Abstract

Biologicals are widely used therapeutic agents for rheumatologic diseases, cancers, and other chronic inflammatory diseases. They are characterized by complex structures and content of variable amounts of foreign regions, which may lead to anti-drug antibodies (ADA) development. ADA onset may limit the clinical usage of biologicals because they may decrease their safety. In fact they are mainly associated with immediate hypersensitivity reactions (HSRs). Development of ADAs is reduced by concomitant immunosuppressive treatment, while it is increased by longer intervals between drug administrations; thus, regular infusion regimens should be preferred to reduce HSRs. Once ADAs have formed, some procedures can be implemented to reduce the risk of HSRs. ADAs may belong to different isotype; the detection of IgE ADA is advisable to be assessed when high and early ADAs are detected, in order to reduce the risk of severe HRs. In patients who need to reintroduce the biological culprit, as alternative therapies are not available, drug desensitization (DD) may be applied. Desensitization should be conceptually dedicated to patients with an IgE-mediated HSR; however, it can be performed also in patients who had developed non-IgE-mediated HSRs. Although the underlying mechanisms behind successful DD has not been fully clarified, the DD procedure is associated with the inhibition of mast cell degranulation and cytokine production. Additionally, some data are emerging about the inhibition of drug-specific immune responses during DD.

Highlights

  • Biologicals are indispensable therapeutic agents in immunological, oncological, and inflammatory diseases, and their application in clinical practice is increasing

  • Taking into account the structural characteristics of biologicals, which differ from traditional drugs, and their ability to elicit anti-drug antibodies (ADA), the mechanisms underlying hypersensitivity reactions (HSRs) to biologicals can be divided into ADA and non-ADA mediated

  • ADA may belong to different isotypes, so ADA-mediated HSR may be classified as IgE- and non-IgE-mediated reactions

Read more

Summary

INTRODUCTION

Biologicals are indispensable therapeutic agents in immunological, oncological, and inflammatory diseases, and their application in clinical practice is increasing. Prevention of Hypersensitivity to Biologicals first lifetime exposure or after repeated administrations and different pathogenic mechanisms are involved. The potential risk of biologicals’ immunogenicity is an important issue in clinical practice, leading to the development of anti-drug antibodies (ADA). Patients with ADA, as IgG or IgE developed during treatment with biologicals or preexisting, are more likely to have increased risk of immediate HSRs [1]. In patients with HSR toward a biological, approaches for avoiding future adverse events differ depending on the mechanism of reactions. These strategies are very important when no alternative therapies are available. In this review we discuss the clinical and diagnostic strategies to prevent and mitigate HSR toward biologicals, especially when related to the development of immunogenicity

MECHANISMS OF HYPERSENSITIVITY REACTIONS TO BIOLOGICALS
Identification of Patients With Clinical Risk Factors for HSR
The Role of Immunomodulatory Therapies to Block ADA Formation
The Role of Premedication
Definition of the Pathogenic Mechanism of HSR
Drug Desensitization to Induce Tolerance in Patients With HSR
Findings
CONCLUSIONS
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call