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10.1186/s13601-018-0213-z

http://scihub22266oqcxt.onion/10.1186/s13601-018-0213-z
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C6050685!6050685!30026908
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suck abstract from ncbi


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pmid30026908      Clin+Transl+Allergy 2018 ; 8 (ä): ä
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  • Anti-IgE therapy for IgE-mediated allergic diseases: from neutralizing IgE antibodies to eliminating IgE+ B cells #MMPMID30026908
  • Hu J; Chen J; Ye L; Cai Z; Sun J; Ji K
  • Clin Transl Allergy 2018[]; 8 (ä): ä PMID30026908show ga
  • Allergic diseases are inflammatory disorders that involve many types of cells and factors, including allergens, immunoglobulin (Ig)E, mast cells, basophils, cytokines and soluble mediators. Among them, IgE plays a vital role in the development of acute allergic reactions and chronic inflammatory allergic diseases, making its control particularly important in the treatment of IgE-mediated allergic diseases. This review provides an overview of the current state of IgE targeted therapy development, focusing on three areas of translational research: IgE neutralization in blood; IgE-effector cell elimination; and IgE+ B cell reduction. IgE-targeted medicines such as FDA approved drug Xolair (Omalizumab) represent a promising avenue for treating IgE-mediated allergic diseases given the pernicious role of IgE in disease progression. Additionally, targeted therapy for IgE-mediated allergic diseases may be advanced through cellular treatments, including the modification of effector cells.
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