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Table 1 Schematic representation of different sources for CAR engineering

From: Strategies to enhance CAR-T persistence

Source selection

Characteristic

Advantage

Disadvantage

Phase

autoCAR-T

Original CAR product

Most effective at the present

Heterogeneity

Product approved

alloCAR-T

Derived from donors

Industrial production; Low cost;

Off-the-shelf

GvHD; HvGD

Product approved

undefined CD4/CD8

Selected by CD3 marker

Without additional process

Heterogeneity

Product approved

constant CD4/CD8

Selected by CD4/CD8 marker

Industrial production;

Evaluable efficacy

Multiple operation steps

Clinical trials

CAR-NKT

Both T and NK features

Multiple modes of antitumor activity;

noGvHD; anti-solid tumor potency

Low abundance

Clinical trials

CAR-γδT

Without MHC restriction

Multiple modes of antitumor;

noGvHD; no ICANS

Low abundance;

Difficult proliferation

Clinical trials

CAR-Treg

Immunosuppression

Curing GvHD & autoimmune diseases

Potential instability

Clinical trials