Clinical and experimental treatment of allergic asthma with an emphasis on allergen immunotherapy and its mechanisms

被引:3
|
作者
Fiala, Scott [1 ]
Fleit, Howard B. [1 ]
机构
[1] SUNY Stony Brook, Dept Pathol, Renaissance Sch Med, Stony Brook, NY 11794 USA
来源
CLINICAL AND EXPERIMENTAL IMMUNOLOGY | 2023年 / 212卷 / 01期
关键词
allergic asthma; allergen immunotherapy (AIT); regulatory T (Treg) cell; subcutaneous allergen immunotherapy (SCIT); sublingual allergen immunotherapy (SLIT); HOUSE-DUST MITE; SUBLINGUAL IMMUNOTHERAPY; SUBCUTANEOUS IMMUNOTHERAPY; IMMUNOLOGICAL MECHANISMS; COMPARATIVE EFFICACY; UNITED-STATES; RHINITIS; COMBINATION; ANAPHYLAXIS; OMALIZUMAB;
D O I
10.1093/cei/uxad031
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Allergen immunotherapy (AIT) is currently the only form of treatment that modifies allergic asthma. Pharmacotherapy alone seeks to control the symptoms of allergic asthma, allergic rhinitis, and other atopic conditions. In contrast, AIT can induce long-term physiological modifications through the immune system. AIT enables individuals to live improved lives many years after treatment ends, where they are desensitized to the allergen(s) used or no longer have significant allergic reactions upon allergen provocation. The leading forms of treatment with AIT involve injections of allergen extracts with increasing doses via the subcutaneous route or drops/tablets via the sublingual route for several years. Since the initial attempts at this treatment as early as 1911 by Leonard Noon, the mechanisms by which AIT operates remain unclear. This literature-based review provides the primary care practitioner with a current understanding of the mechanisms of AIT, including its treatment safety, protocols, and long-term efficacy. The primary mechanisms underlying AIT include changes in immunoglobulin classes (IgA, IgE, and IgG), immunosuppressive regulatory T-cell induction, helper T cell type 2 to helper T cell type 1 cell/cytokine profile shifts, decreased early-phase reaction activity and mediators, and increased production of IL-10, IL-35, TGF-beta, and IFN-gamma. Using the databases PubMed and Embase, a selective literature search was conducted searching for English, full-text, reviews published between 2015 and 2022 using the keywords (with wildcards) "allerg*," "immunotherap*," "mechanis*," and "asthma." Among the cited references, additional references were identified using a manual search. [GRAPHICS] .
引用
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页码:14 / 28
页数:15
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