Targeting Immune Cells.

IF 2 4区 医学 Q3 RESPIRATORY SYSTEM Journal of Aerosol Medicine and Pulmonary Drug Delivery Pub Date : 2024-12-01 DOI:10.1089/jamp.2024.63954.es
Emilie Seydoux, Kleanthis Fytianos, Christophe von Garnier, Barbara Rothen-Rutishauser, Fabian Blank
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Abstract

The respiratory tract with its vast surface area and very thin air-blood tissue barrier presents an extremely large interface for potential interaction with xenobiotics such as inhaled pathogens or medicaments. To protect its large and vulnerable surface, the lung is populated with several different types of immune cells. Pulmonary epithelial cells, macrophages and dendritic cells are key players in shaping the innate and adaptive immune response. Due to their localization, they represent a frontline of cell populations that are among the first to come in contact with inhaled xenobiotics. Furthermore, depending on the lung compartment they populate, these cells show a large variety in morphology, phenotype, and function. These unique characteristics make those cell populations ideal targets for specific immunomodulators that are designed for inhalation. Depending on cell population or lung compartment targeting, a specific immune response may be triggered or modulated. The purpose of a potent carrier for pulmonary immunomodulation is, first, to efficiently target a specific immunocompetent cell and, second, to affect its role in generating an immune response. Immunomodulation may occur at different levels of immune cell-antigen interaction, i.e. antigen uptake, trafficking, processing and presentation. Inhalation of nanosized carriers for drugs or vaccines shows great potential for both prophylactic and therapeutic approaches in order to modulate immune responses locally or systemically, due to the specific deposition and targeting properties of nanoparticles. Immune responses triggered by nanosized particles may be either immunostimulatory or immunosuppressive and depending on the specific purpose, stimulation or suppression may either be desired or unwanted. Meticulous analysis of immunomodulatory potential, pharmacologic and toxicologic testing of inhalable nanocarriers is required in order to find novel and optimal approaches for prophylaxis and therapy of pulmonary diseases. The design and characterization of such nanoparticles requires well-coordinated interdisciplinary research among engineers, biologists and clinicians.

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靶向免疫细胞。
呼吸道具有巨大的表面积和非常薄的空气-血液组织屏障,为吸入病原体或药物等外源性药物提供了一个非常大的潜在相互作用界面。为了保护其大而脆弱的表面,肺中充满了几种不同类型的免疫细胞。肺上皮细胞、巨噬细胞和树突状细胞是形成先天和适应性免疫反应的关键细胞。由于它们的定位,它们代表了第一批与吸入的外源药物接触的细胞群的前线。此外,根据它们所分布的肺间室,这些细胞在形态、表型和功能上表现出很大的变化。这些独特的特性使这些细胞群成为吸入特定免疫调节剂的理想目标。根据细胞群或肺隔室靶向,可以触发或调节特定的免疫反应。一种有效的肺免疫调节载体的目的是,首先,有效地靶向特定的免疫能力细胞,其次,影响其在产生免疫应答中的作用。免疫调节可能发生在免疫细胞-抗原相互作用的不同水平,即抗原摄取、运输、加工和呈递。由于纳米颗粒的特定沉积和靶向特性,吸入纳米级药物或疫苗载体在预防和治疗方面都显示出巨大的潜力,从而可以局部或全身调节免疫反应。纳米颗粒引发的免疫反应可能是免疫刺激或免疫抑制,根据具体目的,刺激或抑制可能是需要的或不需要的。为了找到预防和治疗肺部疾病的新颖和最佳方法,需要对可吸入纳米载体的免疫调节潜力、药理学和毒理学测试进行细致的分析。这种纳米粒子的设计和表征需要工程师、生物学家和临床医生之间良好协调的跨学科研究。
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来源期刊
CiteScore
6.70
自引率
2.90%
发文量
34
审稿时长
>12 weeks
期刊介绍: Journal of Aerosol Medicine and Pulmonary Drug Delivery is the only peer-reviewed journal delivering innovative, authoritative coverage of the health effects of inhaled aerosols and delivery of drugs through the pulmonary system. The Journal is a forum for leading experts, addressing novel topics such as aerosolized chemotherapy, aerosolized vaccines, methods to determine toxicities, and delivery of aerosolized drugs in the intubated patient. Journal of Aerosol Medicine and Pulmonary Drug Delivery coverage includes: Pulmonary drug delivery Airway reactivity and asthma treatment Inhalation of particles and gases in the respiratory tract Toxic effects of inhaled agents Aerosols as tools for studying basic physiologic phenomena.
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