| scholarly article | Q13442814 |
| P2093 | author name string | R Ahmed | |
| L Bhatti | |||
| L D Butler | |||
| P2860 | cites work | The role of mononuclear phagocytes in HTLV-III/LAV infection | Q29618676 |
| Pneumocystis carinii pneumonia and mucosal candidiasis in previously healthy homosexual men: evidence of a new acquired cellular immunodeficiency | Q34055177 | ||
| Antigenic Requirements for Triggering of Cytotoxic T Lymphocytes | Q35497372 | ||
| Both L3T4+ and Lyt-2+ helper T cells initiate cytotoxic T lymphocyte responses against allogenic major histocompatibility antigens but not against trinitrophenyl-modified self | Q36350610 | ||
| Long-term humoral unresponsiveness in vivo, induced by treatment with monoclonal antibody against L3T4. | Q36352864 | ||
| Functional subclasses of T-lymphocytes bearing different Ly antigens. I. The generation of functionally distinct T-cell subclasses is a differentiative process independent of antigen | Q36358156 | ||
| Virus-lymphocyte interaction: T cells of the helper subset are infected with lymphocytic choriomeningitis virus during persistent infection in vivo | Q36887681 | ||
| Mechanism of recovery from acute virus infection: treatment of lymphocytic choriomeningitis virus-infected mice with monoclonal antibodies reveals that Lyt-2+ T lymphocytes mediate clearance of virus and regulate the antiviral antibody response | Q36888736 | ||
| Characteristics and functions of Sendai virus-specific T-cell clones | Q36915283 | ||
| Biology of cloned cytotoxic T lymphocytes specific for lymphocytic choriomeningitis virus: clearance of virus in vivo | Q36918873 | ||
| Immune therapy of a persistent and disseminated viral infection. | Q36920380 | ||
| Effective clearance of a persistent viral infection requires cooperation between virus-specific Lyt2+ T cells and nonspecific bone marrow-derived cells | Q36920387 | ||
| Selective Tropism of Lymphadenopathy Associated Virus (LAV) for Helper-Inducer T Lymphocytes | Q39140204 | ||
| Pathogenesis of infection with human immunodeficiency virus | Q39659930 | ||
| The Virology and Immunobiology of Lymphocytic Choriomeningitis Virus Infection | Q40099207 | ||
| Characterization of the Murine Antigenic Determinant, Designated L3T4a, Recognized by Monoclonal Antibody GK 1.5: Expression of L3T4a by Functional T Cell Clones Appears to Correlate Primarily with Class II MHC Antigen-Reactivity | Q40108126 | ||
| Ly antigens associated with T cell recognition and effector function | Q40215930 | ||
| T-T-cell interactions during the vitro cytotoxic allograft responses. I. Soluble products from activated Lyl+ T cells trigger autonomously antigen-primed Ly23+ T cells to cell proliferation and cytolytic activity | Q40695893 | ||
| Selection of genetic variants of lymphocytic choriomeningitis virus in spleens of persistently infected mice. Role in suppression of cytotoxic T lymphocyte response and viral persistence | Q42937121 | ||
| Properties of purified T cell subsets. I. In vitro responses to class I vs. class II H-2 alloantigens | Q42937851 | ||
| Functional analysis of T lymphocyte subsets in antiviral host defense. | Q44098687 | ||
| Induction of cytotoxic T-cell responses in vivo in the absence of CD4 helper cells | Q44304252 | ||
| Cytoimmunotherapy for persistent virus infection reveals a unique clearance pattern from the central nervous system | Q45834090 | ||
| H-2 compatibility requirement for virus-specific T cell-mediated effector functions in vivo. I. Specificity of T cells conferring antiviral protection against lymphocytic choriomeningitis virus is associated with H-2K and H-2D | Q45888810 | ||
| Expression of interleukin-2 receptors as a differentiation marker on intrathymic stem cells | Q59061491 | ||
| Therapy with monoclonal antibodies by elimination of T-cell subsets in vivo | Q59082223 | ||
| Capacity of purified Lyt-2+ T cells to mount primary proliferative and cytotoxic responses to Ia- tumour cells | Q70300280 | ||
