Definition of CD 11a, b, c, and CD 18 glycoproteins on chemotactically deficient granulocyte membranes in patients affected by myeloid disorders.

Abstract:

:We studied neutrophil chemotaxis and surface membrane glycoproteins in 12 patients suffering from myeloid disorders with abnormal karyotype using in vitro techniques in all 12. Chromosome studies were also carried out virtually simultaneously. We chose to study only patients showing a deficit of chemotaxis (p less than 0.001). Ten of these patients revealed a clonal chromosome abnormality in most of the leukemic cells. The monoclonal antibody technique using MoAb 60.1, 60.3, 60.5, OKM1, LFA-1 and 9E8 demonstrated normal leukocyte membrane glycoproteins CD 11a, b, c and CD 18 and therefore excludes that an abnormality of these is involved in the pathogenesis of altered leukocyte chemotaxis. No correlation between chemotactic deficit and any specific clonal chromosome abnormality was found.

journal_name

Acta Haematol

journal_title

Acta haematologica

authors

Ricevuti G,Mazzone A,Notario A

doi

10.1159/000205543

subject

Has Abstract

pub_date

1989-01-01 00:00:00

pages

126-30

issue

3

eissn

0001-5792

issn

1421-9662

journal_volume

81

pub_type

杂志文章
  • High-dose gammaglobulin therapy for idiopathic thrombocytopenic purpura in adults.

    abstract::High-dose gammaglobulin therapy for patients with idiopathic thrombocytopenic purpura (ITP), introduced by Imbach et al., was applied to 5 adults with chronic refractory ITP to investigate the mechanism of the increase in platelet counts. In 4 of the 5 cases, transient increase in platelet count was observed. Platelet...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206927

    authors: Kurata Y,Tsubakio T,Yonezawa T,Tarui S

    更新日期:1983-01-01 00:00:00

  • Immunoglobulin levels, opsonic activity and phagocytic power in Egyptian thalassemic children.

    abstract::Serum IgG, IgM and IgA were determined in 25 patients with homozygous beta thalassemia and 7 with the trait. The levels were increased in homozygous patients and increased further after splenectomy. Serum opsonic activity against Salmonella typhi and staphylococci was impaired in homozygous patients. Splenectomy cause...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206875

    authors: Khalifa AS,Fattah SA,Maged Z,Sabry F,Mohamed HA

    更新日期:1983-01-01 00:00:00

  • Lymphocytotoxic activity of monoclonal immunoglobulins in plasmalymphocytic diseases.

    abstract::95 of 1,019 (9.3%) sera with monoclonal immunoglobulins (MIg) were found to have cold-reacting lymphocytotoxins (LCT). There was no difference in the prevalence of LCT in multiple myeloma, macroglobulinemia, cancer, lymphoma or benign monoclonal gammopathy. Prevalence of LCT was similar in various classes and types of...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206328

    authors: Pruzanski W,Capes H,Ramirez G,Falk J

    更新日期:1985-01-01 00:00:00

  • Nonchemotherapy Treatment of Immunoglobulin Light Chain Amyloidosis.

    abstract::Immunoglobulin light chain amyloidosis (AL amyloidosis) is a rare, life-threatening disease characterized by the deposition of misfolded proteins in vital organs such as the heart, the lungs, the kidneys, the peripheral nervous system, and the gastrointestinal tract. This causes a direct toxic effect, eventually leadi...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000507724

    authors: Van Doren L,Lentzsch S

    更新日期:2020-01-01 00:00:00

  • Increase of neutrophil alkaline phosphatase in the parents of trisomy 21 children. Hematological and cytogenetic studies.

    abstract::A comparative study of karyotypes, hematological variables and neutrophil alkaline phosphatase (NAP) was performed in 106 parents (53 couples) of children with free, homogeneous trisomy 21 and of 220 parents (110 couples) of normal children. In the parents of trisomy 21 children we found a significant increase of the ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207208

    authors: Grozdea J,Bourrouillou G,Mounie C,Colombies P

    更新日期:1980-01-01 00:00:00

  • Tyramide signal amplification: an enhanced method for immunohistochemistry on methyl-methacrylate-embedded bone marrow trephine sections.

    abstract::The detection of cellular antigens in bone marrow sections depends on the method of embedding, the nature of antigen and antibody, antigen retrieval techniques and the sensitivity of the immunohistochemical method. This study evaluated a fluorescyl-tyramide-enhanced immunostaining method on methyl-methacrylate-embedde...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000097458

    authors: Gaiser T,Bernhards J

    更新日期:2007-01-01 00:00:00

  • Immunological profile after splenectomy in children with beta-thalassaemia major.

