Effect of seasonal allergen exposure on mucosal IL-16 and CD4+ cells in patients with allergic rhinitis.

BACKGROUND: CD4+ T cells constitute a major source of cytokines in allergic diseases such as allergic rhinitis. Interleukin (IL)-16 selectively recruits CD4+ cells. METHODS: We evaluated the effect of natural allergen exposure during a grass-pollen season on IL-16 expression and number of CD4+ cells in nasal mucosa. Patients with allergic rhinitis (n=16) were treated with either a nasal glucocorticoid beclomethasone (BDP; 400 microg/day) or placebo, and gave nasal biopsies prior to and during the grass-pollen season. The evaluated markers in allergic rhinitis patients were also compared to those in healthy control subjects (n=5). RESULTS: Prior to the pollen season, the expression of IL-16, but not the number of CD4+ cells, was significantly higher in patients with allergic rhinitis than in healthy control subjects. The grass-pollen season further increased IL-16 expression and also increased the number of CD4+ cells in placebo-treated, but not in BDP-treated, allergic rhinitis patients. The pollen-season-induced change in IL-16 expression and in CD4+ cells was significantly more pronounced in placebo- than in BDP-treated patients. There was a significant correlation between the change in IL-16 expression and the number of CD4+ cells. CONCLUSIONS: These data suggest that local upregulation of IL-16 expression contributes to the inflammation observed in seasonal allergic rhinitis. Hypothetically, inhibition of IL-16 expression can be one of several mechanisms by which nasal glucocorticoids achieve their anti-inflammatory effect in allergic rhinitis.

Direct energy transfer from the peripheral LH2 antenna to the reaction center in a mutant of Rhodobacter sphaeroides that lacks the core LH1 antenna.

The light-harvesting apparatus of the photosynthetic bacterium Rhodobacter sphaeroides is composed of a peripheral LH2 complex which directs excitation energy to the LH1/reaction center core. The puf BA genes encoding the LH1 polypeptides have been deleted, producing a photosynthetically-competent strain which contains LH2 and reaction centers. Time-resolved absorption and fluorescence measurements demonstrate that energy is efficiently transferred from LH2 to the reaction center, despite the absence of LH1. Energy trapping takes place in 55 +/- 5 ps at room temperature, compared to the result for the wild-type strain of 60 +/- 5 ps. At 77 K, the results for the mutant and wild type are 75 +/- 5 and approximately 35 ps, respectively; the slower time in the mutant is attributed to the small differences in antenna/reaction center contacts and relative distances that are bound to exist as a consequence of LH1 and LH2 being assembled from different alpha- and beta-polypeptides. Measurements with closed reaction centers provided new information on the nature of fast energy transfer within the B850 pigments of LH2. We conclude that the absorption band is inhomogeneously broadened, and the fast (approximately 10 ps) lifetime observed in the 847-857-nm region is interpreted as very rapid (1-5 ps) hopping of the excitation energy from high-energy to low-energy pigments within the B850 absorption band. Time-resolved anisotropy studies demonstrate that energy-transfer events within B850 occur on a subpicosecond to picosecond time scale.(ABSTRACT TRUNCATED AT 250 WORDS)