| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1009618501 |
| P356 | DOI | 10.1038/369648A0 |
| P2888 | exact match | https://scigraph.springernature.com/pub.10.1038/369648a0 |
| P698 | PubMed publication ID | 7516038 |
| P2093 | author name string | Ahmed R | |
| Lau LL | |||
| Jamieson BD | |||
| Somasundaram T | |||
| P2860 | cites work | T cell memory is short-lived in the absence of antigen | Q36230537 |
| Antivirally protective cytotoxic T cell memory to lymphocytic choriomeningitis virus is governed by persisting antigen | Q36231954 | ||
| T cell memory. Long-term persistence of virus-specific cytotoxic T cells | Q36356494 | ||
| Positive selection of CD8+ T cells induced by major histocompatibility complex binding peptides in fetal thymic organ culture | Q36361722 | ||
| The maintenance and regulation of the humoral immune response: persisting antigen and the role of follicular antigen-binding dendritic cells as accessory cells | Q40300507 | ||
| T-cell memory: new perspectives | Q40710707 | ||
| Lifespans of naive, memory and effector lymphocytes | Q40832453 | ||
| 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 | ||
| Virus-specific memory T cells are Pgp-1+ and can be selectively activated with phorbol ester and calcium ionophore | Q43615296 | ||
| Analyses of the cytotoxic T lymphocyte responses to glycoprotein and nucleoprotein components of lymphocytic choriomeningitis virus | Q43816895 | ||
| B-cell memory is short-lived in the absence of antigen. | Q52120670 | ||
| Peptide contributes to the specificity of positive selection of CD8+ T cells in the thymus | Q63363368 | ||
| P433 | issue | 6482 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | cytotoxicity | Q246181 |
| P1104 | number of pages | 5 | |
| P304 | page(s) | 648-652 | |
| P577 | publication date | 1994-06-01 | |
| P1433 | published in | Nature | Q180445 |
| P1476 | title | Cytotoxic T-cell memory without antigen | |
| P478 | volume | 369 |
| Q35957424 | A Single 17D Yellow Fever Vaccination Provides Lifelong Immunity; Characterization of Yellow-Fever-Specific Neutralizing Antibody and T-Cell Responses after Vaccination |
| Q36986726 | A brief history of CD8 T cells. |
| Q35601931 | A comparison of T cell memory against the same antigen induced by virus versus intracellular bacteria. |
| Q35196530 | A highly optimized DNA vaccine confers complete protective immunity against high-dose lethal lymphocytic choriomeningitis virus challenge. |
| Q89973084 | A modeling platform for the lymphatic system |
| Q33905201 | A new theory of cytotoxic T-lymphocyte memory: implications for HIV treatment. |
| Q41074050 | A non-retroviral RNA virus persists in DNA form |
| Q40896159 | A repetitive sequence of Epstein-Barr virus nuclear antigen 6 comprises overlapping T cell epitopes which induce HLA-DR-restricted CD4(+) T lymphocytes |
| Q34572241 | A role for antigen in the maintenance of immunological memory |
| Q73782683 | A simple method for evaluating the rejection of grafted spleen cells by flow cytometry and tracing adoptively transferred cells by light microscopy |
| Q33882896 | Absence of mouse 2B4 promotes NK cell-mediated killing of activated CD8+ T cells, leading to prolonged viral persistence and altered pathogenesis |
| Q33932737 | Accessing complexity: the dynamics of virus-specific T cell responses. |
| Q41672935 | Alpha beta and gamma delta T-cell networks and their roles in natural resistance to viral infections |
| Q58690522 | An Emerging Role for Serine Protease Inhibitors in T Lymphocyte Immunity and Beyond |
| Q41234466 | An HLA-B35-restricted epitope modified at an anchor residue results in an antagonist peptide |
| Q40657844 | Antigen and memory CD8 T cells: were they both right? |
| Q36381049 | Antigen is required for the activation of effector activities, whereas interleukin 2 Is required for the maintenance of memory in ovalbumin-specific, CD8+ cytotoxic T lymphocytes |
| Q41492285 | Antigen localisation regulates immune responses in a dose- and time-dependent fashion: a geographical view of immune reactivity |
| Q45282363 | Antigen-specific CD8+ T cell subset distribution in lymph nodes draining the site of herpes simplex virus infection |
