| P50 | author | Susan L. Swain | Q56754956 |
| P2093 | author name string | K Kai McKinstry | |
| | Tara M Strutt | |
| P2860 | cites work | The immunity-related GTPase Irgm1 promotes the expansion of activated CD4+ T cell populations by preventing interferon-gamma-induced cell death | Q24643456 |
| | Follicular helper T cells: lineage and location | Q24647274 |
| | Antiviral CD4+ memory T cells are IL-15 dependent | Q24676283 |
| | The NF-kappaB regulator Bcl-3 and the BH3-only proteins Bim and Puma control the death of activated T cells | Q24676636 |
| | Puma cooperates with Bim, the rate-limiting BH3-only protein in cell death during lymphocyte development, in apoptosis induction | Q24677017 |
| | Alveolar epithelial type II cell: defender of the alveolus revisited | Q24791750 |
| | Proapoptotic Bcl-2 relative Bim required for certain apoptotic responses, leukocyte homeostasis, and to preclude autoimmunity | Q28138855 |
| | The caspase-8 inhibitor FLIP promotes activation of NF-kappaB and Erk signaling pathways | Q28145665 |
| | Sustained survivin expression from OX40 costimulatory signals drives T cell clonal expansion | Q28250811 |
| | Proapoptotic BAX and BAK: a requisite gateway to mitochondrial dysfunction and death | Q28363890 |
| | Bmi1 regulates memory CD4 T cell survival via repression of the Noxa gene | Q28588527 |
| | TH1 and TH2 cells: different patterns of lymphokine secretion lead to different functional properties | Q29547848 |
| | TNF- and cancer therapy-induced apoptosis: potentiation by inhibition of NF-kappaB | Q29614706 |
| | An essential role for NF-kappaB in preventing TNF-alpha-induced cell death | Q29614707 |
| | Cellular responses to interferon-gamma | Q29618567 |
| | Suppression of TNF-alpha-induced apoptosis by NF-kappaB | Q29618717 |
| | Multifunctional TH1 cells define a correlate of vaccine-mediated protection against Leishmania major | Q29619125 |
| | Dissection of TNF receptor 1 effector functions: JNK activation is not linked to apoptosis while NF-kappaB activation prevents cell death | Q29620021 |
| | T-cell quality in memory and protection: implications for vaccine design | Q30014840 |
| | Multiple dendritic cell populations activate CD4+ T cells after viral stimulation | Q33321258 |
| | bcl-2 transgene inhibits T cell death and perturbs thymic self-censorship | Q57338704 |
| | Quality and Vaccine Efficacy of CD4+ T Cell Responses Directed to Dominant and Subdominant Epitopes in ESAT-6 from Mycobacterium tuberculosis | Q58827803 |
| | Bax and Bak: back-bone of T cell death | Q62817758 |
| | Naive and effector CD4 T cells differ in their requirements for T cell receptor versus costimulatory signals | Q71687726 |
| | Lack of interferon gamma receptor beta chain and the prevention of interferon gamma signaling in TH1 cells | Q71902890 |
| | A role for non-MHC genetic polymorphism in susceptibility to spontaneous autoimmunity | Q72628270 |
| | Bcl-2 is upregulated at the CD4+ CD8+ stage during positive selection and promotes thymocyte differentiation at several control points | Q72628282 |
| | CD44 supports T cell proliferation and apoptosis by apposition of protein kinases | Q73166201 |
| | FasL promoter activation by IL-2 through SP1 and NFAT but not Egr-2 and Egr-3 | Q73170394 |
| | Activation-induced T cell death occurs at G1A phase of the cell cycle | Q73228067 |
| | Broad programming by IL-2 receptor signaling for extended growth to multiple cytokines and functional maturation of antigen-activated T cells | Q73400763 |
| | Mechanisms of CD95 (APO-1/Fas)-mediated apoptosis | Q77485539 |
| | Withdrawal of stimulation may initiate the transition of effector to memory CD4 cells | Q77522350 |
| | Granzyme B is critical for T cell receptor-induced cell death of type 2 helper T cells | Q80092770 |
| | From vanilla to 28 flavors: multiple varieties of T regulatory cells | Q80141724 |
| | CD4 T cell-mediated protection from lethal influenza: perforin and antibody-mediated mechanisms give a one-two punch | Q80142432 |
| | Persistent depots of influenza antigen fail to induce a cytotoxic CD8 T cell response | Q80427869 |
| | Direct interferon-gamma signaling dramatically enhances CD4+ and CD8+ T cell memory | Q80582310 |
| | CD8+ T cells responding to influenza infection reach and persist at higher numbers than CD4+ T cells independently of precursor frequency | Q80591535 |
| | IL-6 increases primed cell expansion and survival | Q81621879 |
| | Effector differentiation is not prerequisite for generation of memory cytotoxic T lymphocytes | Q39912633 |
