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Wyszukujesz frazę ""B-Lymphocytes"" wg kryterium: Wszystkie pola


Tytuł:
Characterization of the alternative splicing landscape in lung adenocarcinoma reveals novel prognosis signature associated with B cells.
Autorzy:
Shao MM; Department of Respiratory and Critical Care Medicine, Beijing Institute of Respiratory Medicine and Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.
Zhai K; Department of Respiratory and Critical Care Medicine, Beijing Institute of Respiratory Medicine and Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.
Huang ZY; Department of Respiratory and Critical Care Medicine, Beijing Institute of Respiratory Medicine and Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.
Yi FS; Department of Respiratory and Critical Care Medicine, Beijing Institute of Respiratory Medicine and Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.
Zheng SC; Department of Respiratory and Critical Care Medicine, Beijing Institute of Respiratory Medicine and Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.
Liu YL; Department of Respiratory and Critical Care Medicine, Beijing Institute of Respiratory Medicine and Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.
Qiao X; Department of Respiratory and Critical Care Medicine, Beijing Institute of Respiratory Medicine and Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.
Chen QY; Department of Respiratory and Critical Care Medicine, Beijing Institute of Respiratory Medicine and Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.
Wang Z; Department of Respiratory and Critical Care Medicine, Beijing Institute of Respiratory Medicine and Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.
Shi HZ; Department of Respiratory and Critical Care Medicine, Beijing Institute of Respiratory Medicine and Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.
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Źródło:
PloS one [PLoS One] 2023 Jul 11; Vol. 18 (7), pp. e0279018. Date of Electronic Publication: 2023 Jul 11 (Print Publication: 2023).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Adenocarcinoma of Lung*/genetics
Lung Neoplasms*/genetics
Pleural Effusion, Malignant*
B-Lymphocytes, Regulatory*
Neoplasms, Second Primary*
Humans ; Alternative Splicing ; Prognosis ; Tumor Microenvironment/genetics
Czasopismo naukowe
Tytuł:
Canine peripheral blood mononuclear cell-derived B lymphocytes pretreated with lipopolysaccharide enhance the immunomodulatory effect through macrophage polarization.
Autorzy:
Jang HW; Laboratory of Veterinary Internal Medicine, Department of Veterinary Clinical Science, College of Veterinary Medicine, Seoul National University, Seoul, Republic of Korea.
An JH; Laboratory of Veterinary Internal Medicine, Department of Veterinary Clinical Science, College of Veterinary Medicine, Seoul National University, Seoul, Republic of Korea.
Kim KB; Laboratory of Veterinary Internal Medicine, Department of Veterinary Clinical Science, College of Veterinary Medicine, Seoul National University, Seoul, Republic of Korea.
Lee JH; Laboratory of Veterinary Internal Medicine, Department of Veterinary Clinical Science, College of Veterinary Medicine, Seoul National University, Seoul, Republic of Korea.
Oh YI; Laboratory of Veterinary Internal Medicine, Department of Veterinary Clinical Science, College of Veterinary Medicine, Seoul National University, Seoul, Republic of Korea.
Park SM; Laboratory of Veterinary Internal Medicine, Department of Veterinary Clinical Science, College of Veterinary Medicine, Seoul National University, Seoul, Republic of Korea.
Chae HK; Laboratory of Veterinary Internal Medicine, Department of Veterinary Clinical Science, College of Veterinary Medicine, Seoul National University, Seoul, Republic of Korea.
Youn HY; Laboratory of Veterinary Internal Medicine, Department of Veterinary Clinical Science, College of Veterinary Medicine, Seoul National University, Seoul, Republic of Korea.
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Źródło:
PloS one [PLoS One] 2021 Nov 22; Vol. 16 (11), pp. e0256651. Date of Electronic Publication: 2021 Nov 22 (Print Publication: 2021).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
B-Lymphocytes/*drug effects
Cell Polarity/*drug effects
Immunomodulation/*drug effects
Leukocytes, Mononuclear/*drug effects
Lipopolysaccharides/*pharmacology
Macrophages/*drug effects
Animals ; B-Lymphocytes/cytology ; Dogs ; Leukocytes, Mononuclear/cytology ; Macrophage Activation/drug effects ; Macrophages/cytology
Czasopismo naukowe
Tytuł:
Establishment and characterization of HBV-associated B lymphocytes with an immortalization potential.
Autorzy:
Qi X; Department of Infectious Diseases, Zhongnan Hospital of Wuhan University, Wuhan, Hubei province, China.
Gui X; Department of Infectious Diseases, Zhongnan Hospital of Wuhan University, Wuhan, Hubei province, China.
Zhuang K; ABSL-III Laboratory at the Center for Animal Experiment, State Key Laboratory of Virology, Wuhan University, Wuhan, Hubei province, China.
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Źródło:
PloS one [PLoS One] 2019 May 23; Vol. 14 (5), pp. e0217161. Date of Electronic Publication: 2019 May 23 (Print Publication: 2019).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
B-Lymphocytes/*pathology
Hepatitis B/*epidemiology
Hepatitis B virus/*isolation & purification
Lymphoma, B-Cell/*complications
Adult ; Aged ; Aged, 80 and over ; B-Lymphocytes/virology ; Case-Control Studies ; Cell Culture Techniques ; Cell Transformation, Viral ; Cells, Cultured ; China/epidemiology ; Clone Cells ; Female ; Hepatitis B/transmission ; Humans ; Lymphoma, B-Cell/virology ; Male ; Middle Aged ; Prevalence ; Retrospective Studies ; Young Adult
Czasopismo naukowe
Tytuł:
A B-cell developmental gene regulatory network is activated in infant AML.
