Quilizumab

Last updated
Quilizumab
Monoclonal antibody
Type Whole antibody
Source Humanized (from mouse)
Target IGHE
Clinical data
ATC code
  • none
Identifiers
CAS Number
ChemSpider
  • none
UNII
KEGG
Chemical and physical data
Formula C6492H10046N1728O2023S44
Molar mass 146082.49 g·mol−1

Quilizumab (INN) is a humanized monoclonal antibody designed for the treatment of asthma. [1] It binds to IGHE. [2] [3] [4] [5] [6] [7]

This drug was developed by Genentech.

Related Research Articles

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<span class="mw-page-title-main">Immunoglobulin E</span> Immunoglobulin E (IgE) Antibody

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Tanox was a biopharmaceutical company based in Houston, Texas. The company was founded by two biomedical research scientists, Nancy T. Chang and Tse Wen Chang in March 1986 with $250,000, which was a large part of their family savings at that time. Both Changs grew up and received college education in chemistry in National Tsing Hua University in Taiwan and obtained Ph.D. degrees from Harvard University. For postdoctoral training, Tse Wen shifted to immunology and did research with Herman N. Eisen at the Center for Cancer Research, M.I.T. The two Changs successively became research managers and worked with a range of monoclonal antibody projects in Centocor, Inc. based in Malvern, Pennsylvania, from 1981 to 1985. The Changs were recruited by Baylor College of Medicine toward the end of 1985 and offered faculty positions in the Division of Molecular Virology. Soon after their arrival, they were encouraged by a high-ranking Baylor official and local business leaders to start a biotech venture in Houston. This was in a period of time when the economy of Houston was in slump as the result of the collapse of the oil industry.

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Ligelizumab is a humanized IgG1 monoclonal antibody designed for the treatment of severe asthma and chronic spontaneous urticaria. It is an anti-IgE that binds to IGHE an acts as an immunomodulator.

Tse Wen Chang is an immunology researcher, whose career spans across academia and industry. His early research involving the Immunoglobulin E (IgE) pathway and antibody-based therapeutics lead to the development of omalizumab, a medication that has been approved for the treatment of severe allergic asthma and severe chronic spontaneous urticaria. Chang is a cofounder of Tanox, a biopharmaceutical company specialized in anti-IgE therapies for the treatment of allergic diseases. After Tanox's tripartite partnership with Genentech and Novartis was forged in 1996, Chang returned to his alma mater, the National Tsing Hua University in Taiwan and served as the Dean (1996–1999) of the College of Life Sciences. Chang was appointed by the Taiwanese government as President of the Development Center for Biotechnology (DCB) in 2000, and served as a Science and Technology Advisor of the Executive Yuan from 2002 to 2006. From 2006 to 2016, he was tenured as Distinguished Research Fellow at the Genomics Research Center, Academia Sinica. He founded Immunwork, Inc. in 2014.

<span class="mw-page-title-main">PLAID syndrome</span> Medical condition

PLAID syndrome is an inherited condition characterised by antibody deficiency and immune dysregulation, first described in 2012. The name is an acronym of "PLCG2-associated antibody deficiency and immune dysregulation". It is characterised by cold-induced urticaria, autoimmunity, atopy and humoral immune deficiency.

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<span class="mw-page-title-main">Autoimmune urticaria</span> Autoimmune disease causing hives and itching

Autoimmune urticaria, also known as chronic autoimmune urticaria, is a type of chronic urticaria characterized by the presence of autoantibodies in the patient's immune system that target the body's own mast cells, leading to episodes of hives (urticaria). This immunologically distinct type of urticaria is considered autoimmune because the immune system, which normally protects the body from foreign organisms, mistakenly attacks the body's own cells, causing inflammation and other symptoms.

References

  1. Statement On A Nonproprietary Name Adopted By The USAN Council - Quilizumab, American Medical Association .
  2. World Health Organization (2011). "International Nonproprietary Names for Pharmaceutical Substances (INN). Proposed INN: List 106" (PDF). WHO Drug Information. 25 (4).
  3. Harris JM, Cabanski CR, Scheerens H, Samineni D, Bradley MS, Cochran C, Staubach P, Metz M, Sussman G, Maurer M (December 2016). "A randomized trial of quilizumab in adults with refractory chronic spontaneous urticaria". J. Allergy Clin. Immunol. 138 (6): 1730–1732. doi:10.1016/j.jaci.2016.06.023. PMID   27567329.
  4. Harris JM, Maciuca R, Bradley MS, Cabanski CR, Scheerens H, Lim J, Cai F, Kishnani M, Liao XC, Samineni D, Zhu R, Cochran C, Soong W, Diaz JD, Perin P, Tsukayama M, Dimov D, Agache I, Kelsen SG (March 2016). "A randomized trial of the efficacy and safety of quilizumab in adults with inadequately controlled allergic asthma". Respir. Res. 17: 29. doi: 10.1186/s12931-016-0347-2 . PMC   4797126 . PMID   26993628.
  5. Gauvreau GM, Harris JM, Boulet LP, Scheerens H, Fitzgerald JM, Putnam WS, Cockcroft DW, Davis BE, Leigh R, Zheng Y, Dahlén B, Wang Y, Maciuca R, Mayers I, Liao XC, Wu LC, Matthews JG, O'Byrne PM (July 2014). "Targeting membrane-expressed IgE B cell receptor with an antibody to the M1 prime epitope reduces IgE production". Sci Transl Med. 6 (243): 243ra85. doi:10.1126/scitranslmed.3008961. PMID   24990880. S2CID   41593528.
  6. Licari A, Castagnoli R, Panfili E, Marseglia A, Brambilla I, Marseglia GL (March 2017). "An Update on Anti-IgE Therapy in Pediatric Respiratory Diseases". Curr Respir Med Rev. 13 (1): 22–29. doi:10.2174/1573398X13666170616110738. PMC   5735517 . PMID   29290750.
  7. Deza G, Ricketti PA, Giménez-Arnau AM, Casale TB (2018). "Emerging Biomarkers and Therapeutic Pipelines for Chronic Spontaneous Urticaria". J Allergy Clin Immunol Pract. 6 (4): 1108–1117. doi:10.1016/j.jaip.2018.02.024. PMID   30033912. S2CID   51710078.