Innate immunity
Adaptive immunity
Mucosal barriers
barrier injury
Comorbidities
Immunodeficiency disorders
one or more components of the adaptive or innate immune response is impaired
- inability to effectively resolve infections
Primary immunodeficiency
inherited immune disorders resulting from genetic mutations
- usually present at birth, childhood
- single gene mutations or unknown genetic susceptibility
Secondary immunodeficiency
Burden of disease
Age associations
Young children diagnosis
B cell immunodeficiencies
T cell immunodeficiencies
Severe combined immune deficiencies (SCID)
Phagocyte (WBC)
Complement defects
Asplenia
Prevention
Treatment
supportive therapy:
- preventative antibiotics and antifungals
- antibody replacement therapy
key vaccines recommended but live vaccines avoided
- herd immunity
SID causes
Asplenia types
post-splenectomy infection bacteria
post-splenectomy infection protozoa
Prevention for post-splenectomy infections