HLA-A, B (Class I) and HLA-DR, DQ (Class II) Antigens in Turkish Patients with Recurrent Aphthous Ulceration and Behçet's Disease
Objective: The aims of the present study were to typify the human leukocyte antigen system (HLA)-A, B (class I) and HLA-DR, DQ (class II) antigens and to assess the frequency of the presence of these antigens in the Turkish population with recurrent aphthous ulceration (RAU) and Behçet's diseas...
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| Published in | Medical principles and practice Vol. 22; no. 5; pp. 464 - 468 |
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| Main Authors | , , , |
| Format | Journal Article |
| Language | English |
| Published |
Basel, Switzerland
S. Karger AG
01.01.2013
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| Subjects | |
| Online Access | Get full text |
| ISSN | 1011-7571 1423-0151 1423-0151 |
| DOI | 10.1159/000348366 |
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| Abstract | Objective: The aims of the present study were to typify the human leukocyte antigen system (HLA)-A, B (class I) and HLA-DR, DQ (class II) antigens and to assess the frequency of the presence of these antigens in the Turkish population with recurrent aphthous ulceration (RAU) and Behçet's disease (BD) compared to healthy subjects. Subjects and Methods: Thirty patients with RAU, 30 with BD, and 15 healthy subjects were included in the study. HLA typing was performed by serology with commercial kits for HLA class I and II (One Lambda, Canoga Park, Calif., USA). Results: The HLA-A23 frequency was 26.7% in the RAU patients, which was significantly higher than the 3.3% frequency in the patients with BD (p < 0.05). The HLA-A24 frequency was 33.3% in the RAU patient group, which was significantly higher (p < 0.05) than the frequency in the healthy subjects (6.7%). Significantly higher frequencies (46.7%) of HLA-A30 were found in the healthy subjects compared to the BD (13.3%) and RAU (3.3%) patients (p < 0.05 and p < 0.01, respectively). A higher frequency of HLA-B13 was observed in the RAU (23.3%) patients compared to the BD (0%) patients (p < 0.01). A decrease was observed in HLA-DR10 and HLA-DR17 in the RAU patients (p < 0.05), while a higher frequency of HLA-DR10 was observed in the BD patients compared to the RAU patients (p < 0.01). Conclusions: These results showed that RAU and BD were not in the same spectrum and the involvement of other genetic and/or environmental factors might be responsible for the development of these diseases and/or disease progression. |
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| AbstractList | Objective: The aims of the present study were to typify the human leukocyte antigen system (HLA)-A, B (class I) and HLA-DR, DQ (class II) antigens and to assess the frequency of the presence of these antigens in the Turkish population with recurrent aphthous ulceration (RAU) and Behçet's disease (BD) compared to healthy subjects. Subjects and Methods: Thirty patients with RAU, 30 with BD, and 15 healthy subjects were included in the study. HLA typing was performed by serology with commercial kits for HLA class I and II (One Lambda, Canoga Park, Calif., USA). Results: The HLA-A23 frequency was 26.7% in the RAU patients, which was significantly higher than the 3.3% frequency in the patients with BD (p < 0.05). The HLA-A24 frequency was 33.3% in the RAU patient group, which was significantly higher (p < 0.05) than the frequency in the healthy subjects (6.7%). Significantly higher frequencies (46.7%) of HLA-A30 were found in the healthy subjects compared to the BD (13.3%) and RAU (3.3%) patients (p < 0.05 and p < 0.01, respectively). A higher frequency of HLA-B13 was observed in the RAU (23.3%) patients compared to the BD (0%) patients (p < 0.01). A decrease was observed in HLA-DR10 and HLA-DR17 in the RAU patients (p < 0.05), while a higher frequency of HLA-DR10 was observed in the BD patients compared to the RAU patients (p < 0.01). Conclusions: These results showed that RAU and BD were not in the same spectrum and the involvement of other genetic and/or environmental factors might be responsible for the development of these diseases and/or disease progression. The aims of the present study were to typify the human leukocyte antigen system (HLA)-A, B (class I) and HLA-DR, DQ (class II) antigens and to assess the frequency of the presence of these antigens in the Turkish population with recurrent aphthous ulceration (RAU) and Behçet's disease (BD) compared to healthy subjects. Thirty patients with RAU, 30 with BD, and 15 healthy subjects were included in the study. HLA typing was performed by serology with commercial kits for HLA class I and II (One Lambda, Canoga Park, Calif., USA). The HLA-A23 frequency was 26.7% in the RAU patients, which was significantly higher than the 3.3% frequency in the patients with BD (p < 0.05). The HLA-A24 frequency was 33.3% in the RAU patient group, which was significantly higher (p < 0.05) than the frequency in the healthy subjects (6.7%). Significantly higher frequencies (46.7%) of HLA-A30 were found in the healthy subjects compared to the BD (13.3%) and RAU (3.3%) patients (p < 0.05 and p < 0.01, respectively). A higher frequency of HLA-B13 was observed in the RAU (23.3%) patients compared to the BD (0%) patients (p < 0.01). A decrease was observed in HLA-DR10 and HLA-DR17 in the RAU patients (p < 0.05), while a higher frequency of HLA-DR10 was observed in the BD patients compared to the RAU patients (p < 0.01). These results showed that RAU and BD were not in the same spectrum and the involvement of other genetic and/or environmental factors might be responsible for the development of these diseases and/or disease progression. The aims of the present study were to typify the human leukocyte antigen system (HLA)-A, B (class I) and HLA-DR, DQ (class II) antigens and to assess the frequency of the presence of these antigens in the Turkish population with recurrent aphthous ulceration (RAU) and Behçet's disease (BD) compared to healthy subjects.OBJECTIVEThe aims of the present study were to typify the human leukocyte antigen system (HLA)-A, B (class I) and HLA-DR, DQ (class II) antigens and to assess the frequency of the presence of these antigens in the Turkish population with recurrent aphthous ulceration (RAU) and Behçet's disease (BD) compared to healthy subjects.Thirty patients with RAU, 30 with BD, and 15 healthy subjects were included in the study. HLA typing was performed by serology with commercial kits for HLA class I and II (One Lambda, Canoga Park, Calif., USA).SUBJECTS AND METHODSThirty patients with RAU, 30 with BD, and 15 healthy subjects were included in the study. HLA typing was performed by serology with commercial kits for HLA class I and II (One Lambda, Canoga Park, Calif., USA).The HLA-A23 frequency was 26.7% in the RAU patients, which was significantly higher than the 3.3% frequency in the patients with BD (p < 0.05). The HLA-A24 frequency was 33.3% in the RAU patient group, which was significantly higher (p < 0.05) than the frequency in the healthy subjects (6.7%). Significantly higher frequencies (46.7%) of HLA-A30 were found in the healthy subjects compared to the BD (13.3%) and RAU (3.3%) patients (p < 0.05 and p < 0.01, respectively). A higher frequency of HLA-B13 was observed in the RAU (23.3%) patients compared to the BD (0%) patients (p < 0.01). A decrease was observed in HLA-DR10 and HLA-DR17 in the RAU patients (p < 0.05), while a higher frequency of HLA-DR10 was observed in the BD patients compared to the RAU patients (p < 0.01).RESULTSThe HLA-A23 frequency was 26.7% in the RAU patients, which was significantly higher than the 3.3% frequency in the patients with BD (p < 0.05). The HLA-A24 frequency was 33.3% in the RAU patient group, which was significantly higher (p < 0.05) than the frequency in the healthy subjects (6.7%). Significantly higher frequencies (46.7%) of