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[Disorders of phagocytic and fungicide function of granulocytes in chronic muco-cutaneous candidiasis]
Abstract:
The granulocytes which are distributed by blood circulation close to the extern and intern body surfaces as well as in all organs protect the organism from microbial perils by phagocytosis and intracellular killing of bacteria and fungi so constituting a very important component of the granulocytic functions seriously impairs the host resistance and may entail a state of persisting infectious disease. As chronic mucocutaneous candidosis (CMCC) represents such a persistent generalized infection, we studied in vitro several functional activities of the granulocytes of 5 patients suffering from CMCC. 2 of them presented a non-familiar type of CMCC, the remaining 3 patients (father and 2 daughters) were subject to the hereditary type of CMCC. For comparison, by the same way we investigated the granulocytic functions of 51 clinically and immunologically healthy adult persons. Each of our 5 patients exhibited a reduced ability of the granulocytes to phagocytize and kill Candida albicans. In the CMCC family, the father had a marked deficiency of the oxidase activity of the granulocytes whereas in his daughters, the oxidase deficiency proved to be of a minor grade. In the sera of both daughters a phagocytosis inhibiting factor could be assumed to exist in addition to the granulocytic abnormalities. When heat-inactivated Candida albicans cells, however, were used for experiments, the granulocytes of each patient were able to phagocytize the germs at the same rate as did the granulocytes taken from the controls. With regard to alterations of the T cell function previously reported in CMCC, in all patients we also could demonstrate various symptoms of a T cell-dependent immunodeficiency. The results of the present in vitro-experiments furnish good evidence of a state of fundamental deficiency of the microphages in patients with CMCC, which may be the dominating cellular factor in the aetiopathogenesis of CMCC.
Insights
Patients with chronic mucocutaneous candidosis (CMCC) show impaired granulocyte function, affecting their ability to fight Candida albicans infections. This study reveals fundamental microphage deficiencies contributing to CMCC pathogenesis.
Area of Science:
- Immunology
- Microbiology
- Genetics
Background:
- Granulocytes are crucial for host defense against microbial pathogens like fungi.
- Chronic mucocutaneous candidosis (CMCC) is a persistent infection linked to impaired immune responses.
- Understanding granulocyte dysfunction in CMCC is vital for elucidating disease mechanisms.
Observation:
- Granulocytes from CMCC patients exhibited reduced phagocytosis and killing of Candida albicans in vitro.
- A hereditary form of CMCC showed granulocyte oxidase deficiency, varying in severity.
- Patients also displayed T cell-dependent immunodeficiency symptoms.
Findings:
- Impaired granulocyte function, including phagocytosis and intracellular killing, was observed in all CMCC patients studied.
- Specific deficiencies in granulocyte oxidase activity were identified in a familial CMCC case.
- The study suggests a potential phagocytosis inhibiting factor in the sera of some patients.
Implications:
- These findings highlight fundamental microphage deficiencies as a key factor in the aetiopathogenesis of CMCC.
- The results underscore the importance of granulocyte function in persistent fungal infections.
- Further research into these cellular defects could lead to targeted therapeutic strategies for CMCC.