HTLV-III/LAV antibody status of spouses and household contacts assisting in home infusion of hemophilia patients.

Abstract:

:Thirty-four adult and pediatric hemophilia A and B patients and 50 nonhemophilic members belonging to 28 families were enrolled in August 1984 in a study of human T cell lymphotropic virus type III/lymphadenopathy-associated virus (HTLV-III/LAV) antibody status and T cell subpopulation numbers. All 50 household contacts, including three spouses of LAV antibody-positive adult hemophiliacs, were immunologically normal and serologically negative with respect to HTLV-III/LAV. Based on Western blot serologic testing of blood samples collected intermittently between July 1981 and August 1984 from 33 representative St Louis hemophiliacs studied during the period from 1981 to 1984, the average time since seroconversion was estimated as 20 months. One spouse of a seropositive hemophiliac and 23 parents of 27 seropositive pediatric hemophiliacs assisted regularly with home infusions. These infusion assistants have collectively experienced 44 person-years of concentrate infusion "exposure" without seroconversion. These results suggest that the likelihood for transmission of HTLV-III/LAV from hemophiliacs to persons assisting in their therapy is extremely low.

journal_name

Blood

journal_title

Blood

authors

Lawrence DN,Jason JM,Bouhasin JD,McDougal JS,Knutsen AP,Evatt BL,Joist JH

subject

Has Abstract

pub_date

1985-09-01 00:00:00

pages

703-5

issue

3

eissn

0006-4971

issn

1528-0020

journal_volume

66

pub_type

杂志文章

相关文献

BLOOD文献大全
  • Single-strand conformation polymorphism analysis is a rapid and effective method for the identification of mutations and polymorphisms in the gene for glycoprotein IIIa.

    abstract::Glanzmann thrombasthenia (GT) is the most common inherited disorder of platelets. Most of the molecular defects previously identified in GT have been caused by point (or other small) mutations in the genes for glycoprotein (GP) IIb or GPIIIa. We have used single-strand conformation polymorphism (SSCP) analysis to rapi...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Jin Y,Dietz HC,Nurden A,Bray PF

    更新日期:1993-10-15 00:00:00

  • How I treat essential thrombocythemia.

    abstract::In the past 5 years we have witnessed significant advances in both the diagnostic process and optimal therapy for patients with essential thrombocythemia (ET). Insights into the underlying molecular mechanisms have been accompanied by the development of new diagnostic tests and by an improved understanding of the rela...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2010-08-270033

    authors: Beer PA,Erber WN,Campbell PJ,Green AR

    更新日期:2011-02-03 00:00:00

  • CD177 modulates human neutrophil migration through activation-mediated integrin and chemoreceptor regulation.

    abstract::CD177 is a glycosylphosphatidylinositol (GPI)-anchored protein expressed by a variable proportion of human neutrophils that mediates surface expression of the antineutrophil cytoplasmic antibody antigen proteinase 3. CD177 associates with β2 integrins and recognizes platelet endothelial cell adhesion molecule 1 (PECAM...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2017-03-768507

    authors: Bai M,Grieshaber-Bouyer R,Wang J,Schmider AB,Wilson ZS,Zeng L,Halyabar O,Godin MD,Nguyen HN,Levescot A,Cunin P,Lefort CT,Soberman RJ,Nigrovic PA

    更新日期:2017-11-09 00:00:00

  • Plasmodium falciparum-infected erythrocytes induce NF-kappaB regulated inflammatory pathways in human cerebral endothelium.

    abstract::Cerebral malaria is a severe multifactorial condition associated with the interaction of high numbers of infected erythrocytes to human brain endothelium without invasion into the brain. The result is coma and seizures with death in more than 20% of cases. Because the brain endothelium is at the interface of these pro...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2009-06-226415

    authors: Tripathi AK,Sha W,Shulaev V,Stins MF,Sullivan DJ Jr

    更新日期:2009-11-05 00:00:00

  • The expanding role(s) of eosinophils in health and disease.