| 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 |
| Q41504874 | Antiviral immunity |
| Q28302762 | Antiviral pressure exerted by HIV-1-specific cytotoxic T lymphocytes (CTLs) during primary infection demonstrated by rapid selection of CTL escape virus |
| Q39580928 | Apoptotic regulation of T cells and absence of immune deficiency in virus-infected gamma interferon receptor knockout mice |
| Q41091852 | Aspects of cytotoxic T cell memory |
| Q42596681 | Assessment of CD4(+) and CD8 (+) T cell responses using MHC class I and II tetramers |
| Q40907781 | Attrition of T cell memory: selective loss of LCMV epitope-specific memory CD8 T cells following infections with heterologous viruses |
| Q81483915 | Augmentation of post transplant immunity: antigen encounter at the time of hematopoietic stem cell transplantation enhances antigen-specific donor T-cell responses in the post transplant repertoire |
| Q41091833 | B-T lymphocyte interactions in the generation and survival of memory cells. |
| Q39589039 | Biology of attenuated modified vaccinia virus Ankara recombinant vector in mice: virus fate and activation of B- and T-cell immune responses in comparison with the Western Reserve strain and advantages as a vaccine |
| Q52562585 | Biomagnetic isolation of antigen-specific CD8+ T cells usable in immunotherapy. |
| Q35835410 | Bone marrow is a major site of long-term antibody production after acute viral infection |
| Q52019514 | Both CD45R(low) and CD45R(high) "revertant" CD4 memory T cells provide help for memory B cells. |
| Q47873807 | Bystander stimulation of T cells in vivo by cytokines |
| Q34003227 | CD4(+) T-cell subsets that mediate immunological memory to Mycobacterium tuberculosis infection in mice |
| Q52040195 | CD4+ T-cell memory, CD45R subsets and the persistence of antigen--a unifying concept. |
| Q47972786 | CD4-CD8-C.B-17 SCID thymocytes enter the CD4+CD8+ stage in the presence of neonatally grafted T cells |
| Q39873438 | CD4-deficient mice have reduced levels of memory cytotoxic T lymphocytes after immunization and show diminished resistance to subsequent virus challenge. |
| Q35873254 | CD40 ligand-deficient mice generate a normal primary cytotoxic T-lymphocyte response but a defective humoral response to a viral infection |
| Q33783902 | CD40 ligand-mediated interactions are involved in the generation of memory CD8(+) cytotoxic T lymphocytes (CTL) but are not required for the maintenance of CTL memory following virus infection |
| Q41898717 | CD40L-deficient mice show deficits in antiviral immunity and have an impaired memory CD8+ CTL response. |
| Q52030364 | CD45 isoform phenotypes of human T cells: CD4(+)CD45RA(-)RO(+) memory T cells re-acquire CD45RA without losing CD45RO. |
| Q42159952 | CD45RC isoforms define two types of CD4 memory T cells, one of which depends on persisting antigen |
| Q36366705 | CD8 T cell memory in B cell-deficient mice |
| Q44126823 | CD8+ T-cell memory to viruses |
| Q34735857 | CTLA4 mediates antigen-specific apoptosis of human T cells |
| Q71785375 | Cellular competition modulates survival and selection of CD8+ T cells |
| Q41468156 | Chitosan hydrogel vaccine generates protective CD8 T cell memory against mouse melanoma |
| Q34869878 | Coadministration of HIV vaccine vectors with vaccinia viruses expressing IL-15 but not IL-2 induces long-lasting cellular immunity |
| Q52040373 | Compartmentalization of bacterial antigens: differential effects on priming of CD8 T cells and protective immunity. |
| Q24657414 | Conserved T cell receptor repertoire in primary and memory CD8 T cell responses to an acute viral infection |
| Q45535661 | Contemporaneous fluctuations in T cell responses to persistent herpes virus infections |
| Q36365305 | Control of CD4 effector fate: transforming growth factor beta 1 and interleukin 2 synergize to prevent apoptosis and promote effector expansion |
| Q34891171 | Coregulation of CD8+ T cell exhaustion by multiple inhibitory receptors during chronic viral infection. |
| Q33971036 | Costimulation in antiviral immunity: differential requirements for CD4(+) and CD8(+) T cell responses |
| Q52040367 | Counting antigen-specific CD8 T cells: a reevaluation of bystander activation during viral infection. |