Autorzy:
Bolouri H; Center for Systems Immunology, Benaroya Research Institute, Seattle, WA, United States of America.
Ries R; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, United States of America.
Pardo L; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, United States of America.; Hematologics Inc., Seattle, WA, United States of America.
Hylkema T; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, United States of America.
Zhou W; Van Andel Research Institute, Grand Rapids, MI, United States of America.
Smith JL; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, United States of America.
Leonti A; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, United States of America.
Loken M; Hematologics Inc., Seattle, WA, United States of America.
Farrar JE; Arkansas Children's Research Institute and University of Arkansas for Medical Sciences, Little Rock, AR, United States of America.
Triche TJ Jr; Van Andel Research Institute, Grand Rapids, MI, United States of America.
Meshinchi S; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, United States of America.
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Źródło:
PloS one [PLoS One] 2021 Nov 18; Vol. 16 (11), pp. e0259197. Date of Electronic Publication: 2021 Nov 18 (Print Publication: 2021).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
B-Lymphocytes/*metabolism
Gene Regulatory Networks/*genetics
Leukemia, Myeloid, Acute/*diagnosis
B-Lymphocytes/cytology ; B-Lymphocytes/immunology ; Cell Cycle Proteins/genetics ; DNA Methylation ; Humans ; Infant ; Leukemia, Myeloid, Acute/genetics ; MicroRNAs/metabolism ; RNA, Messenger/metabolism ; RNA-Binding Proteins/genetics ; Trans-Activators/genetics ; Transcription Factors/genetics ; Up-Regulation
Czasopismo naukowe
Tytuł:
Characterization of microRNA expression in B cells derived from Japanese black cattle naturally infected with bovine leukemia virus by deep sequencing.
Autorzy:
Ochiai C; Cooperative Department of Veterinary Medicine, Faculty of Agriculture, Iwate University, Morioka, Iwate, Japan.
Miyauchi S; Cooperative Department of Veterinary Medicine, Faculty of Agriculture, Iwate University, Morioka, Iwate, Japan.
Kudo Y; Cooperative Department of Veterinary Medicine, Faculty of Agriculture, Iwate University, Morioka, Iwate, Japan.
Naruke Y; Cooperative Department of Veterinary Medicine, Faculty of Agriculture, Iwate University, Morioka, Iwate, Japan.
Yoneyama S; Graduate School of Veterinary Sciences, Iwate University, Morioka, Iwate, Japan.
Tomita K; Graduate School of Veterinary Sciences, Iwate University, Morioka, Iwate, Japan.
Dongze L; Graduate School of Veterinary Sciences, Iwate University, Morioka, Iwate, Japan.
Chiba Y; Graduate School of Veterinary Sciences, Iwate University, Morioka, Iwate, Japan.
Hirata TI; Field Science Center, Faculty of Agriculture, Iwate University, Shizukuishi, Iwate, Japan.
Ichijo T; Cooperative Department of Veterinary Medicine, Faculty of Agriculture, Iwate University, Morioka, Iwate, Japan.
Nagai K; Cooperative Department of Veterinary Medicine, Faculty of Agriculture, Iwate University, Morioka, Iwate, Japan.
Kobayashi S; Division of Bacterial and Parasitic Disease, National Institute of Animal Health, Tsukuba, Ibaraki, Japan.
Yamada S; Cooperative Department of Veterinary Medicine, Faculty of Agriculture, Iwate University, Morioka, Iwate, Japan.; Graduate School of Veterinary Sciences, Iwate University, Morioka, Iwate, Japan.
Hikono H; Department of Animal Sciences, Teikyo University of Science, Adachi, Tokyo, Japan.
Murakami K; Cooperative Department of Veterinary Medicine, Faculty of Agriculture, Iwate University, Morioka, Iwate, Japan.; Graduate School of Veterinary Sciences, Iwate University, Morioka, Iwate, Japan.
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Źródło:
PloS one [PLoS One] 2021 Sep 10; Vol. 16 (9), pp. e0256588. Date of Electronic Publication: 2021 Sep 10 (Print Publication: 2021).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
B-Lymphocytes/*metabolism
Enzootic Bovine Leukosis/*metabolism
Leukemia Virus, Bovine/*isolation & purification
MicroRNAs/*metabolism
Animals ; B-Lymphocytes/cytology ; Cattle ; Proviruses/isolation & purification ; Viral Load
Czasopismo naukowe
Tytuł:
IL-7 treatment augments and prolongs sepsis-induced expansion of IL-10-producing B lymphocytes and myeloid-derived suppressor cells.
Autorzy:
Kulkarni U; Institute of Immunology, Jena University Hospital, Jena, Germany.
Herrmenau C; Institute of Immunology, Jena University Hospital, Jena, Germany.
Win SJ; Institute of Immunology, Jena University Hospital, Jena, Germany.
