Ilaria Floris, Víctor García-González, Belen Palomares, Kurt Appel, Beatrice Lejeune
{"title":"微免疫治疗药物2LARTH®可在体内减轻类风湿关节炎的炎症和症状。","authors":"Ilaria Floris, Víctor García-González, Belen Palomares, Kurt Appel, Beatrice Lejeune","doi":"10.1155/2020/1594573","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Rheumatoid arthritis (RA) is a chronic inflammatory joint disease, which can cause cartilage and bone damages as well as pain and disability. In order to prevent disease progression, reduce pain, and major symptoms of RA, one good strategy consists in targeting proinflammatory cytokines that have the key role in the vicious circle of synovial inflammation and pain. The micro-immunotherapy medicine (MIM) 2LARTH® targets cytokines involved in inflammation.</p><p><strong>Aim: </strong>The aim of the study is to evaluate the effect of the MIM compared to vehicle in an <i>in vivo</i> model of RA, induced in mice after immunization with articular bovine type II collagen.</p><p><strong>Methods: </strong>Vehicle and MIM were dissolved in pure water (1 capsule in 100 ml) and 100 <i>µ</i>l was given by gavage daily for 14 days. To evaluate the severity of arthritis, wrist and ankle thickness was determined, paw edema was measured, and a clinical score from 0 to 4 was established. Furthermore, histological analysis was performed. To evaluate systemic inflammation, circulating levels of IL-1<i>β</i> and TNF-<i>α</i> were measured by ELISA.</p><p><strong>Results: </strong>Ankle thickness was found to be significantly reduced in MIM-treated mice compared to vehicle-treated mice (<i>P</i> < 0.05) and compared to untreated me (<i>P</i> < 0.05) and compared to untreated me (<i>P</i> < 0.05) and compared to untreated me (<i>β</i> and TNF-<i>α</i> were measured by ELISA. <i>P</i> < 0.05) and compared to untreated me (.</p><p><strong>Conclusion: </strong>The results indicate that the tested medicine reduces inflammation, histological, and clinical signs of RA in a CIA model.</p>","PeriodicalId":51715,"journal":{"name":"International Journal of Rheumatology","volume":null,"pages":null},"PeriodicalIF":2.3000,"publicationDate":"2020-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2020/1594573","citationCount":"13","resultStr":"{\"title\":\"The Micro-Immunotherapy Medicine 2LARTH® Reduces Inflammation and Symptoms of Rheumatoid Arthritis <i>In Vivo</i>.\",\"authors\":\"Ilaria Floris, Víctor García-González, Belen Palomares, Kurt Appel, Beatrice Lejeune\",\"doi\":\"10.1155/2020/1594573\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Rheumatoid arthritis (RA) is a chronic inflammatory joint disease, which can cause cartilage and bone damages as well as pain and disability. In order to prevent disease progression, reduce pain, and major symptoms of RA, one good strategy consists in targeting proinflammatory cytokines that have the key role in the vicious circle of synovial inflammation and pain. The micro-immunotherapy medicine (MIM) 2LARTH® targets cytokines involved in inflammation.</p><p><strong>Aim: </strong>The aim of the study is to evaluate the effect of the MIM compared to vehicle in an <i>in vivo</i> model of RA, induced in mice after immunization with articular bovine type II collagen.</p><p><strong>Methods: </strong>Vehicle and MIM were dissolved in pure water (1 capsule in 100 ml) and 100 <i>µ</i>l was given by gavage daily for 14 days. To evaluate the severity of arthritis, wrist and ankle thickness was determined, paw edema was measured, and a clinical score from 0 to 4 was established. Furthermore, histological analysis was performed. To evaluate systemic inflammation, circulating levels of IL-1<i>β</i> and TNF-<i>α</i> were measured by ELISA.</p><p><strong>Results: </strong>Ankle thickness was found to be significantly reduced in MIM-treated mice compared to vehicle-treated mice (<i>P</i> < 0.05) and compared to untreated me (<i>P</i> < 0.05) and compared to untreated me (<i>P</i> < 0.05) and compared to untreated me (<i>β</i> and TNF-<i>α</i> were measured by ELISA. <i>P</i> < 0.05) and compared to untreated me (.</p><p><strong>Conclusion: </strong>The results indicate that the tested medicine reduces inflammation, histological, and clinical signs of RA in a CIA model.</p>\",\"PeriodicalId\":51715,\"journal\":{\"name\":\"International Journal of Rheumatology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2020-01-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1155/2020/1594573\",\"citationCount\":\"13\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Rheumatology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1155/2020/1594573\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2020/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q2\",\"JCRName\":\"RHEUMATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Rheumatology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/2020/1594573","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2020/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"RHEUMATOLOGY","Score":null,"Total":0}
The Micro-Immunotherapy Medicine 2LARTH® Reduces Inflammation and Symptoms of Rheumatoid Arthritis In Vivo.
Background: Rheumatoid arthritis (RA) is a chronic inflammatory joint disease, which can cause cartilage and bone damages as well as pain and disability. In order to prevent disease progression, reduce pain, and major symptoms of RA, one good strategy consists in targeting proinflammatory cytokines that have the key role in the vicious circle of synovial inflammation and pain. The micro-immunotherapy medicine (MIM) 2LARTH® targets cytokines involved in inflammation.
Aim: The aim of the study is to evaluate the effect of the MIM compared to vehicle in an in vivo model of RA, induced in mice after immunization with articular bovine type II collagen.
Methods: Vehicle and MIM were dissolved in pure water (1 capsule in 100 ml) and 100 µl was given by gavage daily for 14 days. To evaluate the severity of arthritis, wrist and ankle thickness was determined, paw edema was measured, and a clinical score from 0 to 4 was established. Furthermore, histological analysis was performed. To evaluate systemic inflammation, circulating levels of IL-1β and TNF-α were measured by ELISA.
Results: Ankle thickness was found to be significantly reduced in MIM-treated mice compared to vehicle-treated mice (P < 0.05) and compared to untreated me (P < 0.05) and compared to untreated me (P < 0.05) and compared to untreated me (β and TNF-α were measured by ELISA. P < 0.05) and compared to untreated me (.
Conclusion: The results indicate that the tested medicine reduces inflammation, histological, and clinical signs of RA in a CIA model.