Autoantibodies, idiotypes, anti-idiotypes and autoimmunity.

Abstract:

:The establishment of mouse and human monoclonal anti-DNA antibodies is described. Common idiotypes were identified on these antibodies employing monoclonal (mouse) and polyclonal anti-idiotypic antibodies. The significance of the presence and titer of the common idiotypes as clinical activity marker was examined in patients with systemic lupus erythematosus. Based on Jerne's network theory [Ann. Immunol. 125c: 373-389, 1974], naturally occurring anti-idiotypic antibodies to anti-DNA antibodies were reported. The utilization of this information to understand autoimmunity is discussed.

journal_name

Acta Haematol

journal_title

Acta haematologica

authors

Isenberg D,Shoenfeld Y

doi

10.1159/000206029

subject

Has Abstract

pub_date

1986-01-01 00:00:00

pages

95-100

issue

2-3

eissn

0001-5792

issn

1421-9662

journal_volume

76

pub_type

杂志文章
  • 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

  • Influence of alpha-thalassemia trait on the prevalence and severity of anemia in pregnancy among women in Kuwait.

    abstract::Alpha-thalassemia is very common in the Kuwaiti population, but its influence on anemia of pregnancy has not been previously investigated. We have screened a group of 59 anemic (Hb < 11 g/dl) pregnant women for the alpha-thal-2 (-alpha-3.7 kb) deletion which is the commonest alpha-thal allele in this community, using ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000039757

    authors: Diejomaoh FM,Haider MZ,Dalal H,Abdulaziz A,D'Souza TM,Adekile AD

    更新日期:2000-01-01 00:00:00

  • Pulmonary hypertension in sickle-cell disease: comorbidities and echocardiographic findings.

    abstract:BACKGROUND:Our aim is to determine comorbidities associated with pulmonary hypertension (PHT) in clinically stable sickle-cell disease (SCD) patients and to evaluate left ventricular (LV) and right ventricular (RV) function in those patients. METHODS:Echocardiography was performed in 87 SCD patients that were divided ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000102588

    authors: Akgül F,Yalçin F,Seyfeli E,Uçar E,Karazincir S,Balci A,Gali E

    更新日期:2007-01-01 00:00:00

  • Role of cytokines in healing chronic skin wounds.

    abstract::In the chronic wound, the normal cascade of inflammation, granulation and reconstruction phases of healing is interrupted. Cytokines are now known to orchestrate different biochemical mediators resulting in the restoration of the healing phases. Growth factors may play a significant role in stimulating wound repair by...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000040833

    authors: Nath C,Gulati SC

    更新日期:1998-01-01 00:00:00

  • Ticarcillin-induced neutropenia corroborated by in vitro CFU-C toxicity.

    abstract::A patient developed a drug rash and neutropenia while receiving tobramycin, ticarcillin and flucloxacillin intravenously for osteomyelitis. Incorporation of these antibiotics into in vitro cultures of bone marrow granulocyte macrophage precursors (CFU-C) showed no inhibition of the patient's marrow or normal marrow by...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206794

    authors: Irvine AE,Morris TC,Kelly GJ,McCracken N

    更新日期:1983-01-01 00:00:00

  • Precursor T-Lymphoblastic Lymphoma Associated with t(8;9)(p11.2;q33): A Case Report and Review of the Literature.

    abstract::The 8p11 myeloproliferative syndrome (EMS) is an aggressive neoplasm associated with chromosomal translocations involving the fibroblast growth factor receptor 1 (FGFR1) tyrosine kinase gene on chromosome 8p11-12. A new case of a 9-year-old boy with leukocytosis, eosinophilia, and general lymphadenopathy is reported i...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000481392

    authors: Lv H,Hu S,Lu J,Zhai Q,Zhai Z,Du Z,Sun Y,Li J,He H,Wang Y

    更新日期:2018-01-01 00:00:00

  • Treatment of iron deficiency anemia with intravenous iron preparations.

