HIV gene therapy research advances.

Abstract:

:In this issue of Blood, Tebas et al report antiviral effects in a clinical trial of multiple infusions of lentiviral vector–modified autologous CD4T lymphocytes in 17 HIV-infected patients aviremic on antiretroviral therapy (ART).

journal_name

Blood

journal_title

Blood

authors

Jacobson JM

doi

10.1182/blood-2013-01-475921

subject

Has Abstract

pub_date

2013-02-28 00:00:00

pages

1483-4

issue

9

eissn

0006-4971

issn

1528-0020

pii

121/9/1483

journal_volume

121

pub_type

评论,杂志文章

相关文献

BLOOD文献大全
  • Paroxysmal nocturnal hemoglobinuria.

    abstract::Paroxysmal nocturnal hemoglobinuria (PNH) is a rare bone marrow failure disorder that manifests with hemolytic anemia, thrombosis, and peripheral blood cytopenias. The absence of two glycosylphosphatidylinositol (GPI)-anchored proteins, CD55 and CD59, leads to uncontrolled complement activation that accounts for hemol...

    journal_title:Blood

    pub_type: 杂志文章,评审

    doi:10.1182/blood-2014-02-522128

    authors: Brodsky RA

    更新日期:2014-10-30 00:00:00

  • How I treat infant leukemia.

    abstract::Leukemia in infants is rare but generates tremendous interest due to its aggressive clinical presentation in a uniquely vulnerable host, its poor response to current therapies, and its fascinating biology. Increasingly, these biological insights are pointing the way toward novel therapeutic approaches. Using represent...

    journal_title:Blood

    pub_type: 杂志文章,随机对照试验

    doi:10.1182/blood-2018-04-785980

    authors: Brown P,Pieters R,Biondi A

    更新日期:2019-01-17 00:00:00

  • Recombinant human interleukin-1 receptor antagonist in the treatment of steroid-resistant graft-versus-host disease.

    abstract::Acute graft-versus-host disease (GVHD) that is resistant to therapy is a highly lethal complication of marrow transplantation. Inflammatory cytokines such as interleukin-1 (IL-1) may be critical mediators of this process. If so, specific inhibition of IL-1 activity with recombinant human IL-1 receptor antagonist (IL-1...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Antin JH,Weinstein HJ,Guinan EC,McCarthy P,Bierer BE,Gilliland DG,Parsons SK,Ballen KK,Rimm IJ,Falzarano G

    更新日期:1994-08-15 00:00:00

  • Plasmic degradation of fibrin rapidly decreases platelet adhesion and spreading.

    abstract::Plasmin cleaves fibrin at or near sites involved in platelet recognition and may modulate platelet adhesion and spreading. Using an in vitro system, we have characterized the effects of limited plasmic degradation of polymerized fibrin on platelet adhesion and spreading. As shown by scanning electron microscopy, expos...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Hamaguchi M,Bunce LA,Sporn LA,Francis CW

    更新日期:1994-08-15 00:00:00

  • The EC domains of human fibrinogen420 contain calcium binding sites but lack polymerization pockets.

    abstract::The extended (E) isoform unique to Fibrinogen420 (Fib420) is distinguished from the conventional chain of Fibrinogen340 by the presence of an additional 236-residue carboxyl terminus globular domain (EC). A recombinant form of EC (rEC), having a predicted mass of 27,653 Daltons, was expressed in yeast (Pichia pastoris...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Applegate D,Haraga L,Hertzberg KM,Steben LS,Zhang JZ,Redman CM,Grieninger G

    更新日期:1998-11-15 00:00:00

  • Control of coronavirus infection through plasmacytoid dendritic-cell-derived type I interferon.

    abstract::This study demonstrates a unique and crucial role of plasmacytoid dendritic cells (pDCs) and pDC-derived type I interferons (IFNs) in the pathogenesis of mouse coronavirus infection. pDCs controlled the fast replicating mouse hepatitis virus (MHV) through the immediate production of type I IFNs. Recognition of MHV by ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2006-05-023770

    authors: Cervantes-Barragan L,Züst R,Weber F,Spiegel M,Lang KS,Akira S,Thiel V,Ludewig B

    更新日期:2007-02-01 00:00:00

  • Long-acting recombinant coagulation factor IX albumin fusion protein (rIX-FP) in hemophilia B: results of a phase 3 trial.

