A novel gene, designated ML-1, was identified front a human genomic DNA clo
ne and human T cell cDNA sequences. The second exon of ML-1 gene shares sig
nificant sequence identity with the gene encoding IL-17 (IL-17). ML-1 gene
expression was upregulated in activated PBMCs, CD4(+) T cells, allergen-spe
cific Th0, Th1, and Th2 clones, activated basophils, and mast cells. Increa
sed expression of the ML-1 gene, but not IL-17, was seen following allergen
challenge in four asthmatic subjects, suggesting its role in allergic infl
ammatory responses. ML-1 from transiently transfected COS-7 cells was able
to induce gene expression and protein production for IL-6 and IL-8 (at 10 n
g/ml of ML-1: for IL-6, 599.6 +/- 19.1 pg/ml; for IL-8, 1724.2 +/- 132.9 pg
/ml; and at 100 ng/ml of ML-1: for IL-6, 1005.3 +/- 55.6 pg/ml; for IL-8, 4
371.4 +/- 280.5 pg/ml; p < 0.05 for both doses vs baseline) in primary bron
chial epithelial (PBE) cells. Furthermore, increased expression of ICAM-1 w
as found in ML-1-stimulated PBE cells (mean fluorescence intensity (MFI) =
31.42 +/- 4.39 vs baseline, MFI = 12.26 +/- 1.77, p < 0.05), a functional f
eature distinct from IL-17 (MFI = 11.07 +/- 1.22). This effect was not inhi
bited by a saturating amount of IL-17. These findings demonstrate that ML-1
is a novel cytokine with a distinct function, and suggest a different rece
ptor for ML-1 on PBE cells.