Department of Physiology and Pharmacology, Karolinska Institutet, Solna, Stockholm County, Sweden.
Centre for Neuroscience Studies, Queen's University, Kingston, Ontario, Canada.
Curr Opin Immunol. 2024 Dec;91:102507. doi: 10.1016/j.coi.2024.102507. Epub 2024 Nov 22.
The immune and nervous systems have co-evolved complex mechanisms to sense environmental dangers and orchestrate a concerted response to safeguard tissue and mobilize host defenses. This sophisticated interplay, marked by a shared repertoire of receptors and ligands, influences disease pathogenesis. Neuro-immune interactions in allergic diseases are pivotal for symptom development, from anaphylaxis to chronic conditions like asthma and atopic dermatitis. This review explores the neuro-immune interplay within the atopic march, emphasizing its role in host defense, inflammation resolution, and tissue repair. We delve into the multifaceted functions of nociceptors in orchestrating type 2 immune responses and the progression of allergic disorders, focusing on key regulators such as CGRP-RAMP1 and SP-MRGPRB2/A2. Additionally, we discuss the potential of nociceptor neuron-blocking drugs to target neuro-immunity, offering the possibility of reversing the progression of the atopic march. Altogether, we underscore the need for targeted interventions to disrupt the pathological processes and enhance therapeutic outcomes at various stages of the atopic march.
免疫系统和神经系统共同进化出复杂的机制来感知环境危险,并协调一致的反应来保护组织和动员宿主防御。这种复杂的相互作用,以共同的受体和配体库为标志,影响疾病的发病机制。神经免疫相互作用在过敏性疾病中对症状的发展至关重要,从过敏反应到哮喘和特应性皮炎等慢性疾病。本综述探讨了特应性进展过程中的神经免疫相互作用,强调了它在宿主防御、炎症消退和组织修复中的作用。我们深入研究了伤害感受器在协调 2 型免疫反应和过敏性疾病进展中的多方面功能,重点关注 CGRP-RAMP1 和 SP-MRGPRB2/A2 等关键调节因子。此外,我们还讨论了伤害感受器神经元阻断药物靶向神经免疫的潜力,为逆转特应性进展提供了可能。总之,我们强调需要有针对性的干预措施来破坏病理过程,并在特应性进展的各个阶段提高治疗效果。