| Characterization of the murine T cell surface molecule, designated L3T4, identified by monoclonal antibody GK1.5: similarity of L3T4 to the human Leu-3/T4 molecule | Q70452024 | ||
| T cell-accessory cell interactions that initiate allospecific cytotoxic T lymphocyte responses: existence of both Ia-restricted and Ia-unrestricted cellular interaction pathways | Q72730534 | ||
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | antibody | Q79460 |
| cytotoxicity | Q246181 | ||
| cell function | Q95674809 | ||
| P304 | page(s) | 2102-2106 | |
| P577 | publication date | 1988-06-01 | |
| P1433 | published in | Journal of Virology | Q1251128 |
| P1476 | title | T4+ T helper cell function in vivo: differential requirement for induction of antiviral cytotoxic T-cell and antibody responses | |
| P478 | volume | 62 |
| Q47982760 | A conditioned dendritic cell can be a temporal bridge between a CD4+ T-helper and a T-killer cell |
| Q33863345 | Activated B cells can deliver help for the in vitro generation of antiviral cytotoxic T cells |
| Q36821295 | Activity of CD4+ T-cell clones of type 1 and type 2 in generation of influenza virus-specific cytotoxic responses in vitro |
| Q33764677 | Anthrax toxin as a molecular tool for stimulation of cytotoxic T lymphocytes: disulfide-linked epitopes, multiple injections, and role of CD4(+) cells |
| Q35212646 | Antiviral CD4 and CD8 T-cell memory: differences in the size of the response and activation requirements |
| Q39874289 | Antiviral cytotoxic T-cell memory by vaccination with recombinant Listeria monocytogenes |
| Q35877771 | Antiviral immune responses in CTLA4 transgenic mice |
| Q36689886 | Antiviral immune responses in gene-targeted mice expressing the immunoglobulin heavy chain of virus-neutralizing antibodies |
| Q36639479 | Antiviral immune responses of lymphocytic choriomeningitis virus-infected mice lacking CD8+ T lymphocytes because of disruption of the beta 2-microglobulin gene |
| Q36362059 | Autoimmune diabetes can be induced in transgenic major histocompatibility complex class II-deficient mice |
| Q35835410 | Bone marrow is a major site of long-term antibody production after acute viral infection |
| Q36380997 | CD4+ T cell help impairs CD8+ T cell deletion induced by cross-presentation of self-antigens and favors autoimmunity |
| Q54194324 | CD4+ T cells are essential in overcoming experimental murine measles encephalitis. |
| Q34234563 | CD4+ T cells are not required for the induction of dengue virus-specific CD8+ T cell or antibody responses but contribute to protection after vaccination |
| Q36637922 | CD4+ T cells are required to sustain CD8+ cytotoxic T-cell responses during chronic viral infection |
| Q77355825 | CD4+ T-cell induction and effector functions: a comparison of immunity against soluble antigens and viral infections |
| Q39873438 | CD4-deficient mice have reduced levels of memory cytotoxic T lymphocytes after immunization and show diminished resistance to subsequent virus challenge. |
| Q45860713 | CD4-positive T lymphocytes are required for the generation of the primary but not the secondary CD8-positive cytolytic T lymphocyte response to herpes simplex virus in C57BL/6 mice |
| Q35873254 | CD40 ligand-deficient mice generate a normal primary cytotoxic T-lymphocyte response but a defective humoral response to a viral infection |
| Q36367895 | CD8(+) T cells mediate CD40-independent maturation of dendritic cells in vivo |
| Q34577200 | Cell-intrinsic transforming growth factor-beta signaling mediates virus-specific CD8+ T cell deletion and viral persistence in vivo |
| Q36577746 | Cellular and Molecular Basis of the Protective Immune Response to Cytomegalovirus Infection |
| Q36414246 | Characterization of CD8+ T cell function and immunodominance generated with an H2O2-inactivated whole-virus vaccine |
| Q34357808 | Cognate CD4(+) T cell licensing of dendritic cells in CD8(+) T cell immunity |
