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New Insights into Anti-allergic, Anti-asthmatic Materials

A special issue of Molecules (ISSN 1420-3049). This special issue belongs to the section "Natural Products Chemistry".

Deadline for manuscript submissions: closed (31 January 2024) | Viewed by 8649

Special Issue Editor


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Guest Editor
Department of Herbology, College of Korean Medicine, Sangji University, 83 Sangjidae-gil, Wonju, Gangwon-do 26339, Republic of Korea
Interests: allergy; asthma; airway inflammation; natural product; chemokines; immune cells
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

Bioactive natural products (plant, animal, and insect extracts) and their active ingredients can play an important role in anti-inflammatory responses by inhibiting inflammatory mediators and are used as a medicine for the treatment of inflammatory diseases, such as allergic diseases and airway inflammation including asthma, allergic dermatitis, COPD, etc. In allergic diseases and airway inflammation, recruitment of inflammatory cells such as T cells, mast cells, eosinophils, and neutrophils is mediated via a number of chemokines and their receptors. They also play a role in activation and differentiation of inflammatory cells by selectively activating Th1 or Th2 cells or by effects on epithelial or endothelial cells. Chemokines and their receptors are crucial therapeutic targets in allergic diseases and COPD because of their central role in immune cell recruitment and activation during inflammation.

This Special Issue on “New Insights into Anti-Allergic, Anti-Asthmatic Materials” welcomes original research and reviews on: (1) characterization of active ingredients of medicinal plants, animals, insects, etc.; (2) the therapeutic effects and mechanisms of natural products on allergic diseases such as allergic asthma, allergic dermatitis and COPD (chronic obstructive pulmonary disease); (3) the multi-ingredient synergistic effects and therapeutic mechanisms of natural products, their active ingredients, their combinations on allergic diseases, etc.; (4) identification of targets and mechanisms of activity of anti-allergic and anti-asthmatic materials; and (5) critical reviews of the historical, preclinical, and clinical research on natural products, and their active ingredients on allergic diseases and COPD.

Prof. Dr. Young Cheol Lee
Guest Editor

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Keywords

  • Anti-allergic materials
  • Anti-asthmatic materials
  • Chemokines
  • Chemokine receptors
  • Cytokines
  • Immune cells
  • Airway inflammation
  • COPD
  • Natural product
  • Insect

Published Papers (3 papers)

