Comprehensive Pharmacology 2022
DOI: 10.1016/b978-0-12-820472-6.00073-6
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Novel Immunomodulatory Therapies for Respiratory Pathologies

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Cited by 10 publications
(5 citation statements)
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References 481 publications
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“…The presence of protection despite a relatively weak humoral immune response is of interest in the context of the discussion on the consequences of an inadequate immune response during infection, as excessive, inappropriate, or altered immune responses can lead to increased tissue damage, impaired lung function, and worsening of respiratory disease [70].…”
Section: Discussionmentioning
confidence: 99%
“…The presence of protection despite a relatively weak humoral immune response is of interest in the context of the discussion on the consequences of an inadequate immune response during infection, as excessive, inappropriate, or altered immune responses can lead to increased tissue damage, impaired lung function, and worsening of respiratory disease [70].…”
Section: Discussionmentioning
confidence: 99%
“…Activation of the lipid-derived molecule leukotriene LTB4 and the consequent production of ROS may contribute to the severity of the inflammatory condition, exacerbating tissue damage and potentially leading to complications such as acute respiratory distress syndrome (ARDS) [ 118 , 119 ]. Furthermore, bronchoconstriction induced by CysLTR1 activation can impair lung function, leading to decreased respiratory capacity and the need for respiratory support [ 120 , 121 ]. Regarding the cytokine imbalance, the increased production of IL-12 and decreased IL-4 suggest that SARS-CoV-2 infection may promote a Th1 immune response associated with inflammation and effector cell activation such as macrophages.…”
Section: Role Of Lipid Droplets In the Viral Infection Cycle And Huma...mentioning
confidence: 99%
“…Эта терапия используется у некоторых пациентов с ХОБЛ и БА. Гетерогенность воспалительных клеток и медиаторов при разных эндофенотипах ХОБЛ и БА требует разработки новых ЛС -антагонистов хемокиновых рецепторов (CXCR2), ингибиторов цитокинов, янус-киназы, селектина, р38 митоген-активированной протеинкиназы и др., которые потенциально могут быть эффективны при АСО с преобладанием фенотипа ХОБЛ или БА с воспалением не-Т2 типа [61].…”
Section: дополнительные лс при Aco опосредованном нет2 воспалениемunclassified