Bauer M; Department of Anesthesiology and Intensive Care Medicine, Jena University Hospital, Jena, Germany.; Center for Sepsis Control & Care, Jena University Hospital, Jena, Germany.
Kamradt T; Institute of Immunology, Jena University Hospital, Jena, Germany.
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Źródło:
PloS one [PLoS One] 2018 Feb 21; Vol. 13 (2), pp. e0192304. Date of Electronic Publication: 2018 Feb 21 (Print Publication: 2018).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
B-Lymphocytes/*drug effects
Interleukin-10/*biosynthesis
Interleukin-7/*pharmacology
Myeloid-Derived Suppressor Cells/*immunology
Sepsis/*pathology
Animals ; Antigens, CD/immunology ; B-Lymphocytes/immunology ; Flow Cytometry ; Mice ; Mice, Inbred C57BL ; Sepsis/immunology ; T-Lymphocytes, Regulatory/immunology
Czasopismo naukowe
Tytuł:
BCR activated CLL B cells use both CR3 (CD11b/CD18) and CR4 (CD11c/CD18) for adhesion while CR4 has a dominant role in migration towards SDF-1.
Autorzy:
Nagy-Baló Z; Department of Immunology, Eötvös Loránd University, Budapest, Hungary.; MTA-ELTE Immunology Research Group, Eötvös Loránd University, Budapest, Hungary.
Kiss R; MTA-SE Momentum Molecular Oncohematology Research Group, First Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.
Demeter J; Department of Internal Medicine and Oncology, Semmelweis University, Budapest, Hungary.
Bödör C; MTA-SE Momentum Molecular Oncohematology Research Group, First Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.
Bajtay Z; Department of Immunology, Eötvös Loránd University, Budapest, Hungary.; MTA-ELTE Immunology Research Group, Eötvös Loránd University, Budapest, Hungary.
Erdei A; Department of Immunology, Eötvös Loránd University, Budapest, Hungary.; MTA-ELTE Immunology Research Group, Eötvös Loránd University, Budapest, Hungary.
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Źródło:
PloS one [PLoS One] 2021 Jul 20; Vol. 16 (7), pp. e0254853. Date of Electronic Publication: 2021 Jul 20 (Print Publication: 2021).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
B-Lymphocytes/*metabolism
CD11b Antigen/*metabolism
CD11c Antigen/*metabolism
Aged ; B-Lymphocytes/immunology ; CD11b Antigen/immunology ; CD11c Antigen/immunology ; CD18 Antigens/metabolism ; Cell Adhesion/immunology ; Cell Movement/physiology ; Chemokine CXCL12/metabolism ; Female ; Fibrinogen/metabolism ; Humans ; Integrin alphaXbeta2 ; Leukemia, Lymphocytic, Chronic, B-Cell/immunology ; Leukemia, Lymphocytic, Chronic, B-Cell/metabolism ; Macrophage-1 Antigen/metabolism ; Macrophages/metabolism ; Male ; Middle Aged ; Phagocytosis
Czasopismo naukowe
Tytuł:
CD200R1 and CD200R1L expression is regulated during B cell development in swine and modulates the Ig production in response to the TLR7 ligand imiquimoid.
Autorzy:
Poderoso T; Departamento de Biotecnología, Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA), Madrid, Spain.
De la Riva PM; Departamento de Biotecnología, Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA), Madrid, Spain.
Álvarez B; Departamento de Biotecnología, Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA), Madrid, Spain.
Ezquerra Á; Departamento de Biotecnología, Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA), Madrid, Spain.
Domínguez J; Departamento de Biotecnología, Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA), Madrid, Spain.
Revilla C; Departamento de Biotecnología, Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA), Madrid, Spain.
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Źródło:
PloS one [PLoS One] 2021 May 07; Vol. 16 (5), pp. e0251187. Date of Electronic Publication: 2021 May 07 (Print Publication: 2021).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
B-Lymphocytes/*metabolism
Imiquimod/*pharmacology
Immunoglobulins/*metabolism
Orexin Receptors/*metabolism
Animals ; B-Lymphocytes/drug effects ; Cell Differentiation/drug effects ; Female ; Leukocytes, Mononuclear/metabolism ; Lymphocyte Activation/drug effects ; Swine
Czasopismo naukowe
Tytuł:
High SLC2A1 expression associated with suppressing CD8 T cells and B cells promoted cancer survival in gastric cancer.
Autorzy:
Min KW; Department of Pathology, Hanyang University Guri Hospital, Hanyang University College of Medicine, Guri, Gyeonggi-do, Republic of Korea.
Kim DH; Department of Pathology, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
Son BK; Department of Internal Medicine, Eulji Hospital, Eulji University School of Medicine, Seoul, Republic of Korea.
Moon KM; Department of Internal Medicine, Gangneung Asan Hospital, University of Ulsan College of Medicine, Gangneung, Gangwon-do, Republic of Korea.
Kim SM; Department of Pharmacology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Intazur Rahaman M; Department of Pharmacology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Kim SW; Department of Pharmacology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Kim EK; Department of Pathology, Eulji Hospital, Eulji University School of Medicine, Seoul, Republic of Korea.
