Literature DB >> 1904328

Activation of complement during apheresis.

G Hetland1, T E Mollnes, P Garred.   

Abstract

C3 activation products and the terminal complement complex (TCC) were examined in plasma during plasmapheresis of patients with Guillain-Barré Syndrome (GBS) (n = 4), Waldenström's syndrome (n = 4), and hypercholesterolaemia (n = 1), or during cytapheresis of platelet (n = 10) and granulocyte (n = 2) donors. Blood specimens were taken before, during and after the procedures. There was a significant activation of complement after apheresis in the GBS patients and one of the patients with Waldenström's syndrome, but not in the other patients. There were no significant differences in complement activation products before compared with after cytapheresis in the healthy donors. This demonstrates the biocompatibility with respect to complement activation of the materials used. The observed complement activation in some of the patients during plasma exchange is probably caused by activation products in the replacement plasma.

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Year:  1991        PMID: 1904328      PMCID: PMC1535422     

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


  11 in total

1.  Effect of time, temperature and anticoagulants on in vitro complement activation: consequences for collection and preservation of samples to be examined for complement activation.

Authors:  T E Mollnes; P Garred; G Bergseth
Journal:  Clin Exp Immunol       Date:  1988-09       Impact factor: 4.330

Review 2.  Activation of the complement system at the interface between blood and artificial surfaces.

Authors:  M D Kazatchkine; M P Carreno
Journal:  Biomaterials       Date:  1988-01       Impact factor: 12.479

3.  First-use syndrome with cuprammonium cellulose dialyzers.

Authors:  T S Ing; J T Daugirdas; S Popli; V C Gandhi
Journal:  Int J Artif Organs       Date:  1983-09       Impact factor: 1.595

4.  Complement and the damaging effects of cardiopulmonary bypass.

Authors:  J K Kirklin; S Westaby; E H Blackstone; J W Kirklin; D E Chenoweth; A D Pacifico
Journal:  J Thorac Cardiovasc Surg       Date:  1983-12       Impact factor: 5.209

5.  Different oxygenators for cardiopulmonary bypass lead to varying degrees of human complement activation in vitro.

Authors:  V Videm; E Fosse; T E Mollnes; O Ellingsen; T Pedersen; H Karlsen
Journal:  J Thorac Cardiovasc Surg       Date:  1989-05       Impact factor: 5.209

6.  Complement activation during cardiopulmonary bypass: evidence for generation of C3a and C5a anaphylatoxins.

Authors:  D E Chenoweth; S W Cooper; T E Hugli; R W Stewart; E H Blackstone; J W Kirklin
Journal:  N Engl J Med       Date:  1981-02-26       Impact factor: 91.245

7.  Complications of therapeutic apheresis, including a fatal case with pulmonary vascular occlusion.

Authors:  M D Rubenstein; R T Wall; G S Wood; M A Edwards
Journal:  Am J Med       Date:  1983-07       Impact factor: 4.965

8.  Quantification of the terminal complement complex in human plasma by an enzyme-linked immunosorbent assay based on monoclonal antibodies against a neoantigen of the complex.

Authors:  T E Mollnes; T Lea; S S Frøland; M Harboe
Journal:  Scand J Immunol       Date:  1985-08       Impact factor: 3.487

9.  Quantification in enzyme-linked immunosorbent assay of a C3 neoepitope expressed on activated human complement factor C3.

Authors:  P Garred; T E Mollnes; T Lea
Journal:  Scand J Immunol       Date:  1988-03       Impact factor: 3.487

10.  the role of autoantibody and immune complexes in the pathogenesis of Guillain-Barré syndrome.

Authors:  S D Cook; P C Dowling
Journal:  Ann Neurol       Date:  1981       Impact factor: 10.422

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  1 in total

1.  Chemotaxins C5a and fMLP induce release of calprotectin (leucocyte L1 protein) from polymorphonuclear cells in vitro.

Authors:  G Hetland; G J Talgö; M K Fagerhol
Journal:  Mol Pathol       Date:  1998-06
  1 in total

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