Anthropological and genetic studies on uveitis in Mongoloids
蒙古人种葡萄膜炎的人类学和遗传学研究
基本信息
- 批准号:07041166
- 负责人:
- 金额:$ 9.92万
- 依托单位:
- 依托单位国家:日本
- 项目类别:Grant-in-Aid for international Scientific Research
- 财政年份:1995
- 资助国家:日本
- 起止时间:1995 至 1997
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Anthropological and molecular genetic studies on intractable uveitis syndromes which are frequently seen in the Mongoloid population were performed in Syria, Jordan, Mongol and Portugal in the fiscal year of 1997.In Syria and Jordan, there were many patients with Behcet's disease, and most of the patients in the Ophthalmology Department as well as the Rheumatology Department were those with Behcet's disease, quite similar to Japan. However, Vogt-Koyanagi-Harada's disease was rarely seen in these countries. In Syria, uveitis survey clinic was not yet established, and we advised them how to establish this for our future cooperative studies. In Jordan, however, a speciality clinic for Behcet's disease was already established, and we could see more than 50 typical cases of Behcet's disease. We could also get blood samples from these patients for the HLA-DNA typing. Molecular genetic analyzes on these samples are now in progress in our laboratory.In Mongolia, there were many patients with i … More ntractable uveitis syndromes, and typical cases with Behcet's disease or Vogt-Koyanagi-Harada's disease were seen. On the other hand, no patients were diagnosed as sarcoidosis in Mongolia. Clinical festures of uveitis in Mongolia was generally similar to Japan, as had been expected. In this investigation, we could establish a scientific basis for future cooperative studies.Portugal is located in the west end of the so-called Silk-Route, and similar to Japan and other Mediterranean countries, there were many Portuguese patients with Behcet's disease. However, Vogt-Koyanagi-Harada's disease or sarcoidosis was not as frequent as in Japan. In the next study, association of HLA-B^<**>5101 is to be studied in Portuguese patients with Behcet's disease.Blood samples collected before from Saudi Arabia or Greece were also HLA-DNA typed in our laboratory this year, and the same HLA class I association with Japanese patients was found in these patients.We can conclude from these results that certain types of intractable uveitis frequently seen in the Mongoloid population are also seen along with the Silk-Route, and these uveitis may have been spread along with the migration of the old Nomadic Tibes. Less
1997年在叙利亚和约旦,在叙利亚,约旦,约旦,蒙古人和葡萄牙在蒙古人种群中经常看到的关于可顽固性葡萄炎综合征的人类学和分子遗传研究。但是,在这些国家很少见到沃格特·卡亚纳吉·哈拉达氏病。在叙利亚,尚未建立葡萄膜炎调查诊所,我们建议他们如何为未来的教练研究建立这一点。然而,在约旦,已经建立了一个贝塞特氏病的专业诊所,我们可以看到50多例Behcet疾病的典型病例。我们还可以从这些患者的HLA-DNA键入中获取血液样本。在我们的实验室中,对这些样品的分子遗传分析现在正在进行中。在蒙古,有许多I…更多令人不安的葡萄炎综合症患者,而Behcet病或Vogt-Koyanagi-Harada病的典型病例被发现。另一方面,在蒙古中没有被诊断为结节病。正如预期的那样,蒙古葡萄膜炎的临床庆典通常与日本相似。这项投资,我们可以为未来的合作研究建立科学基础。然而,沃格特·卡亚纳吉·哈拉达氏病或结节病不像日本那样频繁。在下一项研究中,将在葡萄牙患者中进行HLA-B^<**> 5101的关联。今年还在我们的实验室中键入的HLA-DNA之前,还可以在这些患者中发现了同一类型的人群,也可以在我们的实验室中发现了同样的类型。随着丝绸路线,这些葡萄膜炎可能随着旧游牧锡的迁移而蔓延。较少的
项目成果
期刊论文数量(87)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
工藤成樹: "AIDSに合併したサイトメガロウイルス網膜炎の2症例" 眼臨医報. 89. 34-37 (1995)
工藤茂树:“艾滋病并发巨细胞病毒性视网膜炎两例”眼科报告,89. 34-37 (1995)。
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
Kimura K.: "Prevalence of antibodies against Borrelia species in patients with unclassified uveitis in regions in which lyme disease is endemic and nonendemic" Clin Diagn Lab Immunol. 2. 53-56 (1995)