| Q27469883 | Cross-reactivity between hepatitis C virus and Influenza A virus determinant-specific cytotoxic T cells |
| Q36444180 | Cure of chronic viral infection and virus-induced type 1 diabetes by neutralizing antibodies |
| Q41115176 | Cutaneous leishmaniasis: a model for analysis of the immunoregulation by accessory cells |
| Q42745422 | Cutting edge: CXCR4 is critical for CD8+ memory T cell homeostatic self-renewal but not rechallenge self-renewal |
| Q34979245 | Cytokine detection by ELISPOT: relevance for immunological studies in type 1 diabetes |
| Q47591127 | Cytokine-Mediated Regulation of CD8 T-Cell Responses During Acute and Chronic Viral Infection |
| Q36199934 | Cytomegalovirus Reinfections Stimulate CD8 T-Memory Inflation |
| Q36363678 | Cytotoxic T lymphocyte response to a wild type hepatitis B virus epitope in patients chronically infected by variant viruses carrying substitutions within the epitope. |
| Q34194927 | Cytotoxic and proliferative T cell responses in HIV-1-infected Macaca nemestrina |
| Q35838136 | DNA vaccination against persistent viral infection. |
| Q35129707 | Death and Baxes: mechanisms of lymphotrophic cytokines |
| Q35377489 | Defects in apoptosis increase memory CD8+ T cells following infection of Bim-/-Faslpr/lpr mice |
| Q43760325 | Design of a polyepitope construct for the induction of HLA-A0201-restricted HIV 1-specific CTL responses using HLA-A*0201 transgenic, H-2 class I KO mice |
| Q35865606 | Detection of simian immunodeficiency virus (SIV)-specific CD8+ T cells in macaques protected from SIV challenge by prior SIV subunit vaccination. |
| Q36423118 | Development of a new hydrogen peroxide–based vaccine platform. |
| Q41834240 | Developmental regulation of Lck targeting to the CD8 coreceptor controls signaling in naive and memory T cells |
| Q45710912 | Different Dynamics of CD4+ and CD8+ T Cell Responses During and After Acute Lymphocytic Choriomeningitis Virus Infection |
| Q37429321 | Differential T cell responses to residual viral antigen prolong CD4+ T cell contraction following the resolution of infection |
| Q35689057 | Differential clearance and immune responses to tick cell-derived versus macrophage culture-derived Ehrlichia chaffeensis in mice |
| Q33532640 | Direct presentation is sufficient for an efficient anti-viral CD8+ T cell response |
| Q34644494 | Dissecting the complexity of the memory T cell response |
| Q36376757 | Distinct costimulatory molecules are required for the induction of effector and memory cytotoxic T lymphocytes |
| Q52208717 | Do we need 3 doses of hepatitis B vaccine? |
| Q41540707 | Dynamics of HIV variants and specific cytotoxic T-cell recognition in nonprogressors and progressors. |
| Q24682788 | ENV-specific cytotoxic T lymphocyte responses in HIV seronegative health care workers occupationally exposed to HIV-contaminated body fluids |
| Q79159017 | Effector HIV‐specific cytotoxic T‐lymphocyte activity in long‐term nonprogressors: Associations with viral replication and progression |
| Q35884254 | Effector and memory CD8+ T cells as seen in immunity to malaria. |
| Q46686105 | Enhanced ELISPOT detection of antigen-specific T cell responses from cryopreserved specimens with addition of both IL-7 and IL-15--the Amplispot assay. |
| Q33812288 | Enrichment of immediate-early 1 (m123/pp89) peptide-specific CD8 T cells in a pulmonary CD62L(lo) memory-effector cell pool during latent murine cytomegalovirus infection of the lungs |
| Q49376152 | Epigenetic Maintenance of Acquired Gene Expression Programs during Memory CD8 T Cell Homeostasis. |
| Q92947188 | Epigenetic signature of PD-1+ TCF1+ CD8 T cells that act as resource cells during chronic viral infection and respond to PD-1 blockade |
| Q36367550 | Epitope focusing in the primary cytotoxic T cell response to Epstein-Barr virus and its relationship to T cell memory |
| Q41091825 | Establishment and persistence of virus-specific CD4+ and CD8+ T cell memory |
| Q77296861 | Evaluation of the stability and immunogenicity of autoclaved and nonautoclaved preparations of a vaccine against American tegumentary leishmaniasis |
| Q34019945 | Evolution of the CD8 T-cell repertoire during infections |
