# Dexamethasone inhibits IL-9 production by human T cells

**Authors:** Lauren E Holz, Kristoffer P Jakobsen, Jacques Van Snick, Francoise Cormont, William A Sewell

PMC · DOI: 10.1186/1476-9255-2-3 · 2005-04-20

## TL;DR

Dexamethasone significantly reduces IL-9 production by human T cells, which may explain part of its effectiveness in treating allergic diseases.

## Contribution

The study demonstrates that dexamethasone strongly inhibits IL-9 mRNA and protein levels in activated T cells.

## Key findings

- Dexamethasone reduced IL-9 mRNA levels to 0.7% of control values.
- Protein secretion of IL-9 was reduced to 2.8% of control values.
- The IC50 value of dexamethasone on IL-9 mRNA expression was 4 nM.

## Abstract

Interleukin 9 (IL-9) is produced by activated CD4+ T cells. Its effects include stimulation of mucus production, enhanced mast cell proliferation, enhanced eosinophil function, and IgE production. These effects are consistent with a role in allergic diseases. Glucocorticoids have potent anti-inflammatory effects, including suppression of cytokine synthesis, and are widely used in the treatment of allergic conditions.

We examined the effect of the glucocorticoid dexamethasone (Dex) on IL-9 mRNA expression and protein secretion with real-time RT-PCR and ELISA. Peripheral blood mononuclear cells (PBMC) were prepared from human volunteers and activated with OKT3. CD4+ T cells were purified from PBMC and activated with OKT3 plus PMA.

IL-9 mRNA abundance and protein secretion were both markedly reduced following treatment of activated PBMC with Dex. mRNA levels were reduced to 0.7% of control values and protein secretion was reduced to 2.8% of controls. In CD4+ T cells, Dex reduced protein secretion to a similar extent. The IC50 value of Dex on mRNA expression was 4 nM.

These results indicate that IL-9 production is very markedly inhibited by Dex. The findings raise the possibility that the beneficial effects of glucocorticoids in the treatment of allergic diseases are in part mediated by inhibition of IL-9 production.

## Linked entities

- **Proteins:** IL9 (interleukin 9), CD4 (CD4 molecule)
- **Chemicals:** dexamethasone (PubChem CID 5743), PMA (PubChem CID 171116383)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** IL1RN (interleukin 1 receptor antagonist) [NCBI Gene 3557] {aka CRMO2, DIRA, ICIL-1RA, IL-1RN, IL-1ra, IL-1ra3}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, GATA3 (GATA binding protein 3) [NCBI Gene 2625] {aka HDR, HDRS}, Il9 (interleukin 9) [NCBI Gene 16198] {aka Il-9, P40}, COX8A (cytochrome c oxidase subunit 8A) [NCBI Gene 1351] {aka COX, COX8, COX8-2, COX8L, MC4DN15, VIII}, CSF1 (colony stimulating factor 1) [NCBI Gene 1435] {aka CSF-1, MCSF, PG-M-CSF}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, IL9 (interleukin 9) [NCBI Gene 3578] {aka HP40, IL-9, P40}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, IL13 (interleukin 13) [NCBI Gene 3596] {aka IL-13, P600}, IL11 (interleukin 11) [NCBI Gene 3589] {aka AGIF, IL-11}, CREB1 (cAMP responsive element binding protein 1) [NCBI Gene 1385] {aka CREB, CREB-1}, ICAM1 (intercellular adhesion molecule 1) [NCBI Gene 3383] {aka BB2, CD54, P3.58}, CSF2 (colony stimulating factor 2) [NCBI Gene 1437] {aka CSF, GMCSF}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, JUNB (JunB proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 3726] {aka AP-1}, POTEF (POTE ankyrin domain family member F) [NCBI Gene 728378] {aka A26C1B, POTE2alpha, POTEACTIN}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, IGHE (immunoglobulin heavy constant epsilon) [NCBI Gene 3497] {aka IgE}, IL5 (interleukin 5) [NCBI Gene 3567] {aka EDF, IL-5, TRF}, UNG (uracil DNA glycosylase) [NCBI Gene 7374] {aka DGU, HIGM4, HIGM5, UDG, UNG1, UNG15}
- **Diseases:** airway damage (MESH:D000402), allergic asthma (MESH:D001249), allergic (MESH:D004342), mastocytosis (MESH:D008415), parasitic infection (MESH:D010272), hyperreactivity (MESH:D016535), eosinophilia (MESH:D004802), bronchial hyper-reactivity (MESH:D001982), allergic inflammation (MESH:D007249), goblet cell hyperplasia (MESH:D002276)
- **Chemicals:** KCl (MESH:D011189), L-glutamine (MESH:D005973), EDTA (MESH:D004492), Dex (MESH:D003907), OKT3 (MESH:D016853), prostaglandin (MESH:D011453), MACS Buffer (-), Trizol (MESH:C411644), water (MESH:D014867), PBS (MESH:D007854), NaCl (MESH:D012965), glycine (MESH:D005998), penicillin (MESH:D010406), H2SO4 (MESH:C033158), dGTP (MESH:C029603), dATP (MESH:C026600), agarose (MESH:D012685), DEPC (MESH:D004047), streptomycin (MESH:D013307), Tween-20 (MESH:D011136), dCTP (MESH:C024107), dithiothreitol (MESH:D004229), biotin (MESH:D001710), dUTP (MESH:C027078), trypan blue (MESH:D014343), CO2 (MESH:D002245), HEPES (MESH:D006531), MgCl2 (MESH:D015636)
- **Species:** Homo sapiens (human, species) [taxon 9606], Avian myeloblastosis virus (no rank) [taxon 11866], Orthonairovirus abuminaense (species) [taxon 2843618], Mus musculus (house mouse, species) [taxon 10090]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC1112611/full.md

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Source: https://tomesphere.com/paper/PMC1112611