Table 2.
T1D drug development at present.
| Target pathways | Target | Limitations | Clinical status | References |
|---|---|---|---|---|
| Inhibition of T cell activation | Anti-CD3, anti-CD2, etc. | Broad suppression induces adverse events | Approved by FDA | [53, 54, 57] |
| B cell antagonists | Anti-CD20 | Not universal or persistent | Approved in multiple AIDs | [58] |
| Cytokine antagonists | IL-1, TNF-α, etc. | Focus on the last, more advanced stages of illness pathogenesis rather than their earliest stages; recurrent treatment; off-target effects | Several being tested in phase 1,2 studies of stage 3 T1D patients | [59, 60] |
| Cytokine agonists | IL-2, etc. | Off-target effects; recurrent treatment | Being tested in phase 1, 2 studies of stage 3 T1D patients | [61] |
| Autoantigen therapies | Peptides, nanoparticles, etc. | Mostly disappointing results | Early clinical trials | [62] |
| Adoptive cell therapy | CAR/TCR-Treg, etc. | Challenging drug development | Preclinical and early phase 1 trials underway | [63, 64] |
| β cell regeneration | Islet β cells, pancreatic α cells, etc. | Current therapeutic medicines have limited β cell recovery efficiency | Being tested | [120] |