scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1008726237 |
P356 | DOI | 10.1038/332378A0 |
P698 | PubMed publication ID | 2965306 |
P50 | author | Charles Janeway | Q1065040 |
P2093 | author name string | Poo WJ | |
Conrad L | |||
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Why whip egg whites in copper bowls? | Q56235350 | ||
Evidence for a physical association of CD4 and the CD3: α : β T-cell receptor | Q58974599 | ||
Antigen-specific interaction between T and B cells | Q59063745 | ||
Cooperative interaction of B lymphocytes with antigen-specific helper T lymphocytes is MHC restricted | Q59067228 | ||
The role of B cell surface Ia antigen recognition by T cells in B cell triggering. Analysis of the interaction of cloned helper T cells with normal B cells in differing states of activation and with B cells expressing thexid defect | Q70361979 | ||
Thymus-marrow cell combinations. Synergism in antibody production | Q72797600 | ||
Coclustering of CD4 (L3T4) molecule with the T-cell receptor is induced by specific direct interaction of helper T cells and antigen-presenting cells | Q34340219 | ||
B-cell stimulatory factor 1 and not interleukin 2 is the autocrine growth factor for some helper T lymphocytes | Q34593796 | ||
Cell to cell interaction in the immune response. II. The source of hemolysin-forming cells in irradiated mice given bone marrow and thymus or thoracic duct lymphocytes | Q36269342 | ||
Cell interactions between histoincompatible T and B lymphocytes. II. Failure of physiologic cooperative interactions between T and B lymphocytes from allogeneic donor strains in humoral response to hapten-protein conjugates | Q36272251 | ||
Both a monoclonal antibody and antisera specific for determinants unique to individual cloned helper T cell lines can substitute for antigen and antigen-presenting cells in the activation of T cells | Q36348048 | ||
The Fab fragment of a directly activating monoclonal antibody that precipitates a disulfide-linked heterodimer from a helper T cell clone blocks activation by either allogeneic Ia or antigen and self-Ia | Q36348755 | ||
Antigen presentation by hapten-specific B lymphocytes. I. Role of surface immunoglobulin receptors | Q36349536 | ||
Distinct functional phenotypes of cloned Ia-restricted helper T cells | Q36350297 | ||
Direct interactions between B and T lymphocytes bearing complementary receptors | Q36351526 | ||
The specific direct interaction of helper T cells and antigen-presenting B cells | Q37395408 | ||
The requirement of more than one antigenic determinant for immunogenicity | Q41822375 | ||
Inhibition of in vitro immune response by treatment of spleen cell suspensions with anti-theta serum | Q43926328 | ||
The carrier effect in the secondary response to hapten-protein conjugates. II. Cellular cooperation. | Q51023960 | ||
P433 | issue | 6162 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 378-380 | |
P577 | publication date | 1988-03-01 | |
P1433 | published in | Nature | Q180445 |
P1476 | title | Receptor-directed focusing of lymphokine release by helper T cells | |
P478 | volume | 332 |
Q41842929 | "Cell biology meets physiology: functional organization of vertebrate plasma membranes"--the immunological synapse |
Q51628152 | 3D computation modelling of the influence of cytokine secretion on Th-cell development suggests that negative selection (inhibition of Th1 cells) is more effective than positive selection by IL-4 for Th2 cell dominance. |
Q57962257 | A polarizing situation |
Q50991697 | A role for the immunological synapse in lineage commitment of CD4 lymphocytes. |
Q84081035 | ASMase: the tailor of cytotoxic T cell granule exocytosis |
Q36229864 | Anti-interferon gamma treatment blocks the ability of glutaraldehyde-polymerized allergens to inhibit specific IgE responses |
Q45007253 | Antibody responses to hapten in thymectomized mice: extraordinarily pronounced deficiency in IgG1 production |
Q36531047 | Antigen-receptor complex stimulation triggers protein kinase C-dependent CD11a/CD18-cytoskeleton association in T lymphocytes |
Q37745396 | Assessment of cytokines by immunofluorescence and the paraformaldehyde-saponin procedure |
Q24557336 | Association of intercellular adhesion molecule 1 with the multichain high-affinity interleukin 2 receptor |
Q35732477 | Bacterial toxin-induced cytokine production studied at the single-cell level |
Q59019634 | Between B cells and T cells |
Q34578365 | Biochemical basis of synergy between antigen and T-helper (Th) cell-mediated activation of resting human B cells |
Q67513111 | CD4+ T cell-mediated killing of major histocompatibility complex class II-positive antigen-presenting cells (APC). III. CD4+ cytotoxic T cells induce apoptosis of APC |
Q35670765 | Casein kinase I delta controls centrosome positioning during T cell activation |
Q36228985 | Cdc42-interacting protein-4 functionally links actin and microtubule networks at the cytolytic NK cell immunological synapse. |
Q59044986 | Cell–cell interactions in the antibody response |
Q21245308 | Centriole polarisation to the immunological synapse directs secretion from cytolytic cells of both the innate and adaptive immune systems |
