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1.
Mycoses ; 51(3): 228-35, 2008 May.
Article in English | MEDLINE | ID: mdl-18399903

ABSTRACT

Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) is an autosomal recessive syndrome characterised by chronic mucocutaneous candidiasis (CMC) and multiple endocrine failures. While the spectrum and modalities of autoimmunity are the main objects of current research into APECED, unequivocal data on the efficiency of immune responses to infectious agents are still elusive. The in vitro ability of monocytes and polymorphonuclear leucocytes to phagocytise and kill bacteria and fungi, and the degree of activation of lymphocytes cultured with mitogens and Candida albicans were investigated by flow cytometry in 11 APECED patients and healthy subjects. In addition, a comparison of gamma-globulin and immunoglobulin (Ig) concentrations was performed, and a correlation was sought between oral fungal load and the anti-Candida antibody titre. No difference between APECED patients and healthy subjects was observed in the phagocyte function, although the patients had a larger number of monocytes. Similarly, cultured lymphocytes were equally activated in the two groups. The concentration of gamma-globulins was higher among APECED patients, and anti-Candida IgM and IgG correlated with current and past oral candidiasis respectively. APECED patients have efficient innate and adaptive immune responses against exogenous stimuli, and currently, the mechanisms of mucocutaneous anergy leading to the high prevalence of CMC in this syndrome remain to be elucidated.


Subject(s)
Autoantibodies/analysis , Candidiasis, Chronic Mucocutaneous/immunology , Polyendocrinopathies, Autoimmune/immunology , Adolescent , Adult , Autoimmunity , Female , Humans , Immunity, Innate , Immunoglobulin G , Immunoglobulin M , Male , Polyendocrinopathies, Autoimmune/complications , Polyendocrinopathies, Autoimmune/genetics
2.
Eur J Clin Microbiol Infect Dis ; 25(3): 193-6, 2006 Mar.
Article in English | MEDLINE | ID: mdl-16525775

ABSTRACT

Reported here are the features of a Rhodotorula mucilaginosa outbreak that occurred in a neonatal intensive care unit. Over a period of 19 days, clinical and laboratory signs of sepsis appeared in four premature infants carrying indwelling vascular catheters. After bloodstream infection with R. mucilaginosa was ascertained, the patients underwent amphotericin B therapy and recovered completely. In a retrospective case-control study, the variables displaying a statistical difference between case and control-group neonates were birth weight, gestational age, duration of parenteral nutrition, duration of antibiotic therapy and prophylactic administration of fluconazole. To our knowledge, this is the first reported outbreak caused by yeasts of the Rhodotorula genus.


Subject(s)
Bacteremia/epidemiology , Disease Outbreaks , Infant, Premature, Diseases/epidemiology , Intensive Care Units, Neonatal , Mycoses/epidemiology , Rhodotorula/isolation & purification , Amphotericin B/therapeutic use , Antifungal Agents/therapeutic use , Bacteremia/drug therapy , Bacteremia/microbiology , Case-Control Studies , Catheterization, Central Venous/adverse effects , Catheters, Indwelling/adverse effects , Female , Humans , Infant, Low Birth Weight , Infant, Newborn , Infant, Premature , Infant, Premature, Diseases/drug therapy , Infant, Premature, Diseases/microbiology , Male , Mycoses/drug therapy , Mycoses/microbiology , Rhodotorula/pathogenicity
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