Kwon MJ; Department of Pathology, Hallym University Sacred Heart Hospital, Hallym University College of Medicine, Anyang, Gyeonggi-do, Republic of Korea.
Koh YW; Department of Pathology, Ajou University School of Medicine, Suwon, Gyeonggi-do, Republic of Korea.
Oh IH; Department of Internal Medicine, Eulji Hospital, Eulji University School of Medicine, Seoul, Republic of Korea.
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Źródło:
PloS one [PLoS One] 2021 Mar 18; Vol. 16 (3), pp. e0245075. Date of Electronic Publication: 2021 Mar 18 (Print Publication: 2021).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
B-Lymphocytes/*metabolism
CD8-Positive T-Lymphocytes/*metabolism
Glucose Transporter Type 1/*metabolism
Stomach Neoplasms/*pathology
Aged ; Antineoplastic Agents/pharmacology ; Antineoplastic Agents/therapeutic use ; B-Lymphocytes/cytology ; B-Lymphocytes/immunology ; CD8-Positive T-Lymphocytes/cytology ; CD8-Positive T-Lymphocytes/immunology ; Cell Line, Tumor ; Cell Proliferation/drug effects ; DNA Copy Number Variations ; Disease-Free Survival ; Down-Regulation/drug effects ; Female ; Glucose Transporter Type 1/genetics ; Humans ; Male ; Middle Aged ; Mutation ; Prognosis ; Signal Transduction/drug effects ; Stomach Neoplasms/drug therapy ; Stomach Neoplasms/metabolism ; Stomach Neoplasms/mortality ; Survival Rate ; Tretinoin/pharmacology ; Tretinoin/therapeutic use
Czasopismo naukowe
Tytuł:
B cell and monocyte phenotyping: A quick asset to investigate the immune status in patients with IgA nephropathy.
Autorzy:
Sendic S; Division of Nephrology, Department of Clinical Sciences, Karolinska Institutet, Danderyd Hospital, Stockholm, Sweden.
Mansouri L; Karolinska Institutet, Clinical Science and Education, Södersjukhuset, Stockholm, Sweden.
Lundberg S; Division of Nephrology, Department of Clinical Sciences, Karolinska Institutet, Danderyd Hospital, Stockholm, Sweden.
Nopp A; Karolinska Institutet, Clinical Science and Education, Södersjukhuset, Stockholm, Sweden.
Jacobson SH; Division of Nephrology, Department of Clinical Sciences, Karolinska Institutet, Danderyd Hospital, Stockholm, Sweden.
Lundahl J; Karolinska Institutet, Clinical Science and Education, Södersjukhuset, Stockholm, Sweden.
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Źródło:
PloS one [PLoS One] 2021 Mar 19; Vol. 16 (3), pp. e0248056. Date of Electronic Publication: 2021 Mar 19 (Print Publication: 2021).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
B-Lymphocytes/*immunology
Glomerulonephritis, IGA/*immunology
Monocytes/*immunology
Adult ; B-Lymphocytes/metabolism ; Cross-Sectional Studies ; Cytokines/blood ; Female ; Glomerulonephritis, IGA/blood ; Humans ; Immunophenotyping ; Leukocytes, Mononuclear/immunology ; Leukocytes, Mononuclear/metabolism ; Male ; Middle Aged ; Monocytes/metabolism
Czasopismo naukowe
Tytuł:
The anti-arthritis effect of sulforaphane, an activator of Nrf2, is associated with inhibition of both B cell differentiation and the production of inflammatory cytokines.
Autorzy:
Moon SJ; Division of Rheumatology, Department of Internal Medicine, Uijeongbu St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Uijeongbu, South Korea.
Jhun J; The Rheumatism Research Center, Catholic Research Institute of Medical Science, The Catholic University of Korea, Seoul, South Korea.
Ryu J; The Rheumatism Research Center, Catholic Research Institute of Medical Science, The Catholic University of Korea, Seoul, South Korea.
Kwon JY; The Rheumatism Research Center, Catholic Research Institute of Medical Science, The Catholic University of Korea, Seoul, South Korea.
Kim SY; The Rheumatism Research Center, Catholic Research Institute of Medical Science, The Catholic University of Korea, Seoul, South Korea.
Jung K; Impact Biotech, Seoul, South Korea.
Cho ML; The Rheumatism Research Center, Catholic Research Institute of Medical Science, The Catholic University of Korea, Seoul, South Korea.; Impact Biotech, Seoul, South Korea.; Laboratory of Immune Network, Conversant Research Consortium in Immunologic Disease, College of Medicine, The Catholic University of Korea, Seoul, South Korea.
Min JK; Department of Internal Medicine, and the Clinical Medicine Research Institute of Bucheon St. Mary's Hospital, Bucheon-si, South Korea.
