| Project/Area Number |
02670480
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| Research Category |
Grant-in-Aid for General Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Research Field |
Dermatology
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| Research Institution | Yamaguchi University |
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Principal Investigator |
MUTO Masahiko Yamaguchi Univ. Hosp., Dept. Dermat. Lecturer, 医学部附属病院, 講師 (40175625)
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| Co-Investigator(Kenkyū-buntansha) |
TAKATA Ichiro Yamaguchi Univ. Sch. Med., Dept. Dermat. Assistant, 医学部, 助手 (40216651)
NAKANO Junji Yamaguchi Univ. Hosp., Dept. Dermat. Assistant, 医学部附属病院, 助手 (40198156)
ASAGAMI Chidori Yamaguchi Univ. Sch. Med., Dept. Dermat. Professor, 医学部, 教授 (80035188)
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| Project Period (FY) |
1990 – 1991
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| Project Status |
Completed (Fiscal Year 1991)
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| Budget Amount *help |
¥1,600,000 (Direct Cost: ¥1,600,000)
Fiscal Year 1991: ¥700,000 (Direct Cost: ¥700,000)
Fiscal Year 1990: ¥900,000 (Direct Cost: ¥900,000)
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| Keywords | Psoriatic arthritis / Psoriasis vulgaris / Pustular psotiasis / Disease susceptibility / HLA genes / Anaphylatoxin C4a / Linoleic acid / HLAハプロタイプ / HLA |
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| Research Abstract |
Psoriasis is considered a multifactorial disease, and its clinical manifestations may well reflect this heterogeneous etiology.
In order to elucidate distinct (or universal) haplotypes carrying the susceptibility to psoriasis, we performed serotyping and/or DNA-oligotyping of 154 unrelated Japanese patients with psoriasis. Sixty-two out of the 154 were psoriasis vulgaris (PV), 19 were psoriatic arthritis (PA) and 73 were pustular psoriasis (PP). HLA data on 71 out of the 73 PP patients were cited from a report by A. Ohkawara et al. (1990).
1)HLA-Al-B37-Cw6 and B39-Cw7 haplotypes had association with PV.
2)HLA-A2-Bw46-Cwll-DRw8-DQw6-DPB2.2 (primary associated HLA antigen was HLA-A2) and B27 had association with PA. By using the method proposed by Thomson and Bodmer, the susceptibility gene in linkage disequilibrium with HLA-A2 seems to be inherited in a dominant fashion.
3)There was no difference on DNA polymorphism of HLA-A2 gene between patients with PA and healthy controls, according to RFLP analysis of the HLA-A2 gene.
4)HLA-A2 had association with PP.
5)HLA-DRw13-DQW6 haplotype frequency was decreased both in PA and in PV.
6)No globally universal HLA haplotype was identified as the carrier of susceptibility to psoriasis (PV, PA and PP).
A study on biological roles of the HLA haplotypes in psoriasis revealed the following findings :
1)HLA-A2-Bw46-Cwll-DRw8-D9. w6-DPB2.2 haplotype-positive PA patients had a correlation with increased serum levels of anaphylatoxin C4a derived from complement component C4.
2)HLA-A1-B37-Cw6 haplotype showed association with low serum levels of linoleic acid among patients with PV.
Association between HLA class I antigens and class II antigens and psoriasis supports that some part of psoriasis is recognized as a disease with immunogenetic disorders. Further investigations by using transgenic mice introduced particular HLA alleles might be necessary to clarify the pathogenesis of psoriasis.
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