| | CD44 regulates survival and memory development in Th1 cells | Q40157095 |
| | Antigen-specific and non-specific CD4+ T cell recruitment and proliferation during influenza infection | Q40391424 |
| | Activated T cell death in vivo mediated by proapoptotic bcl-2 family member bim. | Q40717909 |
| | Diversity of epitope and cytokine profiles for primary and secondary influenza a virus-specific CD8+ T cell responses | Q40820376 |
| | Engagement of CD4 before TCR triggering regulates both Bax- and Fas (CD95)-mediated apoptosis | Q40881618 |
| | Establishment and persistence of virus-specific CD4+ and CD8+ T cell memory | Q41091825 |
| | From naive to memory T cells | Q41091863 |
| | Th1 and Th2 subsets equally undergo Fas-dependent and -independent activation-induced cell death | Q41096065 |
| | Mature T lymphocyte apoptosis--immune regulation in a dynamic and unpredictable antigenic environment | Q33652471 |
| | Shutdown of an acute T cell immune response to viral infection is mediated by the proapoptotic Bcl-2 homology 3-only protein Bim | Q33715752 |
| | Lymphocyte survival--the struggle against death | Q33804304 |
| | Autophagy is induced in CD4+ T cells and important for the growth factor-withdrawal cell death | Q33999904 |
| | Cutting Edge: Limiting amounts of IL-7 do not control contraction of CD4+ T cell responses | Q34023803 |
| | In vivo activation of antigen-specific CD4 T cells. | Q34178091 |
| | The many roles of FAS receptor signaling in the immune system | Q34205697 |
| | Unlike Th1, Th17 cells mediate sustained autoimmune inflammation and are highly resistant to restimulation-induced cell death | Q34217243 |
| | CD28 costimulation can promote T cell survival by enhancing the expression of Bcl-XL. | Q34300766 |
| | A role for antigen in the maintenance of immunological memory | Q34572241 |
| | The biology of interleukin-2. | Q34585827 |
| | Differentiation and function of Th17 T cells | Q34618966 |
| | Plasticity of CD4+ T cell lineage differentiation. | Q34982725 |
| | Overview: apoptotic signaling pathways in the immune system | Q35129689 |
| | Activation-induced cell death in T cells | Q35129715 |
| | Similarities and differences in CD4+ and CD8+ effector and memory T cell generation | Q35207085 |
| | Aberrant contraction of antigen-specific CD4 T cells after infection in the absence of gamma interferon or its receptor. | Q35217552 |
| | IL-2-induced activation-induced cell death is inhibited in IL-15 transgenic mice | Q35296962 |
| | Persistent antigen presentation after acute vesicular stomatitis virus infection | Q35635383 |
| | Control of T cell viability | Q35698562 |
| | Virus-specific antigen presentation by different subsets of cells from lung and mediastinal lymph node tissues of influenza virus-infected mice | Q35848499 |
| | T-lymphocyte death during shutdown of an immune response | Q35920529 |
| | Multiple-cytokine-producing antiviral CD4 T cells are functionally superior to single-cytokine-producing cells | Q35947812 |
| | Convergence of TCR and cytokine signaling leads to FOXO3a phosphorylation and drives the survival of CD4+ central memory T cells | Q36228932 |
| | Rapid default transition of CD4 T cell effectors to functional memory cells | Q36229656 |
| | T cell memory is short-lived in the absence of antigen | Q36230537 |
| | Response of naive antigen-specific CD4+ T cells in vitro: characteristics and antigen-presenting cell requirements | Q36231963 |
| | Interleukin-2 enhances CD4+ T cell memory by promoting the generation of IL-7R alpha-expressing cells | Q36267169 |
| | Type I interferons keep activated T cells alive | Q36367751 |
| | Transforming growth factor beta1 inhibits Fas ligand expression and subsequent activation-induced cell death in T cells via downregulation of c-Myc | Q36367920 |
| | Antigen-specific T helper cell function: differential cytokine expression in primary and memory responses | Q36369065 |
| | Protection from respiratory virus infections can be mediated by antigen-specific CD4(+) T cells that persist in the lungs | Q36369221 |
| | CD4 effector T cell subsets in the response to influenza: heterogeneity, migration, and function | Q36371144 |
| | Ligand-induced autoregulation of IFN-gamma receptor beta chain expression in T helper cell subsets | Q41270009 |
| | Costimulatory requirements of naive CD4+ T cells. ICAM-1 or B7-1 can costimulate naive CD4 T cell activation but both are required for optimum response. | Q41332813 |
| | Autocrine T-cell suicide mediated by APO-1/(Fas/CD95) | Q41371079 |