    abstract::A global phase 3 study evaluated the pharmacokinetics, efficacy, and safety of recombinant fusion protein linking coagulation factor IX with albumin (rIX-FP) in 63 previously treated male patients (12-61 years) with severe hemophilia B (factor IX [FIX] activity ≤2%). The study included 2 groups: group 1 patients recei...

    journal_title:Blood

    pub_type: 杂志文章,多中心研究

    doi:10.1182/blood-2015-09-669234

    authors: Santagostino E,Martinowitz U,Lissitchkov T,Pan-Petesch B,Hanabusa H,Oldenburg J,Boggio L,Negrier C,Pabinger I,von Depka Prondzinski M,Altisent C,Castaman G,Yamamoto K,Álvarez-Roman MT,Voigt C,Blackman N,Jacobs I,PROLONG

    更新日期:2016-04-07 00:00:00

  • A small molecule inhibitor of Pim protein kinases blocks the growth of precursor T-cell lymphoblastic leukemia/lymphoma.

    abstract::The serine/threonine Pim kinases are up-regulated in specific hematologic neoplasms, and play an important role in key signal transduction pathways, including those regulated by MYC, MYCN, FLT3-ITD, BCR-ABL, HOXA9, and EWS fusions. We demonstrate that SMI-4a, a novel benzylidene-thiazolidine-2, 4-dione small molecule ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2009-07-233445

    authors: Lin YW,Beharry ZM,Hill EG,Song JH,Wang W,Xia Z,Zhang Z,Aplan PD,Aster JC,Smith CD,Kraft AS

    更新日期:2010-01-28 00:00:00

  • Thrombosis in the setting of obesity or inflammatory bowel disease.

    abstract::Obesity and inflammatory bowel disease (IBD) are systemic inflammatory disorders that predispose to arterial and venous thrombosis through similar prothrombotic mechanisms. Obesity and IBD are chronic risk factors that lead to a persistently elevated risk of thrombosis, although the thrombotic risk with IBD appears to...

    journal_title:Blood

    pub_type: 杂志文章,评审

    doi:10.1182/blood-2016-05-716720

    authors: Lentz SR

    更新日期:2016-11-17 00:00:00

  • Trial of repeated low-dose aspirin in diabetic angiopathy.

    abstract::We compared the ability of aspirin to suppress platelet aggregation and thromboxane synthesis in ten normal subjects and ten patients with diabetic angiopathy and high rate of entry of new platelets into the circulation. When single doses of 100 to 1,000 mg aspirin were ingested daily for 1 month, there were time gaps...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: DiMinno G,Silver MJ,Cerbone AM,Murphy S

    更新日期:1986-10-01 00:00:00

  • Graft failure following bone marrow transplantation for severe aplastic anemia: risk factors and treatment results.

    abstract::Graft failure was analyzed in 625 patients receiving allogeneic bone marrow transplants from HLA-identical sibling donors as treatment for severe aplastic anemia. Sixty-eight (11%) had no or only transient engraftment. Second bone marrow transplants were successful in achieving extended survival in 16 of 27 patients w...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Champlin RE,Horowitz MM,van Bekkum DW,Camitta BM,Elfenbein GE,Gale RP,Gluckman E,Good RA,Rimm AA,Rozman C

    更新日期:1989-02-01 00:00:00

  • A point mutation in the cysteine-rich domain of glycoprotein (GP) IIIa results in the expression of a GPIIb-IIIa (alphaIIbbeta3) integrin receptor locked in a high-affinity state and a Glanzmann thrombasthenia-like phenotype.

    abstract::This article reports a Glanzmann thrombasthenia (GT) patient, N.M., with a point mutation in the third cysteine-rich repeat of beta3-integrin or platelet glycoprotein (GP) IIIa, leading to the expression of a constitutively activated fibrinogen receptor. The diagnosis of GT was based on a severely reduced platelet-agg...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood.v98.8.2432

    authors: Ruiz C,Liu CY,Sun QH,Sigaud-Fiks M,Fressinaud E,Muller JY,Nurden P,Nurden AT,Newman PJ,Valentin N

    更新日期:2001-10-15 00:00:00

  • Long-term remission of Kaposi sarcoma-associated herpesvirus-related multicentric Castleman disease with anti-CD20 monoclonal antibody therapy.

    abstract::Kaposi sarcoma-associated herpesvirus (KSHV)-related multicentric Castleman disease (MCD) is potentially lethal. Growing evidence indicates that, as in Epstein-Barr virus-driven lymphoproliferative disorders after transplantation, KSHV DNA burden in peripheral blood mononuclear cells (PBMCs) may represent the most acc...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood.v98.12.3473

    authors: Corbellino M,Bestetti G,Scalamogna C,Calattini S,Galazzi M,Meroni L,Manganaro D,Fasan M,Moroni M,Galli M,Parravicini C

