Immature human cord blood progenitors engraft and proliferate to high levels in severe combined immunodeficient mice.

Abstract:

:Unseparated or Ficoll-Hypaque (Pharmacia, Piscataway, NJ)--fractionated human cord blood cells were transplanted into sublethally irradiated severe combined immunodeficient (SCID) mice. High levels of multilineage engraftment, including myeloid and lymphoid lineages, were obtained with 80% of the donor samples as assessed by DNA analysis, fluorescence-activated cell sorting (FACS), and morphology. In contrast to previous and concurrent studies with adult human bone marrow (BM), treatment with human cytokines was not required to establish high-level human cell engraftment, suggesting that neonatal cells either respond differently to the murine microenvironment or they provide their own cytokines in a paracrine fashion. Committed and multipotential myelo-erythroid progenitors were detected using in vitro colony assays and FACS analysis of the murine BM showed the presence of immature CD34+ cells. In addition, human hematopoiesis was maintained for at least 14 weeks providing further evidence that immature hematopoietic precursors had engrafted the murine BM. This in vivo model for human cord blood-derived hematopoiesis will be useful to gain new insights into the biology of neonatal hematopoietic cells and to evaluate their role in gene therapy. There is growing evidence that there are ontogeny-related changes in immature human hematopoietic cells, and therefore, the animal models we have developed for adult and neonatal human hematopoiesis provide useful tools to evaluate these changes in vivo.

journal_name

Blood

journal_title

Blood

authors

Vormoor J,Lapidot T,Pflumio F,Risdon G,Patterson B,Broxmeyer HE,Dick JE

subject

Has Abstract

pub_date

1994-05-01 00:00:00

pages

2489-97

issue

9

eissn

0006-4971

issn

1528-0020

journal_volume

83

pub_type

杂志文章

相关文献

BLOOD文献大全
  • Spontaneous heparin-induced thrombocytopenia syndrome: 2 new cases and a proposal for defining this disorder.

    abstract::The existence of spontaneous heparin-induced thrombocytopenia (HIT) syndrome (or autoimmune HIT), defined as a transient prothrombotic thrombocytopenic disorder without proximate heparin exposure serologically indistinguishable from HIT, is controversial. We describe 2 new cases presenting with thrombotic stroke/throm...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2014-01-549741

    authors: Warkentin TE,Basciano PA,Knopman J,Bernstein RA

    更新日期:2014-06-05 00:00:00

  • Isotype switch variants reveal clonally related subpopulations in diffuse large B-cell lymphoma.

    abstract::Primary diffuse large B-cell lymphomas (DLBCLs) are aggressive tumors accounting for approximately 40% of B-cell malignancies. The immunoglobulin (Ig) variable region genes have undergone rearrangement and are commonly somatically mutated. The majority show intraclonal variation which indicates that somatic mutation h...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Ottensmeier CH,Stevenson FK

    更新日期:2000-10-01 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

  • Engineered factor IX variants bypass FVIII and correct hemophilia A phenotype in mice.

    abstract::The complex of the serine protease factor IX (FIX) and its cofactor, factor VIII (FVIII), is crucial for propagation of the intrinsic coagulation cascade. Absence of either factor leads to hemophilia, a disabling disorder marked by excessive hemorrhage after minor trauma. FVIII is the more commonly affected protein, e...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2011-05-353672

    authors: Milanov P,Ivanciu L,Abriss D,Quade-Lyssy P,Miesbach W,Alesci S,Tonn T,Grez M,Seifried E,Schüttrumpf J

    更新日期:2012-01-12 00:00:00

  • Immunophenotypic evidence of leukemia after induction therapy predicts relapse: results from a prospective Children's Cancer Group study of 252 patients with acute myeloid leukemia.

    abstract::Approximately 40% of children with acute myeloid leukemia (AML) who respond to initial therapy subsequently relapse. Multidimensional flow cytometry employing a standardized panel of monoclonal antibodies enables the detection of small numbers of occult leukemic cells that persist during therapy using technology adapt...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2002-10-3064

    authors: Sievers EL,Lange BJ,Alonzo TA,Gerbing RB,Bernstein ID,Smith FO,Arceci RJ,Woods WG,Loken MR

