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Ara h 2-specific IgE epitope-like peptides inhibit the binding of IgE to Ara h 2 and suppress lgE-dependent effector cell activation
ID
Korošec, Peter
(
Avtor
),
ID
Koren, Ana
(
Avtor
),
ID
Debeljak, Jerneja
(
Avtor
),
ID
Zahirović, Abida
(
Avtor
),
ID
Skerbinjek-Kavalar, Maja
(
Avtor
),
ID
Berce, Vojko
(
Avtor
),
ID
Dejanović, Luka
(
Avtor
),
ID
Luzar, Jernej
(
Avtor
),
ID
Štrukelj, Borut
(
Avtor
),
ID
Lunder, Mojca
(
Avtor
)
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MD5: 3F2EEA4596BD6AF30245EB392A4B29B7
URL - Izvorni URL, za dostop obiščite
https://onlinelibrary.wiley.com/doi/10.1111/cea.14314
Galerija slik
Izvleček
Background: Clinical and experimental analyses indicate a pathognomonic role for allergen IgE crosslinking through epitope–paratope interactions as a major initial step in the cascade leading to effector cell activation and clinical manifestations of lgE-mediated food allergies. We aimed to undertake the initial development and assessment of Ara h 2-specific IgE epitope-like peptides that can bind to allergenspecific IgE paratopes and suppress effector cell activation. Methods: We performed biopanning, screening, IgE binding, selection and mapping of peptides. We generated synthetic peptides for use in all functional experiments. ImmunoCAP inhibition, basophil and mast cell activation tests, with LAD2 cells, a human mast cell line were performed. Twenty-six children or young adults who had peanut allergy were studied. Results: We identified and selected three linear peptides (DHPRFNRDNDVA, DHPRYGP and DHPRFST), and immunoblot analyses revealed binding to lgE from peanut-allergic individuals. The peptide sequences were aligned to the disordered region corresponding to the loop between helices 2 and 3 of Ara h 2, and conformational mapping showed that the peptides match the surface of Ara h 2 and h 6 but not other peanut allergens. In ImmunoCAP inhibition experiments, the peptides significantly inhibit the binding of IgE to Ara h 2 (p < .001). In basophil and mast cell activation tests, the peptides significantly suppressed Ara h 2-induced effector cell activation (p < .05) and increased the half-maximal Ara h 2 effective concentration (p < .05). Binding of the peptides to specific IgEs did not induce activation of basophils or mast cells. Conclusions: These studies show that the indicated peptides reduce the allergenic activity of Ara h 2 and suppress lgE-dependent basophil and mast cell activation. These observations may suggest a novel therapeutic strategy for food allergy based on epitope–paratop blocking.
Jezik:
Angleški jezik
Ključne besede:
Ara h 2
,
ImmunoCAP inhibition
,
basophil activation test
,
epitopes
,
mast cell activation test
,
paratopes
,
peanut allergy
,
peptides
,
specific IgE
Vrsta gradiva:
Članek v reviji
Tipologija:
1.01 - Izvirni znanstveni članek
Organizacija:
FFA - Fakulteta za farmacijo
Status publikacije:
Objavljeno
Različica publikacije:
Objavljena publikacija
Leto izida:
2023
Št. strani:
Str. 636-647
Številčenje:
Vol. 53, iss. 6
PID:
20.500.12556/RUL-147382
UDK:
616-056.43
ISSN pri članku:
1365-2222
DOI:
10.1111/cea.14314
COBISS.SI-ID:
151992835
Datum objave v RUL:
03.07.2023
Število ogledov:
1523
Število prenosov:
76
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Objavi na:
Gradivo je del revije
Naslov:
Clinical & experimental allergy
Skrajšan naslov:
Clin. exp. allergy
Založnik:
Wiley
ISSN:
1365-2222
COBISS.SI-ID:
515014681
Licence
Licenca:
CC BY-NC-ND 4.0, Creative Commons Priznanje avtorstva-Nekomercialno-Brez predelav 4.0 Mednarodna
Povezava:
http://creativecommons.org/licenses/by-nc-nd/4.0/deed.sl
Opis:
Najbolj omejujoča licenca Creative Commons. Uporabniki lahko prenesejo in delijo delo v nekomercialne namene in ga ne smejo uporabiti za nobene druge namene.
Sekundarni jezik
Jezik:
Slovenski jezik
Ključne besede:
alergeni
,
Ara h 2
,
test aktivacije bazofilcev
,
epitopi
,
inhibicija ImmunoCAP
,
test aktivacije mastocitov
,
paratopi
,
alergija na arašide
,
peptidi
,
specifični IgE
Projekti
Financer:
ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:
P3-0360
Naslov:
Celostna obravnava alergijskih bolezni in astme v Sloveniji: od epidemiologije do genetike
Financer:
ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:
P4-0127
Naslov:
Farmacevtska biotehnologija: znanost za zdravje
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