Sensitization Prevalence, Antibody Cross-Reactivity and Immunogenic Peptide Profile of Api g 2, the Non-Specific Lipid Transfer Protein 1 of Celery

Background: Celery (Apium graveolens) represents a relevant allergen source that can elicit severe reactions in the adult population. To investigate the sensitization prevalence and cross-reactivity of Api g 2 from celery stalks in a Mediterranean population and in a mouse model. Methodology: 786 non-randomized subjects from Italy were screened for IgE reactivity to rApi g 2, rArt v 3 (mugwort pollen LTP) and nPru p 3 (peach LTP) using an allergen microarray. Clinical data of 32 selected patients with reactivity to LTP under investigation were evaluated. Specific IgE titers and cross-inhibitions were performed in ELISA and allergen microarray. Balb/c mice were immunized with purified LTPs; IgG titers were determined in ELISA and mediator release was examined using RBL-2H3 cells. Simulated endolysosomal digestion was performed using microsomes obtained from human DCs. Results: IgE testing showed a sensitization prevalence of 25.6% to Api g 2, 18.6% to Art v 3, and 28.6% to Pru p 3 and frequent co-sensitization and correlating IgE-reactivity was observed. 10/32 patients suffering from LTP-related allergy reported symptoms upon consumption of celery stalks which mainly presented as OAS. Considerable IgE cross-reactivity was observed between Api g 2, Art v 3, and Pru p 3 with varying inhibition degrees of individual patients' sera. Simulating LTP mono-sensitization in a mouse model showed development of more congruent antibody specificities between Api g 2 and Art v 3. Notably, biologically relevant murine IgE cross-reactivity was restricted to the latter and diverse from Pru p 3 epitopes. Endolysosomal processing of LTP showed generation of similar clusters, which presumably represent T-cell peptides. Conclusions: Api g 2 represents a relevant celery stalk allergen in the LTP-sensitized population. The molecule displays common B cell epitopes and endolysosomal peptides that encompass T cell epitopes with pollen and plant-food derived LTP.

Volvo G-2 puuhiilikaasulaitteiden asennus FC-kansiventtiilimoottoriin

kuv., 15 x 22 cm

Volvo G-2 puuhiilikaasulaitteiden asennus FC-kansiventtiilimoottoriin

15 x 22 cm

Huoltokirja ja varaosaluettelo : Volvo puuhiilikaasulaitteet, tyypit G-1 ja G-2

kuv., 15 x 22 cm

Scalar scenarios contributing to (g-2) mu with enhanced Yukawa couplings

In this work we address contributions from scalars to (g-2)μ. In order to explain the recently measured deviation by the BNL experiment on (g-2)μ, it is necessary that these scalars are either light or couple strongly with muons. Here we explore this last possibility. We show that a scalar with mass of the order of 102 GeV provides significant contribution to (g-2)μ if the Yukawa coupling is about 10-1. We suggest scenarios where this comes about naturally. ©2001 The American Physical Society.

Remarks on higher-order hadronic corrections to the muon g-2

Recently, it was shown that insertions of hadronic vacuum polarization at O(α4) generate non-negligible effects in the calculation of the anomalous magnetic moment of the muon. This result raises the question if other hadronic diagrams at this order might become relevant for the next round of g−2 measurements as well. In this note we show that a potentially enhanced such contribution, hadronic light-by-light scattering in combination with electron vacuum polarization, is already sufficiently suppressed.

Hadronic light-by-light scattering and the muon g−2

The largest uncertainties in the Standard Model calculation of the anomalous magnetic moment of the muon (g − 2)μ come from hadronic contributions. In particular, it can be expected that in a few years the subleading hadronic light-by-light (HLbL) contribution will dominate the theory uncertainty. We present a dispersive description of the HLbL tensor, which is based on unitarity, analyticity, crossing symmetry, and gauge invariance. Such a model-independent Approach opens up an avenue towards a data-driven determination of the HLbL contribution to the (g − 2)μ.

Mus Hs 208 - Sinfonia a 2 violini, 2 oboe, 2 flauti, 2 corni in G, 2 corni in D, 2 fagotti, viola e bassi ; Stimmen zu der Sinfonia von Mozart N. 31, componirt 26. April 1779

del ... Wolfgango Amadeo Mozart

Erläuterung zu den Arbeiten von H. Gerlach in den Blättern XVII, XVIII, XXII, XXIII südlich von der Rhone. 1. Heinrich Gerlach. Sein Leben und Wirken [von Fr. G.] 2. Die penninischen Alpen. Abgedruckt mit Bewilligung der betreffenden Commission der Schweizerischen naturforschenden Gesellschaft ans Band XXIII der Neuen Denkschriften der Schweizerischen naturforschenden Gesellschaft. Mit einer Profiltafel. 3. Bericht über den Bergbau im Kanton Wallis. Durch den hohen Staatsrath autorisirter Abdruck. Im Buchhandel bei Galerini in Sitten.

Mode of access: Internet.

Cell death mechanisms associated with G(2) radiosensitivity in patients with prostate cancer and benign prostatic hyperplasia

Cells respond to genotoxic insults such as ionizing radiation by halting in the G(2) phase of the cell cycle. Delayed cell death (mitotic death) can occur when the cell is released from G(2), and specific spindle defects form endopolyploid cells (endoreduplication/tetraploidy). Enhanced G(2) chromosomal radiosensitivity has been observed in many cancers and genomic instability syndromes, and it is manifested by radiation-induced chromatid aberrations observed in lymphocytes of patients. Here we compare the G(2) chromosomal radiosensitivity in prostate patients with benign prostatic hyperplasia (BPH) or prostate cancer with disease-free controls. We also investigated whether there is a correlation between G(2) chromosomal radiosensitivity and aneuploidy (tetraploidy and endoreduplication), which are indicative of mitotic cell death. The G(2) assay was carried out on all human blood samples. Metaphase analysis was conducted on the harvested chromosomes by counting the number of aberrations and the mitotic errors (endoreduplication/tetraploidy) separately per 100 metaphases. A total of 1/14 of the controls were radiosensitive in G(2) compared to 6/15 of the BPH patients and 15/17 of the prostate cancer patients. Radiation-induced mitotic inhibition was assessed to determine the efficacy of G(2) checkpoint control in the prostate patients. There was no significant correlation of G(2) radiosensitivity scores and mitotic inhibition in BPH patients (P = 0.057), in contrast to prostate cancer patients, who showed a small but significant positive correlation (P = 0.029). Furthermore, there was no significant correlation between G(2) radiosensitivity scores of BPH patients and endoreduplication/ tetraploidy (P = 0.136), which contrasted with an extremely significant correlation observed in prostate cancer patients (P < 0.0001). In conclusion, cells from prostate cancer patients show increased sensitivity to the induction of G(2) aberrations from ionizing radiation exposure but paradoxically show reduced mitotic indices and aneuploidy as a function of aberration frequency.