    abstract:OBJECTIVE:We aimed to determine the effects of intravenous iron therapy on blood parameters in pediatric patients who do not tolerate oral iron therapy for any reason. PATIENTS AND METHODS:The patient group consisted of candidates for elective operations requiring blood transfusions in order to raise hemoglobin (Hb) c...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000092348

    authors: Akarsu S,Taskin E,Yilmaz E,Yilmaz H,Kilic M,Aygun AD

    更新日期:2006-01-01 00:00:00

  • Double esterase staining and other neutrophilic granule abnormalities in 237 patients with the myelodysplastic syndrome studied by the cancer and leukemia group B.

    abstract::We investigated double (specific and nonspecific) esterase (DE) staining in marrow cells of 237 patients with the myelodysplastic syndromes (MDS). Additional abnormalities of neutrophilic granules were examined cytochemically and immunocytochemically for myeloperoxidase activity and antigen elastase, lactoferrin and C...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000040855

    authors: Elghetany MT,Peterson B,MacCallum J,Nelson DA,Varney JF,Sullivan AK,Silverman LR,Schiffer CA,Davey FR,Bloomfield CD

    更新日期:1998-01-01 00:00:00

  • Biological mothers may be dangerous blood donors for their neonates.

    abstract::Premature neonates require blood transfusions, and biological parents may wish to be directed donors. Biological mothers pose a potential danger because their plasma may contain antibodies that will react with blood cell antigens inherited by the infant from the father. We studied 25 healthy, pregnant women at the tim...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000204889

    authors: Elbert C,Strauss RG,Barrett F,Goeken NE,Pittner B,Cordle D

    更新日期:1991-01-01 00:00:00

  • An atypical von Willebrand's disease with hyperreactivity of platelet aggregation.

    abstract::Two family members (daughter and mother) with a bleeding disorder showed prolonged bleeding time and activated partial thromboplastin time associated with decreased plasma levels of factor VIII procoagulant activity, factor VIII-related antigen, and factor VIII-ristocetin cofactor activity. The ristocetin-induced plat...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206579

    authors: Niiya K,Kubonishi I,Taguchi H,Miyoshi I

    更新日期:1984-01-01 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

  • Changes in peripheral blood mononuclear cell subpopulations during antithymocyte globulin therapy for severe aplastic anemia.

    abstract::The short-term effect of a domestically produced equine antithymocyte globulin (ATG) was analyzed in 6 patients with acquired severe aplastic anemia (AA). All patients received 5 doses of ATG every other day in a 60-min intravenous infusion. Five peripheral blood immunoregulatory mononuclear cell (MNC) subsets, define...

    journal_title:Acta haematologica

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1159/000205557

    authors: López-Karpovitch X,Zarzosa ME,Cárdenas MR,Piedras J

    更新日期:1989-01-01 00:00:00

  • Platelet functions before, during and after labor.

    abstract::Platelet functions were evaluated in 20 healthy pregnant women in the last months of pregnancy, during labor, and 5-12 weeks after labor. The results showed an increased platelet count, bleeding time and nitroblue tetrazolium (NBT) test, as well as an increased plasma calcium level postlabor. ADP- and epinephrine-indu...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207151

    authors: Sagi A,Creter D,Goldman J,Djaldetti M

    更新日期:1981-01-01 00:00:00

  • Virus-bearing plasma cells in peripheral blood of a patient with 'hairy cell' leukemia.

    abstract::Electron-microscopic examination of peripheral blood from a patient with 'hairy cell' leukemia revealed classical 'hairy cells', atypical lymphoid cells and numerous pathological plasma cells. Osmiophilic granular material coated the cell surface of 'hairy cells' and lymphoid cells but not the plasmalemma of the plasm...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000208089

    authors: Pedio G,Rüttner JR,Spycher MA,Gut D

    更新日期:1975-01-01 00:00:00

  • Hairy cell leukemia variant.