    abstract::Surprisingly, the role(s) of eosinophils in health and disease is often summarized by clinicians and basic research scientists as a pervasive consensus opinion first learned in medical/graduate school. Eosinophils are rare white blood cells whose activities are primarily destructive and are only relevant in parasitic ...

    journal_title:Blood

    pub_type: 杂志文章,评审

    doi:10.1182/blood-2012-06-330845

    authors: Jacobsen EA,Helmers RA,Lee JJ,Lee NA

    更新日期:2012-11-08 00:00:00

  • HIF1α is required for survival maintenance of chronic myeloid leukemia stem cells.

    abstract::Hypoxia-inducible factor-1α (HIF1α), a master transcriptional regulator of the cellular and systemic hypoxia response, is essential for the maintenance of self-renewal capacity of normal HSCs. It is still unknown whether HIF1α has a role in survival regulation of leukemia stem cells (LSCs) in chronic myeloid leukemia ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2011-10-387381

    authors: Zhang H,Li H,Xi HS,Li S

    更新日期:2012-03-15 00:00:00

  • Fibrinogen Bern I: substitution gamma 337 Asn-->Lys is responsible for defective fibrin monomer polymerization.

    abstract::An inherited fibrinogen variant, fibrinogen Bern I, was isolated from plasma of an asymptomatic woman. Routine coagulation studies showed prolonged thrombin and reptilase clotting times. Fibrinogen concentration was diminished when determined by a functional assay, but was normal by the heat precipitation method. The ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Steinmann C,Reber P,Jungo M,Lämmle B,Heinemann G,Wermuth B,Furlan M

    更新日期:1993-10-01 00:00:00

  • A case of mistaken identity.

    abstract::McCullough and colleagues show that problems with cord banking still exist. To improve the results of cord transplantations, more attention should be given to ensuring quality standards rather than just collecting more units. ...

    journal_title:Blood

    pub_type: 评论,杂志文章

    doi:10.1182/blood-2009-06-226738

    authors: Querol S

    更新日期:2009-08-20 00:00:00

  • Production of laminin B2 chain protein and messenger RNA by a murine neutrophil precursor cell line, 32Dc13.

    abstract::Laminin is a heterotrimeric glycoprotein that plays a central role in promoting neutrophil chemotaxis, motility, and attachment to basement membrane. Rabbit peritoneal exudate neutrophils stain positively for laminin, which is presumed to be of exogenous origin and bound to laminin receptors on the cell surface. We ex...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Tweardy DJ,Sasaki M,Cardamone JJ Jr,McCoy JP Jr,Bonidie MJ,Signorella AP

    更新日期:1990-10-01 00:00:00

  • Human T cells expressing two additional receptors (TETARs) specific for HIV-1 recognize both epitopes.

    abstract::Adoptive TCR transfer against rapidly mutating targets, such as HIV-1 or cancer, must counteract corresponding immune escape. Hence, we generated T cells expressing two additional receptors (TETARs) specific for HIV-1 by TCR mRNA electroporation. An HLA-A2-restricted gag-specific TCR and an HLA-B13-restricted nef-spec...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2011-04-347005

    authors: Hofmann C,Höfflin S,Hückelhoven A,Bergmann S,Harrer E,Schuler G,Dörrie J,Schaft N,Harrer T

    更新日期:2011-11-10 00:00:00

  • Coexistence of multiple mechanisms of PT523 resistance in human leukemia cells harboring 3 reduced folate carrier alleles: transcriptional silencing, inactivating mutations, and allele loss.

    abstract::The reduced folate carrier (RFC) is the dominant route for the uptake of various antifolates including PT523, a potent dihydrofolate reductase inhibitor (Ki = 0.35 pM) and an excellent transport substrate of the RFC (Kt = 0.7 microM). Here, we describe the multiple mechanisms of RFC inactivation in human leukemia PT52...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2005-10-4048

    authors: Kaufman Y,Ifergan I,Rothem L,Jansen G,Assaraf YG

    更新日期:2006-04-15 00:00:00

  • Ferroportin deficiency in erythroid cells causes serum iron deficiency and promotes hemolysis due to oxidative stress.

