Frequent ongoing T-cell receptor rearrangements in childhood B-precursor acute lymphoblastic leukemia: implications for monitoring minimal residual disease.

Abstract:

:Crosslineage T-cell receptor delta (TCR delta) rearrangements are widely used as tumor markers for the follow up of minimal residual disease in childhood B-precursor acute lymphoblastic leukemia (ALL) by polymerase chain reaction (PCR). The major drawback of this approach is the risk of false-negative results due to clonal evolution. We investigated the stability of V delta 2D delta 3 rearrangements in a group of 56 childhood B-precursor ALL patients by PCR and Southern blot analysis. At the PCR level, V delta 2D delta 3-to-J alpha rearranged subclones (one pathway for secondary TCR delta recombination) were demonstrated in 85.2% of V delta 2D delta 3-positive patients tested, which showed that small subclones are present in the large majority of patients despite apparently monoclonal TCR delta Southern blot patterns. Sequence analysis of V delta 2D delta 3J alpha rearrangements showed a biased J alpha gene usage, with HAPO5 and J alpha F in 26 of 32 and 6 of 32 clones, respectively. Comparison of V delta 2D delta 3 rearrangement status between diagnosis and first relapse showed differences in seven of eight patients studied. In contrast, from first relapse onward, no clonal changes were observed in six patients studied. To investigate the occurrence of crosslineage TCR delta rearrangements in normal B and T cells, fluorescence-activated cell sorter-sorted peripheral blood CD19+/CD3- and CD19-/CD3+ cell populations from three healthy donors were analyzed. V delta 2D delta 3 rearrangements were detected at low frequencies in both B and T cells, which suggests that V delta 2-to-D delta 3 joining also occurs during normal B-cell differentiation. A model for crosslineage TCR delta rearrangements in B-precursor ALL is deduced that explains the observed clonal changes between diagnosis and relapse and is compatible with multistep leukemogenesis of B-precursor ALL.

journal_name

Blood

journal_title

Blood

authors

Steenbergen EJ,Verhagen OJ,van Leeuwen EF,van den Berg H,von dem Borne AE,van der Schoot CE

subject

Has Abstract

pub_date

1995-07-15 00:00:00

pages

692-702

issue

2

eissn

0006-4971

issn

1528-0020

journal_volume

86

pub_type

杂志文章

相关文献

BLOOD文献大全
  • Selective expression of CD45 isoforms defines CALLA+ monoclonal B-lineage cells in peripheral blood from myeloma patients as late stage B cells.

    abstract::The peripheral blood lymphocytes from 42 patients with multiple myeloma (MM) and 13 patients with monoclonal gammopathy of undetermined significance (MGUS) were studied by three-color immunofluorescence (IF) using antibodies directed to a broad range of B-cell markers (CD19, CD20, CD21, CD24), CALLA (CD10), PCA-1 (a p...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Jensen GS,Mant MJ,Belch AJ,Berenson JR,Ruether BA,Pilarski LM

    更新日期:1991-08-01 00:00:00

  • The relationship of human platelet density to platelet age: platelet population labeling by monoamine oxidase inhibition.

    abstract::The relationship between platelet density and platelet age appears to vary between species with relatively few labeling studies in humans reported. In this study, irreversible monoamine oxidase (MAO) inhibitors were used to biochemically label the circulating platelet population in 15 humans. Platelet samples were the...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Chamberlain KG,Tong M,Chiu E,Penington DG

    更新日期:1989-04-01 00:00:00

  • Proliferation of diffusion chamber colony-forming units (CFUD) in cultures of normal human bone marrow in diffusion chambers in mice.

    abstract::Normal human bone marrow contains cells capable of forming colonies of hemopoietic cells in fibrin clots in diffusion chambers implanted intraperitoneally (i.p.) into irradiated mice. The present paper describes the proliferation of such colony-forming units (CFUD) in cultures in vivo. Cells harvested from diffusion c...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Jacobsen N

    更新日期:1977-03-01 00:00:00

  • Identification of novel B-lineage cells in human fetal bone marrow that coexpress CD7.

