States News Service, 08/2018
Newspaper Article
States News Service, 10/2017
Newspaper Article
Journal of Infectious Diseases, ISSN 0022-1899, 06/2015, Volume 211, Issue 12, pp. 2014 - 2022
Background. We demonstrated previously that tumor necrosis factor a (TNF-alpha)- producing Chlamydia-specific CD8(+) T cells cause oviduct pathological...
Chlamydia | genital infection | CD8 | oviduct pathology | T cells | TNF receptor 2 | TNF receptor 1 | INFECTIOUS DISEASES | ALPHA | MICROBIOLOGY | IMMUNOLOGY | PATHOGENESIS | PROTECTIVE IMMUNITY | MODELS | UROGENITAL INFECTION | DEFICIENT | CD8(+) T cells | CHRONIC DISEASE MANIFESTATIONS | MICE | MURIDARUM INFECTION | CD8-Positive T-Lymphocytes - chemistry | Chlamydia Infections - pathology | Receptors, Tumor Necrosis Factor, Type II - analysis | Animals | Reproductive Tract Infections - pathology | Mice, Inbred C57BL | Female | Receptors, Tumor Necrosis Factor, Type I - analysis | Mice, Knockout | Chlamydia infections | Prevention | Genetically modified mice | Usage | Care and treatment | Tumor necrosis factor | Research | Major and Brief Reports | CD8+ T cells
Chlamydia | genital infection | CD8 | oviduct pathology | T cells | TNF receptor 2 | TNF receptor 1 | INFECTIOUS DISEASES | ALPHA | MICROBIOLOGY | IMMUNOLOGY | PATHOGENESIS | PROTECTIVE IMMUNITY | MODELS | UROGENITAL INFECTION | DEFICIENT | CD8(+) T cells | CHRONIC DISEASE MANIFESTATIONS | MICE | MURIDARUM INFECTION | CD8-Positive T-Lymphocytes - chemistry | Chlamydia Infections - pathology | Receptors, Tumor Necrosis Factor, Type II - analysis | Animals | Reproductive Tract Infections - pathology | Mice, Inbred C57BL | Female | Receptors, Tumor Necrosis Factor, Type I - analysis | Mice, Knockout | Chlamydia infections | Prevention | Genetically modified mice | Usage | Care and treatment | Tumor necrosis factor | Research | Major and Brief Reports | CD8+ T cells
Journal Article
Pharmaceutical Research, ISSN 0724-8741, 8/2018, Volume 35, Issue 8, pp. 1 - 8
The first CD19 CAR T-cell products, Kymriah and Yescarta, are entering the US market and also being evaluated for marketing authorization in the EU. This...
Biochemistry, general | Biomedical Engineering | T-cells | Biomedicine | Pharmacy | CAR T | antigen receptor | immunotherapy | Medical Law | genetic modification | Pharmacology/Toxicology | THERAPY | B-CELL | METABOLISM | KINETICS | PHARMACOLOGY & PHARMACY | LEUKEMIA | CHEMISTRY, MULTIDISCIPLINARY | Genetic Engineering - methods | Receptors, Chimeric Antigen - therapeutic use | Immunotherapy, Adoptive - methods | Neoplasms - therapy | Animals | Neoplasms - immunology | Humans | Receptors, Chimeric Antigen - immunology | Receptors, Chimeric Antigen - genetics | T-Lymphocytes - immunology | T-Lymphocytes - transplantation | Antigens | Care and treatment | Immunotherapy | Genetically modified organisms | Drug therapy | T cells | Cancer | CD19 antigen | Hematology | Toxicity | Medical services | T cell receptors | Lymphocytes T | Patients | Industrial development | Manufacturing | Solid tumors | Genetic modification | Expert Review
Biochemistry, general | Biomedical Engineering | T-cells | Biomedicine | Pharmacy | CAR T | antigen receptor | immunotherapy | Medical Law | genetic modification | Pharmacology/Toxicology | THERAPY | B-CELL | METABOLISM | KINETICS | PHARMACOLOGY & PHARMACY | LEUKEMIA | CHEMISTRY, MULTIDISCIPLINARY | Genetic Engineering - methods | Receptors, Chimeric Antigen - therapeutic use | Immunotherapy, Adoptive - methods | Neoplasms - therapy | Animals | Neoplasms - immunology | Humans | Receptors, Chimeric Antigen - immunology | Receptors, Chimeric Antigen - genetics | T-Lymphocytes - immunology | T-Lymphocytes - transplantation | Antigens | Care and treatment | Immunotherapy | Genetically modified organisms | Drug therapy | T cells | Cancer | CD19 antigen | Hematology | Toxicity | Medical services | T cell receptors | Lymphocytes T | Patients | Industrial development | Manufacturing | Solid tumors | Genetic modification | Expert Review
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 10/2009, Volume 106, Issue 41, pp. 17469 - 17474
Effector cells derived from central memory CD8⁺ T cells were reported to engraft and survive better than those derived from effector memory populations,...
