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Cryptococcus neoformans and Candida albicans regulate CD4 expression on human monocytes
D Pietrella1, C Monari, C Retini
1Microbiology Section Department of Experimental Medicine, University of Perugia, Italy.
The Journal of Infectious Diseases
|October 21, 1998
Summary
This study shows fungi like Candida albicans can change CD4 receptor levels on human monocytes. This fungal interaction may impact human immunodeficiency virus (HIV) entry.
Area of Science:
- Immunology
- Microbiology
- Cell Biology
Background:
- CD4 receptors on human monocytes are crucial for immune responses.
- Fungal pathogens like Candida albicans and Cryptococcus neoformans can interact with host immune cells.
- Understanding these interactions is vital for host defense and disease pathogenesis.
Purpose of the Study:
- To investigate the ability of Candida albicans and Cryptococcus neoformans to modulate CD4 expression on human monocytes.
- To explore the role of fungal components, such as glucuronoxylomannan, in this modulation.
- To determine the cellular mechanisms involved in fungal-mediated CD4 expression changes.
Main Methods:
- Human monocytes were exposed to different strains of Candida albicans and Cryptococcus neoformans.
- CD4 receptor expression levels on monocytes were quantified.
- The effect of purified glucuronoxylomannan and opsonic factors was assessed.
- Protein synthesis inhibitors were used to investigate the mechanism of CD4 modulation.
Main Results:
- Candida albicans and acapsular Cryptococcus neoformans induced higher CD4 expression than encapsulated strains.
- Glucuronoxylomannan alone did not regulate CD4 expression but down-regulated it when combined with acapsular C. neoformans.
- Fungal cell binding or internalization, facilitated by opsonic factors, appears critical for CD4 overexpression.
- Protein synthesis is necessary for this modulation, ruling out simple receptor redistribution.
Conclusions:
- Fungi can induce novel modulations of CD4 expression on human monocytes.
- This fungal-mediated CD4 modulation may have implications for the entry of human immunodeficiency virus (HIV) via gp120.
- Further research is warranted to explore the clinical relevance of these findings in fungal infections and HIV pathogenesis.