    abstract::In the present study we used multiparameter flow cytometry and cell sorting to evaluate fetal bone marrow, a rich source of cells early in lymphoid development. We found CD7 to be expressed on a subset of CD19+ cells, including some that had matured to cytoplasmic mu+ (pre-B) and surface mu+ (B) cells. In addition, a ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Grümayer ER,Griesinger F,Hummell DS,Brunning RD,Kersey JH

    更新日期:1991-01-01 00:00:00

  • Solid-phase von Willebrand factor contains a conformationally active RGD motif that mediates endothelial cell adhesion through the alpha v beta 3 receptor.

    abstract::The interaction of von Willebrand factor (vWF) with the alpha v beta 3 integrin of human umbilical vein endothelial cells is dependent on the RGD sequence present at residues 1744-1746 of the mature vWF subunit. We compared vWF and its two dimeric fragments, SpIII (residues 1-1365) and SpII (residues 1366-2050), as ad...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Denis C,Williams JA,Lu X,Meyer D,Baruch D

    更新日期:1993-12-15 00:00:00

  • Vav1, but not Vav2, contributes to platelet aggregation by CRP and thrombin, but neither is required for regulation of phospholipase C.

    abstract::We have investigated the role of the Rho and Rac family small guanine triphosphate (GTP) exchange factors (RhoGEFs), Vav1 and Vav2, in the activation of platelets by the immunoreceptor tyrosine-based activation motif (ITAM)-coupled collagen receptor GPVI and by the G protein-coupled receptor agonist thrombin. The glyc...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood.V100.10.3561

    authors: Pearce AC,Wilde JI,Doody GM,Best D,Inoue O,Vigorito E,Tybulewicz VL,Turner M,Watson SP

    更新日期:2002-11-15 00:00:00

  • Distinct hematopoietic progenitor compartments are delineated by the expression of aldehyde dehydrogenase and CD34.

    abstract::A broad range of hematopoietic stem cells and progenitors reside within a fraction of umbilical cord blood (UCB) that exhibits low light scatter properties (SSC(lo)) and high expression of aldehyde dehydrogenase (ALDH(br)). Many SSC(lo) ALDH(br) cells coexpress CD34; however, other cells express either ALDH or CD34. T...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2004-09-3652

    authors: Storms RW,Green PD,Safford KM,Niedzwiecki D,Cogle CR,Colvin OM,Chao NJ,Rice HE,Smith CA

    更新日期:2005-07-01 00:00:00

  • Human hematopoietic stem cells stimulated to proliferate in vitro lose engraftment potential during their S/G(2)/M transit and do not reenter G(0).

    abstract::An understanding of mechanisms regulating hematopoietic stem cell engraftment is of pivotal importance to the clinical use of cultured and genetically modified transplants. Human cord blood (CB) cells with lymphomyeloid repopulating activity in NOD/SCID mice were recently shown to undergo multiple self-renewal divisio...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Glimm H,Oh IH,Eaves CJ

    更新日期:2000-12-15 00:00:00

  • Production and nucleotide sequence of an inhibitory human IgM autoantibody directed against platelet glycoprotein Ia/IIa.

    abstract::Human B-cell lines were derived by limiting dilutions of Epstein-Barr virus (EBV) transformed peripheral B cells from a patient with an autoantibody against glycoprotein (GP)Ia/IIa, and manifesting defective collagen-induced platelet aggregation and a bleeding problem. Antibody-producing clones were selected for their...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Deckmyn H,Zhang J,Van Houtte E,Vermylen J

    更新日期:1994-09-15 00:00:00

  • Somatic mosaicism and compound heterozygosity in female hemophilia B.

    abstract::Sequencing the complete factor IX gene of 2 sisters with hemophilia B with different phenotypes and no family history of hemorrhagic diathesis revealed a common 5' splice site mutation in intron 3 (T6704C) in both and an additional missense mutation (I344T) in one. The presence of dysfunctional antigen in the latter s...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Costa JM,Vidaud D,Laurendeau I,Vidaud M,Fressinaud E,Moisan JP,David A,Meyer D,Lavergne JM

