Innate and acquired immune responses against Candida albicans in congenic B10.D2 mice with deficiency of the C5

Insights

Mice lacking the C5 complement component showed reduced early defense against Candida albicans. However, complement C5 did not impact long-term immunity or the development of acquired immune responses to this fungal infection.

Area of Science:

  • Immunology
  • Microbiology
  • Infectious Diseases

Background:

  • The complement system, particularly the C5 component, plays a crucial role in innate and adaptive immunity.
  • Candida albicans is an opportunistic fungal pathogen that can cause severe infections, especially in immunocompromised individuals.

Purpose of the Study:

  • To investigate the role of complement component C5 in innate and acquired immune responses to Candida albicans infection.
  • To determine if C5 deficiency affects the clearance of C. albicans and the development of protective immunity.

Main Methods:

  • Congenic mice, either sufficient or deficient in C5, were used.
  • Mice were challenged intravenously with Candida albicans.
  • Kidney fungal burden was assessed via cultural analyses at various time points.
  • Delayed hypersensitivity and Candida-specific antibody responses were measured.

Main Results:

  • C5-sufficient mice cleared C. albicans more effectively than C5-deficient mice within the first week post-challenge.
  • While C5 contributed to faster fungal clearance in the early weeks, both groups showed similar fungal loads by week four.
  • No significant differences were observed in the development of delayed hypersensitivity or Candida-specific antibody responses between the two groups.

Conclusions:

  • Complement component C5 is important for early innate immune control of Candida albicans.
  • C5 deficiency does not impair the development of acquired immune responses, including delayed hypersensitivity and antibody production.
  • The later-acting complement components contribute to early fungal growth inhibition but do not affect the ultimate outcome of infection in immunized animals.

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