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Źródło:
PloS one [PLoS One] 2021 Feb 16; Vol. 16 (2), pp. e0245986. Date of Electronic Publication: 2021 Feb 16 (Print Publication: 2021).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Arthritis, Rheumatoid/*drug therapy
B-Lymphocytes/*drug effects
Cell Differentiation/*drug effects
Cytokines/*biosynthesis
Isothiocyanates/*pharmacology
NF-E2-Related Factor 2/*metabolism
Sulfoxides/*pharmacology
Animals ; Arthritis, Rheumatoid/immunology ; Arthritis, Rheumatoid/metabolism ; B-Lymphocytes/pathology ; Cytokines/metabolism ; Inflammation/metabolism ; Isothiocyanates/therapeutic use ; Leukocytes, Mononuclear/drug effects ; Leukocytes, Mononuclear/metabolism ; Male ; Mice ; Sulfoxides/therapeutic use
Czasopismo naukowe
Tytuł:
Deficiency in Cardiolipin Reduces Doxorubicin-Induced Oxidative Stress and Mitochondrial Damage in Human B-Lymphocytes.
Autorzy:
Aryal B; Laboratory of Applied Biochemistry, Division of Biotechnology Review and Research III, Office of Biotechnology Products, Office of Pharmaceutical Quality, Center for Drug Evaluation and Research, U.S. Food and Drug Administration, Silver Spring, Maryland, 20993, United States of America.
Rao VA; Laboratory of Applied Biochemistry, Division of Biotechnology Review and Research III, Office of Biotechnology Products, Office of Pharmaceutical Quality, Center for Drug Evaluation and Research, U.S. Food and Drug Administration, Silver Spring, Maryland, 20993, United States of America.
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Źródło:
PloS one [PLoS One] 2016 Jul 19; Vol. 11 (7), pp. e0158376. Date of Electronic Publication: 2016 Jul 19 (Print Publication: 2016).
Typ publikacji:
Journal Article
MeSH Terms:
Antibiotics, Antineoplastic/*pharmacology
B-Lymphocytes/*drug effects
Cardiolipins/*metabolism
Doxorubicin/*pharmacology
Oxidative Stress/*drug effects
Reactive Oxygen Species/*metabolism
Acyltransferases ; Animals ; B-Lymphocytes/metabolism ; B-Lymphocytes/pathology ; Barth Syndrome/metabolism ; Barth Syndrome/pathology ; Caspase 3/genetics ; Caspase 3/metabolism ; Cell Death/drug effects ; Cell Line ; Humans ; Lipid Peroxidation/drug effects ; Mitochondria/drug effects ; Mitochondria/metabolism ; Myocytes, Cardiac/cytology ; Myocytes, Cardiac/drug effects ; Myocytes, Cardiac/metabolism ; Primary Cell Culture ; Protective Factors ; Protein Carbonylation/drug effects ; RNA, Small Interfering/genetics ; RNA, Small Interfering/metabolism ; Rats ; Transcription Factors/antagonists & inhibitors ; Transcription Factors/genetics ; Transcription Factors/metabolism
Czasopismo naukowe
Tytuł:
B lymphocytes can be activated to act as antigen presenting cells to promote anti-tumor responses.
Autorzy:
Rossetti RAM; Department of Immunology, Instituto de Ciências Biomédicas, Universidade de São Paulo, São Paulo, Brazil.
Lorenzi NPC; Hospital Universitário, Universidade de São Paulo, São Paulo, Brazil.
Yokochi K; Hospital Universitário, Universidade de São Paulo, São Paulo, Brazil.
Rosa MBSF; Instituto do Câncer do Estado de São Paulo, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.
Benevides L; Department of Immunology and Biochemistry, Faculdade de Medicina de Ribeirao Preto, University of Sao Paulo, Ribeirão Preto, Brazil.
Margarido PFR; Hospital Universitário, Universidade de São Paulo, São Paulo, Brazil.
Baracat EC; Hospital Universitário, Universidade de São Paulo, São Paulo, Brazil.; Instituto do Câncer do Estado de São Paulo, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.
Carvalho JP; Instituto do Câncer do Estado de São Paulo, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.
Villa LL; Instituto do Câncer do Estado de São Paulo, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.; Instituto de Radiologia, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.
Lepique AP; Department of Immunology, Instituto de Ciências Biomédicas, Universidade de São Paulo, São Paulo, Brazil.
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Źródło:
PloS one [PLoS One] 2018 Jul 05; Vol. 13 (7), pp. e0199034. Date of Electronic Publication: 2018 Jul 05 (Print Publication: 2018).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
B-Lymphocytes/*immunology
CD40 Ligand/*administration & dosage
Interleukin-4/*administration & dosage
T-Lymphocytes/*immunology
Uterine Cervical Neoplasms/*immunology
Animals ; Antigen-Presenting Cells/immunology ; B7-1 Antigen/immunology ; B7-2 Antigen/immunology ; CD40 Antigens/immunology ; Dendritic Cells/immunology ; Female ; Homeodomain Proteins/immunology ; Humans ; Immunity, Cellular ; Immunotherapy ; Lymphocyte Activation/immunology ; Mice ; Uterine Cervical Neoplasms/pathology ; Uterine Cervical Neoplasms/therapy
Czasopismo naukowe
Tytuł:
Defective Autophagy, Mitochondrial Clearance and Lipophagy in Niemann-Pick Type B Lymphocytes.
Autorzy:
Canonico B; Department of Biomolecular Sciences, University of Urbino Carlo Bo, Urbino, Italy.
Cesarini E; Department of Biomolecular Sciences, University of Urbino Carlo Bo, Urbino, Italy.
Salucci S; Department of Biomolecular Sciences, University of Urbino Carlo Bo, Urbino, Italy.
