Abstract

Anaphylaxis is an acute and life-threatening systemic reaction. Many triggers have been described, including food, drug, and hymenoptera allergens, which are the most frequently involved. The mechanisms described in anaphylactic reactions are complex and implicate a diversity of pathways. Some of these mechanisms may be key to the development of the anaphylactic reaction, while others may only modify its severity. Although specific IgE, mast cells, and basophils are considered the principal players in anaphylaxis, alternative mechanisms have been proposed in non-IgE anaphylactic reactions. Neutrophils, macrophages, as well as basophils, have been involved, as have IgG-dependent, complement and contact system activation. A range of cationic substances can induce antibody-independent mast cells activation through MRGPRX2 receptor. Cofactors and augmenting factors may explain why, in some patients, food allergen exposure can cause anaphylaxis, while in other clinical scenario it can be tolerated or elicits a mild reaction. With the influence of these factors, food allergic reactions may be induced at lower doses of allergen and/or become more severe. Exercise, alcohol, estrogens, and some drugs such as Non-steroidal anti-inflammatory drugs, angiotensin-converting enzyme inhibitors, β-blockers, and lipid-lowering drugs are the main factors described, though their mechanisms and signaling pathways are poorly understood.

Highlights

  • Anaphylaxis is an acute, life-threatening, systemic reaction caused by the mediators released from different cells [1]

  • Mast cells are considered the pivotal cells in IgE-mediated anaphylaxis [6], and the role of macrophages and neutrophils has been described in IgE-independent reactions [6, 7]

  • Muñoz-Cano et al [5] studied patients with anaphylaxis induced by lipid transfer proteins (LTP) and mediated by IgE. They found an increase of specific anti-LTP IgG1 and IgG3 levels and increased expression of the three genes coding for FcγRI (CD64), an activating receptor [5]

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Summary

INTRODUCTION

Anaphylaxis is an acute, life-threatening, systemic reaction caused by the mediators released from different cells [1]. When the signal is sufficiently powerful, mast cell and basophil activation make progress, releasing mediators [11] Those mediators lead to the amplification of the allergic reaction through the recruitment and activation of other cells involved in the IgE immunological response [12,13,14]. Muñoz-Cano et al [5] studied patients with anaphylaxis induced by lipid transfer proteins (LTP) and mediated by IgE They found an increase of specific anti-LTP IgG1 and IgG3 levels and increased expression of the three genes coding for FcγRI (CD64), an activating receptor [5]. Neutrophils, activated through FcγRIV-IgG2, are proposed to play a major role in a mouse model of anaphylaxis [7] They are important PAF producers, and a differential PAF release has been observed in neutrophil-dependent reactions in mice [7, 25]. In the LTP particular case, anaphylaxis may be elicited via IgE, IgG, or both, with the involvement of neutrophils and of mast cells and basophils, other allergens may act

Complement Activation in Anaphylaxis
Contact System Activation in Anaphylaxis
COFACTORS AND AUGMENTING FACTORS IN ANAPHYLAXIS
Findings
CONCLUSION
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