PMID- 26751942 OWN - NLM STAT- MEDLINE DCOM- 20160429 LR - 20170112 IS - 0392-856X (Print) IS - 0392-856X (Linking) VI - 34 IP - 1 DP - 2016 Jan-Feb TI - Hypersensitivity reactions during treatment with biological agents. PG - 129-32 AB - The recent development of biological agents, namely, anti-tumour necrosis factor alpha (TNF-alpha) agents (infliximab, adalimumab and etanercept), anti- CD20 monoclonal antibody (rituximab) and anti-interleukin 6 receptor (IL-6R) monoclonal antibody (tocilizumab), represents a major breakthrough for the treatment of immune-mediated disorders. Given their structural and functional differences, distinct safety profiles can be expected for each of these agents. Evidence in the literature indicates that patients treated with anti-TNF-alpha agents and tocilizumab are at increased risk for bacterial infections. However, an increased therapeutic use of these biological agents has disclosed other side-effects, including immediate hypersensitivity reactions, such as anaphylaxis and urticaria. Both under-diagnosis and over-diagnosis of hypersensitivity reactions to biological agents are potential problems. Thus, it is important to identify these reactions and to adopt the right approach to manage them. This article reviews the general aspects of adverse events during biologic treatment, focusing on IgE-mediated hypersensitivity reactions to anti-TNF-alpha agents, rituximab and tocilizumab, and on the tools for the diagnosis of these life-threatening reactions. FAU - Puxeddu, Ilaria AU - Puxeddu I AD - Immuno-Allergology Unit, Department of Clinical and Experimental Medicine, University of Pisa, Italy. FAU - Caltran, Elena AU - Caltran E AD - Immuno-Allergology Unit, Department of Clinical and Experimental Medicine, University of Pisa, Italy. FAU - Rocchi, Valeria AU - Rocchi V AD - Immuno-Allergology Unit, Department of Clinical and Experimental Medicine, University of Pisa, Italy. FAU - Del Corso, Isabella AU - Del Corso I AD - Immuno-Allergology Unit, Department of Clinical and Experimental Medicine, University of Pisa, Italy. FAU - Tavoni, Antonio AU - Tavoni A AD - Immuno-Allergology Unit, Department of Clinical and Experimental Medicine, University of Pisa, Italy. FAU - Migliorini, Paola AU - Migliorini P AD - Immuno-Allergology Unit, Department of Clinical and Experimental Medicine, University of Pisa, Italy. paola.migliorini@med.unipi.it. LA - eng PT - Journal Article PT - Review DEP - 20160109 PL - Italy TA - Clin Exp Rheumatol JT - Clinical and experimental rheumatology JID - 8308521 RN - 0 (Antibodies, Monoclonal, Humanized) RN - 0 (Biological Products) RN - 0 (Immunosuppressive Agents) RN - 0 (Tumor Necrosis Factor-alpha) RN - 37341-29-0 (Immunoglobulin E) RN - 4F4X42SYQ6 (Rituximab) RN - I031V2H011 (tocilizumab) SB - IM MH - Animals MH - Antibodies, Monoclonal, Humanized/*adverse effects/immunology MH - Biological Products/*adverse effects/immunology MH - Drug Hypersensitivity/classification/diagnosis/*etiology/immunology MH - Humans MH - Immunoglobulin E/immunology MH - Immunologic Tests MH - Immunosuppressive Agents/*adverse effects/immunology MH - Prognosis MH - Risk Factors MH - Rituximab/*adverse effects/immunology MH - Tumor Necrosis Factor-alpha/*antagonists & inhibitors/immunology EDAT- 2016/01/12 06:00 MHDA- 2016/04/30 06:00 CRDT- 2016/01/12 06:00 PHST- 2015/02/12 00:00 [received] PHST- 2015/06/15 00:00 [accepted] PHST- 2016/01/12 06:00 [entrez] PHST- 2016/01/12 06:00 [pubmed] PHST- 2016/04/30 06:00 [medline] AID - 9190 [pii] PST - ppublish SO - Clin Exp Rheumatol. 2016 Jan-Feb;34(1):129-32. Epub 2016 Jan 9.