    更新日期:2001-12-01 00:00:00

  • p53 overexpression as a marker of poor prognosis in mantle cell lymphomas with t(11;14)(q13;q32).

    abstract::The t(11;14)(q13;q32) translocation, which juxtaposes the BCL1 oncogene with the Ig heavy chain locus, has been associated with an uncommon subtype of non-Hodgkin's lymphoma (NHL) termed mantle cell lymphoma (MCL). To date, no molecular marker that serves as an indicator of tumor progression or clinical prognosis has ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Louie DC,Offit K,Jaslow R,Parsa NZ,Murty VV,Schluger A,Chaganti RS

    更新日期:1995-10-15 00:00:00

  • Notch ligands Delta 1 and Jagged1 transmit distinct signals to T-cell precursors.

    abstract::Signaling through the Notch pathway plays an essential role in inducing T-lineage commitment and promoting the maturation of immature thymocytes. Using an in vitro culture system, we show that 2 different classes of Notch ligands, Jagged1 or Delta1, transmit distinct signals to T-cell progenitors. OP9 stromal cells ex...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2004-08-3257

    authors: Lehar SM,Dooley J,Farr AG,Bevan MJ

    更新日期:2005-02-15 00:00:00

  • Steady-state generation of mucosal IgA+ plasmablasts is not abrogated by B-cell depletion therapy with rituximab.

    abstract::The anti-CD20 antibody rituximab depletes human B cells from peripheral blood, but it remains controversial to what extent tissue-resident B cells are affected. In representative patients with rheumatoid arthritis, we here demonstrate that recently activated presumably short-lived plasmablasts expressing HLA-DR(high) ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2010-01-266536

    authors: Mei HE,Frölich D,Giesecke C,Loddenkemper C,Reiter K,Schmidt S,Feist E,Daridon C,Tony HP,Radbruch A,Dörner T

    更新日期:2010-12-09 00:00:00

  • Mapping of genes that control the antibody response to human factor IX in mice.

    abstract::We tested the hypothesis that the antibody response to human factor IX in mice is controlled by genetic factors, especially histocompatibility antigens. Seven inbred mouse strains were immunized against human factor IX by adenoviral gene transfer or serial injections of human factor IX protein. A/J mice had the highes...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2004-03-1126

    authors: Lozier JN,Tayebi N,Zhang P

    更新日期:2005-02-01 00:00:00

  • Traditional beer consumption and the iron status of spouse pairs from a rural community in Zimbabwe.

    abstract::To examine the relationship between dietary iron exposure through the consumption of traditional beer and the presence of iron overload in black Africans not related by birth, we studied 28 husband and wife pairs from a rural Zimbabwean community. Lifetime traditional beer consumption was estimated by questioning subj...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Moyo VM,Gangaidzo IT,Gomo ZA,Khumalo H,Saungweme T,Kiire CF,Rouault T,Gordeuk VR

    更新日期:1997-03-15 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

  • The antitumorigenic trifecta.

    abstract::The laboratory of Judah Folkman identified the potent endogenous antiangiogenic protein angiostatin in 1994.(1) In this issue of Blood, Lee and colleagues propose 2 new mechanisms of action for angiostatin that may represent promising targets for new cancer therapeutics.(2). ...

    journal_title:Blood

    pub_type: 评论,杂志文章

    doi:10.1182/blood-2009-06-226233

    authors: Mowery YM,Pizzo SV

    更新日期:2009-08-27 00:00:00

  • Amino-sugars enhance recognition and phagocytosis of particles by human neutrophils.

    abstract::Neutrophils were examined for their ability to recognize and ingest beads coated with amino-derivatives of glucose, mannose, and galactose. Radioactive or fluorescent beads coated with any of the three sugars were ingested to an extent three times that observed with albumin-coated beads. Enhancement of ingestion of su...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Doolittle RL,Packman CH,Lichtman MA

    更新日期:1983-09-01 00:00:00

  • Discontinuation of fucose therapy in LADII causes rapid loss of selectin ligands and rise of leukocyte counts.

