Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5916865 | Molecular Immunology | 2014 | 11 Pages |
â¢Surprising facts on the clinical relevance of complement activation-related pseudoallergy (CARPA), a hypersensitivity reaction to state-of-art medicines.â¢Evidence for C activation via all three pathways and a tetrad of physiological changes in pigs that models the human reaction.â¢Outline of the likely pathomechanism of CARPA involving multiple signaling and effector pathways with double initial “hit”.â¢A scheme of in vitro and in vivo tests that enables assessing the CARPAgenic potential of drugs.â¢Proposal of a remarkable analogy between the classic stress reaction and CARPA.
Intravenous injection of a variety of nanotechnology enhanced (liposomal, micellar, polymer-conjugated) and protein-based (antibodies, enzymes) drugs can lead to hypersensitivity reactions (HSRs), also known as infusion, or anaphylactoid reactions. The molecular mechanism of mild to severe allergy symptoms may differ from case to case and is mostly not known, however, in many cases a major cause, or contributing factor is activation of the complement (C) system. The clinical relevance of C activation-related HSRs, a non-IgE-mediated pseudoallergy (CARPA), lies in its unpredictability and occasional lethal outcome. Accordingly, there is an unmet medical need to develop laboratory assays and animal models that quantitate CARPA. This review provides basic information on CARPA; a short history, issues of nomenclature, incidence, classification of reactogenic drugs and symptoms, and the mechanisms of C activation via different pathways. It is pointed out that anaphylatoxin-induced mast cell release may not entirely explain the severe reactions; a “second hit” on allergy mediating cells may also contribute. In addressing the increasing requirements for CARPA testing, the review evaluates the available assays and animal models, and proposes a possible algorithm for the screening of reactogenic drugs and hypersensitive patients. Finally, an analogy is proposed between CARPA and the classic stress reaction, suggesting that CARPA represents a “blood stress” reaction, a systemic fight of the body against harmful biological and chemical agents via the anaphylatoxin/mast-cell/circulatory system axis, in analogy to the body's fight of physical and emotional stress via the hypothalamo/pituitary/adrenal axis. In both cases the response to a broad variety of noxious effects are funneled into a uniform pattern of physiological changes.
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