    更新日期:2000-08-15 00:00:00

  • Transplacentally acquired maternal T lymphocytes in severe combined immunodeficiency: a study of 121 patients.

    abstract::A study in 121 infants with severe combined immunodeficiency (SCID) was performed to determine the prevalence of an engraftment by transplacentally acquired maternal T cells and to explore clinical and immunological findings related to this abnormality. Each newly diagnosed patient with SCID presenting with circulatin...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood.v98.6.1847

    authors: Müller SM,Ege M,Pottharst A,Schulz AS,Schwarz K,Friedrich W

    更新日期:2001-09-15 00:00:00

  • Erythropoiesis-inhibiting factor(s) (EIF): methodologic studies.

    abstract::Erythropoiesis-inhibiting factors (EIF) have been demonstrated in plasma from hypertransfused animals and from polycythemic individuals during periods of hyperoxia, but there is a decided discrepancy in the data published. In the present paper methodologic variations of a bioassay for demonstrating the erythropoiesis-...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Lindemann R

    更新日期:1976-01-01 00:00:00

  • Residual amounts of glycoproteins IIb and IIIa may be present in the platelets of most patients with Glanzmann's thrombasthenia.

    abstract::Glanzmann's thrombasthenia is an inherited bleeding disorder characterized by abnormalities of platelet membrane glycoproteins (GP) IIb and IIIa. Most patients, usually designated as type I, have been reported to have undetectable levels of GP IIb and GP IIIa with the assay used. We have used polyclonal rabbit antibod...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Nurden AT,Didry D,Kieffer N,McEver RP

    更新日期:1985-04-01 00:00:00

  • Sustained signaling through the B-cell receptor induces Mcl-1 and promotes survival of chronic lymphocytic leukemia B cells.

    abstract::The clinical course of chronic lymphocytic leukemia (CLL) differs significantly between patients with mutated (M-CLL) and unmutated (U-CLL) immunoglobulin (Ig) variable heavy-chain (V(H)) genes, implying a role for B-cell receptor (BCR) signaling in the pathogenesis of this disease. We have now investigated activation...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2004-07-2669

    authors: Petlickovski A,Laurenti L,Li X,Marietti S,Chiusolo P,Sica S,Leone G,Efremov DG

    更新日期:2005-06-15 00:00:00

  • Non-MALT marginal zone B-cell lymphomas: a description of clinical presentation and outcome in 124 patients.

    abstract::Marginal zone B-cell lymphoma (MZL) is a recently individualized lymphoma that encompasses mucosa-associated lymphoid tissue (MALT) lymphoma, splenic lymphoma with or without villous lymphocytes, and nodal lymphoma with or without monocytoid B-cells. If the clinical description and outcome of MALT lymphoma is well kno...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Berger F,Felman P,Thieblemont C,Pradier T,Baseggio L,Bryon PA,Salles G,Callet-Bauchu E,Coiffier B

    更新日期:2000-03-15 00:00:00

  • Natural history of hereditary spherocytosis during the first year of life.

    abstract::Although hereditary spherocytosis (HS) is a common disorder of the red cell membrane, its clinical and biologic expression at birth and in early infancy has received little attention. In order to obtain insights into the natural history of HS during infancy, we studied 46 neonates, 39 from families in which 1 of the p...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Delhommeau F,Cynober T,Schischmanoff PO,Rohrlich P,Delaunay J,Mohandas N,Tchernia G

    更新日期:2000-01-15 00:00:00

  • Treatment of adult acute lymphoblastic leukemia with intensive cyclical chemotherapy: a follow-up report.

    abstract::We treated 109 patients with adult acute lymphoblastic leukemia (ALL) diagnosed by histochemical and immunologic techniques. Patients were excluded only for age greater than 50 years and Burkitt's leukemia. Treatment included a four-drug remission induction phase followed by alternating cycles of noncrossresistant che...