| Q39737687 | Expansion of pre-existing, lymph node-localized CD8+ T cells during supervised treatment interruptions in chronic HIV-1 infection |
| Q58582058 | Expressionin vivo of CD45RA, CD45RB and CD44 on T cell receptor-transgenic CD8+ T cells following immunization |
| Q41492227 | Factors controlling the turnover of T memory cells |
| Q34083121 | Final report of the phase I/II clinical trial of the E75 (nelipepimut-S) vaccine with booster inoculations to prevent disease recurrence in high-risk breast cancer patients |
| Q52032084 | Following the development of a CD4 T cell response in vivo: from activation to memory formation. |
| Q36951600 | FoxO1 controls effector-to-memory transition and maintenance of functional CD8 T cell memory. |
| Q52037874 | From naive to memory. Development and regulation of CD4+ T cell responses. |
| Q37804530 | From vaccines to memory and back |
| Q35064049 | Functional differences between memory and naive CD8 T cells |
| Q35889447 | Functional management of an antiviral cytotoxic T-cell response |
| Q36452614 | Functional signatures in antiviral T-cell immunity for monitoring virus-associated diseases. |
| Q33649172 | Functionally heterogeneous CD8(+) T-cell memory is induced by Sendai virus infection of mice |
| Q52020873 | Gamma chain required for naïve CD4+ T cell survival but not for antigen proliferation. |
| Q33683440 | General and specific immunosuppression caused by antiviral T-cell responses |
| Q46137070 | Generation and in vivo persistence of polarized Th1 and Th2 memory cells |
| Q34167992 | Generation and maintenance of memory T cells |
| Q41102899 | Generation of T-cell memory |
| Q34527878 | Generation of cytotoxic and humoral immune responses by nonreplicative recombinant Semliki Forest virus. |
| Q37773428 | Generation of effector CD8+ T cells and their conversion to memory T cells |
| Q41073930 | Growth stimulation of tumor-specific cytotoxic T lymphocytes on concanavalin a-immobilized carrier beads |
| Q39906478 | HIV versus the immune system: another apparent victory for the virus |
| Q74265095 | HIV-1 dynamics revisited: biphasic decay by cytotoxic T lymphocyte killing? |
| Q28291024 | HIV-specific cytotoxic T-cells in HIV-exposed but uninfected Gambian women |
| Q37560728 | Heterologous Immunity and Persistent Murine Cytomegalovirus Infection |
| Q35095576 | Heterologous immunity provides a potent barrier to transplantation tolerance |
| Q35946213 | Highly attenuated modified vaccinia virus Ankara (MVA) as an effective recombinant vector: a murine tumor model |
| Q37374676 | Highly efficient antiviral CD8+ T-cell induction by peptides coupled to the surfaces of liposomes |
| Q34180992 | Homeostasis of alpha beta TCR+ T cells. |
| Q36528980 | Homeostasis of memory T cells |
| Q45373528 | Homeostatic Turnover of Virus-Specific Memory CD8 T Cells Occurs Stochastically and Is Independent of CD4 T Cell Help |
| Q36666331 | Host and viral factors in the immunopathogenesis of primary hepatitis C virus infection |
| Q34143952 | Host factors influencing viral persistence. |
| Q33247444 | How does cross-reactive stimulation affect the longevity of CD8+ T cell memory? |
| Q39874178 | Human cytotoxic T-cell memory: long-lived responses to vaccinia virus |
| Q34207616 | Human memory T cells: lessons from stem cell transplantation |
| Q36529005 | Human virus-specific CD8+ T cells: diversity specialists. |
| Q52040025 | Humoral immunity due to long-lived plasma cells. |
| Q33590103 | IFN-gamma induces the erosion of preexisting CD8 T cell memory during infection with a heterologous intracellular bacterium |
| Q33952031 | IL-15 plays a major role in the persistence of Tax-specific CD8 cells in HAM/TSP patients |
| Q34179921 | IL-21 deficiency influences CD8 T cell quality and recall responses following an acute viral infection |
| Q33930706 | IL-7 differentially regulates cell cycle progression and HIV-1-based vector infection in neonatal and adult CD4+ T cells |
| Q40046462 | IL-7 plays a critical role for the homeostasis of allergen-specific memory CD4 T cells in the lung and airways |
| Q35319176 | IL-7 regulates basal homeostatic proliferation of antiviral CD4+T cell memory |