    abstract::Ferroportin (FPN), the only known vertebrate iron exporter, transports iron from intestinal, splenic, and hepatic cells into the blood to provide iron to other tissues and cells in vivo. Most of the circulating iron is consumed by erythroid cells to synthesize hemoglobin. Here we found that erythroid cells not only co...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2018-04-842997

    authors: Zhang DL,Ghosh MC,Ollivierre H,Li Y,Rouault TA

    更新日期:2018-11-08 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

  • The genomic landscape of Waldenstrom macroglobulinemia is characterized by highly recurring MYD88 and WHIM-like CXCR4 mutations, and small somatic deletions associated with B-cell lymphomagenesis.

    abstract::The genetic basis for Waldenström macroglobulinemia (WM) remains to be clarified. Although 6q losses are commonly present, recurring gene losses in this region remain to be defined. We therefore performed whole genome sequencing (WGS) in 30 WM patients, which included germline/tumor sequencing for 10 patients. Validat...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2013-09-525808

    authors: Hunter ZR,Xu L,Yang G,Zhou Y,Liu X,Cao Y,Manning RJ,Tripsas C,Patterson CJ,Sheehy P,Treon SP

    更新日期:2014-03-13 00:00:00

  • Tissue-type plasminogen activator (t-PA) induces stromelysin-1 (MMP-3) in endothelial cells through activation of lipoprotein receptor-related protein.

    abstract::Tissue-type plasminogen activator (t-PA) is approved for treatment of ischemic stroke patients, but it increases the risk of intracranial bleeding (ICB). Previously, we have shown in a mouse stroke model that stromelysin-1 (matrix metalloproteinase-3 [MMP-3]) induced in endothelial cells was critical for ICB induced b...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2009-02-203919

    authors: Suzuki Y,Nagai N,Yamakawa K,Kawakami J,Lijnen HR,Umemura K

    更新日期:2009-10-08 00:00:00

  • Interleukin-10 inhibits interferon-gamma-induced intercellular adhesion molecule-1 gene transcription in human monocytes.

    abstract::Interleukin-10 (IL-10) is a potent monocyte regulatory cytokine that inhibits gene expression of proinflammatory mediators. In this study, we investigated the mechanism by which IL-10 downregulates expression of intercellular adhesion molecule-1 (ICAM-1) on the cell surface of normal human monocytes activated with int...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Song S,Ling-Hu H,Roebuck KA,Rabbi MF,Donnelly RP,Finnegan A

    更新日期:1997-06-15 00:00:00

  • Mammalian homeobox B6 expression can be correlated with erythropoietin production sites and erythropoiesis during development, but not with hematopoietic or nonhematopoietic stem cell populations.

    abstract::There has been increasing interest in the involvement of mammalian homeobox (HOX) genes in hematopoietic regulation. The HOX genes are clustered in 4 chromosomes in mice and humans. In general, 5' end HOX gene expression is predominant in hematopoietic stem cell populations, whereas 3' end HOX gene expression are prim...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Zimmermann F,Rich IN

    更新日期:1997-04-15 00:00:00

  • Warfarin-induced venous limb ischemia/gangrene complicating cancer: a novel and clinically distinct syndrome.

    abstract::Venous limb gangrene (VLG) can occur in cancer patients, but the clinical picture and pathogenesis remain uncertain. We identified 10 patients with metastatic cancer (7 pathologically proven) who developed severe venous limb ischemia (phlegmasia/VLG) after initiating treatment of deep-vein thrombosis (DVT); in 8 patie...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2015-01-622787

    authors: Warkentin TE,Cook RJ,Sarode R,Sloane DA,Crowther MA

    更新日期:2015-07-23 00:00:00

  • Expression of plasma glutathione peroxidase in human liver in addition to kidney, heart, lung, and breast in humans and rodents.

