Literature DB >> 816581

Alternative complement pathway activity in sera from patients with sickle cell disease.

S M Koethe, J T Casper, G E Rodey.   

Abstract

The low molecular weight cobra venom factor (CoVF) was used to activate the terminal sequence of the alternative complement pathway in thirty-one sera from patients with sickle cell disease (SCD). The SCD sera were compared with normal sera as a source of the alternative complement pathway factors C3 proactivator (C3PA) and C3PA convertase. These factors are required for formation of the enzymatically active CoVF-C3PA complex which is capable of cleaving C3 and thus initiating generation of the cytolytic C5b-9 complex. CoVF cofactor activity was significantly less than normal in SCD sera as measured in an indirect lysis assay, indicating reduced C3PA or C3PA convertase activity in these sera. Qualitative (immunoelectrophoresis) and quantitative (radial immunodiffusion) measurement of C3PA showed, however, that this protein is normal or elevated in SCD sera. Taken together, the reduced CoVF cofactor activity and normal or elevated C3PA in SCD sera suggests that sera from patients with sickle cell disease have reduced C3PA convertase activity.

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Year:  1976        PMID: 816581      PMCID: PMC1538371     

Source DB:  PubMed          Journal:  Clin Exp Immunol        ISSN: 0009-9104            Impact factor:   4.330


  14 in total

1.  Immunoreactions involving platelets. I. A steric and kinetic model for formation of a complex from a human antibody, quinidine as a haptene, and platelets; and for fixation of complement by the complex.

Authors:  N R SHULMAN
Journal:  J Exp Med       Date:  1958-05-01       Impact factor: 14.307

2.  The crisis in sickle cell anemia; hematologic studies.

Authors:  L W DIGGS
Journal:  Am J Clin Pathol       Date:  1956-10       Impact factor: 2.493

3.  Deficiency of pneumococcal serum opsonizing activity in sickle-cell disease.

Authors:  J A Winkelstein; R H Drachman
Journal:  N Engl J Med       Date:  1968-08-29       Impact factor: 91.245

4.  Factor D in the alternate pathway of complement activation: purification, physicochemical characterization and functional role.

Authors:  M P Dierich; U Hadding; W König; M Limbert; H U Schorlemmer; D Bitter-Suermann
Journal:  Immunochemistry       Date:  1974-09

5.  C3 proactivator (C3PA) as an acute phase reactant.

Authors:  M Schutte; R DiCamelli; P Murphy; M Sadove; H Gewurz
Journal:  Clin Exp Immunol       Date:  1974-10       Impact factor: 4.330

6.  An abnormality of the alternate pathway of complement activation in sickle-cell disease.

Authors:  R B Johnston; S L Newman; A G Struth
Journal:  N Engl J Med       Date:  1973-04-19       Impact factor: 91.245

7.  Studies of the C3 shunt activation in cobra venom induced lysis of unsensitized erythrocytes.

Authors:  M Brai; A G Osler
Journal:  Proc Soc Exp Biol Med       Date:  1972-07

8.  Activation of the alternate complement pathway by autologous red cell stroma.

Authors:  T R Poskitt; H P Fortwengler; B J Lunskis
Journal:  J Exp Med       Date:  1973-09-01       Impact factor: 14.307

9.  Formation and function of a complex of the C3 proactivator with a protein from cobra venom.

Authors:  N R Cooper
Journal:  J Exp Med       Date:  1973-02-01       Impact factor: 14.307

10.  Properdin factor D: characterization of its active site and isolation of the precursor form.

Authors:  D T Fearon; K F Austen; S Ruddy
Journal:  J Exp Med       Date:  1974-02-01       Impact factor: 14.307

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  15 in total

1.  Factor H: a novel modulator in sickle cell disease.

Authors:  Wassim El Nemer; Bérengère Koehl
Journal:  Haematologica       Date:  2019-05       Impact factor: 9.941

2.  Complement levels in pneumococcal pneumonia.

Authors:  J D Coonrod; B Rylko-Bauer
Journal:  Infect Immun       Date:  1977-10       Impact factor: 3.441

3.  Complement activation in asymptomatic patients with sickle cell anaemia.

Authors:  W A Wilson; E J Thomas; J G Sissons
Journal:  Clin Exp Immunol       Date:  1979-04       Impact factor: 4.330

4.  P-selectin drives complement attack on endothelium during intravascular hemolysis in TLR-4/heme-dependent manner.

Authors:  Nicolas S Merle; Romain Paule; Juliette Leon; Marie Daugan; Tania Robe-Rybkine; Victoria Poillerat; Carine Torset; Véronique Frémeaux-Bacchi; Jordan D Dimitrov; Lubka T Roumenina
Journal:  Proc Natl Acad Sci U S A       Date:  2019-03-08       Impact factor: 11.205

5.  Opsonization of pneumococci by whole serum from sickle cell disease patients.

Authors:  E F Bloch; O Castro; J E Gregory; C Okoh
Journal:  J Natl Med Assoc       Date:  1984-02       Impact factor: 1.798

6.  Nature of complement deficiency in sickle cell disease.

Authors:  W A Wilson
Journal:  Arch Dis Child       Date:  1983-03       Impact factor: 3.791

7.  Rheumatoid arthritis in patients with hemoglobinopathies.

Authors:  Xanthi I Pliakou; Frideriki P Koutsouka; Dimitrios Damigos; Konstantinos L Bourantas; Evangelos C Briasoulis; Paraskevi V Voulgari
Journal:  Rheumatol Int       Date:  2011-09-07       Impact factor: 2.631

8.  Deficiency of serum bactericidal activity against Salmonella typhimurium in sickle cell anaemia.

Authors:  W L Hand; N L King
Journal:  Clin Exp Immunol       Date:  1977-11       Impact factor: 4.330

9.  Restoration by normal human immunoglobulin G of deficient serum opsonization for Streptococcus pneumoniae in sickle cell disease.

Authors:  A B Bjornson; J S Lobel; P I Magnafichi; B C Lampkin
Journal:  Infect Immun       Date:  1981-08       Impact factor: 3.441

10.  Defective yeast opsonisation and functional deficiency of complement in sickle cell disease.

Authors:  V F Larcher; R J Wyke; L R Davis; C E Stroud; R Williams
Journal:  Arch Dis Child       Date:  1982-05       Impact factor: 3.791

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