scholarly journals The use of Omalizumab in Severe Allergic Asthma and Chronic Spontaneous Urticaria: real-life experience

2020 ◽  
Vol 145 (2) ◽  
pp. AB34
Author(s):  
Carla Irani ◽  
Souheil Hallit ◽  
Stephanie Daccache ◽  
Pascale Salameh
Author(s):  
Amelia Licari ◽  
Riccardo Castagnoli ◽  
Chiara Denicolo ◽  
Linda Rossini ◽  
Manuela Seminara ◽  
...  

2018 ◽  
Vol 12 ◽  
pp. 175346661881019 ◽  
Author(s):  
Corrado Pelaia ◽  
Cecilia Calabrese ◽  
Rosa Terracciano ◽  
Francesco de Blasio ◽  
Alessandro Vatrella ◽  
...  

Omalizumab was the first, and for a long time the only available monoclonal antibody for the add-on treatment of severe allergic asthma. In particular, omalizumab selectively targets human immunoglobulin (Ig)E, forming small-size immune complexes that inhibit IgE binding to its high- and low-affinity receptors. Therefore, omalizumab effectively blunts the immune response in atopic asthmatic patients, thus significantly improving the control of asthma symptoms and successfully preventing disease exacerbations. These very positive effects of omalizumab make it possible to drastically decrease both referrals to the emergency room and hospitalizations for asthma exacerbations. Such important therapeutic actions of omalizumab have been documented by several randomized clinical trials, and especially by more than 10 years of real-life experience in daily clinical practice. Omalizumab can also interfere with airway remodelling by inhibiting the activation of IgE receptors located on structural cells such as bronchial epithelial cells and airway smooth muscle cells. Moreover, omalizumab is characterized by a very good safety and tolerability profile. Hence, omalizumab represents a valuable therapeutic option for the add-on biological treatment of severe allergic asthma.


Author(s):  
Rania Abusamra ◽  
Sarah Latham ◽  
Shrabani Chakraborty ◽  
Marc Woodman ◽  
Cara Bossley ◽  
...  

2012 ◽  
Vol 25 (1) ◽  
pp. 77-82 ◽  
Author(s):  
Eleni G. Tzortzaki ◽  
Andreas Georgiou ◽  
Dimitrios Kampas ◽  
Marinos Lemessios ◽  
Miltiadis Markatos ◽  
...  

2020 ◽  
Vol 22 (1) ◽  
pp. 32-45
Author(s):  
Emanuela Martina ◽  
Federico Diotallevi ◽  
Tommaso Bianchelli ◽  
Matteo Paolinelli ◽  
Annamaria Offidani

Background: Chronic Spontaneous Urticaria (CSU) is a disease characterized by the onset of wheals and/or angioedema over 6 weeks. The pathophysiology for CSU is very complex, involving mast cells and basophils with a multitude of inflammatory mediators. For many years the treatment of CSU has been based on the use of antihistamines, steroids and immunosuppressive agents with inconstant and frustrating results. The introduction of omalizumab, the only licensed biologic for antihistamine- refractory CSU, has changed the management of the disease. Objective: The aim of this article is to review the current state of the art of CSU, the real-life experience with omalizumab and the promising drugs that are under development. Methods:: An electronic search was performed to identify studies, case reports, guidelines and reviews focused on the new targets for the treatment of chronic spontaneous urticaria, both approved or under investigation. The search was limited to articles published in peer-reviewed journals in the English Language in the PubMed database and trials registered in Clinicaltrials.gov. Results:: Since the advent of omalizumab, the search for new therapies for chronic spontaneous urticaria has had a new impulse. Anti-IgE drugs will probably still be the cornerstone of therapy, but new targets may prove effective in syndromic urticaria or refractory cases. Conclusion:: Although omalizumab has been a breakthrough in the treatment of CSU, many patients do not completely get benefit and even require more effective treatments. Novel drugs are under investigation with promising results.


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