| Q45000674 | Comparison of activation versus induction of unresponsiveness of virus-specific CD4+ and CD8+ T cells upon acute versus persistent viral infection |
| Q64250220 | Complexities of Type I Interferon Biology: Lessons from LCMV |
| Q33971036 | Costimulation in antiviral immunity: differential requirements for CD4(+) and CD8(+) T cell responses |
| Q36648449 | Cross-protection against lymphocytic choriomeningitis virus mediated by a CD4+ T-cell clone specific for an envelope glycoprotein epitope of Lassa virus |
| Q45738849 | Cytokine responses to human immunodeficiency virus type 1 (HIV-1) induced by immunization with live recombinant canarypox virus vaccine expressing HIV-1 genes boosted by HIV-1(SF-2) recombinant GP120. |
| Q35873118 | Different roles for CD4+ and CD8+ T lymphocytes and macrophage subsets in the control of a generalized virus infection |
| Q37812033 | Dissection of an inflammatory process induced by CD8+ T cells |
| Q36783416 | Effective clearance of mouse hepatitis virus from the central nervous system requires both CD4+ and CD8+ T cells |
| Q36793382 | Efficacious control of cytomegalovirus infection after long-term depletion of CD8+ T lymphocytes |
| Q36623371 | Enhanced establishment of a virus carrier state in adult CD4+ T-cell-deficient mice. |
| Q52061868 | Environmental modulation of the autonomy of cytotoxic T lymphocytes. |
| Q36631176 | Expression of seven herpes simplex virus type 1 glycoproteins (gB, gC, gD, gE, gG, gH, and gI): comparative protection against lethal challenge in mice. |
| Q35080684 | Functional CD8+ but not CD4+ T cell responses develop independent of thymic epithelial MHC. |
| Q47982749 | Help for cytotoxic-T-cell responses is mediated by CD40 signalling |
| Q46351727 | Helper interleukins are produced by both CD4 and CD8 splenic T cells after mitogen stimulation |
| Q34143952 | Host factors influencing viral persistence. |
| Q39589096 | Human immunodeficiency virus type 1- and cytomegalovirus-specific cytotoxic T lymphocytes can persist at high frequency for prolonged periods in the absence of circulating peripheral CD4(+) T cells. |
| Q52040025 | Humoral immunity due to long-lived plasma cells. |
| Q40951379 | Immune conflicts in lymphocytic choriomeningitis virus |
| Q93511968 | Immunity to viruses |
| Q41935553 | Immunological tolerance to LCMV antigens differently affects control of acute and chronic virus infection in mice. |
| Q36375719 | In vivo cytotoxic T lymphocyte elicitation by mycobacterial heat shock protein 70 fusion proteins maps to a discrete domain and is CD4(+) T cell independent |
| Q35857176 | Indirect regulation of CD4 T-cell responses by tumor necrosis factor receptors in an acute viral infection. |
| Q36380318 | Induction of a CD8+ cytotoxic T lymphocyte response by cross-priming requires cognate CD4+ T cell help |
| Q56967605 | Influence of CD4 T cells and the source of major histocompatibility complex class II-restricted peptides on cytotoxic T-cell priming by dendritic cells |
| Q47551035 | Innate and adaptive T cells in influenza disease |
| Q36478934 | Insertion signal sequence fused to minimal peptides elicits specific CD8+ T-cell responses and prolongs survival of thymoma-bearing mice. |
| Q44465948 | Limiting dilution analysis of virus-specific memory B cells by an ELISPOT assay |
| Q36366666 | Long-lasting CD8 T cell memory in the absence of CD4 T cells or B cells. |
| Q33784950 | Long-term CD4 Th1 and Th2 memory following acute lymphocytic choriomeningitis virus infection |
| Q41195152 | Long-term humoral immunity against viruses: revisiting the issue of plasma cell longevity |
| Q33630150 | Longitudinal requirement for CD4+ T cell help for adenovirus vector-elicited CD8+ T cell responses |
| Q72815556 | Lysis of infected cells in vivo by antiviral cytolytic T cells demonstrated by release of cell internal viral proteins |
