Cargando…
Design, synthesis, and LFA-1/ICAM-1 antagonist activity evaluation of Lifitegrast analogues
The interaction between Lymphocyte function-associated antigen 1 (LFA-1) and intercellular-adhesion molecule-1 (ICAM-1) plays important roles in the cell-mediated immune response and inflammation associated with dry eye disease. LFA-1/ICAM-1 antagonists can be used for the treatment of dry eye disea...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8853157/ https://www.ncbi.nlm.nih.gov/pubmed/35194364 http://dx.doi.org/10.1007/s00044-022-02851-9 |
_version_ | 1784653175506075648 |
---|---|
author | Du, Guoxin Du, Weiwei An, Yuanlong Wang, Minnan Hao, Feifei Tong, Xiaochu Gong, Qi He, Xiangdong Jiang, Hualiang He, Wei Zheng, Mingyue Zhang, Donglei |
author_facet | Du, Guoxin Du, Weiwei An, Yuanlong Wang, Minnan Hao, Feifei Tong, Xiaochu Gong, Qi He, Xiangdong Jiang, Hualiang He, Wei Zheng, Mingyue Zhang, Donglei |
author_sort | Du, Guoxin |
collection | PubMed |
description | The interaction between Lymphocyte function-associated antigen 1 (LFA-1) and intercellular-adhesion molecule-1 (ICAM-1) plays important roles in the cell-mediated immune response and inflammation associated with dry eye disease. LFA-1/ICAM-1 antagonists can be used for the treatment of dry eye disease, such as Lifitegrast which has been approved by the FDA in 2016 as a new drug for the treatment of dry eye disease. In this study, we designed and synthesized some new structure compounds that are analogues to Lifitegrast, and their biological activities were evaluated by in vitro cell-based assay and also by in vivo mouse dry eye model. Our results demonstrated that one of these analogues of Lifitegrast (compound 1b) showed good LFA-1/ICAM-1 antagonist activity in in vitro assay; meanwhile, it also significantly reduced ocular surface epithelial cells damage, increased goblet cell density in dry eye mouse and highly improved the symptoms of dry eye mouse. [Figure: see text] |
format | Online Article Text |
id | pubmed-8853157 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-88531572022-02-18 Design, synthesis, and LFA-1/ICAM-1 antagonist activity evaluation of Lifitegrast analogues Du, Guoxin Du, Weiwei An, Yuanlong Wang, Minnan Hao, Feifei Tong, Xiaochu Gong, Qi He, Xiangdong Jiang, Hualiang He, Wei Zheng, Mingyue Zhang, Donglei Med Chem Res Original Research The interaction between Lymphocyte function-associated antigen 1 (LFA-1) and intercellular-adhesion molecule-1 (ICAM-1) plays important roles in the cell-mediated immune response and inflammation associated with dry eye disease. LFA-1/ICAM-1 antagonists can be used for the treatment of dry eye disease, such as Lifitegrast which has been approved by the FDA in 2016 as a new drug for the treatment of dry eye disease. In this study, we designed and synthesized some new structure compounds that are analogues to Lifitegrast, and their biological activities were evaluated by in vitro cell-based assay and also by in vivo mouse dry eye model. Our results demonstrated that one of these analogues of Lifitegrast (compound 1b) showed good LFA-1/ICAM-1 antagonist activity in in vitro assay; meanwhile, it also significantly reduced ocular surface epithelial cells damage, increased goblet cell density in dry eye mouse and highly improved the symptoms of dry eye mouse. [Figure: see text] Springer US 2022-02-17 2022 /pmc/articles/PMC8853157/ /pubmed/35194364 http://dx.doi.org/10.1007/s00044-022-02851-9 Text en © The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Original Research Du, Guoxin Du, Weiwei An, Yuanlong Wang, Minnan Hao, Feifei Tong, Xiaochu Gong, Qi He, Xiangdong Jiang, Hualiang He, Wei Zheng, Mingyue Zhang, Donglei Design, synthesis, and LFA-1/ICAM-1 antagonist activity evaluation of Lifitegrast analogues |
title | Design, synthesis, and LFA-1/ICAM-1 antagonist activity evaluation of Lifitegrast analogues |
title_full | Design, synthesis, and LFA-1/ICAM-1 antagonist activity evaluation of Lifitegrast analogues |
title_fullStr | Design, synthesis, and LFA-1/ICAM-1 antagonist activity evaluation of Lifitegrast analogues |
title_full_unstemmed | Design, synthesis, and LFA-1/ICAM-1 antagonist activity evaluation of Lifitegrast analogues |
title_short | Design, synthesis, and LFA-1/ICAM-1 antagonist activity evaluation of Lifitegrast analogues |
title_sort | design, synthesis, and lfa-1/icam-1 antagonist activity evaluation of lifitegrast analogues |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8853157/ https://www.ncbi.nlm.nih.gov/pubmed/35194364 http://dx.doi.org/10.1007/s00044-022-02851-9 |
work_keys_str_mv | AT duguoxin designsynthesisandlfa1icam1antagonistactivityevaluationoflifitegrastanalogues AT duweiwei designsynthesisandlfa1icam1antagonistactivityevaluationoflifitegrastanalogues AT anyuanlong designsynthesisandlfa1icam1antagonistactivityevaluationoflifitegrastanalogues AT wangminnan designsynthesisandlfa1icam1antagonistactivityevaluationoflifitegrastanalogues AT haofeifei designsynthesisandlfa1icam1antagonistactivityevaluationoflifitegrastanalogues AT tongxiaochu designsynthesisandlfa1icam1antagonistactivityevaluationoflifitegrastanalogues AT gongqi designsynthesisandlfa1icam1antagonistactivityevaluationoflifitegrastanalogues AT hexiangdong designsynthesisandlfa1icam1antagonistactivityevaluationoflifitegrastanalogues AT jianghualiang designsynthesisandlfa1icam1antagonistactivityevaluationoflifitegrastanalogues AT hewei designsynthesisandlfa1icam1antagonistactivityevaluationoflifitegrastanalogues AT zhengmingyue designsynthesisandlfa1icam1antagonistactivityevaluationoflifitegrastanalogues AT zhangdonglei designsynthesisandlfa1icam1antagonistactivityevaluationoflifitegrastanalogues |