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Assessing Anti-fungal Activity of Isolated Alveolar Macrophages by Confocal Microscopy
Published on: July 9, 2014
CARD9 Is Required for Classical Macrophage Activation and the Induction of Protective Immunity against Pulmonary
Althea Campuzano1, Natalia Castro-Lopez1, Amanda J Martinez1
1Department of Biology, South Texas Center for Emerging Infectious Diseases, The University of Texas at San Antonio, San Antonio, Texas, USA.
Insights
Caspase recruitment domain-containing protein 9 (CARD9) is essential for vaccine-induced immunity against fungal infections. CARD9 deficiency impairs protective responses against Cryptococcus neoformans by altering immune cell activation and cytokine production.
Area of Science:
- Immunology
- Mycology
- Infectious Diseases
Background:
- Caspase recruitment domain-containing protein 9 (CARD9) is a key adaptor protein in innate immunity, crucial for sensing fungal pathogens via C-type lectin receptors (CLRs).
- CARD9 plays a vital role in regulating protective immunity against fungal infections, including Cryptococcus neoformans, an opportunistic pathogen causing severe infections in immunocompromised individuals.
- The precise role of CARD9 in vaccine-mediated immunity against C. neoformans remains largely unknown.
Purpose of the Study:
- To investigate the necessity of CARD9 for inducing protective immune responses against C. neoformans infection following vaccination.
- To elucidate the impact of CARD9 deficiency on immune cell function and cytokine profiles after immunization with a C. neoformans vaccine candidate.
Main Methods:
- Utilized CARD9-deficient and wild-type mice immunized with a C. neoformans mutant (LW10).
- Assessed immune responses, including cytokine production (IL-17, IL-4, IL-5, IL-13), leukocyte infiltration, and macrophage activation phenotypes (M1/M2).
- Evaluated the fungicidal capacity of macrophages and nitric oxide production in response to C. neoformans infection and stimulation.
Main Results:
- CARD9 deficiency significantly abrogated vaccine-induced protection against C. neoformans challenge.
- CARD9-deficient mice showed reduced IL-17 and increased Th2-type cytokine production post-vaccination.
- Macrophages from CARD9-deficient mice exhibited an M2-skewed phenotype, impaired fungicidal activity, and failed to produce nitric oxide.
Conclusions:
- CARD9 is indispensable for mounting effective vaccine-mediated immunity against C. neoformans.
- CARD9 signaling is critical for M1 macrophage activation and fungicidal function, essential for controlling C. neoformans infection.
- These findings highlight CARD9 as a crucial host factor in antifungal defense and vaccine development.
Abstract:
Caspase recruitment domain-containing protein 9 (CARD9) is a critical adaptor molecule triggered by the interaction of C-type lectin receptors (CLRs) with carbohydrate motifs found in fungi. Consequently, clinical and animal studies indicate that CARD9 is an important regulator of protective immunity against fungal pathogens. Previous studies suggest that CARD9 is important for the induction of protection against Cryptococcus neoformans, an opportunistic fungal pathogen that causes life-threatening infections of the central nervous system in immunocompromised patients. However, the effect of CARD9 deficiency on the induction of protective immune responses against C. neoformans is unknown. Immunization with a C. neoformans mutant that overexpresses the transcription factor zinc finger 2, denoted LW10, results in protection against an otherwise lethal challenge with wild-type (WT) C. neoformans Our results showed that CARD9 is essential for the induction of vaccine-mediated immunity against C. neoformans infection. We observed significant decreases in interleukin-17 (IL-17) production and significant increases in Th2-type cytokine (IL-4, IL-5, and IL-13) production in CARD9-deficient mice after inoculation with strain LW10. While leukocyte infiltration to the lungs of CARD9-deficient mice was similar in LW10 and WT C. neoformans-infected mice, macrophages derived from CARD9-deficient mice inherently skewed toward an M2 activation phenotype, were unable to contain the growth of LW10, and failed to produce nitric oxide in response to infection with LW10 or stimulation with lipopolysaccharide. These results suggest that CARD9-mediated signaling is required for M1 macrophage activation and fungicidal activity necessary for the induction of vaccine-mediated immunity against C. neoformansIMPORTANCECryptococcus neoformans is a fungal pathogen that is found throughout the environment and can cause life-threatening infections of the lung and central nervous system in severely immunocompromised individuals. Caspase recruitment domain-containing protein 9 (CARD9) is a critical molecule that is activated after interactions of C-type lectin receptors (CLRs) found on the surfaces of specific immune cells, with carbohydrate structures associated with fungi. Patients with defects in CARD9 are significantly more susceptible to a multitude of fungal infections. C. neoformans contains several carbohydrate structures that interact with CLRs on immune cells and activate CARD9. Consequently, these studies evaluated the necessity of CARD9 for the induction of protective immunity against C. neoformans infection. These results are important, as they advance our understanding of cryptococcal pathogenesis and host factors necessary for the induction of protective immunity against C. neoformans.
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