    更新日期:2003-05-01 00:00:00

  • Endogenous platelet factor 4 stimulates activated protein C generation in vivo and improves survival after thrombin or lipopolysaccharide challenge.

    abstract::Pharmacologic infusion of activated protein C (APC) improves survival in severe sepsis, and platelet factor 4 (PF4) accelerates APC generation in a primate thrombin-infusion model. We now tested whether endogenous platelet PF4 content affects APC generation. Mice completely deficient in PF4 (mPF4(-/-)) had impaired AP...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2007-03-081901

    authors: Kowalska MA,Mahmud SA,Lambert MP,Poncz M,Slungaard A

    更新日期:2007-09-15 00:00:00

  • Tissue inhibitor of metalloproteinases 1 is an autocrine and paracrine survival factor, with additional immune-regulatory functions, expressed by Hodgkin/Reed-Sternberg cells.

    abstract::Tissue inhibitor of metalloproteinases (TIMP)-1 and TIMP-2 are proteins with proteinase-inhibiting and cytokine properties. TIMP-1 is active primarily in B cells and B-cell lymphomas, whereas TIMP-2 expression is restricted to T cells. The expression of TIMP-1 and TIMP-2 in lymph nodes from patients with Hodgkin disea...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood.v99.1.258

    authors: Oelmann E,Herbst H,Zühlsdorf M,Albrecht O,Nolte A,Schmitmann C,Manzke O,Diehl V,Stein H,Berdel WE

    更新日期:2002-01-01 00:00:00

  • JAK2V617F homozygosity arises commonly and recurrently in PV and ET, but PV is characterized by expansion of a dominant homozygous subclone.

    abstract::Subclones homozygous for JAK2V617F are more common in polycythemia vera (PV) than essential thrombocythemia (ET), but their prevalence and significance remain unclear. The JAK2 mutation status of 6495 BFU-E, grown in low erythropoietin conditions, was determined in 77 patients with PV or ET. Homozygous-mutant colonies...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2012-05-431791

    authors: Godfrey AL,Chen E,Pagano F,Ortmann CA,Silber Y,Bellosillo B,Guglielmelli P,Harrison CN,Reilly JT,Stegelmann F,Bijou F,Lippert E,McMullin MF,Boiron JM,Döhner K,Vannucchi AM,Besses C,Campbell PJ,Green AR

    更新日期:2012-09-27 00:00:00

  • P-selectin binds to the D'-D3 domains of von Willebrand factor in Weibel-Palade bodies.

    abstract::It has recently been shown that the ultralarge platelet-recruiting von Willebrand factor (VWF) strings formed immediately at exocytosis from endothelial cells may be anchored to the cell surface by interaction with the integral membrane protein P-selectin. This finding of a new binding partner for VWF immediately prom...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2005-09-3635

    authors: Michaux G,Pullen TJ,Haberichter SL,Cutler DF

    更新日期:2006-05-15 00:00:00

  • A clonally distinct recurrence of Burkitt's lymphoma at 15 years.

    abstract::A human immunodeficiency virus-negative male was successfully treated for two occurrences of Burkitt's lymphoma, 15 years apart. As consolidation of his second remission, he underwent high-dose chemotherapy with peripheral blood stem cell transplantation. In an effort to prove whether the second lymphoma was a relapse...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Lister J,Miklos JA,Swerdlow SH,Bahler DW

    更新日期:1996-08-15 00:00:00

  • Autoreactive MZ and B-1 B-cell activation by Faslpr is coincident with an increased frequency of apoptotic lymphocytes and a defect in macrophage clearance.

    abstract::Murine autoreactive anti-Smith (Sm) B cells are negatively regulated by anergy and developmental arrest, but are also positively selected into the marginal zone (MZ) and B-1 B-cell populations. Despite positive selection, anti-Sm production occurs only in autoimmune-prone mice. To investigate autoreactive B-cell activ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2005-12-006858

    authors: Qian Y,Conway KL,Lu X,Seitz HM,Matsushima GK,Clarke SH

    更新日期:2006-08-01 00:00:00

  • A key role for G-CSF-induced neutrophil production and trafficking during inflammatory arthritis.

