Table 1.
Cell type | Size of the TCR repertoire | Polymorphism of restricting element | TCR cross-pairing potential * | Difficulties of ex vivo expansion | Risk of off-tumor on target recognition | Reported or expected risk of GVHD | Universality score (lowest is best) | Intrinsic immune activity | References |
---|---|---|---|---|---|---|---|---|---|
αβ-TCR T cells | |||||||||
VST | ++ | +++ | ++ | – | – | – | 7 | Anti-viral | (11, 12) |
iNKT | + | + | + | – | + | – | 4 | Anti-tumoral, pro-inflammatory, protect from GVHD | (13–16) |
dNKT | +++ | + | +++ | ++ | ++ | + | 12 | Immune suppressive | (7, 17, 18) |
CD1a-restricted | +++ | + | +++ | + | ++ | + | 11 | Unknown | (19–21) |
CD1b GEM | + | + | ++ | + | ++ | + | 8 | Unknown | (22, 23) |
CD1b LDN5-like | + | + | ++ | + | ++ | + | 8 | Unknown | (22, 23) |
CD1b-restricted | ++ | + | +++ | + | ++ | + | 10 | Unknown | (19–21) |
CD1c-restricted | +++ | + | +++ | + | ++ | + | 11 | Unknown | (19–21) |
MAIT | + | + | +++ | +++ | ++ | + | 11 | Unknown | |
γδ-TCR T cells | |||||||||
Vγ9Vδ2 | – | + | – | – | + | – | 2 | Anti-tumoral, pro-inflammatory, APC | (24–27) |
Vδ1 | +++ | Unknown (non-HLA) | – | – | + | – | 4 | Anti-tumoral, pro-inflammatory | (28) |
Table summarizing the different features restricting the use of a T cell subset as universal donor cells. The amplitude of each restricting feature is depicted as none/extremely low (–), low (+), intermediate (++) and high (+++). The addition of each (+) is reported in the “Universality score” column, which represents the universal potential of each T cell subset, with a lower score corresponding to higher universality.
Upon introduction of a transgenic TCR.
TCR, T cell receptor; VST, virus-specific T cell; MAIT, mucosal-associated invariant T cell; GEM, germline-encoded mycolyl lipid-reactive; dNKT, diverse natural killer T cells; iNKT, invariant natural killer T cells; HLA, human leukocyte antigen; GVHD, graft-versus-host disease; APC, antigen-presenting cell.