Q70646356 | Characterization of cytokine production in infectious mononucleosis studied at a single-cell level in tonsil and peripheral blood |
Q30489790 | Choreography of cell motility and interaction dynamics imaged by two-photon microscopy in lymphoid organs |
Q41654061 | Ciprofloxacin enhances T cell function by modulating interleukin activities |
Q28289165 | Clonal sketches of the immune response |
Q73327643 | Co-development of naive CD4+ cells towards T helper type 1 or T helper type 2 cells induced by a combination of IL-12 and IL-4 |
Q41532456 | Collaboration of helper and cytotoxic T lymphocytes |
Q39170851 | Commonality of the IL-4/IL-13 pathway in atopic diseases |
Q72349595 | Comparative analysis of the ability of leucocytes, endothelial cells and platelets to degrade the subendothelial basement membrane: evidence for cytokine dependence and detection of a novel sulfatase |
Q36296177 | Comprehensive Analysis of Immunological Synapse Phenotypes Using Supported Lipid Bilayers |
Q72410202 | Concomitant in vivo production of 19 different cytokines in human tonsils |
Q67234965 | Concomitant production of different lymphokines in activated T cells |
Q24806593 | Control of T lymphocyte morphology by the GTPase Rho. |
Q37697703 | Cross-linking Fc receptors stimulate splenic non-B, non-T cells to secrete interleukin 4 and other lymphokines |
Q37808729 | Cytokine reporter mice in immunological research: perspectives and lessons learned |
Q34579927 | Cytokines and anti-cytokine therapy: clinical potential for treatment of feline disease |
Q57240716 | Cytokines: Principles and prospects |
Q36276679 | Cytoskeletal polarization of T cells is regulated by an immunoreceptor tyrosine-based activation motif-dependent mechanism |
Q42676587 | Cytotoxic T lymphocyte-associated molecule-4, a high-avidity receptor for CD80 and CD86, contains an intracellular localization motif in its cytoplasmic tail |
Q30514126 | Cytotoxic immunological synapses do not restrict the action of interferon-γ to antigenic target cells. |
Q68237460 | Direct helper T cell-induced B cell differentiation involves interaction between T cell antigen CD28 and B cell activation antigen B7 |
Q52082839 | Direct interaction with primed CD4+ CD45R0+ memory T lymphocytes induces expression of endothelial leukocyte adhesion molecule-1 and vascular cell adhesion molecule-1 on the surface of vascular endothelial cells |
Q35815993 | Directed exocytosis of secretory granules containing apolipoprotein E to the adherent surface and basal vacuoles of macrophages spreading on immobile immune complexes |
Q36539209 | Diversity of cytokine synthesis and function of mouse CD4+ T cells |
Q73133839 | Down-regulation of Listeria monocytogenes-specific Th1 cytokine response by treatment of mice with goat antibody to mouse IgD |
Q37470914 | Dynamics of membrane trafficking downstream of B and T cell receptor engagement: impact on immune synapses |
Q41012876 | Dynein Separately Partners with NDE1 and Dynactin To Orchestrate T Cell Focused Secretion. |
Q28316111 | Effects of FK506 and cyclosporin A on cytokine production studied in vitro at a single-cell level |
Q36222548 | Endothelial cell-associated platelet-activating factor: a novel mechanism for signaling intercellular adhesion |
Q44798096 | Endotoxin and staphylococcus aureus enterotoxin a induce different patterns of cytokines |
Q39526082 | Exacerbation of experimental murine cutaneous leishmaniasis with CD4+Leishmania major-specific T cell lines or clones which secrete interferon-γ and mediate parasite-specific delayed-type hypersensitivity |
Q28208110 | Exclusion of CD43 from the immunological synapse is mediated by phosphorylation-regulated relocation of the cytoskeletal adaptor moesin |
Q35263067 | Expression of cytokines by recombinant vaccinia viruses: a model for studying cytokines in virus infections in vivo |
Q34088786 | Functional anatomy of the thymic microenvironment |
Q93512205 | Functional and phenotypic analysis of human T-cell clones which stimulate IgE production in vitro |
Q58981012 | Global or directed exocytosis? |
Q37796606 | HIV-1 Virological Synapse is not Simply a Copycat of the Immunological Synapse |
Q36539242 | Heterogeneity in lymphokine profiles of CD4+ and CD8+ T cells and clones activated in vivo and in vitro |
Q30815346 | Highly restricted expression of a stromal cell determinant in mouse bone marrow in vivo |
Q42731039 | Hiways and byways to the secretory synapse |
Q34353214 | How B cells capture, process and present antigens: a crucial role for cell polarity |
Q36928394 | Human interleukin-4: An immunomodulator with potential therapeutic applications |
Q68726063 | IL-2-like activity in lymph fluid following in vivo antigen challenge |
Q40360998 | IL-4 Haploinsufficiency Specifically Impairs IgE Responses against Allergens in Mice. |
Q24675460 | Identification of a novel surface protein on activated CD4+ T cells that induces contact-dependent B cell differentiation (help) |
Q52114558 | Idiotypic networks incorporating T-B cell co-operation. The conditions for percolation. |
