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April 18, 2026Cells0 citationsOpen Access

Expression of Human CEACAM Receptors Promotes Inflammation and Organ Damage During Systemic Candida albicans Infection in Mice

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EKEsther KlaileMMMario Marco MüllerJSJohannes Sonnberger

Key Points

  • To investigate the role of human CEACAM receptors in inflammation and organ damage during systemic Candida albicans infections in mice.
  • Used CEABAC10 transgenic mice expressing CEACAM3, CEACAM5, and CEACAM6 receptors.
  • Conducted murine infection model with Candida albicans.
  • Analyzed survival rates, cytokine levels, and organ inflammation in infected mice.
  • CEABAC10 mice exhibited shorter survival periods after C. albicans infection compared to wild-type mice.
  • Infected CEABAC10 mice had heightened levels of pro-inflammatory cytokines during an early cytokine storm.
  • Liver and kidney tissue showed severe inflammatory responses, with increased neutrophil and macrophage infiltration.

Abstract

Invasive candidiasis is a fungal infection characterized by a high mortality rate. Carcinoembryonic antigen-related cell adhesion molecule (CEACAM) family receptors play a crucial role in regulating innate responses of both leukocytes and epithelia. Human CEACAM3, CEACAM5 and CEACAM6 receptors recognize Candida albicans and are expressed in transgenic CEABAC10 mice. In a murine C. albicans infection model, CEABAC10 mice exhibited a shortened survival period attributed to an early cytokine storm, an exacerbated acute phase response, and heightened systemic inflammation compared to their wild-type littermates. The livers and kidneys of CEABAC10 mice displayed intensified purulent necrotizing inflammation, accompanied by increased infiltration of neutrophils and macrophages. Our in vivo and in vitro data indicated that the expression of CEACAM6 on monocytes of CEABAC10 mice caused the elevated cytokine levels and the subsequent exacerbation of the acute phase response upon C. albicans infection, resulting in decreased survival.

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Cite This Study

Klaile et al. (2026) studied this question.

synapsesocial.com/papers/69e3207940886becb653f849https://doi.org/10.3390/cells15080707
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