    abstract::The in vitro immune functions of peripheral blood lymphocytes have been studied in 12 children with beta-thalassaemia major and hypersplenism. The study was performed prior to splenectomy and on the 2nd, 6th, 15th and 30th day after splenectomy. It was found that before splenectomy, patients had low numbers of blood l...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000205886

    authors: Mandalenaki-Lambrou K,Vrachnou E,Calogeropoulou C,Ladis V,Kattamis C

    更新日期:1987-01-01 00:00:00

  • Evidence for an erythropoietin-stimulating factor in patients with renal and hepatic disease.

    abstract::Recently, a factor was discovered in the serum of hepatectomized animals which was capable of augmenting the hepatic erythropoietin response to hypoxia when injected into normal rats. This substance was localized in the liver via an in situ perfusion technique and was termed the hepatic erythropoietic factor (HEF). Pa...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206884

    authors: Naughton BA,Liu P,Naughton GK,Gordon AS

    更新日期:1983-01-01 00:00:00

  • Acquired C1-inhibitor deficiency in essential cryoglobulinemia and macrocryoglobulinemia.

    abstract::In 5 patients with mixed cryoglobulinemia, 3 with Waldenström's disease and 2 with essential cryoglobulinemia, a C1-inhibitor (C1-INH) deficiency was discovered. The complement profile was characteristic of the acquired type: the total hemolytic activity and the early components were reduced, C3 was diminished in 1 pa...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207773

    authors: Casali P,Borzini P,Pioltelli P,Invernizzi F,Zanussi C

    更新日期:1978-01-01 00:00:00

  • Mediastinal bulky tumour in Hodgkin's disease and prognostic value of positron emission tomography in the evaluation of post-treatment residual masses.

    abstract::Among the 193 patients (82 female, 111 male) treated primarily for Hodgkin's disease at our clinic between 1990 and 2001 and followed up until 2003, 42 (22%) had mediastinal bulky tumours (MBTs) by the Cotswolds criteria. The rate of MBT diagnosis was significantly greater in the early stage of the disease, these pati...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000081271

    authors: Keresztes K,Lengyel Z,Devenyi K,Vadasz G,Miltenyi Z,Illes A

    更新日期:2004-01-01 00:00:00

  • Absence of mutations on the SNF5 gene in hematological neoplasms with chromosome 22 abnormalities.

    abstract:BACKGROUND:The relation with SNF5 mutation and chromosome 22 abnormalities is not clear in hematological neoplasms. METHODS:To elucidate the relevance of the SNF5 gene on 22q11.2, karyotypes were reviewed in 283 hematological neoplasms. Loss of heterozygosity (LOH) on 22q was analyzed in 21 plasma cell myelomas withou...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000324932

    authors: Mori N,Inoue K,Okada M,Motoji T

    更新日期:2011-01-01 00:00:00

  • Chemotherapeutic remissions in Wistar Furth rat acute myelogenous leukemia: a model for human AML.

    abstract::Acute myelogenous leukemia (AML) of the inbred Wistar/Furth (W/Fu) rat is pathophysiologically similar to human AML. Subcutaneous transplantation of 1.0 X 10(6) cells of a clonal tissue culture line of W/Fu AML into 6- to 8-week-old rats produced local myeloblastomas in 8--10 days which progressed to infiltration of r...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207886

    authors: Greenberger JS,Bocaccino CA,Szot SJ,Moloney WC

    更新日期:1977-03-01 00:00:00

  • Acquired pure red-cell aplasia associated with an increase of T cells bearing receptors for the Fc of IgG.

    abstract::A case of steroid-resistant acquired pure red-cell aplasia associated with a relative and absolute increase of TG cells is described. Removal of T cells enhanced erythroid colony and burst formation in vitro, and it is suggested that TG cells may be implicated in the pathogenesis of this case of acquired pure red-cell...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207191

    authors: Linch DC,Cawley JC,MacDonald SM,Masters G,Roberts BE,Antonis AH,Waters AK,Sieff C,Lydyard PM

    更新日期:1981-01-01 00:00:00

  • Cytochemical detection of erythroblastic enzymes in acquired dyserythropoiesis.

    abstract::We have studied the amount and intracellular distribution of erythroblastic alkaline and acid phosphatase, nonspecific esterase, and N-acetyl-beta-glucosaminidase in 50 patients with acquired dyserythropoiesis. 19 morphologically normal bone marrow smears served as controls. Alkaline phosphatase was found in all contr...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206406

    authors: Woessner S,Lafuente R,Florensa L,Sans-Sabrafen J

    更新日期:1984-01-01 00:00:00

  • A new method for the detection of the plasminogen activator content of vein walls.

    abstract::The plasminogen activator content of a vein wall has been measured by estimating the radio-activity released from a 125I-tagged fibrin clot by incubating that clot with a known weight of the vein wall. This method could be used in the investigation of the fibrinolytic system of the body in its normal distribution and ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207720

    authors: Johnson RH,Mansfield AO

    更新日期:1978-01-01 00:00:00

  • In situ hybridization studies of cytomegalovirus and Epstein-Barr virus in reactive histiocytic hyperplasia with hemophagocytosis.

