TABLE 3.
PID with indicated level of susceptibility: | ||
---|---|---|
High | Intermediate | Low |
Defects of IL-12/IL-23-IFN-γ axisa,b,c (14, 33, 36, 42, 85, 96) | X-linked hyper-IgM syndrome (CD40L deficiency) (66) | Predominantly antibody deficiencies (19, 21, 22, 64, 67, 72, 91) |
All SCID typesa (11, 12, 105) | Complement deficiencies (43, 107) | |
Idiopathic CD4 lymphocytopeniab (103) | Neutropenias (9, 25) | |
Defects of NEMO-dependent NF-κB activation | Leukocyte adhesion deficiencies (LADs) (97) | |
(X-EDA-ID)b (83) | MHC-I deficiencies (32, 47, 69, 73, 119) | |
Chronic granulomatous diseasea,c (1, 15, 63, 65, 74) | IRAK-4 deficiency (23, 38, 61, 70, 86, 110) | |
Asplenia (48, 99) |
The most frequently isolated mycobacterium with this PID was BCG.
The most frequently isolated mycobacterium with this PID was NTM.
The most frequently isolated mycobacterium with this PID was M. tuberculosis.