| | Interleukin 15 controls both proliferation and survival of a subset of memory-phenotype CD8(+) T cells | Q41773432 |
| | Heterogeneity of intracellular cytokine synthesis at the single-cell level in polarized T helper 1 and T helper 2 populations | Q41840721 |
| | Functionally diverse subsets in CD4 T cell responses against influenza. | Q42282182 |
| | IL-15 and IL-2: a matter of life and death for T cells in vivo | Q42639989 |
| | Fas(CD95)/FasL interactions required for programmed cell death after T-cell activation. | Q42830166 |
| | Membrane Fas ligand kills human peripheral blood T lymphocytes, and soluble Fas ligand blocks the killing | Q42951871 |
| | Interleukin-2 programs mouse alpha beta T lymphocytes for apoptosis | Q43539775 |
| | High antigen density and IL-2 are required for generation of CD4 effectors secreting Th1 rather than Th0 cytokines. | Q44959196 |
| | Termination of antigen-specific immunity by CD95 ligand (Fas ligand) and IL-10. | Q44987433 |
| | Heterogeneity of effector phenotype for acute phase and memory influenza A virus-specific CTL. | Q45402819 |
| | Different Dynamics of CD4+ and CD8+ T Cell Responses During and After Acute Lymphocytic Choriomeningitis Virus Infection | Q45710912 |
| | Virus-specific CD8 T cells in peripheral tissues are more resistant to apoptosis than those in lymphoid organs. | Q45723560 |
| | TNF receptor 1 (TNFR1) and CD95 are not required for T cell deletion after virus infection but contribute to peptide-induced deletion under limited conditions | Q45744528 |
| | Bystander virus infection prolongs activated T cell survival | Q45750055 |
| | Functionally distinct T cells in three compartments of the respiratory tract after influenza virus infection. | Q45768117 |
| | Influenza virus RNA in the lung and lymphoid tissue of immunologically intact and CD4-depleted mice | Q45860583 |
| | The roles of Fas/APO-1 (CD95) and TNF in antigen-induced programmed cell death in T cell receptor transgenic mice. | Q46110412 |
| | Differential regulation of antiviral T-cell immunity results in stable CD8+ but declining CD4+ T-cell memory | Q46347403 |
| | IL-2 induces a competitive survival advantage in T lymphocytes | Q46466198 |
| | Lymphoid reservoirs of antigen-specific memory T helper cells | Q46609740 |
| | Granzyme B, a new player in activation-induced cell death, is down-regulated by vasoactive intestinal peptide in Th2 but not Th1 effectors | Q46859572 |
| | Altered T cell receptor signaling and disrupted T cell development in mice lacking Itk. | Q46862843 |
| | Cell-autonomous Fas (CD95)/Fas-ligand interaction mediates activation-induced apoptosis in T-cell hybridomas. | Q46925453 |
| | Biochemical mechanisms of IL-2-regulated Fas-mediated T cell apoptosis | Q47992184 |
| | IL-4 potentiates activated T cell apoptosis via an IL-2-dependent mechanism | Q48024933 |
| | Immunological adjuvants promote activated T cell survival via induction of Bcl-3. | Q48367905 |
| | Memory CD4 T cells emerge from effector T-cell progenitors | Q48887186 |
| | IFN-gamma mediates the death of Th1 cells in a paracrine manner. | Q51968174 |
| | Asymmetric T lymphocyte division in the initiation of adaptive immune responses. | Q51977375 |
| | Anatomical heterogeneity of memory CD4+ T cells due to reversible adaptation to the microenvironment. | Q51995867 |
| | High numbers of IL-2-producing CD8+ T cells during viral infection: correlation with stable memory development. | Q52011061 |
| | Distinct lineages of T(H)1 cells have differential capacities for memory cell generation in vivo. | Q52011176 |
| | CD4(+) T cell effectors can become memory cells with high efficiency and without further division. | Q52018427 |
| | Class II-independent generation of CD4 memory T cells from effectors. | Q52031200 |
| | Following the development of a CD4 T cell response in vivo: from activation to memory formation. | Q52032084 |
| | OX-40: life beyond the effector T cell stage. | Q52036718 |
| | Visualization of peptide-specific T cell immunity and peripheral tolerance induction in vivo. | Q52057633 |
| | IFNgamma sensitizes for apoptosis by upregulating caspase-8 expression through the Stat1 pathway. | Q52545841 |
| | Soluble TNF-alpha but not transmembrane TNF-alpha sensitizes T cells for enhanced activation-induced cell death. | Q53377749 |
| | CD28 engagement and proinflammatory cytokines contribute to T cell expansion and long-term survival in vivo | Q56908416 |
| | CD28/B7 interactions deliver a unique signal to naive T cells that regulates cell survival but not early proliferation | Q56908745 |