    abstract::We studied 14 adult patients presenting with fever and cytopenia of the peripheral blood and histiocytic hyperplasia with hemophagocytosis (HHH) in the bone marrow regarding an association of cytomegalovirus (CMV) and Epstein-Barr virus (EBV) by using in situ hybridization (ISH) and also evaluated the clinical and lab...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000203746

    authors: Han K,Kim Y,Kahng J,Lee J,Moon Y,Kang C,Shim S

    更新日期:1996-01-01 00:00:00

  • Hodgkin lymphoma accompanied by aplastic anemia and polyclonal expansion of large granular lymphocytes.

    abstract::Immunologic abnormalities have been described in patients with Hodgkin lymphoma, including autoimmune hemolytic anemia and immune thrombocytopenic purpura. The concurrent diagnoses of Hodgkin lymphoma and acquired aplastic anemia, however, is extremely rare. We report a 56-year-old Japanese female patient with severe ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000100038

    authors: Saitoh T,Matsushima T,Yamane A,Sakuraya M,Irisawa H,Yokohama A,Handa H,Tsukamoto N,Karasawa M,Nojima Y,Murakami H

    更新日期:2007-01-01 00:00:00

  • Concomitant Primary Hyperparathyroidism in Patients with Multiple Myeloma: A Possible Link?

    abstract::Hypercalcemia is a significant feature of patients with active multiple myeloma (MM) with extensive bone disease. Among the causes of non-neoplastic hypercalcemia, primary hyperparathyroidism (PHPT) is one of the most common, leading to osteoporosis and bone fractures. Interestingly, some preclinical data indicate tha...

    journal_title:Acta haematologica

    pub_type:

    doi:10.1159/000509768

    authors: Notarfranchi L,Marchica V,Dalla Palma B,Pelagatti L,Burroughs-Garcia J,Pedrazzoni M,Ruffini L,Cetani F,Marcocci C,Giuliani N

    更新日期:2020-09-09 00:00:00

  • Idiopathic thrombocytopenic purpura in Egyptian children.

    abstract::350 patients with idiopathic thrombocytopenic purpura (ITP) aged 2/12-15 years (mean 6.3 +/- 2.7) were followed up during the period January 1st, 1975 to March 31, 1992. They constituted 40% of cases with hemorrhagic diathesis attending the Hematology/Oncology Clinic, Children's Hospital, Ain Shams University (relativ...

    journal_title:Acta haematologica

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1159/000204392

    authors: Khalifa AS,Tolba KA,el-Alfy MS,Gadallah M,Ibrahim FH

    更新日期:1993-01-01 00:00:00

  • Micromegakaryocytes in Human Bone Marrow.

    abstract::Micromegakaryocytes (MMK) were defined morphologically by the cell area, nucleus form and cytoplasmic structure. Bone marrow smears of 7,156 patients were retrospectively analyzed. MMK were found most frequently and abundantly in acute non-lymphatic leukaemia, chronic myeloid leukaemia and pre-leukaemia. The presence ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207213

    authors: Wiesneth M,Pflieger H,Kubanek B,Heimpel H

    更新日期:1980-01-01 00:00:00

  • Amylase-producing Bence Jones multiple myeloma with pancreatitis-like symptoms.

    abstract::Amylase-producing tumors are mainly adenocarcinomas and, in rare instances, multiple myelomas. We describe here a first case of amylase-producing Bence Jones type myeloma with pancreatitis-like symptoms and the second in a Caucasian patient. The finding of salivary-type hyperamylasemia in a 72-year-old female with a p...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000204384

    authors: Lopez J,Ulibarrena C,Gonzalez-Porque P,Navas G,Roldan E,Cancelas JA,Perez-Oteyza J,Burgaleta C,García-Laraña J,Sastre JL

    更新日期:1993-01-01 00:00:00

  • Avascular necrosis of the hip in children with sickle cell disease and high Hb F: magnetic resonance imaging findings and influence of alpha-thalassemia trait.

    abstract::Avascular necrosis (AVN) of the hip is a common cause of morbidity in sickle cell disease (SCD). Its prevalence increases with age and predisposing factors include coexistent alpha-thalassemia trait, frequent vaso-occlusive crisis and a high hematocrit (Hct). SCD is relatively mild among Kuwaiti patients because of th...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000046529

    authors: Adekile AD,Gupta R,Yacoub F,Sinan T,Al-Bloushi M,Haider MZ

    更新日期:2001-01-01 00:00:00

  • Effects of cryoglobulin on fibrin clot formation and fibrinolysis.

