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. 2021 Jun 23;12:678744. doi: 10.3389/fimmu.2021.678744

Table 4.

Preclinical attempts to target T lymphocytes for treating AIS.

Mechanism Drug Molecular targets Outcomes Reference
Infiltration inhibition Anti-VLA-4 antibody CD49d Reduced infarct size and neurological deficit (271)
FTY720/Fingolimod S1P R Reduced hemorrhagic transformation (272, 273)
Immune homeostasis regulation JPI-289 PARP-1 Reduced BBB leakage, infarct size, and neurological deficit (274)
PJ34 (275)
FR247304 Reduced infarct size, neurological deficit (276)
MP-124 (277)
IL-33 ST2R (278280)
vitamin D 3 vitamin D receptor (281)
atorvastatin HMG-CoA reductase (282)
resveratrol PPARγ (283)
Gut microbiota modulation resveratrol Microbiota formation Reduced BBB leakage, infarct size, neurological deficit (284)
fecal microbiota transplantation (225, 285)
NaB HDAC (227)
VPA (228)

VLA-4, very late antigen-4; CD49d, cluster of differentiation 49d; S1P R, sphingosine 1-phosphate receptor; BBB, blood brain barrier; PARP-1, Poly (ADP-ribose) (PAR) polymerase-1; IL-33, interleukin-33; ST2R, simultaneous translation on 2 rods; PPARγ, peroxisome proliferator-activated receptor gamma; NaB, Sodium butyrate; HDAC, histone deacetylase; VPA, valproic acid.