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Review

Drug Hypersensitivity and Desensitizations: Mechanisms and New Approaches

1
Division of Rheumatology, Immunology and Allergy, Department of Medicine, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA 02115, USA
2
Department of Allergy, Marqués de Valdecilla University Hospital-IDIVAL, 39011 Santander, Spain
3
Department of Medicine, College of Medicine, King Saud University, Riyadh 12372, Saudi Arabia
4
Master of Medical Sciences in Immunology Program, Harvard Medical School, Boston, MA 02115, USA
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2017, 18(6), 1316; https://0-doi-org.brum.beds.ac.uk/10.3390/ijms18061316
Received: 2 May 2017 / Revised: 13 June 2017 / Accepted: 14 June 2017 / Published: 20 June 2017
(This article belongs to the Special Issue Drug Hypersensitivity)
Drug hypersensitivity reactions (HSRs) are increasing in the 21st Century with the ever expanding availability of new therapeutic agents. Patients with cancer, chronic inflammatory diseases, cystic fibrosis, or diabetes can become allergic to their first line therapy after repeated exposures or through cross reactivity with environmental allergens. Avoidance of the offending allergenic drug may impact disease management, quality of life, and life expectancy. Precision medicine provides new tools for the understanding and management of hypersensitivity reactions (HSRs), as well as a personalized treatment approach for IgE (Immunoglobuline E) and non-IgE mediated HSRs with drug desensitization (DS). DS induces a temporary hyporesponsive state by incremental escalation of sub-optimal doses of the offending drug. In vitro models have shown evidence that IgE desensitization is an antigen-specific process which blocks calcium flux, impacts antigen/IgE/FcεRI complex internalization and prevents the acute and late phase reactions as well as mast cell mediator release. Through a “bench to bedside” approach, in vitro desensitization models help elucidate the molecular pathways involved in DS, providing new insights to improved desensitization protocols for all patients. The aim of this review is to summarize up to date information on the drug HSRs, the IgE mediated mechanisms of desensitization, and their clinical applications. View Full-Text
Keywords: drug hypersensitivity; desensitization; precision medicine; mast cells; desensitization models; high affinity IgE Fcε receptor I; IgE drug hypersensitivity; desensitization; precision medicine; mast cells; desensitization models; high affinity IgE Fcε receptor I; IgE
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MDPI and ACS Style

De las Vecillas Sánchez, L.; Alenazy, L.A.; Garcia-Neuer, M.; Castells, M.C. Drug Hypersensitivity and Desensitizations: Mechanisms and New Approaches. Int. J. Mol. Sci. 2017, 18, 1316. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms18061316

AMA Style

De las Vecillas Sánchez L, Alenazy LA, Garcia-Neuer M, Castells MC. Drug Hypersensitivity and Desensitizations: Mechanisms and New Approaches. International Journal of Molecular Sciences. 2017; 18(6):1316. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms18061316

Chicago/Turabian Style

De las Vecillas Sánchez, Leticia; Alenazy, Leila A.; Garcia-Neuer, Marlene; Castells, Mariana C. 2017. "Drug Hypersensitivity and Desensitizations: Mechanisms and New Approaches" Int. J. Mol. Sci. 18, no. 6: 1316. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms18061316

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Note that from the first issue of 2016, MDPI journals use article numbers instead of page numbers. See further details here.

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