Regulatory T cells differentially modulate the maturation and apoptosis of human CD8+ T-cell subsets.

Abstract:

:The balanced manifestation of effector functions and the generation of long-living memory cells is a hallmark of efficient CD8(+) T-cell response. Accumulating data pinpoint CD4(+) CD25(high) regulatory T (Treg) cells as a key factor for the inefficiency of CD8(+) T-cell responses in viral persistence. Little is known about the effects of Treg cells on the homeostasis of healthy donor CD8(+) T cells. The present study demonstrates that Treg cells exert differential effects on CD8(+) T-cell subsets. Treg cells inhibited mostly the polyclonal proliferation of CD27(-) effector cells compared with CD27(+) memory CD8(+) T cells. Moreover, they inhibited the polyclonal and antigen-driven differentiation of memory cells into functional effectors as defined by IFN-gamma secretion and induction of CD160 expression. Finally, Treg cells reduced the apoptosis of memory but not of effector and terminal effector cell populations. These effects were at least in part mediated by a decreased expression of PD-L1, but not of programmed death 1 (PD-1), on CD8(+) T cells after activation. Thus, in the setting of a healthy immune system, Treg cells fine-tune the memory/effector cell balance and promote the accumulation of long-living memory cells in case of strong stimulation.

journal_name

Blood

journal_title

Blood

authors

Nikolova M,Lelievre JD,Carriere M,Bensussan A,Lévy Y

doi

10.1182/blood-2008-04-151407

subject

Has Abstract

pub_date

2009-05-07 00:00:00

pages

4556-65

issue

19

eissn

0006-4971

issn

1528-0020

pii

blood-2008-04-151407

journal_volume

113

pub_type

杂志文章

相关文献

BLOOD文献大全
  • A hematopoietic cell L-selectin ligand that is distinct from PSGL-1 and displays N-glycan-dependent binding activity.

    abstract::Human hematopoietic progenitor cells express L-selectin and also express PSGL-1, a ligand for all selectins. Using a shear-based adhesion assay, a hematopoietic cell L-selectin ligand (HCLL) that is expressed on the hematopoietic cell line KG1a and on normal human hematopoietic progenitors was previously identified. T...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Sackstein R,Dimitroff CJ

    更新日期:2000-10-15 00:00:00

  • Transient receptor potential vanilloid 1 mediates pain in mice with severe sickle cell disease.

    abstract::Pain is the leading cause of emergency department visits, hospitalizations, and daily suffering in individuals with sickle cell disease (SCD). The pathologic mechanisms leading to the perception of pain during acute RBC sickling episodes and development of chronic pain remain poorly understood and ineffectively treate...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2010-12-327429

    authors: Hillery CA,Kerstein PC,Vilceanu D,Barabas ME,Retherford D,Brandow AM,Wandersee NJ,Stucky CL

    更新日期:2011-09-22 00:00:00

  • Immunologic stimulation of early murine hematopoiesis and its abrogation by cyclosporin A.

    abstract::Mice injected chronically with antiplatelet serum develop an increase in the number of megakaryocytic progenitor cells compared to animals given normal rabbit serum. To examine the specificity of this response, progenitor cells giving rise to megakaryocyte, granulocyte-macrophage, erythroid, and mixed-cell colonies we...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Burstein SA,Erb SK,Adamson JW,Harker LA

    更新日期:1982-04-01 00:00:00

  • A recombinant murine meizothrombin precursor, prothrombin R157A/R268A, inhibits thrombosis in a model of acute carotid artery injury.

    abstract::Mutations in human prothrombin that generate a stable form of meizothrombin or meizothrombin(desF1) cause dysprothrombinemia in both the homozygous and heterozygous state, suggesting that meizothrombin has dominant anticoagulant effects in vivo. The enzymatic characterization of recombinant mouse meizothrombin, meizot...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2004-02-0478

    authors: Shim K,Zhu H,Westfield LA,Sadler JE

    更新日期:2004-07-15 00:00:00

  • Changing antigen receptor gene rearrangements in a case of early pre-B cell leukemia: evidence for a tumor progenitor cell with stem cell features and implications for monitoring residual disease.