T lymphocytes | Phenotypes | Memory | Stem cells | Cell lines | Immunity | Adoptive transfer | Cells | Tumors | T cell antigen receptors | THERAPY | PROTECTION | IMMUNOTHERAPY | AUTOIMMUNITY | MULTIDISCIPLINARY SCIENCES | TUMOR-REGRESSION | DIFFERENTIATION | CANCER | VIRAL-INFECTION | ANTIGEN | LYMPHOCYTES | Immunotherapy, Adoptive - methods | Animals, Genetically Modified | Humans | Immunophenotyping | Survival Rate | Adoptive Transfer | Animals | Neoplasms - immunology | Autoantigens - immunology | Neoplasms, Experimental - immunology | Primates - immunology | Immunologic Memory | Receptors, Antigen, T-Cell - immunology | Receptors, Antigen, T-Cell - genetics | CD8-Positive T-Lymphocytes - immunology | Biological Sciences
T lymphocytes | Phenotypes | Memory | Stem cells | Cell lines | Immunity | Adoptive transfer | Cells | Tumors | T cell antigen receptors | THERAPY | PROTECTION | IMMUNOTHERAPY | AUTOIMMUNITY | MULTIDISCIPLINARY SCIENCES | TUMOR-REGRESSION | DIFFERENTIATION | CANCER | VIRAL-INFECTION | ANTIGEN | LYMPHOCYTES | Immunotherapy, Adoptive - methods | Animals, Genetically Modified | Humans | Immunophenotyping | Survival Rate | Adoptive Transfer | Animals | Neoplasms - immunology | Autoantigens - immunology | Neoplasms, Experimental - immunology | Primates - immunology | Immunologic Memory | Receptors, Antigen, T-Cell - immunology | Receptors, Antigen, T-Cell - genetics | CD8-Positive T-Lymphocytes - immunology | Biological Sciences
Journal Article
European Journal of Immunology, ISSN 0014-2980, 09/2015, Volume 45, Issue 9, pp. 2457 - 2469
Tumors originate from a number of genetic events that deregulate homeostatic mechanisms controlling normal cell behavior. The immune system, devoted to patrol...
Genetic engineering | T‐cell receptor | Chimeric antigen receptor | T cells | Immunotherapy | Adoptive T‐cell therapy | T-cell receptor | Adoptive T-cell therapy | TARGETS TUMOR | IMMUNOLOGY | ANTITUMOR-ACTIVITY | VERSUS-HOST-DISEASE | SUICIDE-GENE | MOUSE MODELS | TUMOR-INFILTRATING LYMPHOCYTES | METASTATIC MELANOMA | HEMATOPOIETIC STEM-CELLS | DONOR LYMPHOCYTES | Antigens, Neoplasm - genetics | Cell- and Tissue-Based Therapy - methods | Gene Expression | Immunotherapy, Adoptive - methods | Genes, Transgenic, Suicide | Antigens, Neoplasm - immunology | Humans | Mutant Chimeric Proteins - genetics | Forecasting | Immunotherapy, Adoptive - trends | T-Lymphocytes - transplantation | Neoplasms - therapy | Cell Engineering - methods | Neoplasms - genetics | T-Lymphocytes - metabolism | Neoplasms - immunology | Mutant Chimeric Proteins - immunology | Receptors, Antigen, T-Cell - immunology | T-Lymphocytes - immunology | Receptors, Antigen, T-Cell - genetics | Neoplasms - pathology | Genetic Therapy - methods | Care and treatment | Health aspects | Genetically modified organisms | Cancer
Genetic engineering | T‐cell receptor | Chimeric antigen receptor | T cells | Immunotherapy | Adoptive T‐cell therapy | T-cell receptor | Adoptive T-cell therapy | TARGETS TUMOR | IMMUNOLOGY | ANTITUMOR-ACTIVITY | VERSUS-HOST-DISEASE | SUICIDE-GENE | MOUSE MODELS | TUMOR-INFILTRATING LYMPHOCYTES | METASTATIC MELANOMA | HEMATOPOIETIC STEM-CELLS | DONOR LYMPHOCYTES | Antigens, Neoplasm - genetics | Cell- and Tissue-Based Therapy - methods | Gene Expression | Immunotherapy, Adoptive - methods | Genes, Transgenic, Suicide | Antigens, Neoplasm - immunology | Humans | Mutant Chimeric Proteins - genetics | Forecasting | Immunotherapy, Adoptive - trends | T-Lymphocytes - transplantation | Neoplasms - therapy | Cell Engineering - methods | Neoplasms - genetics | T-Lymphocytes - metabolism | Neoplasms - immunology | Mutant Chimeric Proteins - immunology | Receptors, Antigen, T-Cell - immunology | T-Lymphocytes - immunology | Receptors, Antigen, T-Cell - genetics | Neoplasms - pathology | Genetic Therapy - methods | Care and treatment | Health aspects | Genetically modified organisms | Cancer
Journal Article
7.
