Local nasal immunotherapy for allergic rhinitis: A systematic review and meta-analysis

dc.contributor.authorKasemsuk N.
dc.contributor.authorNgaotepprutaram P.
dc.contributor.authorKanjanawasee D.
dc.contributor.authorSuwanwech T.
dc.contributor.authorDurham S.R.
dc.contributor.authorCanonica G.W.
dc.contributor.authorTantilipikorn P.
dc.contributor.otherMahidol University
dc.date.accessioned2023-06-18T17:39:24Z
dc.date.available2023-06-18T17:39:24Z
dc.date.issued2022-12-01
dc.description.abstractIntroduction: Local nasal immunotherapy (LNIT), an alternative noninjection immunotherapy method, is theoretically an efficient method for inducing immunotolerance directly in the affected organ. LNIT is more convenient and less invasive than injection immunotherapy, with fewer systemic reactions. The development of adjuvants to overcome LNIT's limitations raises the possibility of it being an alternative allergen immunotherapy. Objectives: To evaluate the clinical and immunological efficacy and safety of LNIT for patients with allergic rhinitis. Methods: A systematic search for randomized controlled trials comparing LNIT and placebo was performed using OVID Medline and Embase. Outcomes were total nasal symptom score (TNSS), symptom–medication score (SMS), medication score, immunological assessment, and nasal provocation threshold. Data were pooled for meta-analysis. Results: A total of 20 studies with 698 participants were included. The LNIT group had greater posttreatment improvement in TNSS, SMS, and medication score than control (TNSS: standardized mean difference [SMD], –1.37 [95% confidence interval [CI], –2.04 to –0.69]; SMS: SMD, –1.55 [95% CI, –2.83 to –0.28]; and medication score: SMD, –1.09 [95% CI, –1.35 to –0.83]). Immunological assessments showed no significant differences in serum-specific IgE (mean difference [MD], 6.35; 95% CI, –4.62 to 17.31), nasal IgE (MD, –0.59; 95% CI, –1.99 to 0.81), or nasal eosinophil cationic protein (MD, 7.63; 95% CI, –18.65 to 33.91). Only serum IgG significantly increased with LNIT (MD, 0.45; 95% CI, 0.20, 0.70). Posttreatment, nasal provocation threshold was higher with LNIT (MD, 27.30; 95% CI, 10.13–44.46). No significant adverse events were reported. Conclusions: LNIT is a safe alternative allergen immunotherapy route without significant adverse events. It improves clinical symptoms, reduces medication usage, and increases the nasal provocation threshold.
dc.identifier.citationInternational Forum of Allergy and Rhinology Vol.12 No.12 (2022) , 1503-1516
dc.identifier.doi10.1002/alr.23011
dc.identifier.eissn20426984
dc.identifier.issn20426976
dc.identifier.pmid35543418
dc.identifier.scopus2-s2.0-85130262365
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/85312
dc.rights.holderSCOPUS
dc.subjectMedicine
dc.titleLocal nasal immunotherapy for allergic rhinitis: A systematic review and meta-analysis
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85130262365&origin=inward
oaire.citation.endPage1516
oaire.citation.issue12
oaire.citation.startPage1503
oaire.citation.titleInternational Forum of Allergy and Rhinology
oaire.citation.volume12
oairecerif.author.affiliationSiriraj Hospital
oairecerif.author.affiliationHumanitas University
oairecerif.author.affiliationHumanitas Research Hospital
oairecerif.author.affiliationImperial College London
oairecerif.author.affiliationFaculty of Medicine Siriraj Hospital, Mahidol University

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