The MRC OX-22- CD4+ T cells that help B cells in secondary immune responses derive from naive precursors with the MRC OX-22+ CD4+ phenotype.
about
Evidence that the T cell repertoire of normal rats contains cells with the potential to cause diabetes. Characterization of the CD4+ T cell subset that inhibits this autoimmune potentialOX-22high CD4+ T cells induce wasting disease with multiple organ pathology: prevention by the OX-22low subsetCellular and molecular mechanisms for reduced interleukin 4 and interferon-gamma production by neonatal T cells.Changes in CD45 isoform expression accompany antigen-induced murine T-cell activationThe physiological role of regulatory T cells in the prevention of autoimmunity: the function of the thymus in the generation of the regulatory T cell subset.Qualitative differences between naïve and memory T cells.Characterization of rat T helper cell clones specific for Bacteroides gingivalis antigen.Major histocompatibility complex-expressing nonhematopoietic astroglial cells prime only CD8+ T lymphocytes: astroglial cells as perpetuators but not initiators of CD4+ T cell responses in the central nervous systemT cell memory is short-lived in the absence of antigenSpecific unresponsiveness in rats with prolonged cardiac allograft survival after treatment with cyclosporine. III. Further characterization of the CD4+ suppressor cell and its mechanisms of action.Age-related factors in cyclosporine-induced syngeneic graft-versus-host disease: regulatory role of marrow-derived T lymphocytes.Subsets of CD4+ T cells and their roles in the induction and prevention of autoimmunity.Effect of adoptive transfer of cloned Actinobacillus actinomycetemcomitans-specific T helper cells on periodontal disease.Experimental hypersensitivity pneumonitis in the rat: histopathology and T-cell subset compartmentalization.The changing preference of T and B cells for partners as T-dependent antibody responses develop.Gamma interferon treatment in vivo provokes accumulation of activated monocytes in the venous circulation of rats.CD45RC isoforms define two types of CD4 memory T cells, one of which depends on persisting antigen.Immunopathology of diabetes in the RT6-depleted diabetes-resistant BB/Wor rat.T-helper subset function in the gut of rats: differential stimulation of eosinophils, mucosal mast cells and antibody-forming cells by OX8- OX22- and OX8- OX22+ cells.T lymphocytes in rat germinal centres belong to an ER3+ subpopulation of CD4+ cells.Genetic control of HgCl2-induced IgE and autoimmunity by a 117-kb interval on rat chromosome 9 through CD4 CD45RChigh T cells.Lymphocyte trafficking: CD4 T cells with a 'memory' phenotype (CD45RC-) freely cross lymph node high endothelial venules in vivo.Identical expression of CD45R isoforms by CD45RC+ 'revertant' memory and CD45RC+ naive CD4 T cells.
P2860
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P2860
The MRC OX-22- CD4+ T cells that help B cells in secondary immune responses derive from naive precursors with the MRC OX-22+ CD4+ phenotype.
description
1989 nî lūn-bûn
@nan
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
1989年论文
@zh
1989年论文
@zh-cn
name
The MRC OX-22- CD4+ T cells th ...... the MRC OX-22+ CD4+ phenotype.
@en
type
label
The MRC OX-22- CD4+ T cells th ...... the MRC OX-22+ CD4+ phenotype.
@en
prefLabel
The MRC OX-22- CD4+ T cells th ...... the MRC OX-22+ CD4+ phenotype.
@en
P2860
P356
P1476
The MRC OX-22- CD4+ T cells th ...... the MRC OX-22+ CD4+ phenotype.
@en
P2093
P2860
P304
P356
10.1084/JEM.169.3.653
P407
P577
1989-03-01T00:00:00Z