    abstract::A case of acute lymphoblastic leukemia (ALL) was encountered in which the two clonal gamma T-cell receptor gene (TCR gamma) rearrangements found in bone marrow (BM) samples at relapse both differed from the single clonal TCR gamma rearrangement present in BM obtained at diagnosis 5 years previously. In contrast, two c...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Tycko B,Ritz J,Sallan S,Sklar J

    更新日期:1992-01-15 00:00:00

  • Hematopoietic stem cell-based gene therapy for acquired immunodeficiency syndrome: efficient transduction and expression of RevM10 in myeloid cells in vivo and in vitro.

    abstract::Gene delivery via the hematopoietic stem cell (HSC) offers an attractive means to introduce antiviral genes into both T cells and macrophages for acquired immunodeficiency syndrome (AIDS) gene therapy. An amphotropic retroviral vector encoding a bicistronic gene coexpressing RevM10 and the murine CD8alpha' chain (lyt2...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Su L,Lee R,Bonyhadi M,Matsuzaki H,Forestell S,Escaich S,Böhnlein E,Kaneshima H

    更新日期:1997-04-01 00:00:00

  • Cytologic characterization and significance of normal karyotypes in t(8;21) acute myeloblastic leukemia.

    abstract::A cytologic and cytogenetic study of 10 cases of acute myeloblastic leukemia with maturation and t(8;21) translocation is reported. Despite a certain polymorphic appearance, the characteristic cytologic picture, consisting essentially of large myeloblasts with an abundant cytoplasma containing a large Auer rod, allowe...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Berger R,Bernheim A,Daniel MT,Valensi F,Sigaux F,Flandrin G

    更新日期:1982-01-01 00:00:00

  • Amelioration of Sardinian beta0 thalassemia by genetic modifiers.

    abstract::Sardinian beta-thalassemia patients all are homozygotes for the same null allele in the beta-globin gene, but the clinical manifestations are extremely variable in severity. Previous studies have shown that the coinheritance of alpha-thalassemia or the presence of genetic variants that sustain fetal hemoglobin product...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2009-04-217901

    authors: Galanello R,Sanna S,Perseu L,Sollaino MC,Satta S,Lai ME,Barella S,Uda M,Usala G,Abecasis GR,Cao A

    更新日期:2009-10-29 00:00:00

  • Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype.

    abstract::Since their discovery in patients with autosomal dominant (AD) chronic mucocutaneous candidiasis (CMC) in 2011, heterozygous STAT1 gain-of-function (GOF) mutations have increasingly been identified worldwide. The clinical spectrum associated with them needed to be delineated. We enrolled 274 patients from 167 kindreds...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2015-11-679902

    authors: Toubiana J,Okada S,Hiller J,Oleastro M,Lagos Gomez M,Aldave Becerra JC,Ouachée-Chardin M,Fouyssac F,Girisha KM,Etzioni A,Van Montfrans J,Camcioglu Y,Kerns LA,Belohradsky B,Blanche S,Bousfiha A,Rodriguez-Gallego C,Meyts

    更新日期:2016-06-23 00:00:00

  • Three cycles of adriamycin, bleomycin, vinblastine, and dacarbazine (ABVD) or epirubicin, bleomycin, vinblastine, and methotrexate (EBVM) plus extended field radiation therapy in early and intermediate Hodgkin disease: 10-year results of a randomized tria

    abstract::From 1990 to 1996, a total of 386 adult patients with early/intermediate Hodgkin disease (HD) were randomly assigned to receive 3 cycles of adriamycin, bleomycin, vinblastine, dacarbazine (an alkylating agent), and methylprednisolone (ABVDm, arm A) or epirubicin, bleomycin, vinblastine, methotrexate, and methylprednis...

    journal_title:Blood

    pub_type: 临床试验,杂志文章,多中心研究,随机对照试验

    doi:10.1182/blood-2003-05-1611

    authors: le Maignan C,Desablens B,Delwail V,Dib M,Berthou C,Vigier M,Ghandour C,Atmani S,Casassus P,Maisonneuve H,Le Mevel A,Traulle C,Bernard M,Briere J,Colonna P,Andrieu JM

    更新日期:2004-01-01 00:00:00

  • The significance of bcr-abl molecular detection in chronic myeloid leukemia patients "late," 18 months or more after transplantation.