    abstract::Leukocyte adhesion deficiency type II (LADII) is a rare inherited disorder of fucose metabolism. Patients with LADII lack fucosylated glycoconjugates, including the carbohydrate ligands of the selectins, leading to an immunodeficiency caused by the lack of selectin-mediated leukocyte-endothelial interactions. A simple...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood.v97.1.330

    authors: Lühn K,Marquardt T,Harms E,Vestweber D

    更新日期:2001-01-01 00:00:00

  • Expression and functional characterization of an abnormal platelet membrane glycoprotein Ib alpha (Met239 --> Val) reported in patients with platelet-type von Willebrand disease.

    abstract::Platelet-type von Willebrand disease (vWD) is a congenital bleeding disorder characterized by heightened ristocetin-induced platelet aggregation caused by abnormally high affinity between the platelet membrane glycoprotein (GP) Ib/IX complex and von Willebrand factor (vWF). Two distinct point mutations, Gly233 to Val ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Moriki T,Murata M,Kitaguchi T,Anbo H,Handa M,Watanabe K,Takahashi H,Ikeda Y

    更新日期:1997-07-15 00:00:00

  • The secretory pathway of bovine platelets.

    abstract::Human platelets contain tortuous channels in their cytoplasm, the surface-connected or open canalicular system (OCS), that communicate directly with the surrounding medium through openings on the surface membrane. Some workers have suggested that the OCS serves as the egress route for products secreted during the rele...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: White JG

    更新日期:1987-03-01 00:00:00

  • Lysosome-associated small Rab GTPase Rab7b negatively regulates TLR4 signaling in macrophages by promoting lysosomal degradation of TLR4.

    abstract::Toll-like receptor 4 (TLR4) initiates both myeloid differentiation factor 88 (MyD88)-dependent and Toll/interleukin (IL)-1R domain-containing adapter, inducing interferon (IFN)-beta-dependent signaling, leading to production of proinflammatory mediators and type I interferon (IFN) to eliminate pathogens. However, unco...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2007-01-066027

    authors: Wang Y,Chen T,Han C,He D,Liu H,An H,Cai Z,Cao X

    更新日期:2007-08-01 00:00:00

  • Restoration of superoxide generation to a chronic granulomatous disease-derived B-cell line by retrovirus mediated gene transfer.

    abstract::Failure of a superoxide generating system, the NADPH oxidase, present in neutrophils and other phagocytes gives rise to chronic granulomatous disease (CGD), a group of single-gene inherited disorders all characterized by an extreme susceptibility to pyogenic infection, with potentially fatal consequences. About 30% of...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Thrasher A,Chetty M,Casimir C,Segal AW

    更新日期:1992-09-01 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

  • CD44 is a RAS/STAT5-regulated invasion receptor that triggers disease expansion in advanced mastocytosis.

    abstract::The Hermes receptor CD44 is a multifunctional adhesion molecule that plays an essential role in the homing and invasion of neoplastic stem cells in various myeloid malignancies. Although mast cells (MCs) reportedly express CD44, little is known about the regulation and function of this receptor in neoplastic cells in ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2018-02-833582

    authors: Mueller N,Wicklein D,Eisenwort G,Jawhar M,Berger D,Stefanzl G,Greiner G,Boehm A,Kornauth C,Muellauer L,Sehner S,Hoermann G,Sperr WR,Staber PB,Jaeger U,Zuber J,Arock M,Schumacher U,Reiter A,Valent P

    更新日期:2018-11-01 00:00:00

  • Heterogeneity of the T-cell receptor delta gene indicating subclone formation in acute precursor B-cell leukemias.

    abstract::Precursor B-cell acute lymphoblastic leukemias (B-ALLs) have been shown to be oligoclonal at the Ig heavy-chain (IgH) gene level in up to 40% of cases by Southern blot hybridization. In contrast, oligoclonality as deduced from diversity of T-cell receptor (TcR)-delta gene rearrangements of the immature types (ie, V de...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Ghali DW,Panzer S,Fischer S,Argyriou-Tirita A,Haas OA,Kovar H,Gadner H,Panzer-Grümayer ER

    更新日期:1995-05-15 00:00:00

  • Immunophenotypic analysis of B cells in PNH: insights into the generation of circulating naive and memory B cells.

    abstract::Peripheral blood B cells in patients with paroxysmal nocturnal hemoglobinuria (PNH) comprise variable mixtures of normal B cells produced before the onset of disease and glycosylphosphatidylinositol (GPI)-deficient B cells derived from the PNH hematopoietic stem cell. In a detailed phenotypic analysis of 29 patients w...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Richards SJ,Morgan GJ,Hillmen P

    更新日期:2000-11-15 00:00:00