Literature DB >> 3924449

Inherited C8 beta subunit deficiency in a patient with recurrent meningococcal infections: in vivo functional kinetic analysis of C8.

C P Rao, J O Minta, B Laski, C A Alper, E W Gelfand.   

Abstract

A 16 year old with recurrent meningococcal infections is reported. Absence of haemolytic activity in both the classical and alternative pathways resulted from an absence of functional C8. Addition of functional C8 restored hemolytic activity. Antigenically deficient C8 was present in the serum and isoelectric focusing of serum confirmed the absence of the C8 beta chain. Following the infusion of fresh frozen plasma, we followed the decay in C8 functional activity as well as total haemolytic activity. C8 activity peaked at about 3 h with a half-life survival estimated to be 28 h. The kinetics of total haemolytic activity showed a slower decay with an exponential decline over 72 h and a half-life of 55 h. Fresh frozen plasma may be of value in the treatment of patients with C8 deficiency and acute Neisserial infections.

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Year:  1985        PMID: 3924449      PMCID: PMC1577010     

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


  26 in total

1.  Selective deficiency of the second component of complement in a patient with anaphylactoid purpura.

Authors:  E W Gelfand; J E Clarkson; J O Minta
Journal:  Clin Immunol Immunopathol       Date:  1975-07

2.  C8 deficiency in a family with xeroderma pigmentosum. Lack of linkage to the HLA region.

Authors:  G Giraldo; L Degos; E Beth; M Sasportes; A Marcelli; R Gharbi; N K Day
Journal:  Clin Immunol Immunopathol       Date:  1977-11

3.  Absence of the eighth component of complement in association with systemic lupus erythematosus-like disease.

Authors:  H E Jasin
Journal:  J Clin Invest       Date:  1977-09       Impact factor: 14.808

4.  A simple one-step hemolytic assay for C2 with C2-deficient human serum.

Authors:  B Y Ngan; E W Gelfand; J O Minta
Journal:  J Immunol       Date:  1977-03       Impact factor: 5.422

5.  Activation of the alternate pathway of human complements by rabbit cells.

Authors:  T A Platts-Mills; K Ishizaka
Journal:  J Immunol       Date:  1974-07       Impact factor: 5.422

6.  Human deficiency of the eighth component of complement. The requirement of C8 for serum Neisseria gonorrhoeae bactericidal activity.

Authors:  B H Petersen; J A Graham; G F Brooks
Journal:  J Clin Invest       Date:  1976-02       Impact factor: 14.808

7.  Genetic polymorphism in C8 beta-chains. Evidence for two unlinked genetic loci for the eighth component of human complement (C8).

Authors:  C A Alper; D Marcus; D Raum; B H Petersen; T J Spira
Journal:  J Clin Invest       Date:  1983-11       Impact factor: 14.808

8.  Genetic polymorphism of the third component of human complement (C'3).

Authors:  C A Alper; R P Propp
Journal:  J Clin Invest       Date:  1968-09       Impact factor: 14.808

9.  Inherited structural polymorphism in human C2: evidence for genetic linkage between C2 and Bf.

Authors:  C A Alper
Journal:  J Exp Med       Date:  1976-10-01       Impact factor: 14.307

10.  The membrane attack mechanism of complement: the three polypeptide chain structure of the eigth component (C8).

Authors:  W P Klob; H J Müller-Eberhard
Journal:  J Exp Med       Date:  1976-05-01       Impact factor: 14.307

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  2 in total

Review 1.  Infectious diseases associated with complement deficiencies.

Authors:  J E Figueroa; P Densen
Journal:  Clin Microbiol Rev       Date:  1991-07       Impact factor: 26.132

2.  Paradoxical reconstitution of complement activity following plasma transfusion of an individual with deficiency of the seventh component of complement.

Authors:  A E Platonov; R Würzner; B Beloborodov; A M Jones; D V Troshansky; I V Vershinina; P J Lachmann; A Orren
Journal:  Immunology       Date:  1994-01       Impact factor: 7.397

  2 in total

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