| Q33750857 | ITK tunes IL-4-induced development of innate memory CD8+ T cells in a γδ T and invariant NKT cell-independent manner |
| Q38577713 | Immune Memory and Exhaustion: Clinically Relevant Lessons from the LCMV Model |
| Q33718350 | Immune deficiency, immune silencing, and clonal exhaustion of T cell responses during viral infections |
| Q39589794 | Immune responses following neonatal DNA vaccination are long-lived, abundant, and qualitatively similar to those induced by conventional immunization |
| Q39430336 | Immunization with the Leishmania infantum recombinant cyclophilin protein 1 confers partial protection to subsequent parasite infection and generates specific memory T cells. |
| Q51129415 | Immunogenicity and persistence of a targeted anti-caries DNA vaccine. |
| Q45758136 | Immunohistological characterization of the local cellular response directed against pseudorabies virus in pigs |
| Q52804916 | Immunological memories of the bone marrow. |
| Q73458972 | Immunological memory |
| Q52057680 | Immunology. Memories are made of this? |
| Q41225463 | Immunopathology or organ-specific autoimmunity as a consequence of virus infection |
| Q34370427 | In vivo estimates of division and death rates of human T lymphocytes |
| Q35557069 | In vivo proliferation of naïve and memory influenza-specific CD8(+) T cells |
| Q46486509 | Induction of bystander T cell proliferation by viruses and type I interferon in vivo |
| Q71803068 | Induction of human autologous cytotoxic T lymphocytes on formalin-fixed and paraffin-embedded tumour sections |
| Q36366635 | Induction of long-lived germinal centers associated with persisting antigen after viral infection |
| Q39028785 | Induction of multifunctional human immunodeficiency virus type 1 (HIV-1)-specific T cells capable of proliferation in healthy subjects by using a prime-boost regimen of DNA- and modified vaccinia virus Ankara-vectored vaccines expressing HIV-1 Gag c |
| Q34612543 | Influence of effector molecules on the CD8(+) T cell response to infection |
| Q33768584 | Initial T cell frequency dictates memory CD8+ T cell lineage commitment |
| Q28390068 | Integrated defense system overlaps as a disease model: with examples for multiple chemical sensitivity |
| Q36053149 | Interaction between unrelated viruses during in vivo co-infection to limit pathology and immunity |
| Q42265302 | Interconnected subsets of memory follicular helper T cells have different effector functions |
| Q52034883 | Interferon-beta mediates stromal cell rescue of T cells from apoptosis. |
| Q36369770 | Interleukin (IL)-15 and IL-7 jointly regulate homeostatic proliferation of memory phenotype CD8+ cells but are not required for memory phenotype CD4+ cells |
| Q36267169 | Interleukin-2 enhances CD4+ T cell memory by promoting the generation of IL-7R alpha-expressing cells |
| Q34089124 | Interplay between regulatory T cells and PD-1 in modulating T cell exhaustion and viral control during chronic LCMV infection |
| Q39239465 | Interpreting the effect of vaccination on steady state infection in animals challenged with Simian immunodeficiency virus |
| Q45869584 | Intra-pinna anti-tumor vaccination with self-replicating infectious RNA or with DNA encoding a model tumor antigen and a cytokine |
| Q82271563 | Intrathecal immune responses to EBV in early MS |
| Q40173243 | Kinetics of Lymphocyte Proliferation during Primary Immune Response in Macaques Infected with Pathogenic Simian Immunodeficiency Virus SIVmac251: Preliminary Report of the Effect of Early Antiviral Therapy |
| Q44506505 | Kinetics of expansion of SIV Gag-specific CD8+ T lymphocytes following challenge of vaccinated macaques |
| Q77952319 | Kinetics of the response of naive and memory CD8 T cells to antigen: similarities and differences |
| Q37492847 | Kinetics of virus-specific CD8+ T cells and the control of human immunodeficiency virus infection |
| Q34104222 | Lifelong protection against hepatitis B: the role of vaccine immunogenicity in immune memory |
| Q40414738 | Lifespan of lymphocytes |
| Q44465948 | Limiting dilution analysis of virus-specific memory B cells by an ELISPOT assay |
| Q28206693 | Lineage relationship and protective immunity of memory CD8 T cell subsets |
| Q36386097 | Local immunity by tissue-resident CD8(+) memory T cells. |