    abstract::A 59-year-old man presented with lymphocytosis with huge splenomegaly. The abnormal lymphocytes had a high nucleoplasm:cytoplasm ratio, a prominent nucleolus and hairy cytoplasmic projections. Immunophenotyping revealed B-cell leukemia with negative reactions to CD5 and CD25. Cytogenetic study showed 46,XY,der(5)t(5;6...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000203984

    authors: Dunn P,Shih LY,Ho YS,Tien HF

    更新日期:1995-01-01 00:00:00

  • Rhinophyma-like cryptococcal infection as an early manifestation of AIDS in a hemophilia B patient.

    abstract::A hemophilia B patient, seropositive for HIV antibodies since 1984, came to us in March 1989 with a severe necrotizing lesion of the nose. It was an erythematous lesion and looked like rhinophyma. Microbiological examination of the skin biopsy showed the presence of Cryptococcus neoformans. At the time of the study, t...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000205038

    authors: Mares M,Sartori MT,Carretta M,Bertaggia A,Girolami A

    更新日期:1990-01-01 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

  • Sickle cell anemia identified in a multiple-transfused patient through analysis of mRNA with an RT-PCR-based technique.

    abstract::We report the identification of an Hb S homozygosity in a 29-year-old multiple-transfused patient with severe kidney disease using a new reverse-transcription polymerase chain reaction (RT-PCR) technique with mRNA as starting template. The procedure requires considerably less time than sequencing of genomic DNA and is...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000204121

    authors: Smetanina NS,Gu LH,Leonova JYe,Huisman TH

    更新日期:1995-01-01 00:00:00

  • Aplastic anemia: assessment of myeloid progenitor cells in the bone marrow and blood provides prognostic information.

    abstract::15 patients with aplastic anemia were prospectively followed after having measurements of myeloid progenitor cells in bone marrow and blood. Treatment included androgens, low or high dose steroids and standardized supportive care. The median length of survival was 5.8 months. When patients were grouped according to th...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206263

    authors: Hinterberger W,Geissler K,Fischer M,Lechner K,Kabrna E

    更新日期:1985-01-01 00:00:00

  • Benign Bence Jones gammopathy.

    abstract::A case of isolated lambda-light chain proteinemia and proteinuria is reported. During a 42-month follow-up, no sign of myelomatosis or amyloidosis developed and Bence Jones proteinuria remained nearly of the same magnitude. This case of apparently idiopathic Bence Jones gammopathy, the first lambda-type so far reporte...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207409

    authors: Paladini G,Sala PG,Santini PA

    更新日期:1980-01-01 00:00:00

  • Scanning immunoelectron microscopy of hairy cell leukemia.

    abstract::Scanning electron microscopy has shown a typical cell surface morphology in hairy cell leukemia. Scanning immunoelectron microscope techniques, utilizing monoclonal antibodies and colloidal gold particles, have recently become available. Eight patients with hairy cell leukemia have been studied with a panel of monoclo...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206218

    authors: Soligo D,Lambertenghi-Deliliers G,Nava MT,Polli N,Cattoretti G,Polli EE

    更新日期:1985-01-01 00:00:00

  • Routine screening of (--(SEA)) alpha-thalassemia deletion by an enzyme-linked immunosorbent assay for embryonic zeta-globin chains.

    abstract::We evaluated an enzyme-linked immunosorbent assay (ELISA) for embryonic zeta-globin chains as a routine screening test for (--(SEA)) alpha-thalassemia deletion (SEA deletion). A total of 174 consecutive patient samples with a request for Hb analysis were recruited. The ELISA method was evaluated against a polymerase c...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000063060

    authors: Ma SK,Ma V,Chan AY,Chan LC,Chui DH

    更新日期:2002-01-01 00:00:00

  • Molecular Understanding of Non-Transfusion-Dependent Thalassemia Associated with Hemoglobin E-β-Thalassemia in Northeast Thailand.

    abstract::Non-transfusion-dependent thalassemia (NTDT) is associated with various forms of thalassemia and genetic modifiers. We report the molecular basis of NTDT in hemoglobin (Hb) E-β-thalassemia disease. This study was done in 73 adult patients encountered at the prenatal diagnosis center of Khon Kaen University, Northeast ...

