Clonal anergy blocks in vivo growth of mature T cells and can be reversed in the absence of antigen.
about
Inhibition of NF-kappa B during human dendritic cell differentiation generates anergy and regulatory T-cell activity for one but not two human leukocyte antigen DR mismatchesThe impact of T cell intrinsic antigen adaptation on peripheral immune tolerance.Basal gene expression by lung CD4+ T cells in chronic obstructive pulmonary disease identifies independent molecular correlates of airflow obstruction and emphysema extentMechanisms of self-nonself discrimination and possible clinical relevance.Role of dendritic cells in the induction and maintenance of autoimmune diseases.Impact of HLA-G in the outcome of vitiligo in Tunisian patientsNonmyeloablative immunosuppressive regimen prolongs In vivo persistence of gene-modified autologous T cells in a nonhuman primate model.Survival of mouse pancreatic islet allografts in recipients treated with allogeneic small lymphocytes and antibody to CD40 ligand.Extra-thymically induced regulatory T cells: do they have potential in disease prevention?Autologous apoptotic cells preceding transplantation enhance survival in lethal murine graft-versus-host models.Peripheral T-cell tolerance defined through transgenic mouse studies.TRAIL-expressing CD8+ T cells mediate tolerance following soluble peptide-induced peripheral T cell deletion.Neonatal helper-dependent adenoviral vector gene therapy mediates correction of hemophilia A and tolerance to human factor VIIIAntigen-specific immunotherapy for autoimmune disease: fighting fire with fire?Induction of immune tolerance by dendritic cells: implications for preventative and therapeutic immunotherapy of autoimmune disease.Specific T-cell tolerance may be preceded by a primary response.Lymphocytes from orally tolerized mice display enhanced susceptibility to death by apoptosis when cultured in the absence of antigen in vitroLangerhans cells protect from allergic contact dermatitis in mice by tolerizing CD8(+) T cells and activating Foxp3(+) regulatory T cells.Augmentation of transgene-encoded protein after neonatal injection of adeno-associated virus improves hepatic copy number without immune responses.Peripheral CD8+ T cell tolerance to self-proteins is regulated proximally at the T cell receptor.Broadly expressed tumour-associated proteins as targets for cytotoxic T lymphocyte-based cancer immunotherapy.Different use of T cell receptor transducing modules in two populations of gut intraepithelial lymphocytes are related to distinct pathways of T cell differentiationAnergy and exhaustion are independent mechanisms of peripheral T cell toleranceCD8(+) T cell tolerance to a tumor-associated antigen is maintained at the level of expansion rather than effector function.Signal 3 determines tolerance versus full activation of naive CD8 T cells: dissociating proliferation and development of effector function.Conditions that induce tolerance in mature CD4+ T cellsPeripheral selection of T cell repertoires: the role of continuous thymus output.Viral and bacterial infections interfere with peripheral tolerance induction and activate CD8+ T cells to cause immunopathologyTGFβ-dependent expression of PD-1 and PD-L1 controls CD8(+) T cell anergy in transplant tolerancemTOR at the crossroads of T cell proliferation and tolerance.Immune tolerance: mechanisms and application in clinical transplantation.Adenosine and anergy.Regulatory function of in vivo anergized CD4(+) T cellsManipulating the immune system for anti-tumor responses and transplant tolerance via mixed hematopoietic chimerism.Human V delta 2+ gamma delta T-cell tolerance to foreign antigens of Toxoplasma gondii.Posttranscriptional silencing of effector cytokine mRNA underlies the anergic phenotype of self-reactive T cells.Intravenous injection of soluble antigen induces thymic and peripheral T-cells apoptosis.Balancing immunity and tolerance: deleting and tuning lymphocyte repertoires.Tolerance and exhaustion: defining mechanisms of T cell dysfunction.Self-reactivity as the necessary cost of maintaining a diverse memory T-cell repertoire.
P2860
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P2860
Clonal anergy blocks in vivo growth of mature T cells and can be reversed in the absence of antigen.
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年学术文章
@wuu
1993年学术文章
@zh-cn
1993年学术文章
@zh-hans
1993年学术文章
@zh-my
1993年学术文章
@zh-sg
1993年學術文章
@yue
1993年學術文章
@zh
1993年學術文章
@zh-hant
name
Clonal anergy blocks in vivo g ...... sed in the absence of antigen.
@ast
Clonal anergy blocks in vivo g ...... sed in the absence of antigen.
@en
type
label
Clonal anergy blocks in vivo g ...... sed in the absence of antigen.
@ast
Clonal anergy blocks in vivo g ...... sed in the absence of antigen.
@en
prefLabel
Clonal anergy blocks in vivo g ...... sed in the absence of antigen.
@ast
Clonal anergy blocks in vivo g ...... sed in the absence of antigen.
@en
P2093
P2860
P356
P1476
Clonal anergy blocks in vivo g ...... sed in the absence of antigen.
@en
P2093
P2860
P304
P356
10.1084/JEM.177.5.1517
P407
P577
1993-05-01T00:00:00Z