    abstract::The bcr-abl chimeric messenger RNA is frequently detected in chronic myeloid leukemia (CML) patients after bone marrow transplantation. It was previously reported that the relapse risk of bcr-abl detection 6 to 12 months after transplantation was greater than 40%. This risk decreased as the time between transplantatio...

    journal_title:Blood

    pub_type: 临床试验,杂志文章

    doi:10.1182/blood.v98.6.1701

    authors: Radich JP,Gooley T,Bryant E,Chauncey T,Clift R,Beppu L,Edmands S,Flowers ME,Kerkof K,Nelson R,Appelbaum FR

    更新日期:2001-09-15 00:00:00

  • Inhibition of immature erythroid progenitor cell proliferation by macrophage inflammatory protein-1alpha by interacting mainly with a C-C chemokine receptor, CCR1.

    abstract::Several lines of evidence indicate that macrophage inflammatory protein-1alpha (MIP-1alpha) modulates the proliferation of hematopoietic progenitor cells, depending on their maturational stages. To clarify the mechanisms for the modulation of hematopoiesis by this chemokine, we examined the expression of a receptor fo...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Su S,Mukaida N,Wang J,Zhang Y,Takami A,Nakao S,Matsushima K

    更新日期:1997-07-15 00:00:00

  • Phenotypic markers and BCL-1 gene rearrangements in B-cell chronic lymphocytic leukemia: a Cancer and Leukemia Group B study.

    abstract::The markers, CD11b, CD11c, CD14, CD21, CD23, CD25, CD38, and FMC7 were correlated with morphologic and other laboratory and clinical characteristics of 127 patients with untreated CD5+ chronic lymphocytic leukemia (CLL). Only CD38 and CD21 were significantly associated with atypical CLL morphology. The integrin associ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Newman RA,Peterson B,Davey FR,Brabyn C,Collins H,Brunetto VL,Duggan DB,Weiss RB,Royston I,Millard FE

    更新日期:1993-08-15 00:00:00

  • Involvement of bcl-2 gene in Japanese follicular lymphoma.

    abstract::A t(14;18) (q32;q21) chromosome translocation is closely associated with the follicular lymphoma, which is prevalent in the United States, and the t(14;18) causes the juxtaposition of a bcl-2 gene on chromosome 18 with an immunoglobulin heavy-chain gene locus on chromosome 14. Genomic DNAs from 30 Japanese patients wi...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Amakawa R,Fukuhara S,Ohno H,Doi S,Oguma S,Tanabe S,Yamabe H,Edamura S,Tomono N,Nasu K

    更新日期:1989-02-15 00:00:00

  • Genetic heterogeneity in heterocellular hereditary persistence of fetal hemoglobin.

    abstract::A large English pedigree in which heterocellular hereditary persistence of fetal hemoglobin (HPFH) segregates is described. beta-globin cluster deletions and gamma gene promoter mutations associated with HPFH have been excluded. Of particular importance in this pedigree is the absence of any cosegregating hemoglobinop...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Craig JE,Rochette J,Sampietro M,Wilkie AO,Barnetson R,Hatton CS,Demenais F,Thein SL

    更新日期:1997-07-01 00:00:00

  • The embryonic origins of erythropoiesis in mammals.

    abstract::Erythroid (red blood) cells are the first cell type to be specified in the postimplantation mammalian embryo and serve highly specialized, essential functions throughout gestation and postnatal life. The existence of 2 developmentally and morphologically distinct erythroid lineages, primitive (embryonic) and definitiv...

    journal_title:Blood

    pub_type: 杂志文章,评审

    doi:10.1182/blood-2012-01-153486

    authors: Baron MH,Isern J,Fraser ST

    更新日期:2012-05-24 00:00:00

  • The hypercoagulable state in thalassemia.

    abstract::Thalassemia is a congenital hemolytic disorder caused by a partial or complete deficiency of alpha- or beta-globin chain synthesis. Homozygous carriers of beta-globin gene defects suffer from severe anemia and other serious complications from early childhood. The disease is treated by chronic blood transfusion. Howeve...

    journal_title:Blood

    pub_type: 杂志文章,评审

    doi:10.1182/blood.v99.1.36

    authors: Eldor A,Rachmilewitz EA

    更新日期:2002-01-01 00:00:00

  • Mutual inhibition of murine erythropoiesis and granulopoiesis during combined erythropoietin, granulocyte colony-stimulating factor, and stem cell factor administration: in vivo interactions and dose-response surfaces.

