Literature DB >> 1432488

Immunoblotting analysis of sera from patients with candidal vaginitis and healthy females.

A Ishiguro1, M Homma, T Sukai, K Higashide, S Torii, K Tanaka.   

Abstract

Antigenic components of Candida albicans were extracted from whole cells with a buffer containing SDS and 2-mercaptoethanol, and separated by SDS-polyacrylamide gel electrophoresis. The components reactive with IgG, IgA, IgM and IgE antibodies in sera from patients with (14 subjects) and without (15 subjects) C. albicans in the vagina, and from healthy females (34 subjects), were investigated by immunoblotting using immunoglobulin class-specific antibodies. Many components reacted with IgG and IgA in all sera tested; the major antigens that reacted strongly with the sera were 67, 62, 29 and 25 kDa components. Several components were observed which reacted with IgM in 63% of the sera; the 67, 62 and 25 kDa components that reacted with IgG and IgA also reacted with IgM. No components reacting with IgE were detected in any of the sera. No striking differences in antibody binding profiles to whole cell antigens were detected among the C. albicans positive and negative patients or the healthy subjects. On the other hand, IgG against extracellular proteinase was more frequently detected in the C. albicans positive patients than in the C. albicans negative group or the healthy subjects. This may suggest that vaginal infection with C. albicans contributes to a rise in anti-proteinase antibody levels.

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Year:  1992        PMID: 1432488     DOI: 10.1080/02681219280000371

Source DB:  PubMed          Journal:  J Med Vet Mycol        ISSN: 0268-1218


  8 in total

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Authors:  B K Na; C Y Song
Journal:  Clin Diagn Lab Immunol       Date:  1999-11

Review 2.  Serologic response to cell wall mannoproteins and proteins of Candida albicans.

Authors:  J P Martínez; M L Gil; J L López-Ribot; W L Chaffin
Journal:  Clin Microbiol Rev       Date:  1998-01       Impact factor: 26.132

3.  Disruption of each of the secreted aspartyl proteinase genes SAP1, SAP2, and SAP3 of Candida albicans attenuates virulence.

Authors:  B Hube; D Sanglard; F C Odds; D Hess; M Monod; W Schäfer; A J Brown; N A Gow
Journal:  Infect Immun       Date:  1997-09       Impact factor: 3.441

4.  Isolation and preliminary characterization of the 14- to 18-kilodalton Candida albicans antigen as a phospholipomannan containing beta-1,2-linked oligomannosides.

Authors:  P A Trinel; M Borg-von-Zepelin; G Lepage; T Jouault; D Mackenzie; D Poulain
Journal:  Infect Immun       Date:  1993-10       Impact factor: 3.441

5.  Evidence for adhesin activity in the acid-stable moiety of the phosphomannoprotein cell wall complex of Candida albicans.

Authors:  T Kanbe; J E Cutler
Journal:  Infect Immun       Date:  1994-05       Impact factor: 3.441

Review 6.  Production and function of cytokines in natural and acquired immunity to Candida albicans infection.

Authors:  R B Ashman; J M Papadimitriou
Journal:  Microbiol Rev       Date:  1995-12

7.  Diagnosis of systemic candidiasis by enzyme immunoassay detection of specific antibodies to mycelial phase cell wall and cytoplasmic candidal antigens.

Authors:  D Navarro; E Monzonis; J L López-Ribot; P Sepúlveda; M Casanova; J M Nogueira; J P Martínez
Journal:  Eur J Clin Microbiol Infect Dis       Date:  1993-11       Impact factor: 3.267

8.  Effectiveness of a vaccine composed of heat-killed Candida albicans and a novel mucosal adjuvant, LT(R192G), against systemic candidiasis.

Authors:  L Cárdenas-Freytag; E Cheng; P Mayeux; J E Domer; J D Clements
Journal:  Infect Immun       Date:  1999-02       Impact factor: 3.441

  8 in total

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