Luchetti F; Department of Biomolecular Sciences, University of Urbino Carlo Bo, Urbino, Italy.
Falcieri E; Department of Biomolecular Sciences, University of Urbino Carlo Bo, Urbino, Italy.; IGM, CNR, Rizzoli Orthopaedic Institute, Bologna, Italy; Department of Biomolecular Sciences, University of Urbino Carlo Bo, Urbino, Italy.
Di Sario G; Department of Biomolecular Sciences, University of Urbino Carlo Bo, Urbino, Italy.
Palma F; Department of Biomolecular Sciences, University of Urbino Carlo Bo, Urbino, Italy.
Papa S; Department of Biomolecular Sciences, University of Urbino Carlo Bo, Urbino, Italy.
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Źródło:
PloS one [PLoS One] 2016 Oct 31; Vol. 11 (10), pp. e0165780. Date of Electronic Publication: 2016 Oct 31 (Print Publication: 2016).
Typ publikacji:
Journal Article
MeSH Terms:
Autophagy*
Lipid Metabolism*
B-Lymphocytes/*metabolism
Mitochondria/*metabolism
Niemann-Pick Diseases/*metabolism
B-Lymphocytes/ultrastructure ; Biomarkers ; Cell-Derived Microparticles/metabolism ; Endocytosis ; Exocytosis ; Extracellular Space/metabolism ; Flow Cytometry ; Humans ; Intracellular Space/metabolism ; Lysosomes/metabolism ; Mitochondria/ultrastructure ; Mitophagy ; Phagosomes
Czasopismo naukowe
Tytuł:
Rapid identification of anti-idiotypic mAbs with high affinity and diverse epitopes by rabbit single B-cell sorting-culture and cloning technology.
Autorzy:
Lin W; Department of Antibody Engineering, Genentech Inc., South San Francisco, CA, United States of America.
Liang WC; Department of Antibody Engineering, Genentech Inc., South San Francisco, CA, United States of America.
Nguy T; DevSci BioAnalytical Sciences, Genentech Inc., South San Francisco, CA, United States of America.
Maia M; DevSci BioAnalytical Sciences, Genentech Inc., South San Francisco, CA, United States of America.
Tyagi T; Department of Antibody Engineering, Genentech Inc., South San Francisco, CA, United States of America.
Chiu C; Department of Antibody Engineering, Genentech Inc., South San Francisco, CA, United States of America.
Hoi KH; Department of Antibody Engineering, Genentech Inc., South San Francisco, CA, United States of America.
Chen Y; Department of Antibody Engineering, Genentech Inc., South San Francisco, CA, United States of America.
Wu Y; Department of Antibody Engineering, Genentech Inc., South San Francisco, CA, United States of America.
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Źródło:
PloS one [PLoS One] 2020 Dec 21; Vol. 15 (12), pp. e0244158. Date of Electronic Publication: 2020 Dec 21 (Print Publication: 2020).
Typ publikacji:
Journal Article
MeSH Terms:
Antibody Affinity*
Antibodies, Anti-Idiotypic/*immunology
Antibodies, Monoclonal/*immunology
B-Lymphocytes/*immunology
Cell Separation/*methods
Epitopes/*immunology
Animals ; Antibodies, Anti-Idiotypic/genetics ; Antibodies, Monoclonal/genetics ; B-Lymphocytes/classification ; Cells, Cultured ; Cloning, Molecular/methods ; Epitopes/genetics ; Humans ; Immunoglobulin Variable Region/genetics ; Immunoglobulin Variable Region/immunology ; Rabbits
Czasopismo naukowe
Tytuł:
Trogocytosis with monocytes associated with increased α2,3 sialic acid expression on B cells during H5N1 influenza virus infection.
Autorzy:
Kongsomros S; Department of Microbiology, Faculty of Science, Mahidol University, Bangkok, Thailand.
Thanunchai M; Department of Clinical Pathology, Faculty of Medicine, Vajira Hospital, Navamindradhiraj University, Bangkok, Thailand.
Manopwisedjaroen S; Department of Microbiology, Faculty of Science, Mahidol University, Bangkok, Thailand.
Na-Ek P; School of Medicine, Walailak University, Thasala, Nakhon Si Thammarat, Thailand.
Wang SF; Department of Medical Laboratory Sciences and Biotechnology, College of Health Sciences, Kaohsiung Medical University, Kaohsiung City, Taiwan.
Taechalertpaisarn T; Department of Microbiology, Faculty of Science, Mahidol University, Bangkok, Thailand.
Thitithanyanont A; Department of Microbiology, Faculty of Science, Mahidol University, Bangkok, Thailand.
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Źródło:
PloS one [PLoS One] 2020 Sep 18; Vol. 15 (9), pp. e0239488. Date of Electronic Publication: 2020 Sep 18 (Print Publication: 2020).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
B-Lymphocytes/*immunology
B-Lymphocytes/*virology
Influenza A Virus, H5N1 Subtype/*immunology
Influenza A Virus, H5N1 Subtype/*pathogenicity
Influenza, Human/*immunology
Influenza, Human/*virology
Monocytes/*immunology
N-Acetylneuraminic Acid/*immunology
Animals ; Antigen Presentation ; B-Lymphocytes/metabolism ; Birds ; Cell Communication/immunology ; Coculture Techniques ; Humans ; Influenza in Birds/immunology ; Influenza in Birds/virology ; Monocytes/metabolism ; Monocytes/virology ; N-Acetylneuraminic Acid/metabolism ; Receptors, Virus/immunology ; Receptors, Virus/metabolism
Czasopismo naukowe
Tytuł:
A MALT1 inhibitor suppresses human myeloid DC, effector T-cell and B-cell responses and retains Th1/regulatory T-cell homeostasis.