| | Reactive Oxygen Species Regulate Activation-Induced T Cell Apoptosis | Q56922123 |
| | T-cell survival | Q56922138 |
| | IL-6 rescues resting mouse T cells from apoptosis | Q56922159 |
| | Experimental Models to Study Molecular Mechanisms Underlying Intestinal Inflammation | Q57197678 |
| | Minimal activation of memory CD8+ T cell by tissue-derived dendritic cells favors the stimulation of naive CD8+ T cells | Q57227696 |
| | Interferon gamma is required for activation-induced death of T lymphocytes | Q36371148 |
| | Interleukin 7 regulates the survival and generation of memory CD4 cells | Q36371578 |
| | IL-7 promotes the transition of CD4 effectors to persistent memory cells | Q36371590 |
| | Interleukin 2, but not other common gamma chain-binding cytokines, can reverse the defect in generation of CD4 effector T cells from naive T cells of aged mice | Q36375375 |
| | High level expression of CD43 inhibits T cell receptor/CD3-mediated apoptosis | Q36375645 |
| | Unequal death in T helper cell (Th)1 and Th2 effectors: Th1, but not Th2, effectors undergo rapid Fas/FasL-mediated apoptosis | Q36377260 |
| | CD4 regulates susceptibility to Fas ligand- and tumor necrosis factor-mediated apoptosis | Q36400376 |
| | Unexpected prolonged presentation of influenza antigens promotes CD4 T cell memory generation | Q36402838 |
| | Repeated stimulation of CD4 effector T cells can limit their protective function | Q36403433 |
| | cFLIP regulation of lymphocyte activation and development | Q36405075 |
| | Long-lived virus-reactive memory T cells generated from purified cytokine-secreting T helper type 1 and type 2 effectors. | Q36446889 |
| | CD4+ T-cell memory: generation and multi-faceted roles for CD4+ T cells in protective immunity to influenza. | Q36494486 |
| | The microbial mimic poly IC induces durable and protective CD4+ T cell immunity together with a dendritic cell targeted vaccine | Q36497412 |
| | Apoptosis regulators Fas and Bim cooperate in shutdown of chronic immune responses and prevention of autoimmunity | Q36501636 |
| | Control of CD4+ T-cell memory by cytokines and costimulators | Q36528927 |
| | Not all CD4+ memory T cells are long lived | Q36528938 |
| | Immunisation with BCG and recombinant MVA85A induces long-lasting, polyfunctional Mycobacterium tuberculosis-specific CD4+ memory T lymphocyte populations | Q36628376 |
| | Protective influenza-specific CD8 T cell responses require interactions with dendritic cells in the lungs | Q36742280 |
| | Life and death in peripheral T cells | Q36858872 |
| | IFN-gamma acts directly on activated CD4+ T cells during mycobacterial infection to promote apoptosis by inducing components of the intracellular apoptosis machinery and by inducing extracellular proapoptotic signals | Q36867809 |
| | CD8 T cell dysfunction during chronic viral infection. | Q36893050 |
| | Type II collagen autoimmunity in a mouse model of human rheumatoid arthritis | Q36984686 |
| | The effector to memory transition of CD4 T cells. | Q37063091 |
| | Concepts of activated T cell death | Q37090795 |
| | Antigen-experienced T cells limit the priming of naive T cells during infection with Leishmania major | Q37227400 |
| | Abundant c-Fas-associated death domain-like interleukin-1-converting enzyme inhibitory protein expression determines resistance of T helper 17 cells to activation-induced cell death | Q37291626 |
| | IL-10 deficiency unleashes an influenza-specific Th17 response and enhances survival against high-dose challenge | Q37297787 |
| | Plasmodium falciparum apical membrane antigen 1 vaccine elicits multifunctional CD4 cytokine-producing and memory T cells | Q37349074 |
| | Interleukin-2 in the development and control of inflammatory disease | Q37374918 |
| | Different routes of bacterial infection induce long-lived TH1 memory cells and short-lived TH17 cells | Q37483184 |
| | Heterogeneity of CD4+ memory T cells: functional modules for tailored immunity | Q37578374 |
| | The T lymphocyte in experimental allergic encephalomyelitis | Q37925549 |
| | Rapid culling of the CD4+ T cell repertoire in the transition from effector to memory | Q38574697 |
| | Interleukin-2: inception, impact, and implications | Q39603037 |
| | T-lymphocyte downregulation after acute viral infection is not dependent on CD95 (Fas) receptor-ligand interactions. | Q39877053 |
| P304 | page(s) | 110-124 | |
| P577 | publication date | 2010-07-01 | |
| P1433 | published in | Immunological Reviews | Q15724582 |
| P1476 | title | Regulation of CD4+ T-cell contraction during pathogen challenge | |
| P478 | volume | 236 | |