    journal_title:Blood

    pub_type: 临床试验,杂志文章

    doi:

    authors: Linker CA,Levitt LJ,O'Donnell M,Forman SJ,Ries CA

    更新日期:1991-12-01 00:00:00

  • Identification of normal human peripheral blood monocytes and liver as sites of synthesis of coagulation factor XIII a-chain.

    abstract::Factor XIII is the fibrin-stabilizing factor that covalently cross-links fibrin monomers to form a highly organized, stable fibrin clot. The plasma form of factor XIII is a heterodimer, a2b2, consisting of two a-chains and two b-chains; the intracellular form, such as in platelets and placenta, is a dimer, a2, consist...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Weisberg LJ,Shiu DT,Conkling PR,Shuman MA

    更新日期:1987-08-01 00:00:00

  • Murine myeloproliferative disorder as a consequence of impaired collaboration between dendritic cells and CD4 T cells.

    abstract::Dendritic cells (DCs) are a key cell type in the initiation of the adaptive immune response. Recently, an additional role for DCs in suppressing myeloproliferation was discovered. Myeloproliferative disorder (MPD) was observed in murine studies with constitutive depletion of DCs, as well as in patients with congenital...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2018-05-850321

    authors: Humblet-Baron S,Barber JS,Roca CP,Lenaerts A,Koni PA,Liston A

    更新日期:2019-01-24 00:00:00

  • Differentiation of type 1 T regulatory cells (Tr1) by tolerogenic DC-10 requires the IL-10-dependent ILT4/HLA-G pathway.

    abstract::Type 1 T regulatory (Tr1) cells suppress immune responses in vivo and in vitro and play a key role in maintaining tolerance to self- and non-self-antigens. Interleukin-10 (IL-10) is the crucial driving factor for Tr1 cell differentiation, but the molecular mechanisms underlying this induction remain unknown. We identi...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2009-07-234872

    authors: Gregori S,Tomasoni D,Pacciani V,Scirpoli M,Battaglia M,Magnani CF,Hauben E,Roncarolo MG

    更新日期:2010-08-12 00:00:00

  • Pseudo-Bernard-Soulier syndrome: thrombocytopenia caused by autoantibody to platelet glycoprotein Ib.

    abstract::The Bernard-Soulier syndrome is an inherited bleeding disorder that is due to a deficiency in platelet glycoprotein Ib. Bernard-Soulier platelets fail to agglutinate in response to ristocetin despite normal levels of factor VIII:von Willebrand factor. We report a patient who developed severe refractory thrombocytopeni...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Devine DV,Currie MS,Rosse WF,Greenberg CS

    更新日期:1987-08-01 00:00:00

  • CD3/CD28-costimulated T1 and T2 subsets: differential in vivo allosensitization generates distinct GVT and GVHD effects.

    abstract::Adoptive T-cell therapy using CD3/CD28 co-stimulation likely requires in vivo generation of antigen specificity. Because CD28 promotes TH1/TC1 (T1) or TH2/TC2 (T2) differentiation, costimulation may generate donor T1 or T2 cells capable of differentially mediating allogeneic graft-versus-tumor (GVT) effects and graft-...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2002-12-3936

    authors: Jung U,Foley JE,Erdmann AA,Eckhaus MA,Fowler DH

    更新日期:2003-11-01 00:00:00

  • Fibronectin is required for platelet adhesion and for thrombus formation on subendothelium and collagen surfaces.

    abstract::Fibronectin (FN) plays a role in several adhesion mediated functions including the interaction of platelets with subendothelium. We investigated the role of plasma FN in platelet adhesion and platelet thrombus formation under flow conditions. We used two different perfusion models: the annular chamber with alpha-chymo...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Bastida E,Escolar G,Ordinas A,Sixma JJ

    更新日期:1987-11-01 00:00:00

  • Leukocyte ligands for endothelial selectins: specialized glycoconjugates that mediate rolling and signaling under flow.