Autorzy:
Dumont C; Research & Early Development, Respiratory, Inflammation & Autoimmune, R&D BioPharmaceuticals, AstraZeneca, Gothenburg, Sweden.
Sivars U; Research & Early Development, Respiratory, Inflammation & Autoimmune, R&D BioPharmaceuticals, AstraZeneca, Gothenburg, Sweden.
Andreasson T; Research & Early Development, Respiratory, Inflammation & Autoimmune, R&D BioPharmaceuticals, AstraZeneca, Gothenburg, Sweden.
Odqvist L; Research & Early Development, Respiratory, Inflammation & Autoimmune, R&D BioPharmaceuticals, AstraZeneca, Gothenburg, Sweden.
Mattsson J; Research & Early Development, Respiratory, Inflammation & Autoimmune, R&D BioPharmaceuticals, AstraZeneca, Gothenburg, Sweden.
DeMicco A; Research & Early Development, Respiratory, Inflammation & Autoimmune, R&D BioPharmaceuticals, AstraZeneca, Gothenburg, Sweden.
Pardali K; Research & Early Development, Respiratory, Inflammation & Autoimmune, R&D BioPharmaceuticals, AstraZeneca, Gothenburg, Sweden.
Johansson G; Research & Early Development, Respiratory, Inflammation & Autoimmune, R&D BioPharmaceuticals, AstraZeneca, Gothenburg, Sweden.
Yrlid L; Research & Early Development, Respiratory, Inflammation & Autoimmune, R&D BioPharmaceuticals, AstraZeneca, Gothenburg, Sweden.
Cox RJ; Research & Early Development, Respiratory, Inflammation & Autoimmune, R&D BioPharmaceuticals, AstraZeneca, Gothenburg, Sweden.
Seeliger F; Clinical Pharmacology & Safety Sciences, R&D BioPharmaceuticals Gothenburg, Sweden.
Larsson M; Clinical Pharmacology & Safety Sciences, R&D BioPharmaceuticals Gothenburg, Sweden.
Gehrmann U; Research & Early Development, Respiratory, Inflammation & Autoimmune, R&D BioPharmaceuticals, AstraZeneca, Gothenburg, Sweden.
Davis AM; Research & Early Development, Respiratory, Inflammation & Autoimmune, R&D BioPharmaceuticals, AstraZeneca, Gothenburg, Sweden.
Vaarala O; Research & Early Development, Respiratory, Inflammation & Autoimmune, R&D BioPharmaceuticals, AstraZeneca, Gothenburg, Sweden.
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Źródło:
PloS one [PLoS One] 2020 Sep 01; Vol. 15 (9), pp. e0222548. Date of Electronic Publication: 2020 Sep 01 (Print Publication: 2020).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
B-Lymphocytes/*drug effects
Dendritic Cells/*drug effects
Mucosa-Associated Lymphoid Tissue Lymphoma Translocation 1 Protein/*antagonists & inhibitors
Protease Inhibitors/*pharmacology
T-Lymphocytes, Cytotoxic/*drug effects
Allosteric Regulation/drug effects ; Animals ; B-Lymphocytes/immunology ; B-Lymphocytes/metabolism ; Cells, Cultured ; Dendritic Cells/immunology ; Female ; Fluorescence Resonance Energy Transfer ; Healthy Volunteers ; Humans ; Injections, Intraperitoneal ; Interferon-gamma/immunology ; Interferon-gamma/metabolism ; Lymphocyte Activation/drug effects ; Mice ; Mice, Knockout ; Mucosa-Associated Lymphoid Tissue Lymphoma Translocation 1 Protein/genetics ; Mucosa-Associated Lymphoid Tissue Lymphoma Translocation 1 Protein/immunology ; Mucosa-Associated Lymphoid Tissue Lymphoma Translocation 1 Protein/metabolism ; Phenothiazines/pharmacology ; Primary Cell Culture ; Signal Transduction/drug effects ; Signal Transduction/immunology ; T-Lymphocytes, Cytotoxic/immunology ; T-Lymphocytes, Cytotoxic/metabolism ; T-Lymphocytes, Regulatory/drug effects ; T-Lymphocytes, Regulatory/immunology ; T-Lymphocytes, Regulatory/metabolism ; Th1 Cells/drug effects ; Th1 Cells/immunology ; Th1 Cells/metabolism
Czasopismo naukowe
Tytuł:
Mycophenolic acid and 6-mercaptopurine both inhibit B-cell proliferation in granulomatosis with polyangiitis patients, whereas only mycophenolic acid inhibits B-cell IL-6 production.
