Muneer Abbas, Noureddine Berka, Mozna Khraiwesh, Ali Ramadan, Victor Apprey, Paulette Furbert-Harris, Thomas Quinn, Hassan Brim, Georgia Dunston
{"title":"TLR4和MICA基因多态性与坦桑尼亚沙眼病的严重程度相关","authors":"Muneer Abbas, Noureddine Berka, Mozna Khraiwesh, Ali Ramadan, Victor Apprey, Paulette Furbert-Harris, Thomas Quinn, Hassan Brim, Georgia Dunston","doi":"10.16966/2470-1025.116","DOIUrl":null,"url":null,"abstract":"<p><strong>Aim: </strong>To examine the association of TLR4 Asp299Gly and MICA exon 5 microsatellites polymorphisms with severity of trachoma in a sub-Saharan East Africa population of Tanzanian villagers.</p><p><strong>Methods: </strong>The samples were genotyped for MICA exon 5 microsatellites and the TLR4 299 A/G polymorphism by Restriction Fragment Length Polymorphism (RFLP), and GeneScan<sup>®</sup>, respectively. The association of TLR4 Asp299Gly and MICA exon 5 microsatellites with inflammatory trachoma (TI) and trichiasis (TI) were examined.</p><p><strong>Results: </strong>The results showed an association between TLR4 and MICA polymorphisms and trachoma disease severity, as well as with protection. TLR4 an allele was significantly associated with inflammatory trachoma (p=0.0410), while the G allele (p=0.0410) was associated with protection.</p><p><strong>Conclusion: </strong>TLR4 and MICA may modulate the risk of severity to trachoma disease by modulating the immune response to <i>Ct.</i> In addition; the increased frequency of MICA-A9 heterozygote in controls may suggest a positive selection of these alleles in adaptation to environments where <i>Ct</i> is endemic.</p>","PeriodicalId":8657,"journal":{"name":"Autoimmune and Infectious Diseases: Open Access","volume":"2 3","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2016-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4993598/pdf/","citationCount":"3","resultStr":"{\"title\":\"Genetic Polymorphisms of TLR4 and MICA are Associated with Severity of Trachoma Disease in Tanzania.\",\"authors\":\"Muneer Abbas, Noureddine Berka, Mozna Khraiwesh, Ali Ramadan, Victor Apprey, Paulette Furbert-Harris, Thomas Quinn, Hassan Brim, Georgia Dunston\",\"doi\":\"10.16966/2470-1025.116\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Aim: </strong>To examine the association of TLR4 Asp299Gly and MICA exon 5 microsatellites polymorphisms with severity of trachoma in a sub-Saharan East Africa population of Tanzanian villagers.</p><p><strong>Methods: </strong>The samples were genotyped for MICA exon 5 microsatellites and the TLR4 299 A/G polymorphism by Restriction Fragment Length Polymorphism (RFLP), and GeneScan<sup>®</sup>, respectively. The association of TLR4 Asp299Gly and MICA exon 5 microsatellites with inflammatory trachoma (TI) and trichiasis (TI) were examined.</p><p><strong>Results: </strong>The results showed an association between TLR4 and MICA polymorphisms and trachoma disease severity, as well as with protection. TLR4 an allele was significantly associated with inflammatory trachoma (p=0.0410), while the G allele (p=0.0410) was associated with protection.</p><p><strong>Conclusion: </strong>TLR4 and MICA may modulate the risk of severity to trachoma disease by modulating the immune response to <i>Ct.</i> In addition; the increased frequency of MICA-A9 heterozygote in controls may suggest a positive selection of these alleles in adaptation to environments where <i>Ct</i> is endemic.</p>\",\"PeriodicalId\":8657,\"journal\":{\"name\":\"Autoimmune and Infectious Diseases: Open Access\",\"volume\":\"2 3\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4993598/pdf/\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Autoimmune and Infectious Diseases: Open Access\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.16966/2470-1025.116\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2016/6/3 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Autoimmune and Infectious Diseases: Open Access","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.16966/2470-1025.116","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2016/6/3 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
Genetic Polymorphisms of TLR4 and MICA are Associated with Severity of Trachoma Disease in Tanzania.
Aim: To examine the association of TLR4 Asp299Gly and MICA exon 5 microsatellites polymorphisms with severity of trachoma in a sub-Saharan East Africa population of Tanzanian villagers.
Methods: The samples were genotyped for MICA exon 5 microsatellites and the TLR4 299 A/G polymorphism by Restriction Fragment Length Polymorphism (RFLP), and GeneScan®, respectively. The association of TLR4 Asp299Gly and MICA exon 5 microsatellites with inflammatory trachoma (TI) and trichiasis (TI) were examined.
Results: The results showed an association between TLR4 and MICA polymorphisms and trachoma disease severity, as well as with protection. TLR4 an allele was significantly associated with inflammatory trachoma (p=0.0410), while the G allele (p=0.0410) was associated with protection.
Conclusion: TLR4 and MICA may modulate the risk of severity to trachoma disease by modulating the immune response to Ct. In addition; the increased frequency of MICA-A9 heterozygote in controls may suggest a positive selection of these alleles in adaptation to environments where Ct is endemic.