However, most of the studies used skin fibroblasts as the... 
Feeder cells | Induced pluripotent stem cells | Somatic cells | Cell lines | Multipotent stem cells | Stem cells | Fibroblasts | Adults | Pluripotent stem cells | Mesenchymal stem cells | Differentiation | Pluripotency | Reprogramming | reprogramming | differentiation | KRUPPEL-LIKE FACTOR-5 | MULTIDISCIPLINARY SCIENCES | MOUSE | HUMAN FIBROBLASTS | GENERATION | pluripotency | INDUCTION | HUMAN SOMATIC-CELLS | Cell Line | Adult Stem Cells - cytology | Gene Expression | Cell Dedifferentiation - physiology | Pluripotent Stem Cells - cytology | Pluripotent Stem Cells - immunology | Humans | Middle Aged | Alkaline Phosphatase - metabolism | Proteoglycans - metabolism | Adipocytes - cytology | Cell Separation - methods | Cell Culture Techniques - methods | Adult Stem Cells - immunology | Antigens, CD - metabolism | Pluripotent Stem Cells - metabolism | Adult Stem Cells - metabolism | Adipocytes - metabolism | Antigens, Surface - metabolism | Adult | Aged | Cell Dedifferentiation - immunology | Cell Dedifferentiation - genetics | Adipocytes - immunology | Physiological aspects | Transcription factors | Genetic aspects | Research
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5. Full Text In Vitro Expansion of Human Gastric Epithelial Stem Cells and Their Responses to Bacterial Infection
by Bartfeld, Sina and Bayram, Tülay and van de Wetering, Marc and Huch, Meritxell and Begthel, Harry and Kujala, Pekka and Vries, Robert and Peters, Peter J and Clevers, Hans
Gastroenterology, ISSN 0016-5085, 2015, Volume 148, Issue 1, pp. 126 - 136.e6
Background & Aims We previously established long-term, 3-dimensional culture of organoids from mouse tissues (intestine, stomach, pancreas, and liver) and... 
Gastroenterology and Hepatology | Stomach Cancer | Gastric Epithelium | Primary Cells | Tissue Engineering | Cell Proliferation | Biological Markers | Humans | Middle Aged | Male | Wnt Proteins | Helicobacter Infections | Stem Cells | Helicobacter pylori | Organoids | Time Factors | Aged, 80 and over | Adult | Female | Cell Culture Techniques | Niacinamide | Stomach | Cell Separation | Cells, Cultured | Gene Expression Regulation | Epithelial Cells | Cell Lineage | Phenotype | Ploidies | Aged | PROGENITOR CELLS | HOMEOSTASIS | PATHOGENICITY ISLAND | BETA-CATENIN | IDENTIFICATION | CANCER | STOMACH EPITHELIUM | DISEASE | INTESTINAL CRYPT | HELICOBACTER-PYLORI-INFECTION | GASTROENTEROLOGY & HEPATOLOGY | Helicobacter pylori - immunology | Stem Cells - immunology | Epithelial Cells - metabolism | Stomach - immunology | Epithelial Cells - drug effects | Helicobacter pylori - pathogenicity | Stomach - metabolism | Stem Cells - metabolism | Wnt Proteins - metabolism | Helicobacter Infections - pathology | Stem Cells - microbiology | Helicobacter Infections - metabolism | Stomach - drug effects | Biomarkers - metabolism | Stomach - pathology | Epithelial Cells - pathology | Helicobacter Infections - immunology | Epithelial Cells - immunology | Epithelial Cells - microbiology | Stem Cells - drug effects | Stem Cells - pathology | Niacinamide - pharmacology | Stomach - microbiology | Helicobacter Infections - microbiology | Stem cell research | Bacterial infections | Developmental biology | Health aspects | Stem cells | gastric epithelium | tissue engineering | stomach cancer | primary cells
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6. Full Text A novel view of the adult bone marrow stem cell hierarchy and stem cell trafficking
by Ratajczak, M.Z
Leukemia, ISSN 0887-6924, 04/2015, Volume 29, Issue 4, pp. 776 - 782
This review presents a novel view and working hypothesis about the hierarchy within the adult bone marrow stem cell compartment and the still-intriguing... 
PROGENITOR CELLS | SDF-1 GRADIENT | HEMATOPOIETIC STEM/PROGENITOR CELLS | IN-VITRO | COMPLEMENT | ONCOLOGY | MOBILIZATION | GERM-CELLS | CORD BLOOD | REGENERATIVE MEDICINE | HEMATOLOGY | INNATE IMMUNITY | Gene Expression | Bone Marrow - immunology | Bone Marrow Cells - cytology | Humans | Hematopoietic Stem Cell Transplantation | Hematopoietic Stem Cells - metabolism | Bone Marrow Cells - classification | Hematopoietic Stem Cells - immunology | Chemokine CXCL12 - genetics | Bone Marrow - metabolism | Bone Marrow Cells - immunology | Hematopoietic Stem Cells - cytology | Adult | Complement System Proteins - genetics | Germ Cells - cytology | Germ Cells - metabolism | Hematopoietic Stem Cell Mobilization | Bone Marrow Cells - metabolism | Cell Lineage - genetics | Chemokine CXCL12 - immunology | Germ Cells - immunology | Cell Lineage - immunology | Cell Movement | Physiological aspects | Care and treatment | Genetic aspects | Research | Leukemia | Hematopoietic stem cells | Review
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7. Full Text T memory stem cells in health and disease
by Gattinoni, Luca and Speiser, Daniel E and Lichterfeld, Mathias and Bonini, Chiara
Nature Medicine, ISSN 1078-8956, 2017, Volume 23, Issue 1, pp. 18 - 27
T memory stem (TscM) cells are a rare subset of memory lymphocytes endowed with the stem cell like ability to self-renew and the multipotent capacity to... 