| Q36366666 | Long-lasting CD8 T cell memory in the absence of CD4 T cells or B cells. |
| Q37359318 | Long-lasting memory T cell responses following self-limited acute hepatitis B |
| Q36367536 | Long-lived cytotoxic T lymphocyte memory in mucosal tissues after mucosal but not systemic immunization |
| Q40575688 | Long-lived memory T lymphocyte responses after hantavirus infection |
| Q51982621 | Long-lived memory T lymphocyte responses against SARS coronavirus nucleocapsid protein in SARS-recovered patients. |
| Q33784950 | Long-term CD4 Th1 and Th2 memory following acute lymphocytic choriomeningitis virus infection |
| Q35979288 | Long-term T cell memory requires the surface expression of self-peptide/major histocompatibility complex molecules |
| Q41195152 | Long-term humoral immunity against viruses: revisiting the issue of plasma cell longevity |
| Q45771097 | Long-term restoration of immunity against Epstein-Barr virus infection by adoptive transfer of gene-modified virus-specific T lymphocytes |
| Q52053471 | Lymphocyte memory and affinity selection. |
| Q46609740 | Lymphoid reservoirs of antigen-specific memory T helper cells |
| Q34770383 | Maintaining the norm: T-cell homeostasis |
| Q34157833 | Making memories that last a lifetime: heritable functions of self-renewing memory CD8 T cells |
| Q37419599 | Massive expansion of antigen-specific CD8+ T cells during an acute virus infection |
| Q34885695 | Mathematical modeling provides kinetic details of the human immune response to vaccination. |
| Q35883539 | Maturation of the cellular and humoral immune responses to persistent infection in horses by equine infectious anemia virus is a complex and lengthy process. |
| Q41681561 | Mechanisms of viral clearance and persistence |
| Q72797875 | Membrane CD45R isoform exchange on CD4 T cells is rapid, frequent and dynamic in vivo |
| Q58581969 | Memory CD44int CD8 T cells show increased proliferative responses and IFN-γ production following antigenic challenge in vitro |
| Q35659317 | Memory CD8 T cell transcriptional plasticity |
| Q36455241 | Memory CD8 T cells specific for plasmodia liver-stage antigens maintain protracted protection against malaria |
| Q34152220 | Memory CD8 T-cell differentiation during viral infection |
| Q27480404 | Memory CD8+ T cells are gatekeepers of the lymph node draining the site of viral infection |
| Q38202729 | Memory T cells maintain protracted protection against malaria. |
| Q34241501 | Memory T cells persisting within the brain after local infection show functional adaptations to their tissue of residence |
| Q52046277 | Memory alloreactive cytotoxic T cells do not require costimulation for activation in vitro. |
| Q36528984 | Memory of mice and men: CD8+ T-cell cross-reactivity and heterologous immunity |
| Q42604544 | Memory phenotype CD8+ T cells with innate function selectively develop in the absence of active Itk. |
| Q36377209 | Minimal bystander activation of CD8 T cells during the virus-induced polyclonal T cell response |
| Q39240571 | Model with two types of CTL regulation and experiments on CTL dynamics |
| Q38255612 | Modeling T cell responses to antigenic challenge |
| Q36014942 | Modeling the mechanisms of acute hepatitis B virus infection |
| Q28137842 | Modelling T-cell memory by genetic marking of memory T cells in vivo |
| Q36758155 | Models of immune memory: on the role of cross-reactive stimulation, competition, and homeostasis in maintaining immune memory |
| Q34625185 | Natural killer T cell and TLR9 agonists as mucosal adjuvants for sublingual vaccination with clade C HIV-1 envelope protein |
| Q52035177 | Naïve cytotoxic T lymphocytes spontaneously acquire effector function in lymphocytopenic recipients: A pitfall for T cell memory studies? |
| Q34136406 | No one is naive: the significance of heterologous T-cell immunity. |
| Q36121046 | Non-malignant clonal expansions of CD8+ memory T cells in aged individuals |
| Q36528999 | Not-so-great expectations: re-assessing the essence of T-cell memory. |
| Q37444300 | OX40 costimulatory signals potentiate the memory commitment of effector CD8+ T cells |
| Q38958324 | On Peptides and Altered Peptide Ligands: From Origin, Mode of Action and Design to Clinical Application (Immunotherapy). |