    abstract::We have previously shown that G-CSF-deficient (G-CSF(-/-)) mice are markedly protected from collagen-induced arthritis (CIA), which is the major murine model of rheumatoid arthritis, and now investigate the mechanisms by which G-CSF can promote inflammatory disease. Serum G-CSF levels were significantly elevated durin...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2008-02-139535

    authors: Eyles JL,Hickey MJ,Norman MU,Croker BA,Roberts AW,Drake SF,James WG,Metcalf D,Campbell IK,Wicks IP

    更新日期:2008-12-15 00:00:00

  • In vivo delivery of a microRNA-regulated transgene induces antigen-specific regulatory T cells and promotes immunologic tolerance.

    abstract::We previously showed that incorporating target sequences for the hematopoietic-specific microRNA miR-142 into an antigen-encoding transgene prevents antigen expression in antigen-presenting cells (APCs). To determine whether this approach induces immunologic tolerance, we treated mice with a miR-142-regulated lentivir...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2009-04-214569

    authors: Annoni A,Brown BD,Cantore A,Sergi LS,Naldini L,Roncarolo MG

    更新日期:2009-12-10 00:00:00

  • Vav proteins regulate peripheral B-cell survival.

    abstract::Mice lacking all 3 Vav proteins fail to produce significant numbers of recirculating follicular or marginal zone B cells. Those B cells that do mature have shortened lifespans. The constitutive nuclear factor-kappaB (NF-kappaB) activity of resting naive B cells required Vav function and expression of cellular reticulo...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2004-12-4894

    authors: Vigorito E,Gambardella L,Colucci F,McAdam S,Turner M

    更新日期:2005-10-01 00:00:00

  • Disease characteristics and clinical outcome in young adults with essential thrombocythemia versus early/prefibrotic primary myelofibrosis.

    abstract::In the present study, we investigated disease characteristics and clinical outcome in young patients (< 40 years) with World Health Organization (WHO)-defined essential thrombocythemia (ET) compared with early/prefibrotic primary myelofibrosis (PMF) with presenting thrombocythemia. We recruited 213 young patients (med...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2012-01-407981

    authors: Barbui T,Thiele J,Carobbio A,Passamonti F,Rumi E,Randi ML,Bertozzi I,Vannucchi AM,Gisslinger H,Gisslinger B,Finazzi G,Ruggeri M,Rodeghiero F,Rambaldi A,Gangat N,Tefferi A

    更新日期:2012-07-19 00:00:00

  • ICAM-1-activated Src and eNOS signaling increase endothelial cell surface PECAM-1 adhesivity and neutrophil transmigration.

    abstract::Polymorphonuclear neutrophil (PMN) extravasation requires selectin-mediated tethering, intercellular adhesion molecule-1 (ICAM-1)-dependent firm adhesion, and platelet/endothelial cell adhesion molecule 1 (PECAM-1)-mediated transendothelial migration. An important unanswered question is whether ICAM-1-activated signal...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2011-12-397430

    authors: Liu G,Place AT,Chen Z,Brovkovych VM,Vogel SM,Muller WA,Skidgel RA,Malik AB,Minshall RD

    更新日期:2012-08-30 00:00:00

  • Dual mTORC1/mTORC2 inhibition diminishes Akt activation and induces Puma-dependent apoptosis in lymphoid malignancies.

    abstract::The mammalian target of rapamycin (mTOR) plays crucial roles in proliferative and antiapoptotic signaling in lymphoid malignancies. Rapamycin analogs, which are allosteric mTOR complex 1 (mTORC1) inhibitors, are active in mantle cell lymphoma and other lymphoid neoplasms, but responses are usually partial and short-li...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2011-04-346601

    authors: Gupta M,Hendrickson AE,Yun SS,Han JJ,Schneider PA,Koh BD,Stenson MJ,Wellik LE,Shing JC,Peterson KL,Flatten KS,Hess AD,Smith BD,Karp JE,Barr S,Witzig TE,Kaufmann SH