Full Text
Regulatory T cells selectively control CD8+ T cell effector pool size via IL-2 restriction
Journal of Immunology, ISSN 0022-1767, 09/2011, Volume 187, Issue 6, pp. 3186 - 3197
Regulatory T cells (Treg) are key players in maintaining immune homeostasis but have also been shown to regulate immune responses against infectious pathogens....
INTERLEUKIN-2 | RESPONSES | DENDRITIC CELLS | MEMORY | TOLERANCE | MODIFIED VACCINIA VIRUS | IN-VIVO | IMMUNE REGULATION | INFECTION | CTLA-4 | IMMUNOLOGY | T-Lymphocyte Subsets - immunology | Mice, Inbred C57BL | Mice, Transgenic | Reverse Transcriptase Polymerase Chain Reaction | Vaccinia virus - immunology | Mice, Knockout | T-Lymphocytes, Regulatory - immunology | Animals | Interleukin-2 - immunology | Female | Mice | CD8-Positive T-Lymphocytes - immunology | Viral Vaccines - immunology | Immunologic Memory - immunology
INTERLEUKIN-2 | RESPONSES | DENDRITIC CELLS | MEMORY | TOLERANCE | MODIFIED VACCINIA VIRUS | IN-VIVO | IMMUNE REGULATION | INFECTION | CTLA-4 | IMMUNOLOGY | T-Lymphocyte Subsets - immunology | Mice, Inbred C57BL | Mice, Transgenic | Reverse Transcriptase Polymerase Chain Reaction | Vaccinia virus - immunology | Mice, Knockout | T-Lymphocytes, Regulatory - immunology | Animals | Interleukin-2 - immunology | Female | Mice | CD8-Positive T-Lymphocytes - immunology | Viral Vaccines - immunology | Immunologic Memory - immunology
Journal Article
Frontiers in Immunology, ISSN 1664-3224, 06/2018, Volume 9, p. 1301
In recent years, immunotherapy has shown considerable promise in the management of several malignancies. However, the majority of preclinical studies have been...
Comparative oncology | Antitumor immunity | T cells | Translational immunology | Porcine cancer model | Immunotherapy | Neoplasms - metabolism | T-Lymphocyte Subsets - immunology | Neoplasms - etiology | Proto-Oncogene Proteins p21(ras) - genetics | Biomarkers, Tumor | Tumor Microenvironment - genetics | Forkhead Transcription Factors - metabolism | Swine | Lymphocytes, Tumor-Infiltrating - metabolism | Disease Models, Animal | T-Lymphocytes, Cytotoxic - immunology | Gene Expression | Genetic Predisposition to Disease | Receptors, Antigen, T-Cell, gamma-delta - metabolism | Animals, Genetically Modified | Immunomodulation | Tumor Microenvironment - immunology | Animals | Lymphocytes, Tumor-Infiltrating - pathology | T-Lymphocytes, Cytotoxic - metabolism | T-Lymphocyte Subsets - metabolism | Biomarkers | Neoplasms - pathology | Cytotoxicity, Immunologic | Lymphocytes, Tumor-Infiltrating - immunology | translational immunology | antitumor immunity | porcine cancer model | immunotherapy | comparative oncology
Comparative oncology | Antitumor immunity | T cells | Translational immunology | Porcine cancer model | Immunotherapy | Neoplasms - metabolism | T-Lymphocyte Subsets - immunology | Neoplasms - etiology | Proto-Oncogene Proteins p21(ras) - genetics | Biomarkers, Tumor | Tumor Microenvironment - genetics | Forkhead Transcription Factors - metabolism | Swine | Lymphocytes, Tumor-Infiltrating - metabolism | Disease Models, Animal | T-Lymphocytes, Cytotoxic - immunology | Gene Expression | Genetic Predisposition to Disease | Receptors, Antigen, T-Cell, gamma-delta - metabolism | Animals, Genetically Modified | Immunomodulation | Tumor Microenvironment - immunology | Animals | Lymphocytes, Tumor-Infiltrating - pathology | T-Lymphocytes, Cytotoxic - metabolism | T-Lymphocyte Subsets - metabolism | Biomarkers | Neoplasms - pathology | Cytotoxicity, Immunologic | Lymphocytes, Tumor-Infiltrating - immunology | translational immunology | antitumor immunity | porcine cancer model | immunotherapy | comparative oncology
Journal Article
INTERNATIONAL JOURNAL OF CANCER, ISSN 0020-7136, 09/2018, Volume 143, Issue 5, pp. 1212 - 1223
Previous studies have shown that soluble common -chain (sc) modulates CD4(+) T cell immunity with antagonistic functions in c cytokine signaling. However, the...
