“…9,[27][28][29] Immunosuppression with glucocorticoid treatment can reactivate latent diseases such as tuberculosis, 29 Chagas disease, 30 leishmaniasis, 31 toxoplasmosis, 32 cryptosporidiosis, 33 amebiasis, 34 and strongyloidiasis. 35,36 The antiinflammatory activity of glucocorticoids is caused by interactions between the drug and the glucocorticoid receptor within the cytoplasm, which then translocates into the nucleus where it promotes the transcription of several inflammatory genes encoding cytokines, enzymes, receptors, and adhesion molecules. The major consequence of glucocorticoids that affect the transcription factors, such as nuclear factor-κB (NF-κB) and AP-1, is the potent reduction in the synthesis of the cytokines IL-1, IL-2, IL-3, IL-4, IL-5, IL-6, IL-9, IL-13, and GM-CSF, the chemokines IL-8, RANTES, MCP-1, MCP-3, MCP-4, and eotaxin, 9,13,37 and the antibodies IgG, IgM, and IgA.…”