| Q41091839 | On T cell memory: arguments for antigen dependence |
| Q34712736 | On differences between immunity and immunological memory |
| Q52055385 | On the cellular basis of immunological T cell memory |
| Q37361402 | On the role of antigen in maintaining cytotoxic T-cell memory |
| Q46925820 | Origin and differentiation of human memory CD8 T cells after vaccination |
| Q27478466 | Patients with chronic hepatitis C have circulating cytotoxic T cells which recognize hepatitis C virus-encoded peptides binding to HLA-A2.1 molecules |
| Q52015249 | Peptide-pulsed splenic dendritic cells prime long-lasting CD8(+) T cell memory in the absence of cross-priming by host APC. |
| Q33632396 | Peripheral T cell survival |
| Q34235888 | Perpetuation of immunological memory: a relay hypothesis |
| Q35726474 | Persistence of lymphocytic choriomeningitis virus at very low levels in immune mice. |
| Q34070814 | Persistence of viral infection despite similar killing efficacy of antiviral CD8(+) T cells during acute and chronic phases of infection |
| Q37128771 | Persistent parasites and immunologic memory in cutaneous leishmaniasis: implications for vaccine designs and vaccination strategies. |
| Q35636065 | Plasticity of T cell memory responses to viruses |
| Q33803386 | Polyomavirus-infected dendritic cells induce antiviral CD8(+) T lymphocytes |
| Q35111246 | Potent induction of long-term CD8+ T cell memory by short-term IL-4 exposure during T cell receptor stimulation |
| Q33593103 | Preferential amplification of CD8 effector-T cells after transcutaneous application of an inactivated influenza vaccine: a randomized phase I trial |
| Q45751279 | Priming of CD8+ CTL effector cells in mice by immunization with a stress protein-influenza virus nucleoprotein fusion molecule |
| Q52012309 | Programmed contraction of CD8(+) T cells after infection. |
| Q27488288 | Prophylactic DNA vaccine for hepatitis C virus (HCV) infection: HCV-specific cytotoxic T lymphocyte induction and protection from HCV-recombinant vaccinia infection in an HLA-A2.1 transgenic mouse model. |
| Q35959154 | Protection against immunopathological consequences of a viral infection by activated but not resting cytotoxic T cells: T cell memory without "memory T cells"? |
| Q35780228 | Protective antifungal memory CD8(+) T cells are maintained in the absence of CD4(+) T cell help and cognate antigen in mice |
| Q34007297 | Protective efficacy of H antigen from Histoplasma capsulatum in a murine model of pulmonary histoplasmosis |
| Q36401710 | Protective heterologous antiviral immunity and enhanced immunopathogenesis mediated by memory T cell populations |
| Q36410459 | Protective immunity against hepatitis C virus infection |
| Q37290484 | Protective long-term antibody memory by antigen-driven and T help-dependent differentiation of long-lived memory B cells to short-lived plasma cells independent of secondary lymphoid organs |
| Q34669540 | Qualitative differences between naïve and memory T cells |
| Q36806548 | Quantifying T lymphocyte turnover |
| Q35635463 | Quantitating the magnitude of the lymphocytic choriomeningitis virus-specific CD8 T-cell response: it is even bigger than we thought |
| Q33647962 | Quantitative analysis of the acute and long-term CD4(+) T-cell response to a persistent gammaherpesvirus |
| Q33839044 | Quintuple deglycosylation mutant of simian immunodeficiency virus SIVmac239 in rhesus macaques: robust primary replication, tightly contained chronic infection, and elicitation of potent immunity against the parental wild-type strain |
| Q41603477 | Recombinant Listeria monocytogenes as a live vaccine vehicle and a probe for studying cell-mediated immunity |
| Q34400216 | Recombinant Listeria monocytogenes as a live vaccine vehicle for the induction of protective anti-viral cell-mediated immunity |
| Q39683041 | Recombinant vaccinia virus-induced T-cell immunity: quantitation of the response to the virus vector and the foreign epitope |
| Q74082715 | Reconstitution of gammadelta T cell repertoire diversity after human allogeneic hematopoietic cell transplantation and the role of peripheral expansion of mature T cell population in the graft |