cytokine | INTERLEUKIN-2 | NATURAL-KILLER | HOMEOSTASIS | ACTIVATION | PHENOTYPE | IL-15 | IL-2 | NAIVE | adoptive T cell transfer | soluble common gamma chain receptor | ONCOLOGY | cancer immunotherapy | IN-VIVO | COMMON GAMMA-CHAIN | EXPRESSION | Antigens | Oncology, Experimental | Immunotherapy | Genetically modified organisms | Research | T cells | Cancer | Tumors
cytokine | INTERLEUKIN-2 | NATURAL-KILLER | HOMEOSTASIS | ACTIVATION | PHENOTYPE | IL-15 | IL-2 | NAIVE | adoptive T cell transfer | soluble common gamma chain receptor | ONCOLOGY | cancer immunotherapy | IN-VIVO | COMMON GAMMA-CHAIN | EXPRESSION | Antigens | Oncology, Experimental | Immunotherapy | Genetically modified organisms | Research | T cells | Cancer | Tumors
Journal Article
Journal of Infectious Diseases, ISSN 0022-1899, 2015, Volume 212, Issue 10, pp. 1743 - 1751
Background. All 4 dengue virus (DENV) serotypes are now simultaneously circulating worldwide and responsible for up to 400 million human infections each year....
Serotype specific | Nicaragua | Sri Lanka | CD8 | Brazil | Dengue virus | T cells | sup | INFECTIOUS DISEASES | EFFICACY | dengue virus | VACCINE | CLASS-I SUPERTYPES | MICROBIOLOGY | IMMUNOLOGY | serotype specific | INHIBITION | SECONDARY INFECTION | PROTECTIVE ROLE | CD8(+) T cells | EPIDEMIC | Dengue Virus - classification | Dengue Virus - immunology | Humans | Dengue - epidemiology | Serogroup | Viral Proteins - immunology | CD8-Positive T-Lymphocytes - immunology | Dengue - immunology | Genetically modified mice | Research | Children | Health aspects | Dengue viruses | Major and Brief Reports | CD8+ T cells
Serotype specific | Nicaragua | Sri Lanka | CD8 | Brazil | Dengue virus | T cells | sup | INFECTIOUS DISEASES | EFFICACY | dengue virus | VACCINE | CLASS-I SUPERTYPES | MICROBIOLOGY | IMMUNOLOGY | serotype specific | INHIBITION | SECONDARY INFECTION | PROTECTIVE ROLE | CD8(+) T cells | EPIDEMIC | Dengue Virus - classification | Dengue Virus - immunology | Humans | Dengue - epidemiology | Serogroup | Viral Proteins - immunology | CD8-Positive T-Lymphocytes - immunology | Dengue - immunology | Genetically modified mice | Research | Children | Health aspects | Dengue viruses | Major and Brief Reports | CD8+ T cells
Journal Article
Current Opinion in Pharmacology, ISSN 1471-4892, 08/2018, Volume 41, pp. 96 - 103
T-cell receptors (TCRs) can be used to re-direct patients’ immune system to cancer. Directed evolution can enhance TCR affinity towards cancer antigens....