Kimura K.:“莱姆病流行和非流行地区未分类葡萄膜炎患者中抗疏螺旋体抗体的流行率”Clin Diagn Lab Nutrition。
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
Shindo Y,et al: "Clinical and immunogenetic investigation of a laotian patient with Vogt-Koyanagi-Harada's disease" Ophthalmologica. 210. 112-114 (1996)
Shindo Y 等人:“一名患有 Vogt-Koyanagi-Harada 病的老挝患者的临床和免疫遗传学研究”眼科。
- DOI:
- 发表时间:
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- 影响因子:0
- 作者:
- 通讯作者:
Uchio E.: "Suppression of actively induced experimental autoimmune uveoretinitis by CD4+T cells" Graefe's Arch Clin Exp Ophthalmol. 235. 97-102 (1997)
Uchio E.:“CD4 T 细胞对主动诱导的实验性自身免疫性葡萄膜视网膜炎的抑制”Graefe 的 Arch Clin Exp Ophamol。
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
Asako M.: "A juvenile case of Vogt-Koyanagi-Harada's disease with calcific band keratopathy" Jpn J Clin Ophthalmol. 51 : 3. 395-398 (1997)
Asako M.:“伴有钙化带状角膜病的 Vogt-Koyanagi-Harada 病青少年病例”Jpn J Clin Ophthalmol。
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OHNO Shigeaki其他文献
OHNO Shigeaki的其他文献
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{{ truncateString('OHNO Shigeaki', 18)}}的其他基金
Comprhensive examination for serum autoantigens in endogenous uveitis patients
内源性葡萄膜炎患者血清自身抗原的综合检查
- 批准号:
23592602 - 财政年份:2011
- 资助金额:
$ 9.92万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Investigation of disease susceptibility genes associated with intractable intraocular inflammation with racial differences and development of new antioxidant therapy
具有种族差异的顽固性眼内炎症相关疾病易感基因的研究及新型抗氧化疗法的开发
- 批准号:
19406028 - 财政年份:2007
- 资助金额:
$ 9.92万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Molecular genetics and molecular epidemiology of intractable intraocular inflammation frequently found in Mongoloids for prevention of blindness.
蒙古人种中常见的难治性眼内炎症的分子遗传学和分子流行病学,用于预防失明。
- 批准号:
16406032 - 财政年份:2004
- 资助金额:
$ 9.92万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
New development in molecular genetic and molecular pharmacological studies on intractable intraocular inflammation.
难治性眼内炎症的分子遗传学和分子药理学研究新进展。
- 批准号:
16209051 - 财政年份:2004
- 资助金额:
$ 9.92万 - 项目类别:
Grant-in-Aid for Scientific Research (A)
Molecule genetic and molecule immunologic investigations on the mechanisms of viral ocular inflammation
病毒性眼部炎症机制的分子遗传学和分子免疫学研究
- 批准号:
14370550 - 财政年份:2002
- 资助金额:
$ 9.92万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
ANTHROPOLOGICAL AND MOLECULAR GENETIC STUDIES ON THE EPIDEMIOLOGY OF INTRACTABLE OCULAR DISEASES
难治性眼病流行病学的人类学和分子遗传学研究
- 批准号:
12576022 - 财政年份:2000
- 资助金额:
$ 9.92万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Studies on molecular genetic mechanism of intractable immune-mediated inflammatory diseases of the eye by genomic analyses
通过基因组分析研究难治性免疫介导的眼部炎症性疾病的分子遗传机制
- 批准号:
12307038 - 财政年份:2000
- 资助金额:
$ 9.92万 - 项目类别:
Grant-in-Aid for Scientific Research (A)
Anthhropological and genetic studies on ocular inflammatory diseases in Mongoloids
蒙古人种眼部炎症疾病的人类学和遗传学研究
- 批准号:
10041203 - 财政年份:1998
- 资助金额:
$ 9.92万 - 项目类别:
Grant-in-Aid for Scientific Research (A).
Molecular mechanism of intractable ocular diseases
眼部难治性疾病的分子机制
- 批准号:
10671650 - 财政年份:1998
- 资助金额:
$ 9.92万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Molecular genetic studies on Behcet's disease
白塞病的分子遗传学研究
- 批准号:
08457466 - 财政年份:1996
- 资助金额:
$ 9.92万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
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