Q34476426 | IgE receptor-positive non-B/non-T cells dominate the production of interleukin 4 and interleukin 6 in immunized mice |
Q45852364 | Immunodeficient mice recover from infection with vaccinia virus expressing interferon-gamma. |
Q42942148 | Immunoglobulin signal transduction guides the specificity of B cell-T cell interactions and is blocked in tolerant self-reactive B cells |
Q67294462 | Immunoglobulin-specific T-B cell interaction. III. B cell activation by immunoglobulin-recognizing T cell clones |
Q36650242 | Importance of interferons in recovery from mousepox |
Q34075330 | In TH2 cells the Il4 gene has a series of accessibility states associated with distinctive probabilities of IL-4 production. |
Q40755086 | In VitroT-Cell Proliferative Response to the Flavivirus, West Nile |
Q52024167 | In silico simulations suggest that Th-cell development is regulated by both selective and instructive mechanisms. |
Q40696454 | In the immune synapse, ZAP-70 controls T cell polarization and recruitment of signaling proteins but not formation of the synaptic pattern. |
Q37592267 | In vitro activity of CD4+ and CD8+ T lymphocytes from mice immunized with a synthetic malaria peptide |
Q36973798 | In vivo effects of anticytokine antibodies on isotype restriction in Mesocestoides corti-infected BALB/c mice. |
Q36356982 | Induction of human IgE synthesis by CD4+ T cell clones. Requirement for interleukin 4 and low molecular weight B cell growth factor |
Q42155789 | Induction of human IgE synthesis requires interleukin 4 and T/B cell interactions involving the T cell receptor/CD3 complex and MHC class II antigens |
Q34117443 | Information transfer at the immunological synapse. |
Q43047959 | Interferon-gamma, interleukin (IL)-2 and IL-2 receptor expressions in hepatitis C virus-infected liver |
Q45777299 | Interleukin-5 expressed by a recombinant virus vector enhances specific mucosal IgA responses in vivo. |
Q73573505 | Interleukin-6, interleukin-8, and interleukin-10 in kidney transplantation: improved risk strategy? |
Q56908957 | Intracellular trafficking of CTLA-4 and focal localization towards sites of TCR engagement |
Q54606011 | LACK-reactive CD4+ T cells require autocrine IL-2 to mediate susceptibility to Leishmania major. |
Q41703357 | Lymphocytes infected with Theileria parva require both cell-cell contact and growth factor to proliferate. |
Q37049244 | Malaria antigens expressed on the surface of infected hepatocytes: a role in protective immunity? |
Q59052484 | Mast cell lines produce lymphokines in response to cross-linkage of FcεRI or to calcium ionophores |
Q40878841 | Mechanism of self-tolerance to endocrine tissue |
Q37553914 | Mechanisms and functions for the duration of intercellular contacts made by lymphocytes |
Q37111968 | Mechanisms of regulatory T-cell suppression - a diverse arsenal for a moving target |
Q38718470 | Membrane Ig-mediated triggering of B cell tolerance and B cell clonal expansion: implications for rheumatoid factor production in rheumatoid synovitis |
Q38051634 | Microtubule-organizing center polarity and the immunological synapse: protein kinase C and beyond |
Q37779176 | Pathways for cytokine secretion. |
Q41202887 | Polarity of T cell shape, motility, and sensitivity to antigen |
Q37384846 | Polarized expression of cytokines in cell conjugates of helper T cells and splenic B cells |
Q36354723 | Probabilistic regulation of IL-4 production |
Q41736190 | Production and regulation of interleukin 6 in human B lymphoid cells |
Q53959507 | Production and secretion of interferon-gamma (IFN-gamma) in children with atopic dermatitis. |
Q34447939 | Prolactin production by immune cells |
Q41882222 | Rapid up-regulation and granule-independent transport of perforin to the immunological synapse define a novel mechanism of antigen-specific CD8+ T cell cytotoxic activity. |
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Q30478093 | Recruitment of dynein to the Jurkat immunological synapse |
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Q57363719 | Shmoos, Rafts, and Uropods— The Many Facets of Cell Polarity |
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Q90044436 | Stochastic Model of T Cell Repolarization during Target Elimination I |
Q34548289 | Super-resolution imaging of remodeled synaptic actin reveals different synergies between NK cell receptors and integrins |
Q33957034 | Sustained signaling by canonical helper T cell cytokines throughout the reactive lymph node. |
Q58785757 | Synaptic Interactions in Germinal Centers |
Q70177796 | T and B cell collaboration: induction of motility in small, resting B cells by interleukin 4 |
Q37945207 | T cell polarization at the virological synapse |
Q45948164 | T cells use two directionally distinct pathways for cytokine secretion. |
Q43819457 | T helper cells grown with hapten-modified cultured Langerhans' cells produce interleukin 4 and stimulate IgE production by B cells |
Q37929568 | T lymphocyte-derived colony-stimulating factors |
Q37084875 | T-cell activation through immunological synapses and kinapses |
Q36980439 | T-cell hybridomas reveal two distinct mechanisms of antileishmanial defense |
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