    abstract::We analyzed the expression of plasma glutathione peroxidase (GSHPx-P) messenger RNA (mRNA) in mouse, rat, and human tissues, using a human GSHPx-P cDNA clone as the probe. Unlike the classical cellular glutathione peroxidase (GSHPx-1), GSHPx-P expression appears to be tissue-specific. In the mouse and rat, kidney expr...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Chu FF,Esworthy RS,Doroshow JH,Doan K,Liu XF

    更新日期:1992-06-15 00:00:00

  • Transgenic overexpression of human IL-17E results in eosinophilia, B-lymphocyte hyperplasia, and altered antibody production.

    abstract::We have identified and cloned a novel human cytokine with homology to cytokines of the interleukin-17 (IL-17) family, which we have termed human IL-17E (hIL-17E). With the identification of several IL-17 family members, it is critical to understand the in vivo function of these molecules. We have generated transgenic ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2002-01-0012

    authors: Kim MR,Manoukian R,Yeh R,Silbiger SM,Danilenko DM,Scully S,Sun J,DeRose ML,Stolina M,Chang D,Van GY,Clarkin K,Nguyen HQ,Yu YB,Jing S,Senaldi G,Elliott G,Medlock ES

    更新日期:2002-10-01 00:00:00

  • Runx1 deficiency predisposes mice to T-lymphoblastic lymphoma.

    abstract::Chromosomal rearrangements affecting RUNX1 and CBFB are common in acute leukemias. These mutations result in the expression of fusion proteins that act dominant-negatively to suppress the normal function of the Runt-related transcription factor 1 (RUNX)/core binding factor beta (CBFbeta) complexes. In addition, loss-o...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2005-04-1447

    authors: Kundu M,Compton S,Garrett-Beal L,Stacy T,Starost MF,Eckhaus M,Speck NA,Liu PP

    更新日期:2005-11-15 00:00:00

  • Fibrinogen Mitaka II: a hereditary dysfibrinogen with defective thrombin binding caused by an A alpha Glu-11 to Gly substitution.

    abstract::A new type of A alpha Glu-11 to Gly substitution has been identified in a congenitally abnormal fibrinogen, fibrinogen Mitaka II, derived from a 14-year-old female suffering from easy bruising since childhood. Plasma of the patient and fibrinogen purified therefrom were found to clot slowly by thrombin but in a normal...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Niwa K,Yaginuma A,Nakanishi M,Wada Y,Sugo T,Asakura S,Watanabe N,Matsuda M

    更新日期:1993-12-15 00:00:00

  • Proteins encoded by genes involved in chromosomal alterations in lymphoma and leukemia: clinical value of their detection by immunocytochemistry.

    abstract::Acquired chromosomal anomalies (most commonly translocations) in lymphoma and leukemia usually result in either activation of a quiescent gene (by means of immunoglobulin or T-cell-receptor promotors) and expression of an intact protein product, or creation of a fusion gene encoding a chimeric protein. This review sum...

    journal_title:Blood

    pub_type: 杂志文章,评审

    doi:10.1182/blood.v99.2.409

    authors: Falini B,Mason DY

    更新日期:2002-01-15 00:00:00

  • Rare RHCE phenotypes in black individuals of Afro-Caribbean origin: identification and transfusion safety.

    abstract::The molecular backgrounds of variants encountered in Afro-Caribbean black individuals and associated with the production of clinically significant antibodies against high-incidence antigens (anti-RH18, anti-RH34) and against Rhe epitopes were determined. We showed that RH:-18 phenotypes are produced by 3 distinct RHCE...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2002-01-0229

    authors: Noizat-Pirenne F,Lee K,Pennec PY,Simon P,Kazup P,Bachir D,Rouzaud AM,Roussel M,Juszczak G,Ménanteau C,Rouger P,Kotb R,Cartron JP,Ansart-Pirenne H