    abstract::It was confirmed that activation of the kallikrein-kinin enzyme system in cryoglobulinemia might be initiated by activation of factor XII to factor XIIa by cryoglobulin. It was also demonstrated that cryoglobulin or fibrin clots lost their ability to redissolve on warming to 37 degrees C, and consequently the lysis ti...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206563

    authors: Kataoka K,Yamada S,Toki N

    更新日期:1984-01-01 00:00:00

  • Hyper-CVAD regimen in routine management of adult acute lymphoblastic leukemia: a retrospective multicenter study.

    abstract::Treatment of acute lymphoblastic leukemia is unsatisfactory in adults due to disease and patient-related factors and probably because adult chemotherapy regimens are weaker than pediatric protocols. Worries about inadequacy of adult regimens urged many hematologists, including us, to reconsider their routine treatment...

    journal_title:Acta haematologica

    pub_type: 临床试验,杂志文章,多中心研究

    doi:10.1159/000351172

    authors: Buyukasik Y,Acar K,Kelkitli E,Uz B,Serefhanoglu S,Ozdemir E,Pamukcuoglu M,Atay H,Bektas O,Sucak GT,Turgut M,Aksu S,Yagci M,Sayınalp N,Ozcebe OI,Goker H,Haznedaroglu IC

    更新日期:2013-01-01 00:00:00

  • Pseudo-Chediak-Higashi anomaly in acute myeloid leukaemia. An electron microscopical study.

    abstract::2 cases of acute myeloid leukaemia with inclusion bodies are presented. The inclusions were found mainly in the blast cells but could also be encountered in lymphocytes and plasma cells. Cytochemical and ultrastructural studies showed a great resemblance of these inclusions to the ones found in Chediak-Higashi anomaly...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207670

    authors: Efrati P,Nir E,Kaplan H,Dvilanski A

    更新日期:1979-01-01 00:00:00

  • Changes in serum thrombopoietin levels after splenectomy.

    abstract::To clarify the role of thrombopoietin (c-Mpl ligand, TPO) in 'hypersplenic' thrombocytopenia, we used an enzyme-linked immunosorbent assay to examine changes in serum TPO levels accompanied with splenectomy in 6 patients with liver cirrhosis, 4 patients with gastric cancer, and 2 patients with lymphoid malignancies. W...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000040888

    authors: Ichikawa N,Kitano K,Shimodaira S,Ishida F,Ito T,Kajikawa S,Tahara T,Kato T,Kiyosawa K

    更新日期:1998-12-01 00:00:00

  • Defective terminal maturation along monocyte-macrophage lineage in chronic myelomonocytic leukemia.

    abstract::The maturation process of leukemic myelomonocytoid cells derived from peripheral blood of two typical cases of chronic myelomonocytic leukemia was investigated in vitro. In both cases, liquid culture of the leukemic cells in the presence or absence of 12-o-tetradecanoyl phorbol-13-acetate yielded either monocyte-macro...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206382

    authors: Takuwa N,Kanegasaki S,Asano S,Tomita T,Nakayama E,Sato N,Shinohara T,Miwa S

    更新日期:1984-01-01 00:00:00

  • T cell prolymphocytic leukemia with new chromosome rearrangements.

    abstract::A 77-year-old woman presented to the outpatient hematology clinic in August 2001 with leukocytosis, recurrent bacterial infections, sweating and weight loss. Bone marrow biopsy showed 80% infiltration with lymphoid cells having a prolymphocytic morphology. Flow-cytometric immunophenotype analysis showed that over 80% ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000076527

    authors: Zver S,Kokalj Vokac N,Zagradisnik B,Erjavec A,Zagorac A,Zupan IP,Cernelc P

    更新日期:2004-01-01 00:00:00

  • Initial clonal acute lymphoblastic transformation of chronic lymphocytic leukemia with (11;14) and (8;12) chromosome translocations and acquired homozygosity.

    abstract::A 69-year-old woman presented with chronic lymphocytic leukemia (CLL) diagnosed after bone marrow recovery following intensive chemotherapy for acute lymphoblastic leukemia. The retrospective diagnosis of initial blastic transformation of CLL was made. The patient eventually died, 5 months after initial blastic phase,...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000205751

    authors: Archimbaud E,Charrin C,Gentilhomme O,Rimokh R,Guyotat D,Fiere D,Germain D

    更新日期:1988-01-01 00:00:00

  • Circulating platelet aggregates and thrombocytopenia induced by intravenous infusions of arachidonic and lauric acids in guinea pigs.

    abstract::Slow intravenous infusion of Na laurate (NaL) into guinea pigs caused a rapid appearance of platelet aggregates in the arterial blood and a precipitous fall in platelet counts. During the infusion of Na arachidonate (NaA) thrombocytopenia developed slowly, and few and smaller platelet aggregates appeared in the arteri...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207864

    authors: Rafflenbeul D,Zbinden G

    更新日期:1977-01-01 00:00:00