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. 2010 Jul 29;2(8):1963–1983. doi: 10.3390/toxins2081963

Table 1.

Small nonpeptide therapeutics for SEB-induced shock.

Pharmacologic agent Target Biological effects against SEB
Rapamycin FDA-approved for prevention of renal graft rejection Immunophilin FK506BP12 Blocked SEB-induced MCP-1 and IL-6 in vitro and in vivo [125].
Protected mice from lethality even when administered 24 h after SEB.
Dexamethasone FDA-approved for treating inflammatory diseases NF-κB Inhibited SEB-induced proinflammatory cytokines and chemokines in PBMC [72] and adhesion molecules (ICAM, ELAM, VCAM) on endothelial cells [121].
Reduced serum levels of cytokines, attenuated hypothermia due to SEB, improved survival of mice [72,97].
Pentoxifylline FDA-approved for treating peripheral arterial disease Phosphodiesterase Attenuated SEB-induced proinflammatory cytokines and chemokines in PBMC [17,97].
Blocked cytokine release in vivo and prevented SEB-induced lethal shock in SEB + LPS murine models [97].
Pirfenidone Inhibition of TGFβ (exact mechanism unknown) Inhibited SEB-stimulated cytokines in vitro and in vivo [96].
Improved survival of mice [96].
Niacinamide Nitric oxide synthase Inhibited serum IL-2 and IFNγ [94].
Prevented death of mice from SEB-mediated shock [94].
D609 Phospholipase C Blocked SEB-stimulated cytokines, chemokines and proliferation in human PBMC [48].
Improved survival of mice [103].