HLA-A30 were found in the healthy subjects compared to the BD (13.3%) and RAU (3.3%) patients (p < 0.05 and p < 0.01, respectively). A higher frequency of HLA-B13 was observed in the RAU (23.3%) patients compared to the BD (0%) patients (p < 0.01). A decrease was observed in HLA-DR10 and HLA-DR17 in the RAU patients (p < 0.05), while a higher frequency of HLA-DR10 was observed in the BD patients compared to the RAU patients (p < 0.01).These results showed that RAU and BD were not in the same spectrum and the involvement of other genetic and/or environmental factors might be responsible for the development of these diseases and/or disease progression.CONCLUSIONSThese results showed that RAU and BD were not in the same spectrum and the involvement of other genetic and/or environmental factors might be responsible for the development of these diseases and/or disease progression. |
| Author | Aytugar, Emre Demirel, Gülderen Yanikkaya Borahan, M. Oğuz Pekiner, Filiz Namdar |
| AuthorAffiliation | a Department of Oral Diagnosis and Radiology, Faculty of Dentistry, Marmara University Istanbul, Turkey b Immunology Section, Department of Medical Microbiology, Yeditepe University, Istanbul, Turkey |
| AuthorAffiliation_xml | – name: a Department of Oral Diagnosis and Radiology, Faculty of Dentistry, Marmara University Istanbul, Turkey – name: b Immunology Section, Department of Medical Microbiology, Yeditepe University, Istanbul, Turkey |
| Author_xml | – sequence: 1 givenname: Filiz Namdar surname: Pekiner fullname: Pekiner, Filiz Namdar email: fpekiner@yahoo.com – sequence: 2 givenname: Emre surname: Aytugar fullname: Aytugar, Emre – sequence: 3 givenname: Gülderen Yanikkaya surname: Demirel fullname: Demirel, Gülderen Yanikkaya – sequence: 4 givenname: M. Oğuz surname: Borahan fullname: Borahan, M. Oğuz |
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| CitedBy_id | crossref_primary_10_4049_jimmunol_1301415 crossref_primary_10_3390_biomedicines11071882 crossref_primary_10_1159_000351798 crossref_primary_10_1128_JVI_03419_14 crossref_primary_10_1159_000499593 crossref_primary_10_1097_MD_0000000000009131 crossref_primary_10_4049_jimmunol_1402606 crossref_primary_10_1016_j_humimm_2014_04_016 crossref_primary_10_3390_jcm13185440 crossref_primary_10_1016_j_cden_2013_12_002 crossref_primary_10_1159_000489340 crossref_primary_10_51479_cspzl_2017_004 crossref_primary_10_4274_turkderm_galenos_2024_37999 |
| Cites_doi | 10.1111/j.1399-0039.1992.tb01925.x 10.1111/j.1365-2230.2009.03384.x 10.1016/0030-4220(85)90061-1 10.1159/000085737 10.1093/rheumatology/40.6.668 10.1111/j.1744-313X.2008.00801.x 10.1007/s00296-008-0787-1 10.1034/j.1399-0039.1999.540605.x 10.1111/j.1399-0039.2004.00280.x 10.1001/archopht.125.10.1375 10.1016/0007-117X(77)90006-3 10.1001/archotol.127.2.184 10.1111/j.1365-2133.2007.08116.x 10.1016/j.jaad.2007.10.452 10.1016/0198-8859(86)90281-8 10.1034/j.1600-0714.2001.300704.x 10.1007/s10384-007-0473-y 10.1016/S0198-8859(00)00249-4 10.1001/archopht.1986.01050220049024 10.1111/j.1756-185X.2011.01601.x 10.1111/j.1601-0825.2005.01143.x 10.1111/j.1399-0039.1987.tb01599.x 10.1016/0030-4220(72)90211-3 10.1016/j.imlet.2004.03.017 10.1111/j.1600-0714.1993.tb00044.x |
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| Keywords | Antigen HLA class I HLA class II Recurrent aphthous ulceration Behçet's disease |
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| SubjectTerms | Adolescent Adult Behcet Syndrome - blood Behcet Syndrome - immunology Female HLA-A Antigens - blood HLA-DQ Antigens - blood HLA-DR Antigens - blood Humans Male Middle Aged Original Paper Recurrence Stomatitis, Aphthous - blood Stomatitis, Aphthous - immunology Turkey - epidemiology Young Adult |
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| Title | HLA-A, B (Class I) and HLA-DR, DQ (Class II) Antigens in Turkish Patients with Recurrent Aphthous Ulceration and Behçet's Disease |
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