| Q33848737 | Recruitment times, proliferation, and apoptosis rates during the CD8(+) T-cell response to lymphocytic choriomeningitis virus |
| Q48535536 | Recruitment, activation and proliferation of CD8+ memory T cells in an immunoprivileged site. |
| Q41195473 | Reduction of otherwise remarkably stable virus-specific cytotoxic T lymphocyte memory by heterologous viral infections. |
| Q37998155 | Regulating naïve and memory CD8 T cell homeostasis--a role for protein tyrosine phosphatases |
| Q30440743 | Regulation of cytokine production by virus-specific CD8 T cells in the lungs |
| Q34515843 | Regulation of naïve and memory T-cell homeostasis |
| Q35180166 | Remembrance of antigens past: new insights into memory T cells. |
| Q37135496 | Requirement of B cells for generating CD4+ T cell memory |
| Q77719570 | Requirements for memory maintenance |
| Q36228023 | Resolution of a chronic viral infection after interleukin-10 receptor blockade |
| Q36377398 | Resting memory CD8+ T cells are hyperreactive to antigenic challenge in vitro |
| Q24336998 | Retracted: The protein LEM promotes CD8⁺ T cell immunity through effects on mitochondrial respiration |
| Q35212655 | Role of B cells in maintaining helper T-cell memory |
| Q40077061 | Role of Different Subpopulations of CD8+ T Cells during HIV Exposure and Infection. |
| Q36432691 | Role of lymphocytic choriomeningitis virus (LCMV) in understanding viral immunology: past, present and future |
| Q37747298 | Role of tumor necrosis factor receptors in regulating CD8 T-cell responses during acute lymphocytic choriomeningitis virus infection |
| Q36228495 | Secondary memory CD8+ T cells are more protective but slower to acquire a central-memory phenotype. |
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| Q57351531 | Single-step, multiple retroviral transduction of human T cells |
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| Q36401170 | Stability and diversity of T cell receptor repertoire usage during lymphocytic choriomeningitis virus infection of mice |
| Q33846357 | Stimulation of memory T cells by cytokines |
| Q33776104 | Stimulation of naïve and memory T cells by cytokines |
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| Q35768790 | The Nucleoprotein Is Required for Lymphocytic Choriomeningitis Virus-Based Vaccine Vector Immunogenicity |
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| Q45767731 | The hepatitis B virus persists for decades after patients' recovery from acute viral hepatitis despite active maintenance of a cytotoxic T-lymphocyte response. |
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| Q33879538 | The role of antigen-independent persistence of memory cytotoxic T lymphocytes |
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| Q34120067 | The role of mTOR in memory CD8 T-cell differentiation |
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| Q33766848 | Theoretical analysis of the evolution of immune memory |
| Q73263520 | Therapeutic use of IL-2 to enhance antiviral T-cell responses in vivo |
| Q52047566 | Tickling memory T cells. |
| Q40874040 | Tracking genetically engineered lymphocytes long-term reveals the dynamics of T cell immunological memory. |
| Q37167757 | Transience of MHC Class I-restricted antigen presentation after influenza A virus infection |
| Q41455911 | Tumor recognition by the cellular immune system: new aspects of tumor immunology. |
| Q34792441 | Uncertainties - discrepancies in immunology |
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| Q39169186 | Understanding memory CD8+ T cells |
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| Q34138324 | Use of booster inoculations to sustain the clinical effect of an adjuvant breast cancer vaccine: from US Military Cancer Institute Clinical Trials Group Study I-01 and I-02. |
| Q41225504 | Using transgenic mouse models to dissect the pathogenesis of virus-induced autoimmune disorders of the islets of Langerhans and the central nervous system |
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| Q36229254 | Viral antigen and extensive division maintain virus-specific CD8 T cells during chronic infection |
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