    更新日期:2002-12-01 00:00:00

  • Local development of mast cells from bone marrow-derived precursors in the skin of mice.

    abstract::A mechanism to control development of mast cells was investigated in mice. Although mast cells in the skin of normal C57BL/6 mice were still of host type 290 days after irradiation and injection of bone marrow cells from beige (Chediak-Higashi syndrome, C57BL/6 bgJ/bgJ) mice, donor-type mast cells with giant granules ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Hatanaka K,Kitamura Y,Nishimune Y

    更新日期:1979-01-01 00:00:00

  • Notch1 as a potential therapeutic target in cutaneous T-cell lymphoma.

    abstract::Deregulation of Notch signaling has been linked to the development of T-cell leukemias and several solid malignancies. Yet, it is unknown whether Notch signaling is involved in the pathogenesis of mycosis fungoides and Sézary syndrome, the most common subtypes of cutaneous T-cell lymphoma. By immunohistochemistry of 4...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2009-12-260216

    authors: Kamstrup MR,Gjerdrum LM,Biskup E,Lauenborg BT,Ralfkiaer E,Woetmann A,Ødum N,Gniadecki R

    更新日期:2010-10-07 00:00:00

  • HIV-1 reprograms the migration of macrophages.

    abstract::Macrophages are motile leukocytes, targeted by HIV-1, thought to play a critical role in host dissemination of the virus. However, whether infection impacts their migration capacity remains unknown. We show that 2-dimensional migration and the 3-dimensional (3D) amoeboid migration mode of HIV-1-infected human monocyte...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2014-08-596775

    authors: Vérollet C,Souriant S,Bonnaud E,Jolicoeur P,Raynaud-Messina B,Kinnaer C,Fourquaux I,Imle A,Benichou S,Fackler OT,Poincloux R,Maridonneau-Parini I

    更新日期:2015-03-05 00:00:00

  • Small noncleaved cell lymphoma and leukemia in adults. A retrospective study of 65 adults treated with the LMB pediatric protocols.

    abstract::In France, more than 80% of children with Burkitt's lymphoma or Burkitt's leukemia (ALL3) are now cured with the LMB (B-cell non-Hodgkin's lymphoma and B-ALL) protocols of the Société Française d'Oncologie Pédiatrique, but so far, poor results have been obtained in the few adult studies available. We have analyzed the...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Soussain C,Patte C,Ostronoff M,Delmer A,Rigal-Huguet F,Cambier N,Leprisé PY,François S,Cony-Makhoul P,Harousseau JL

    更新日期:1995-02-01 00:00:00

  • Genomic analysis of hairy cell leukemia identifies novel recurrent genetic alterations.

    abstract::Classical hairy cell leukemia (cHCL) is characterized by a near 100% frequency of the BRAFV600E mutation, whereas ∼30% of variant HCLs (vHCLs) have MAP2K1 mutations. However, recurrent genetic alterations cooperating with BRAFV600E or MAP2K1 mutations in HCL, as well as those in MAP2K1 wild-type vHCL, are not well def...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2017-01-765107

    authors: Durham BH,Getta B,Dietrich S,Taylor J,Won H,Bogenberger JM,Scott S,Kim E,Chung YR,Chung SS,Hüllein J,Walther T,Wang L,Lu SX,Oakes CC,Tibes R,Haferlach T,Taylor BS,Tallman MS,Berger MF,Park JH,Zenz T,Abdel-Waha

    更新日期:2017-10-05 00:00:00

  • Antibiotics impair murine hematopoiesis by depleting the intestinal microbiota.

    abstract::Bone marrow suppression is an adverse effect associated with many antibiotics, especially when administered for prolonged treatment courses. Recent advances in our understanding of steady-state hematopoiesis have allowed us to explore the effects of antibiotics on hematopoietic progenitors in detail using a murine mod...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2016-03-708594

    authors: Josefsdottir KS,Baldridge MT,Kadmon CS,King KY

    更新日期:2017-02-09 00:00:00