Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1969 Jun;98(3):996-1004.
doi: 10.1128/jb.98.3.996-1004.1969.

Interaction of Candida albicans with human leukocytes and serum

Interaction of Candida albicans with human leukocytes and serum

R I Lehrer et al. J Bacteriol. 1969 Jun.

Abstract

A quantitative assay of candidacidal activity based on differential staining of non-viable Candida albicans by methylene blue was developed and applied to studies of leukocytes from normal individuals and patients with fungal and other infections. Serum factors were necessary for optimal phagocytosis of C. albicans but lacked direct candidacidal activity. Normal human neutrophils (38 studies) killed 29.0 +/- 7.4% of ingested C. albicans in 1 hr. Eosinophils and monocytes killed a smaller percentage. Neutrophil candidacidal activity did not require protein or ribonucleic acid synthesis by the leukocyte but was inhibited by anaerobic conditions, potassium cyanide, and colchicine. Leukocytes of a patient with hereditary myeloperoxidase deficiency and of three children with chronic granulomatous disease phagocytized C. albicans normally, yet failed to kill them. Our data suggest that the neutrophil can play an important role in resistance to Candida infection and that the lysosomal enzyme myeloperoxidase and its oxidant substrate hydrogen peroxide are the major participants in neutrophil candidacidal activity.

PubMed Disclaimer

References

    1. J Immunol. 1964 Jan;92:145-54 - PubMed
    1. Sabouraudia. 1965 Jun;4(2):126-30 - PubMed
    1. J Okla State Med Assoc. 1964 Mar;57:104-8 - PubMed
    1. J Chronic Dis. 1966 Jun;19(6):667-87 - PubMed
    1. Biochim Biophys Acta. 1968 Feb 1;156(1):168-78 - PubMed

MeSH terms