    abstract::We investigated the in vivo effects of erythropoietin (EPO) on granulopoiesis and, conversely, the effect of granulocyte colony-stimulating factor (G-CSF) treatment on erythropoiesis. Recombinant human EPO at four different doses in combination with recombinant human G-CSF also at four different doses was simultaneous...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: de Haan G,Engel C,Dontje B,Nijhof W,Loeffler M

    更新日期:1994-12-15 00:00:00

  • Inhibition of cell adhesion by anti-P-selectin aptamer: a new potential therapeutic agent for sickle cell disease.

    abstract::Adhesive interactions between circulating sickle red blood cells (RBCs), leukocytes, and endothelial cells are major pathophysiologic events in sickle cell disease (SCD). To develop new therapeutics that efficiently inhibit adhesive interactions, we generated an anti-P-selectin aptamer and examined its effects on cell...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2010-05-285718

    authors: Gutsaeva DR,Parkerson JB,Yerigenahally SD,Kurz JC,Schaub RG,Ikuta T,Head CA

    更新日期:2011-01-13 00:00:00

  • A20 protects endothelial cells from TNF-, Fas-, and NK-mediated cell death by inhibiting caspase 8 activation.

    abstract::A20 is a stress response gene in endothelial cells (ECs). A20 serves a dual cytoprotective function, protecting from tumor necrosis factor (TNF)-mediated apoptosis and inhibiting inflammation via blockade of the transcription factor nuclear factor-kappaB (NF-kappaB). In this study, we evaluated the molecular basis of ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2003-02-0635

    authors: Daniel S,Arvelo MB,Patel VI,Longo CR,Shrikhande G,Shukri T,Mahiou J,Sun DW,Mottley C,Grey ST,Ferran C

    更新日期:2004-10-15 00:00:00

  • PEBP2-beta/CBF-beta-dependent phosphorylation of RUNX1 and p300 by HIPK2: implications for leukemogenesis.

    abstract::The heterodimeric transcription factor RUNX1/PEBP2-beta (also known as AML1/CBF-beta) is essential for definitive hematopoiesis. Here, we show that interaction with PEBP2-beta leads to the phosphorylation of RUNX1, which in turn induces p300 phosphorylation. This is mediated by homeodomain interacting kinase 2 (HIPK2)...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2008-01-134122

    authors: Wee HJ,Voon DC,Bae SC,Ito Y

    更新日期:2008-11-01 00:00:00

  • Development of the glycosylphosphatitylinositol-anchoring defect characteristic for paroxysmal nocturnal hemoglobinuria in patients with aplastic anemia.

    abstract::The introduction of immunosuppressive therapy for treatment of aplastic anemia has led to a considerable improvement in the prognosis of this disease. However, long-term follow-up of these patients showed a high incidence of "late" hematologic complications such as myelodysplasia and paroxysmal nocturnal hemoglobinuri...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Schubert J,Vogt HG,Zielinska-Skowronek M,Freund M,Kaltwasser JP,Hoelzer D,Schmidt RE

    更新日期:1994-04-15 00:00:00

  • The PI3K/mTOR inhibitor PF-04691502 induces apoptosis and inhibits microenvironmental signaling in CLL and the Eµ-TCL1 mouse model.

    abstract::Current treatment strategies for chronic lymphocytic leukemia (CLL) involve a combination of conventional chemotherapeutics, monoclonal antibodies, and targeted signaling inhibitors. However, CLL remains largely incurable, with drug resistance and treatment relapse a common occurrence, leading to the search for novel ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2014-11-610329

    authors: Blunt MD,Carter MJ,Larrayoz M,Smith LD,Aguilar-Hernandez M,Cox KL,Tipton T,Reynolds M,Murphy S,Lemm E,Dias S,Duncombe A,Strefford JC,Johnson PW,Forconi F,Stevenson FK,Packham G,Cragg MS,Steele AJ

    更新日期:2015-06-25 00:00:00

  • Hypermetaphase fluorescence in situ hybridization for quantitative monitoring of Philadelphia chromosome-positive cells in patients with chronic myelogenous leukemia during treatment.