| Q36231639 | Mechanisms of mouse spleen dendritic cell function in the generation of influenza-specific, cytolytic T lymphocytes |
| Q36086689 | Mice deficient in STAT1 but not STAT2 or IRF9 develop a lethal CD4+ T-cell-mediated disease following infection with lymphocytic choriomeningitis virus. |
| Q39873666 | Modulation by gamma interferon of antiviral cell-mediated immune responses in vivo |
| Q86190175 | Normal development and function but impaired memory phenotype of CD8⁺ T cells in transgenic mice expressing HIV-1 Nef in its natural target cells |
| Q28511808 | Normal development and function of CD8+ cells but markedly decreased helper cell activity in mice lacking CD4 |
| Q30310748 | Not all effector CD8+ T cells are alike |
| Q36806516 | Persistence of restricted CD4 T cell expansions in SIV-infected macaques resistant to SHIV89.6P superinfection. |
| Q33803386 | Polyomavirus-infected dendritic cells induce antiviral CD8(+) T lymphocytes |
| Q36697826 | Preventive effects of early anti-CD4 or anti-CD8 treatment on Borna disease in rats |
| Q36659320 | Recombinant parvovirus-like particles as an antigen carrier: a novel nonreplicative exogenous antigen to elicit protective antiviral cytotoxic T cells. |
| Q91014164 | Residual LCMV antigen in transiently CD4+ T cell-depleted mice induces high levels of virus-specific antibodies but only limited B-cell memory |
| Q35838647 | Responses against complex antigens in various models of CD4 T-cell deficiency: surprises from an anti-CD4 antibody transgenic mouse |
| Q36797996 | Role of immune cells in protection against and control of reovirus infection in neonatal mice |
| Q36356034 | Site-restricted persistent cytomegalovirus infection after selective long-term depletion of CD4+ T lymphocytes. |
| Q52075240 | Specific epitope-induced conversion of CD8+ memory cells into effector cytotoxic T lymphocytes in vitro: presentation of peptide antigen by CD8+ T cells |
| Q36356494 | T cell memory. Long-term persistence of virus-specific cytotoxic T cells |
| Q43881895 | T helper cells in cytotoxic T lymphocyte development: Analysis of the cellular basis for deficient T helper cell function in the L3T4-independent T helper cell pathway |
| Q72370400 | T lymphocyte-mediated antiviral immune responses in mice are diminished by treatment with monoclonal antibody directed against the interleukin-2 receptor |
| Q37783263 | The Role of Precursor Frequency in the Differentiation of Memory T Cells: Memory by Numbers |
| Q41870329 | The critical need for CD4 help in maintaining effective cytotoxic T lymphocyte responses |
| Q44783914 | The generation and activation of memory class I MHC restricted cytotoxic T cell responses to influenza A virus in vivo do not require CD4+ T cells |
| Q40708500 | The nucleoprotein of Pichinde virus expressed by a vaccinia-Pichinde virus recombinant partially protects hamsters from lethal virus challenge |
| Q35941639 | The regulation and maturation of antiviral immune responses |
| Q33971012 | The role of CD4(+) T helper cells in the cytotoxic T lymphocyte response to HIV-1. |
| Q36611354 | Timing and magnitude of type I interferon responses by distinct sensors impact CD8 T cell exhaustion and chronic viral infection |
| Q45346306 | Upregulation of OX40 ligand on monocytes contributes to early virological control in patients with chronic hepatitis C. |
| Q24646943 | Viral immune evasion due to persistence of activated T cells without effector function |
| Q72707998 | Viral induction of co-stimulatory activity on antigen-presenting cells bypasses the need for CD4+ T-cell help in CD8+ T-cell responses |
| Q33854007 | Virus-induced delayed-type hypersensitivity reaction is sequentially mediated by CD8+ and CD4+ T lymphocytes |
| Q35981115 | Wild-type coxsackievirus infection dramatically alters the abundance, heterogeneity, and immunostimulatory capacity of conventional dendritic cells in vivo |
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