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.

Mbio
|January 9, 2020
PubMed

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.

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