    abstract::Using Philadelphia chromosome-positive (Ph+) chronic myelogenous leukemia (CML) as a model, our aim has been to develop a molecular cytogenetic method of high resolution analysis for monitoring the frequency of cells with nonrandom chromosome rearrangements in the bone marrow of patients receiving treatment for hemato...

    journal_title:Blood

    pub_type: 临床试验,杂志文章

    doi:

    authors: Seong DC,Kantarjian HM,Ro JY,Talpaz M,Xu J,Robinson JR,Deisseroth AB,Champlin RE,Siciliano MJ

    更新日期:1995-09-15 00:00:00

  • Hematopoiesis and leukemogenesis in mice expressing oncogenic NrasG12D from the endogenous locus.

    abstract::NRAS is frequently mutated in hematologic malignancies. We generated Mx1-Cre, Lox-STOP-Lox (LSL)-Nras(G12D) mice to comprehensively analyze the phenotypic, cellular, and biochemical consequences of endogenous oncogenic Nras expression in hematopoietic cells. Here we show that Mx1-Cre, LSL-Nras(G12D) mice develop an in...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2010-04-280750

    authors: Li Q,Haigis KM,McDaniel A,Harding-Theobald E,Kogan SC,Akagi K,Wong JC,Braun BS,Wolff L,Jacks T,Shannon K

    更新日期:2011-02-10 00:00:00

  • Selection of patients for bone marrow transplantation in severe aplastic anemia.

    abstract::Despite androgens and intensive supportive care, satisfactory survival in severe aplastic anemia remains at 20% or less. Histocompatible bone marrow transplantation can restore normal hematopoiesis in approximately 40% of similarly severe individuals. Delay of transplantation for 3 wk after diagnosis allows time for p...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Camitta BM,Rappeport JM,Parkman R,Nathan DG

    更新日期:1975-03-01 00:00:00

  • Diferric transferrin regulates transferrin receptor 2 protein stability.

    abstract::Transferrin receptor 2 (TfR2) is a type 2 transmembrane protein expressed in hepatocytes that binds iron-bound transferrin (Tf). Mutations in TfR2 cause one form of hereditary hemochromatosis, a disease in which excessive absorption of dietary iron can lead to liver cirrhosis, diabetes, arthritis, and heart failure. T...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2004-06-2477

    authors: Johnson MB,Enns CA

    更新日期:2004-12-15 00:00:00

  • Prolonged defects of interleukin-2 production, responsiveness, and receptor expression in patients with acute lymphoblastic leukemia.

    abstract::The proliferative responsiveness to, production of, and the expression of cell-surface receptors for interleukin-2 (IL-2) were examined in 14 children with acute lymphoblastic leukemia (ALL) in remission and receiving maintenance chemotherapy for 6 to 35 months; in 19 children with ALL in remission and off all therapy...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Borzy MS,Ridgway D

    更新日期:1989-05-01 00:00:00

  • Inducing iron deficiency improves erythropoiesis and photosensitivity in congenital erythropoietic porphyria.

    abstract::Congenital erythropoietic porphyria (CEP) is an autosomal recessive disorder of heme synthesis characterized by reduced activity of uroporphyrinogen III synthase and the accumulation of nonphysiologic isomer I porphyrin metabolites, resulting in ineffective erythropoiesis and devastating skin photosensitivity. Managem...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2014-07-584664

    authors: Egan DN,Yang Z,Phillips J,Abkowitz JL

    更新日期:2015-07-09 00:00:00

  • Generation of EBV-specific cytotoxic T cells that are resistant to calcineurin inhibitors for the treatment of posttransplantation lymphoproliferative disease.

    abstract::Epstein-Barr virus (EBV)-driven posttransplantation lymphoproliferative disease (PTLD) is a serious complication of immunosuppression after either stem cell transplantation (SCT) or solid organ transplantation (SOT). Adoptive transfer of EBV-specific cytotoxic T lymphocytes (EBV-CTLs) is an effective prophylaxis and t...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2009-07-228387

    authors: Brewin J,Mancao C,Straathof K,Karlsson H,Samarasinghe S,Amrolia PJ,Pule M

    更新日期:2009-11-26 00:00:00