    abstract::Reversible interactions of glycoconjugates on leukocytes with P- and E-selectin on endothelial cells mediate tethering and rolling of leukocytes in inflamed vascular beds, the first step in their recruitment to sites of injury. Although selectin ligands on hematopoietic precursors have been identified, here we review ...

    journal_title:Blood

    pub_type: 杂志文章,评审

    doi:10.1182/blood-2011-07-343566

    authors: Zarbock A,Ley K,McEver RP,Hidalgo A

    更新日期:2011-12-22 00:00:00

  • Mast cells are crucial for early inflammation, migration of Langerhans cells, and CTL responses following topical application of TLR7 ligand in mice.

    abstract::Until recently, IgE-activated mast cells have been regarded merely as effector cells of adaptive immune responses, involved in allergic reactions and mucosal immunity to parasites. Herein, we report that murine dermal mast cells, activated by local administration of a cream containing the synthetic TLR7 ligand imiquim...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2006-07-036889

    authors: Heib V,Becker M,Warger T,Rechtsteiner G,Tertilt C,Klein M,Bopp T,Taube C,Schild H,Schmitt E,Stassen M

    更新日期:2007-08-01 00:00:00

  • A monoclonal antibody specific to the granulocyte-derived elastase-fragment D species of human fibrinogen and fibrin: its application to the measurement of granulocyte-derived elastase digests in plasma.

    abstract::When granulocytes are stimulated under certain clinical conditions, elastase is released therefrom and digests fibrin(ogen) independently of the plasmin system, which may also be mobilized simultaneously. Thus, discrimination of these 2 systems becomes urgent for the diagnosis and treatment of the underlying diseases....

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Kohno I,Inuzuka K,Itoh Y,Nakahara K,Eguchi Y,Sugo T,Soe G,Sakata Y,Murayama H,Matsuda M

    更新日期:2000-03-01 00:00:00

  • The role of endothelial PI3Kgamma activity in neutrophil trafficking.

    abstract::Phosphoinositide 3-kinase gamma (PI3Kgamma) in neutrophils plays a critical role in the directed migration of these cells into inflamed tissues. In this study, we demonstrate the importance of the endothelial component of PI3Kgamma activity relative to its leukocyte counterpart in supporting neutrophil interactions wi...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2005-01-0023

    authors: Puri KD,Doggett TA,Huang CY,Douangpanya J,Hayflick JS,Turner M,Penninger J,Diacovo TG

    更新日期:2005-07-01 00:00:00

  • Constitutively activated STAT3 promotes cell proliferation and survival in the activated B-cell subtype of diffuse large B-cell lymphomas.

    abstract::Diffuse large B-cell lymphoma (DLBCL) consists of at least 2 phenotypic subtypes; that is, the germinal center B-cell-like (GCB-DLBCL) and the activated B-cell-like (ABC-DLBCL) groups. It has been shown that GCB-DLBCL responds favorably to chemotherapy and expresses high levels of BCL6, a transcription repressor known...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2007-04-087734

    authors: Ding BB,Yu JJ,Yu RY,Mendez LM,Shaknovich R,Zhang Y,Cattoretti G,Ye BH

    更新日期:2008-02-01 00:00:00

  • The effect of the plasticizer di(2-ethylhexyl)phthalate on red cell deformability.

    abstract::Red cell concentrates (RCC) are stored for 35 to 42 days in plastic containers manufactured with the liquid plasticizer di(2-ethylhexyl)phthalate (DEHP). DEHP leaches from the polyvinylchloride (PVC) plastic bag, then binds to and stabilizes the RC membrane. This study was undertaken to determine the deformability of ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Labow RS,Card RT,Rock G

    更新日期:1987-07-01 00:00:00

  • Two-faced T cells in CLL.

    abstract::In this issue of Blood, Bagnara et al describe the development of a reliable and convincing xenograft model of CLL that recapitulates aspects of the leukemic microenvironment and gives intriguing insights into disease biology. ...

    journal_title:Blood

    pub_type: 评论,杂志文章

    doi:10.1182/blood-2011-03-342709

    authors: Devereux S

    更新日期:2011-05-19 00:00:00