Autorzy:
von Borstel A; Department of Internal Medicine, Division of Nephrology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
Abdulahad WH; Department of Rheumatology and Clinical Immunology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.; Department of Pathology and Medical Biology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
Dekkema G; Department of Pathology and Medical Biology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
Rutgers A; Department of Rheumatology and Clinical Immunology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
Stegeman CA; Department of Internal Medicine, Division of Nephrology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
Veldman J; Department of Pathology and Medical Biology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
Heeringa P; Department of Pathology and Medical Biology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
Sanders JS; Department of Internal Medicine, Division of Nephrology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
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Źródło:
PloS one [PLoS One] 2020 Jul 09; Vol. 15 (7), pp. e0235743. Date of Electronic Publication: 2020 Jul 09 (Print Publication: 2020).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Granulomatosis with Polyangiitis*/drug therapy
Granulomatosis with Polyangiitis*/immunology
B-Lymphocytes/*immunology
Immunosuppressive Agents/*pharmacology
Mycophenolic Acid/*pharmacology
Adult ; Aged ; Azathioprine/pharmacology ; B-Lymphocyte Subsets/immunology ; B-Lymphocytes/drug effects ; B-Lymphocytes/metabolism ; Cell Proliferation/drug effects ; Cytokines/metabolism ; Female ; Flow Cytometry ; Humans ; Interleukin-6/metabolism ; Male ; Mercaptopurine/pharmacology ; Middle Aged
Czasopismo naukowe
Tytuł:
ZBTB38 is dispensable for antibody responses.
Autorzy:
Wong R; Division of Biological and Biomedical Sciences, Washington University in St. Louis, Saint Louis, MO, United States of America.; Department of Immunobiology, University of Arizona, Tucson, AZ, United States of America.
Bhattacharya D; Department of Immunobiology, University of Arizona, Tucson, AZ, United States of America.
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Źródło:
PloS one [PLoS One] 2020 Sep 21; Vol. 15 (9), pp. e0235183. Date of Electronic Publication: 2020 Sep 21 (Print Publication: 2020).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms:
Antibody Formation*
B-Lymphocytes/*immunology
Repressor Proteins/*immunology
Animals ; B-Lymphocytes/cytology ; Gene Deletion ; Gene Expression ; Hematopoiesis ; Immunization ; Mice ; Mice, Knockout ; Repressor Proteins/genetics
Czasopismo naukowe
Tytuł:
Differential effects of disease modifying drugs on peripheral blood B cell subsets: A cross sectional study in multiple sclerosis patients treated with interferon-β, glatiramer acetate, dimethyl fumarate, fingolimod or natalizumab.
Autorzy:
Kemmerer CL; Department of Neurology & Stroke, and Hertie-Institute for Clinical Brain Research, Eberhard-Karls University of Tübingen, Tübingen, Germany.
Pernpeintner V; Department of Neurology, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Ruschil C; Department of Neurology & Stroke, and Hertie-Institute for Clinical Brain Research, Eberhard-Karls University of Tübingen, Tübingen, Germany.
Abdelhak A; Department of Neurology & Stroke, and Hertie-Institute for Clinical Brain Research, Eberhard-Karls University of Tübingen, Tübingen, Germany.
Scholl M; Department of Neurology & Stroke, and Hertie-Institute for Clinical Brain Research, Eberhard-Karls University of Tübingen, Tübingen, Germany.
Ziemann U; Department of Neurology & Stroke, and Hertie-Institute for Clinical Brain Research, Eberhard-Karls University of Tübingen, Tübingen, Germany.
Krumbholz M; Department of Neurology & Stroke, and Hertie-Institute for Clinical Brain Research, Eberhard-Karls University of Tübingen, Tübingen, Germany.
Hemmer B; Department of Neurology, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.; Munich Cluster for Systems Neurology (SyNergy), Munich, Germany.
Kowarik MC; Department of Neurology & Stroke, and Hertie-Institute for Clinical Brain Research, Eberhard-Karls University of Tübingen, Tübingen, Germany.; Department of Neurology, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
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Źródło:
PloS one [PLoS One] 2020 Jul 27; Vol. 15 (7), pp. e0235449. Date of Electronic Publication: 2020 Jul 27 (Print Publication: 2020).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
B-Lymphocyte Subsets/*drug effects
B-Lymphocytes/*drug effects
Immunologic Memory/*drug effects
Multiple Sclerosis/*drug therapy
Adult ; Aged ; Aged, 80 and over ; Antigens, CD/classification ; Antigens, CD/immunology ; Antigens, CD19 ; B-Lymphocyte Subsets/classification ; B-Lymphocyte Subsets/immunology ; B-Lymphocytes/immunology ; Cross-Sectional Studies ; Dimethyl Fumarate/administration & dosage ; Female ; Fingolimod Hydrochloride/administration & dosage ; Flow Cytometry ; Glatiramer Acetate/administration & dosage ; Humans ; Immunologic Memory/immunology ; Immunophenotyping ; Immunosuppressive Agents/administration & dosage ; Immunosuppressive Agents/immunology ; Interferon-beta/administration & dosage ; Male ; Middle Aged ; Multiple Sclerosis/blood ; Multiple Sclerosis/immunology ; Multiple Sclerosis/pathology ; Natalizumab/administration & dosage ; Young Adult
Czasopismo naukowe

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