{"title":"自然免疫与眼部炎症。","authors":"Koh-Hei Sonoda","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>We have focused on the role of innate immunity during the formation oföchoroidal neovascularization\n(CNV) -related diseasesù. Inflammation affects the formation and the progression of various\nvitreoretinal diseases. We performed a comprehensive analysis of inflammatory immune mediators in\nthe vitreous fluids with diabetic macular edema, proliferative diabetic retinopathy, branch retinal vein\nocclusion, central retinal vein occlusion and rhegmatogenous retinal detachment. The concentrations\nof 20 soluble factors (nine cytokines, six chemokines, and five growth factors) were measured\nsimultaneously by multiplex bead analysis system. Out of 20 soluble factors, three factors :\ninterleukin-6 (IL-6), interleukin-8 (IL-8), and monocyte chemoattractant protein-1 (MCP-1) were\nsignificantly elevated in all groups of vitreoretinal diseases compared with control group. According to\nthe correlation analysis in the individual patientʼs level, these three factors that were simultaneously\nincreased, did not show any independent upregulation in all the examined diseases.\nWe also elucidated the role of natural killer (NK)T cells, which restricted CD1 molecule and\nparticipate in the innate immune response, in laser-induced experimental CNV. We examined CNV\nformation in independent two NKT cell-deficient mice, either CD1 knockout (KO) mice or Ja18 KO\nmice, and found that both KO mice showed significant reduction of experimental CNV.\nDuring the clinical process of CNV-related diseases, not only CNV formation, subretinal scaring is\nthought to be another important step. We thus established the experimental model of subretinal\nscaring by injecting peritoneal exudating macrophages into subretinal space. Subretinal fibrous tissue\nwas observed by fundus scope in PEC-inoculated mice after seven days. The tissue was consisted of\nmonotonous and low cell-density area, which expressed a-SMA with collagen synthesis. Because\nPEC-inoculated MCP-1 KO mice showed less amount of glial residual, not only exogenous\nmacrophages, but also intrinsic macrophages are critical. Activated macrophages directly induced\nmyofibrotic changes in RPE cells in vitro.</p>","PeriodicalId":12665,"journal":{"name":"Fukuoka igaku zasshi = Hukuoka acta medica","volume":"107 12","pages":"205-12"},"PeriodicalIF":0.0000,"publicationDate":"2016-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Natural Immunity and Ocular Inflammation.\",\"authors\":\"Koh-Hei Sonoda\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>We have focused on the role of innate immunity during the formation oföchoroidal neovascularization\\n(CNV) -related diseasesù. Inflammation affects the formation and the progression of various\\nvitreoretinal diseases. We performed a comprehensive analysis of inflammatory immune mediators in\\nthe vitreous fluids with diabetic macular edema, proliferative diabetic retinopathy, branch retinal vein\\nocclusion, central retinal vein occlusion and rhegmatogenous retinal detachment. The concentrations\\nof 20 soluble factors (nine cytokines, six chemokines, and five growth factors) were measured\\nsimultaneously by multiplex bead analysis system. Out of 20 soluble factors, three factors :\\ninterleukin-6 (IL-6), interleukin-8 (IL-8), and monocyte chemoattractant protein-1 (MCP-1) were\\nsignificantly elevated in all groups of vitreoretinal diseases compared with control group. According to\\nthe correlation analysis in the individual patientʼs level, these three factors that were simultaneously\\nincreased, did not show any independent upregulation in all the examined diseases.\\nWe also elucidated the role of natural killer (NK)T cells, which restricted CD1 molecule and\\nparticipate in the innate immune response, in laser-induced experimental CNV. We examined CNV\\nformation in independent two NKT cell-deficient mice, either CD1 knockout (KO) mice or Ja18 KO\\nmice, and found that both KO mice showed significant reduction of experimental CNV.\\nDuring the clinical process of CNV-related diseases, not only CNV formation, subretinal scaring is\\nthought to be another important step. We thus established the experimental model of subretinal\\nscaring by injecting peritoneal exudating macrophages into subretinal space. Subretinal fibrous tissue\\nwas observed by fundus scope in PEC-inoculated mice after seven days. The tissue was consisted of\\nmonotonous and low cell-density area, which expressed a-SMA with collagen synthesis. Because\\nPEC-inoculated MCP-1 KO mice showed less amount of glial residual, not only exogenous\\nmacrophages, but also intrinsic macrophages are critical. Activated macrophages directly induced\\nmyofibrotic changes in RPE cells in vitro.</p>\",\"PeriodicalId\":12665,\"journal\":{\"name\":\"Fukuoka igaku zasshi = Hukuoka acta medica\",\"volume\":\"107 12\",\"pages\":\"205-12\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Fukuoka igaku zasshi = Hukuoka acta medica\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fukuoka igaku zasshi = Hukuoka acta medica","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
We have focused on the role of innate immunity during the formation oföchoroidal neovascularization
(CNV) -related diseasesù. Inflammation affects the formation and the progression of various
vitreoretinal diseases. We performed a comprehensive analysis of inflammatory immune mediators in
the vitreous fluids with diabetic macular edema, proliferative diabetic retinopathy, branch retinal vein
occlusion, central retinal vein occlusion and rhegmatogenous retinal detachment. The concentrations
of 20 soluble factors (nine cytokines, six chemokines, and five growth factors) were measured
simultaneously by multiplex bead analysis system. Out of 20 soluble factors, three factors :
interleukin-6 (IL-6), interleukin-8 (IL-8), and monocyte chemoattractant protein-1 (MCP-1) were
significantly elevated in all groups of vitreoretinal diseases compared with control group. According to
the correlation analysis in the individual patientʼs level, these three factors that were simultaneously
increased, did not show any independent upregulation in all the examined diseases.
We also elucidated the role of natural killer (NK)T cells, which restricted CD1 molecule and
participate in the innate immune response, in laser-induced experimental CNV. We examined CNV
formation in independent two NKT cell-deficient mice, either CD1 knockout (KO) mice or Ja18 KO
mice, and found that both KO mice showed significant reduction of experimental CNV.
During the clinical process of CNV-related diseases, not only CNV formation, subretinal scaring is
thought to be another important step. We thus established the experimental model of subretinal
scaring by injecting peritoneal exudating macrophages into subretinal space. Subretinal fibrous tissue
was observed by fundus scope in PEC-inoculated mice after seven days. The tissue was consisted of
monotonous and low cell-density area, which expressed a-SMA with collagen synthesis. Because
PEC-inoculated MCP-1 KO mice showed less amount of glial residual, not only exogenous
macrophages, but also intrinsic macrophages are critical. Activated macrophages directly induced
myofibrotic changes in RPE cells in vitro.