    更新日期:2012-01-12 00:00:00

  • Identification of base substitutions in the promoter regions of the A gamma- and G gamma-globin genes in A gamma- (or G gamma-) beta+-HPFH heterozygotes using the DNA-amplification-synthetic oligonucleotide procedure.

    abstract::DNA amplification combined with hybridization with 32P-labeled synthetic oligonucleotide probes has been used to identify base substitutions in the 5' promoter region of the A gamma globin gene in members of eleven families from China, Sardinia, Canada, and the United States who had a heterozygosity for the A gamma-be...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Yang KG,Stoming TA,Fei YJ,Liang S,Wong SC,Masala B,Huang RB,Wei ZP,Huisman TH

    更新日期:1988-05-01 00:00:00

  • Clinical and molecular characterization of 6 patients affected by severe deficiency of coagulation factor V: Broadening of the mutational spectrum of factor V gene and in vitro analysis of the newly identified missense mutations.

    abstract::Severe factor V (FV) deficiency is a rare bleeding disorder, whose genetic bases have been characterized only in a limited number of cases. We investigated 6 unrelated patients with extremely reduced plasma FV levels, associated with a bleeding tendency ranging from moderately severe to severe. Clinical manifestations...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2003-03-0922

    authors: Montefusco MC,Duga S,Asselta R,Malcovati M,Peyvandi F,Santagostino E,Mannucci PM,Tenchini ML

    更新日期:2003-11-01 00:00:00

  • Combination of 4Ts score and PF4/H-PaGIA for diagnosis and management of heparin-induced thrombocytopenia: prospective cohort study.

    abstract::Rapid exclusion of heparin-induced thrombocytopenia (HIT) is needed to determine which patients can continue to receive heparin. In this prospective management study, 526 participants had a 4Ts score, rapid particle gel immunoassay (platelet factor 4/heparin [PF4/H]-PaGIA), and serotonin-release assay (SRA) performed....

    journal_title:Blood

    pub_type: 临床试验,杂志文章

    doi:10.1182/blood-2014-12-618165

    authors: Linkins LA,Bates SM,Lee AY,Heddle NM,Wang G,Warkentin TE

    更新日期:2015-07-30 00:00:00

  • An essential role for IL-17 in preventing pathogen-initiated bone destruction: recruitment of neutrophils to inflamed bone requires IL-17 receptor-dependent signals.

    abstract::IL-17 and its receptor are founding members of a novel family of inflammatory cytokines. IL-17 plays a pathogenic role in rheumatoid arthritis (RA)-associated bone destruction. However, IL-17 is also an important regulator of host defense through granulopoiesis and neutrophil trafficking. Therefore, the role of IL-17 ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2005-09-010116

    authors: Yu JJ,Ruddy MJ,Wong GC,Sfintescu C,Baker PJ,Smith JB,Evans RT,Gaffen SL

    更新日期:2007-05-01 00:00:00

  • The architecture of the IgG anti-carbohydrate repertoire in primary antibody deficiencies.

    abstract::Immune system failure in primary antibody deficiencies (PADs) has been linked to recurrent infections, autoimmunity, and cancer, yet clinical judgment is often based on the reactivity to a restricted panel of antigens. Previously, we demonstrated that the human repertoire of carbohydrate-specific immunoglobulin G (IgG...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood.2019001705

    authors: Jandus P,Boligan KF,Smith DF,de Graauw E,Grimbacher B,Jandus C,Abdelhafez MM,Despont A,Bovin N,Simon D,Rieben R,Simon HU,Cummings RD,von Gunten S

    更新日期:2019-11-28 00:00:00

  • Expression of myelomonocytic antigens on chronic lymphocytic leukemia B cells correlates with their ability to produce interleukin 1.

    abstract::We analyzed the expression of myelomonocytic-associated antigens on lymphocytes from B cell chronic lymphocytic leukemia (B-CLL) patients. Blood mononuclear cells were depleted of monocytes by one-step Percoll density gradient centrifugation and tested for antigen expression by fluorescent microscopy and flow cytometr...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Morabito F,Prasthofer EF,Dunlap NE,Grossi CE,Tilden AB