REGRESSION | BINDING-AFFINITY | REACTIVITY | PHARMACOLOGY & PHARMACY | PERIPHERAL-BLOOD | GENE-THERAPY | GENERATION | TOXICITY | IDENTIFICATION | ANTIGEN RECEPTOR | LYMPHOCYTES | Immunotherapy - methods | Neoplasms - therapy | Antigens, Neoplasm - immunology | Neoplasms - immunology | Humans | Protein Engineering | Receptors, Antigen, T-Cell - immunology | T-Lymphocytes - immunology | Receptors, Antigen, T-Cell - genetics | Medical colleges | Care and treatment | Immunotherapy | Genomics | Genetically modified organisms | Genetic engineering | Drug therapy | T cells | Cancer
REGRESSION | BINDING-AFFINITY | REACTIVITY | PHARMACOLOGY & PHARMACY | PERIPHERAL-BLOOD | GENE-THERAPY | GENERATION | TOXICITY | IDENTIFICATION | ANTIGEN RECEPTOR | LYMPHOCYTES | Immunotherapy - methods | Neoplasms - therapy | Antigens, Neoplasm - immunology | Neoplasms - immunology | Humans | Protein Engineering | Receptors, Antigen, T-Cell - immunology | T-Lymphocytes - immunology | Receptors, Antigen, T-Cell - genetics | Medical colleges | Care and treatment | Immunotherapy | Genomics | Genetically modified organisms | Genetic engineering | Drug therapy | T cells | Cancer
Journal Article
Journal of Virology, ISSN 0022-538X, 08/2018, Volume 92, Issue 16
Herpes simplex virus 1 (HSV-1) is a prevalent human pathogen that infects the cornea, causing potentially blinding herpetic disease. A clinical herpes vaccine...
CXCL10 | HSV-1 | HLA transgenic rabbit | Ocular | Prime/pull vaccine | CD8 | T cell | Prime/pull | Herpes | Herpes simplex | GLYCOPROTEIN B | EYE DISEASE | CD8(+) T cell | prime/pull vaccine | PERIOCULAR VACCINATION | ocular | herpes simplex | EFFECTOR | STROMAL KERATITIS | VIROLOGY | herpes | prime/pull | GENITAL HERPES | SYSTEMIC VACCINATION | ANIMAL-MODELS | INFECTION | TYPE-1 LATENCY | T-Lymphocyte Subsets - immunology | Humans | Cornea - immunology | HLA Antigens - genetics | Herpes Simplex Virus Vaccines - immunology | Viral Load | Epitopes - immunology | Keratitis, Herpetic - pathology | Herpes Simplex Virus Vaccines - administration & dosage | Disease Models, Animal | Rabbits | Keratitis, Herpetic - virology | Animals, Genetically Modified | Keratitis, Herpetic - prevention & control | Vaccines, Subunit - immunology | HLA Antigens - metabolism | Trigeminal Ganglion - immunology | Lysosomal-Associated Membrane Protein 1 - analysis | Chemokine CXCL10 - administration & dosage | Interferon-gamma - analysis | Animals | Vaccines, Subunit - administration & dosage | Simplexvirus - isolation & purification | Simplexvirus - immunology | CD8-Positive T-Lymphocytes - immunology | Chemokine CXCL10 - metabolism
CXCL10 | HSV-1 | HLA transgenic rabbit | Ocular | Prime/pull vaccine | CD8 | T cell | Prime/pull | Herpes | Herpes simplex | GLYCOPROTEIN B | EYE DISEASE | CD8(+) T cell | prime/pull vaccine | PERIOCULAR VACCINATION | ocular | herpes simplex | EFFECTOR | STROMAL KERATITIS | VIROLOGY | herpes | prime/pull | GENITAL HERPES | SYSTEMIC VACCINATION | ANIMAL-MODELS | INFECTION | TYPE-1 LATENCY | T-Lymphocyte Subsets - immunology | Humans | Cornea - immunology | HLA Antigens - genetics | Herpes Simplex Virus Vaccines - immunology | Viral Load | Epitopes - immunology | Keratitis, Herpetic - pathology | Herpes Simplex Virus Vaccines - administration & dosage | Disease Models, Animal | Rabbits | Keratitis, Herpetic - virology | Animals, Genetically Modified | Keratitis, Herpetic - prevention & control | Vaccines, Subunit - immunology | HLA Antigens - metabolism | Trigeminal Ganglion - immunology | Lysosomal-Associated Membrane Protein 1 - analysis | Chemokine CXCL10 - administration & dosage | Interferon-gamma - analysis | Animals | Vaccines, Subunit - administration & dosage | Simplexvirus - isolation & purification | Simplexvirus - immunology | CD8-Positive T-Lymphocytes - immunology | Chemokine CXCL10 - metabolism
Journal Article
European Journal of Immunology, ISSN 0014-2980, 01/2010, Volume 40, Issue 1, pp. 279 - 290
Modified vaccinia Ankara‐expressing Ag85A (MVA85A) is a new tuberculosis (TB) vaccine aimed at enhancing immunity induced by BCG. We investigated the safety...