    journal_title:Acta haematologica

    pub_type: 临床试验,杂志文章

    doi:10.1159/000449120

    authors: Yamsri S,Pakdee N,Fucharoen G,Sanchaisuriya K,Fucharoen S

    更新日期:2016-01-01 00:00:00

  • Future directions in haematology: beyond multiple myeloma.

    abstract::Thalidomide acts on the microenvironment of myelodysplastic syndromes (MDS) by influencing cytokine networks, and growing evidence supports thalidomide's usefulness in the management of haematological malignancies, such as MDS. The European Collaboration Group on Myelofibrosis with Myeloid Metaplasia reviewed patients...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000087042

    authors: Prentice HG,Sacchi S,Russell N

    更新日期:2005-01-01 00:00:00

  • Characterization of the fibrinolytic state by measuring stable cross-linked fibrin degradation products in disseminated intravascular coagulation associated with acute promyelocytic leukemia.

    abstract::Plasma samples from patients with disseminated intravascular coagulation (DIC) associated with acute promyelocytic leukemia (APL) exhibited higher levels of the D-fragment of fibrin and fibrinogen degradation products [FDP(D)], with relatively lower levels of cross-linked fibrin degradation products (XDP), than sample...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000205392

    authors: Okajima K,Koga S,Okabe H,Inoue M,Takatsuki K

    更新日期:1989-01-01 00:00:00

  • Strategies and clinical implications of chimerism diagnostics after allogeneic hematopoietic stem cell transplantation.

    abstract::Analysis of donor chimerism has become a routine method for the documentation of engraftment after allogeneic hematopoietic stem cell transplantation (HSCT). In recent years several groups have also focused on the application of this technique for the detection of relapsing disease after allogeneic HSCT. This review a...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000077555

    authors: Thiede C,Bornhäuser M,Ehninger G

    更新日期:2004-01-01 00:00:00

  • DNA polymorphism in the beta-globin gene cluster in Saudi Arabs: relation to severity of sickle cell anaemia.

    abstract::Significant DNA polymorphisms have been reported in the beta-globin gene cluster of epsilon-G gamma-A gamma-psi beta-delta-beta-gene region, in normal (Hb AA) individuals and in patients with sickle cell anaemia (SCA). Investigations of the extent of the DNA polymorphisms in the beta A- and beta S-globin gene cluster ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000204653

    authors: el-Hazmi MA,Bahakim HM,Warsy AS

    更新日期:1992-01-01 00:00:00

  • Serological and biochemical analyses of M components in patients with transitional cell carcinoma of the urinary bladder.

    abstract::Serological and biochemical studies were performed on M components isolated from 3 patients with transitional cell carcinoma of the urinary bladder (TCC). All were IgG1(K) proteins. 2 of the 3 belonged to the VKI subgroup, and these 2 also possessed cross-reactive idiotypic determinants. These findings are consistent ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206983

    authors: Pick AI,Wang AC,Frohlichman R,Fudenberg HH

    更新日期:1982-01-01 00:00:00

  • JAK2 and MPL mutations in myeloproliferative neoplasms.

    abstract::The Philadelphia chromosome-negative myeloproliferative disorders (MPDs) polycythemia vera (PV), essential thrombocytosis (ET) and primary myelofibrosis (PMF) are characterized by increased proliferation of terminally differentiated myeloid cells. Although these disorders were recognized as clonal hematopoietic stem c...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000140634

    authors: Koppikar P,Levine RL

    更新日期:2008-01-01 00:00:00

  • Acute promyelocytic leukemia in childhood. Report of a case with a review of the literature.

    abstract::A rare case of acute promyelcytic leukemia (APL) is reported in a 7-year-old boy. The patient displayed the typical features of APL including impaction of the marrow with promyelocytes, marked elevation of the serum vitamin B12 and transcobalamin I levels and a hemorrhagic diathesis. The bleeding diathesis in the case...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207589

    authors: Engelhard D,Yatziv S,Rachmilewitz EA,Polliack A

    更新日期:1979-01-01 00:00:00