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Research

14 pages, 3930 KiB  
Article
The Immuno-Modulatory Activities of Pentaherbs Formula on Ovalbumin-Induced Allergic Rhinitis Mice via the Activation of Th1 and Treg Cells and Inhibition of Th2 and Th17 Cells
by Peiting Li, Miranda Sin-Man Tsang, Lea Ling-Yu Kan, Tianheng Hou, Sharon Sze-Man Hon, Ben Chung-Lap Chan, Ida Miu-Ting Chu, Christopher Wai-Kei Lam, Ping-Chung Leung and Chun-Kwok Wong
Molecules 2022, 27(1), 239; https://0-doi-org.brum.beds.ac.uk/10.3390/molecules27010239 - 31 Dec 2021
Cited by 9 | Viewed by 3122
Abstract
Allergic rhinitis (AR) is a highly prevalent allergic disease induced by immunoglobulin (Ig) E-mediated hypersensitivity reaction at the nasal epithelium against inhaled allergens. Previous studies have demonstrated that Pentaherbs formula (PHF), a modified herbal formula comprising five herbal medicines (Flos Lonicerae, [...] Read more.
Allergic rhinitis (AR) is a highly prevalent allergic disease induced by immunoglobulin (Ig) E-mediated hypersensitivity reaction at the nasal epithelium against inhaled allergens. Previous studies have demonstrated that Pentaherbs formula (PHF), a modified herbal formula comprising five herbal medicines (Flos Lonicerae, Herba Menthae, Cortex Phellodendri, Cortex Moutan and Rhizoma Atractylodis), could suppress various immune effector cells to exert anti-inflammatory and anti-allergic effects in allergic asthma and atopic dermatitis. The present study aimed to further determine the anti-inflammatory activities of PHF in an ovalbumin (OVA)-induced AR BALB/c mouse model. Nasal symptoms such as sneezing and nose rubbing were recorded and the serum total IgE and OVA-specific IgG1, as well as interleukin (IL)-4, IL-5, IL-10, IL-13, chemokines CXCL9 CXCL10, and tumor necrosis factor (TNF)-α concentrations in nasal lavage fluid (NALF) were measured during different treatments. Effects of PHF on the expression of inflammatory mediators in the sinonasal mucosa were quantified using real-time QPCR. PHF was found to suppress allergic symptoms, infiltration of inflammatory cells, and hyperplasia of goblet cells in the nasal epithelium of the OVA-induced AR mice. PHF could reduce OVA-specific IgG1 level in serum, and TNF-α and IL-10 in nasal lavage fluid (NALF), significantly up-regulate the splenic regulatory T (Treg) cell level, increase the Type 1 helper T cell (Th1)/Type 2 helper T cell (Th2) ratio, and reduce the Th17 cells (all p < 0.05). PHF could also alleviate in situ inflammation in sinonasal mucosa of OVA-induced AR mice. In conclusion, oral treatment of PHF showed immuno-modulatory activities in the OVA-induced AR mice by regulating the splenic T cell population to suppress the nasal allergy symptoms and modulating inflammatory mediators, implicating that PHF could be a therapeutic strategy for allergic rhinitis. Full article
(This article belongs to the Special Issue New Insights into Anti-allergic, Anti-asthmatic Materials)
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18 pages, 2383 KiB  
Article
Blockade of NF-κB Translocation and of RANKL/RANK Interaction Decreases the Frequency of Th2 and Th17 Cells Capable of IL-4 and IL-17 Production, Respectively, in a Mouse Model of Allergic Asthma
by Izabela Gregorczyk, Agnieszka Jasiecka-Mikołajczyk and Tomasz Maślanka
Molecules 2021, 26(11), 3117; https://0-doi-org.brum.beds.ac.uk/10.3390/molecules26113117 - 23 May 2021
Cited by 11 | Viewed by 2216
Abstract
The main purpose of this study was to investigate whether the blockade of the interaction between the receptor activator of nuclear factor-κB (NF-ĸB) ligand (RANKL) and its receptor RANK as well as the blockade of NF-κB inhibitor kinase (IKK) and of NF-κB translocation [...] Read more.
The main purpose of this study was to investigate whether the blockade of the interaction between the receptor activator of nuclear factor-κB (NF-ĸB) ligand (RANKL) and its receptor RANK as well as the blockade of NF-κB inhibitor kinase (IKK) and of NF-κB translocation have the potential to suppress the pathogenesis of allergic asthma by inhibition and/or enhancement of the production by CD4+ and CD8+ T cells of important cytokines promoting (i.e., IL-4 and IL-17) and/or inhibiting (i.e., IL-10 and TGF-β), respectively, the development of allergic asthma. Studies using ovalbumin(OVA)-immunized mice have demonstrated that all the tested therapeutic strategies prevented the OVA-induced increase in the absolute number of IL-4- and IL-17-producing CD4+ T cells (i.e., Th2 and Th17 cells, respectively) indirectly, i.e., through the inhibition of the clonal expansion of these cells in the mediastinal lymph nodes. Additionally, the blockade of NF-κB translocation and RANKL/RANK interaction, but not IKK, prevented the OVA-induced increase in the percentage of IL-4-, IL-10- and IL-17-producing CD4+ T cells. These latter results strongly suggest that both therapeutic strategies can directly decrease IL-4 and IL-17 production by Th2 and Th17 cells, respectively. This action may constitute an important mechanism underlying the anti-asthmatic effect induced by the blockade of NF-κB translocation and of RANKL/RANK interaction. Thus, in this context, both these therapeutic strategies seem to have an advantage over the blockade of IKK. None of the tested therapeutic strategies increased both the absolute number and frequency of IL-10- and TGF-β-producing Treg cells, and hence they lacked the potential to inhibit the development of the disease via this mechanism. Full article
(This article belongs to the Special Issue New Insights into Anti-allergic, Anti-asthmatic Materials)
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23 pages, 13741 KiB  
Article
Cryptotympana pustulata Extract and Its Main Active Component, Oleic Acid, Inhibit Ovalbumin-Induced Allergic Airway Inflammation through Inhibition of Th2/GATA-3 and Interleukin-17/RORγt Signaling Pathways in Asthmatic Mice
by Seung-Hyung Kim, Jung-Hee Hong, Won-Kyung Yang, Hyo-Jung Kim, Hyo-Jin An and Young-Cheol Lee
Molecules 2021, 26(7), 1854; https://0-doi-org.brum.beds.ac.uk/10.3390/molecules26071854 - 25 Mar 2021
Cited by 13 | Viewed by 2582
Abstract
Cicadae Periostracum (CP), derived from the slough of Cryptotympana pustulata, has been used as traditional medicine in Korea and China because of its diaphoretic, antipyretic, anti-inflammatory, antioxidant, and antianaphylactic activities. The major bioactive compounds include oleic acid (OA), palmitic acid, and linoleic [...] Read more.
Cicadae Periostracum (CP), derived from the slough of Cryptotympana pustulata, has been used as traditional medicine in Korea and China because of its diaphoretic, antipyretic, anti-inflammatory, antioxidant, and antianaphylactic activities. The major bioactive compounds include oleic acid (OA), palmitic acid, and linoleic acid. However, the precise therapeutic mechanisms underlying its action in asthma remain unclear. The objective of this study was to determine the antiasthmatic effects of CP in an ovalbumin (OVA)-induced asthmatic mouse model. CP and OA inhibited the inflammatory cell infiltration, airway hyperresponsiveness (AHR), and production of interleukin (IL)7 and Th2 cytokines (IL-5) in the bronchoalveolar lavage fluid and OVA-specific imunoglobin E (IgE) in the serum. The gene expression of IL-5, IL-13, CCR3, MUC5AC, and COX-2 was attenuated in lung tissues. CP and OA might inhibit the nuclear translocation of GATA-binding protein 3 (GATA-3) and retinoic acid receptor-related orphan receptor γt (RORγt) via the upregulation of forkhead box p3 (Foxp3), thereby preventing the activation of GATA-3 and RORγt. In the in vitro experiment, a similar result was observed for Th2 and GATA-3. These results suggest that CP has the potential for the treatment of asthma via the inhibition of the GATA-3/Th2 and IL-17/RORγt signaling pathways. Full article
(This article belongs to the Special Issue New Insights into Anti-allergic, Anti-asthmatic Materials)
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