HSCs |
Genetic correction |
Quiescent |
WASP |
[2–5] |
Multipotent |
X-LINKED SCID |
[6, 7] |
Long persistence (years to life-long) |
Artemis SCID |
[8] |
Genotoxicity risks |
|
|
T cells |
Targeting of immune responses to antigens |
Naïve or memory T cell |
TCRs |
Highly replicative |
Melanoma (CG) |
[9, 10] |
Terminally differentiated |
CAR T |
Central memory T cells have long-term persistence (months to years) |
Leukemia (CD19, CD123, FcμR, CD5) |
[11–14] |
Risks of cytokine release syndrome, off-target effects |
Adenocarcinoma (Tn-MUC1) |
[15] |
Viral infections (gB) |
[16] |
Dendritic cells |
Enhancement of antigenic processing and activation of adaptive responses |
DC precursors (monocytes) |
Cancer |
Immature DCs |
Melanoma |
[17–19] |
Quiescent |
Leukemia |
[20] |
Short half-life (days to weeks) |
Prostate cancer |
[21] |
Co-expression of cytokines and maturation factors possible |
Colon cancer |
[22] |
Migration to lymph nodes |
Chronic infections |
Systemic administration (i.v) possible |
HIV |
[23] |
HCV |
[24] |
HCMV |
[25] |
HPV |
[26] |