Vaccine | Tuberculosis | IL‐17 | Polyfunctional | Modified vaccinia Ankara‐expressing Ag85A | Modified vaccinia ankara-expressing Ag85A | IL-17 | MYCOBACTERIUM-TUBERCULOSIS | IMMUNE-RESPONSE | Modified vaccinia Ankara-expressing Ag85A | BCG | CYTOKINE | IMMUNOLOGY | VIRUS ANKARA | TUMOR-NECROSIS-FACTOR | IMMUNOGENICITY | RECOMBINANT | INFECTION | ANTIGEN 85A | Tuberculosis Vaccines - adverse effects | Humans | Antigens, Bacterial - immunology | Child, Preschool | Acyltransferases - immunology | Infant | Male | Acyltransferases - genetics | Antigens, Bacterial - genetics | Vaccinia virus - genetics | CD4-Positive T-Lymphocytes - immunology | Tuberculosis - immunology | Tuberculosis - prevention & control | Adolescent | Female | Immunologic Memory | Tuberculosis Vaccines - immunology | Child
Vaccine | Tuberculosis | IL‐17 | Polyfunctional | Modified vaccinia Ankara‐expressing Ag85A | Modified vaccinia ankara-expressing Ag85A | IL-17 | MYCOBACTERIUM-TUBERCULOSIS | IMMUNE-RESPONSE | Modified vaccinia Ankara-expressing Ag85A | BCG | CYTOKINE | IMMUNOLOGY | VIRUS ANKARA | TUMOR-NECROSIS-FACTOR | IMMUNOGENICITY | RECOMBINANT | INFECTION | ANTIGEN 85A | Tuberculosis Vaccines - adverse effects | Humans | Antigens, Bacterial - immunology | Child, Preschool | Acyltransferases - immunology | Infant | Male | Acyltransferases - genetics | Antigens, Bacterial - genetics | Vaccinia virus - genetics | CD4-Positive T-Lymphocytes - immunology | Tuberculosis - immunology | Tuberculosis - prevention & control | Adolescent | Female | Immunologic Memory | Tuberculosis Vaccines - immunology | Child
Journal Article
Blood, ISSN 0006-4971, 04/2015, Volume 125, Issue 15, pp. 2418 - 2427
Coagulation factor replacement therapy for the X-linked bleeding disorder hemophilia is severely complicated by antibody ("inhibitor") formation. We previously...
INHIBITOR FORMATION | B-CELL | DENDRITIC CELLS | LETTUCE CHLOROPLASTS | FACTOR-IX | FACTOR-VIII | LONG-TERM TOLERANCE | ANTIGEN-SPECIFIC EFFECTOR | GENE-TRANSFER | HEMATOLOGY | IMMUNOLOGICAL-TOLERANCE | Hemophilia B - therapy | Recombinant Fusion Proteins - immunology | Transforming Growth Factor beta - immunology | Factor IX - administration & dosage | Hemophilia B - immunology | Factor IX - immunology | Plants, Genetically Modified - genetics | Administration, Oral | Factor IX - therapeutic use | Humans | Recombinant Fusion Proteins - therapeutic use | Factor IX - genetics
INHIBITOR FORMATION | B-CELL | DENDRITIC CELLS | LETTUCE CHLOROPLASTS | FACTOR-IX | FACTOR-VIII | LONG-TERM TOLERANCE | ANTIGEN-SPECIFIC EFFECTOR | GENE-TRANSFER | HEMATOLOGY | IMMUNOLOGICAL-TOLERANCE | Hemophilia B - therapy | Recombinant Fusion Proteins - immunology | Transforming Growth Factor beta - immunology | Factor IX - administration & dosage | Hemophilia B - immunology | Factor IX - immunology | Plants, Genetically Modified - genetics | Administration, Oral | Factor IX - therapeutic use | Humans | Recombinant Fusion Proteins - therapeutic use | Factor IX - genetics