    更新日期:1987-12-01 00:00:00

  • Arg2074Cys missense mutation in the C2 domain of factor V causing moderately severe factor V deficiency: molecular characterization by expression of the recombinant protein.

    abstract::Factor V (FV) deficiency is a rare bleeding disorder whose genetic basis has been described in a relatively small number of cases. Among a total of 12 genetic defects reported in severely or moderately severe deficient patients, 3 were missense mutations and in no case was the mechanism underlying the deficiency explo...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2002-06-1928

    authors: Duga S,Montefusco MC,Asselta R,Malcovati M,Peyvandi F,Santagostino E,Mannucci PM,Tenchini ML

    更新日期:2003-01-01 00:00:00

  • T(14;18)(q32;q21) involving IGH and MALT1 is a frequent chromosomal aberration in MALT lymphoma.

    abstract::T(11;18)(q21;q21) is the most common structural abnormality in extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue (MALT lymphoma) leading to the fusion of the apoptosis inhibitor-2 (API2) gene and the MALT lymphoma-associated translocation (MALT1) gene. In 2 patients with MALT lymphoma of th...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2002-09-2963

    authors: Streubel B,Lamprecht A,Dierlamm J,Cerroni L,Stolte M,Ott G,Raderer M,Chott A

    更新日期:2003-03-15 00:00:00

  • Natural killer cell-derived human granzyme H induces an alternative, caspase-independent cell-death program.

    abstract::Granzyme H (GzmH) belongs to a family of 5 human serine proteases that are expressed by cytotoxic immune effector cells. Although GzmH is most closely related to the caspase-activating granzyme B (GzmB), neither a natural substrate nor a role in immune defense reactions has been demonstrated for this orphan granzyme. ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2006-10-051649

    authors: Fellows E,Gil-Parrado S,Jenne DE,Kurschus FC

    更新日期:2007-07-15 00:00:00

  • Mechanism of transcriptional activation of the immediate early gene Egr-1 in response to PIXY321.

    abstract::Studies with the granulocyte-macrophage colony-stimulating factor (GM-CSF)/interleukin-3 (IL-3) fusion protein, PIXY321, demonstrated enhanced biological activity of this molecule in comparison with GM-CSF or IL-3 alone or in combination. Experiments were performed to study the mechanisms resulting in PIXY321-induced ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Mignacca RC,Lee HJ,Kwon EM,Sakamoto KM

    更新日期:1996-08-01 00:00:00

  • Factor IX ectopically expressed in platelets can be stored in alpha-granules and corrects the phenotype of hemophilia B mice.

    abstract::We developed 2bF9 transgenic mice in a hemophilia B mouse model with the expression of human factor IX (FIX) under control of the platelet-specific integrin alphaIIb promoter, to determine whether ectopically expressing FIX in megakaryocytes can enable the storage of FIX in platelet alpha-granules and corrects the mur...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2009-11-255612

    authors: Zhang G,Shi Q,Fahs SA,Kuether EL,Walsh CE,Montgomery RR

    更新日期:2010-08-26 00:00:00

  • The chemotherapy of lymphoblastic lymphoma.

    abstract::Thirty-two patients treated on consecutive Southwest Oncology Group (SWOG) protocols for malignant lymphoma were subsequently diagnosed as having lymphoblastic lymphoma. Combination chemistry, usually adriamycin-based, produced complete responses (CR) in 17 patients (53%). Median survival was 15 mo. Patients achieving...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Voakes JB,Jones SE,McKelvey EM

    更新日期:1981-01-01 00:00:00

  • Tissue distribution of target antigen has a decisive influence on the outcome of adoptive cancer immunotherapy.

    abstract::Adoptive transfer of allogeneic T cells has unmatched efficacy to eradicate leukemic cells. We therefore sought to evaluate in kinetic terms interactions between T cells and allogeneic leukemic cells. T cells primed against the model B6(dom1) minor histocompatibility antigen were adoptively transferred in irradiated B...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2002-04-1032

    authors: Meunier MC,Roy-Proulx G,Labrecque N,Perreault C

    更新日期:2003-01-15 00:00:00