MEDICINE, RESEARCH & EXPERIMENTAL | LINEAGE RELATIONSHIP | BIOCHEMISTRY & MOLECULAR BIOLOGY | BONE-MARROW | SELF-RENEWAL | ANTIRETROVIRAL THERAPY | ANTITUMOR-ACTIVITY | HOMEOSTATIC PROLIFERATION | YELLOW-FEVER | CUTTING EDGE | CELL BIOLOGY | PROTECTIVE IMMUNITY | B-CELL | Cell Self Renewal - immunology | Stem Cells - immunology | Leukemia, T-Cell - immunology | Humans | Autoimmune Diseases - immunology | Adoptive Transfer | T-Lymphocytes - transplantation | HIV Infections - immunology | Animals | Autoimmune Diseases - therapy | HIV Infections - therapy | T-Lymphocytes - immunology | Cell Differentiation | Leukemia, T-Cell - therapy | Immunologic Memory - immunology | Medical research | Immune response | Stem cells | Medicine, Experimental | Research | T cells | Health aspects | Autoimmunity | Communicable diseases | Leukemia | B cells | HIV (Viruses) | Adult T cell leukemia | Immunological memory | Memory cells | Stem cell transplantation | Immune reconstitution | Lymphocytes T | Vaccines | Computer memory | Infectious diseases | Allografts | Lymphocytes | Human immunodeficiency virus--HIV | Primates | Autoimmune diseases | Cancer
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8. Full Text Why are MSCs therapeutic? New data: new insight
by Caplan, AI
The Journal of Pathology, ISSN 0022-3417, 01/2009, Volume 217, Issue 2, pp. 318 - 324
Adult marrow‐derived mesenchymal stem cells (MSCs) are able to differentiate into bone, cartilage, muscle, marrow stroma, tendon–ligament, fat and other... 
mesenchymal stem cell | therapeutics | CFU‐F | bone marrow | Mesenchymal stem cell | Bone marrow | CFU-F | Therapeutics | PROGENITOR CELLS | BONE-MARROW | HEMATOPOIETIC MICROENVIRONMENT | INFUSION | PATHOLOGY | MESENCHYMAL STEM-CELLS | ONCOLOGY | IN-VIVO | OSTEOGENESIS IMPERFECTA | SKELETAL MYOBLAST TRANSPLANTATION | EXPRESSION | MARROW STROMAL CELLS | Autoimmunity | Mesenchymal Stem Cells - immunology | Stem Cell Transplantation | Pericytes - immunology | Immune System - physiology | Stem Cell Niche | Pericytes - pathology | Humans | Adult | Adult Stem Cells - pathology | Adult Stem Cells - immunology | Mesenchymal Stem Cells - pathology
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9. Full Text Human adult stem cells derived from adipose tissue protect against experimental colitis and sepsis
by Gonzalez-Rey, E and Anderson, P and González, M A and Rico, L and Büscher, D and Delgado, M
Gut, ISSN 0017-5749, 07/2009, Volume 58, Issue 7, pp. 929 - 939
Background and aims:Inflammatory bowel diseases (IBDs) are associated with uncontrolled innate and adaptive immunity against normal constituents, including... 
INTESTINAL INFLAMMATION | RESPONSES | INFLAMMATORY-BOWEL-DISEASE | LYMPHOCYTE | IN-VIVO | REGULATORY T-CELLS | CD4(+) | DIFFERENTIATION | GASTROENTEROLOGY & HEPATOLOGY | VERSUS-HOST-DISEASE | INHIBIT | Sepsis - immunology | Endotoxemia - prevention & control | Down-Regulation | Humans | Inflammatory Bowel Diseases - immunology | Mice, Inbred C57BL | Cells, Cultured | Adipose Tissue - cytology | Colitis - surgery | Adult Stem Cells - immunology | Mesenchymal Stromal Cells - immunology | T-Lymphocytes, Regulatory - immunology | Animals | Inflammatory Bowel Diseases - surgery | Mice | Colitis - immunology | Mesenchymal Stem Cell Transplantation | Sepsis - surgery | Prevention | Inflammatory bowel diseases | Care and treatment | Usage | Animal models in research | Patient outcomes | Stem cells | Sepsis | Transplantation | Research | Antigens | Drinking water | Cytokines | Mortality | Inflammation | Molecular weight | Inflammatory bowel disease | Cell growth | Lymphocytes | Rodents | Colon | Laboratory animals | Chemokines
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