2015
DOI: 10.1016/j.cyto.2015.03.019
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Long-term sublingual immunotherapy for Japanese cedar pollinosis and the levels of IL-17A and complement components 3a and 5a

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Cited by 9 publications
(7 citation statements)
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“…The results of our study revealed that the serum IL-17 levels decreased after 6 months of cluster immunotherapy compared with levels measured before immunotherapy and compared with levels taken from those who did not receive immunotherapy ( Table 4 ). This result agreed with Ding et al , 30 who showed that the mechanism of action of sublingual immunotherapy (SLIT) for the treatment of AR and asthma may be associated with inhibition of IL-17 expression and also agreed with Sakashita et al , 31 who showed that long-term SLIT reduced the serum levels of IL-17. So, the serum level of IL-17A might prove useful as a biologic parameter to ascertain the effectiveness of SLIT.…”
Section: Discussionsupporting
confidence: 91%
“…The results of our study revealed that the serum IL-17 levels decreased after 6 months of cluster immunotherapy compared with levels measured before immunotherapy and compared with levels taken from those who did not receive immunotherapy ( Table 4 ). This result agreed with Ding et al , 30 who showed that the mechanism of action of sublingual immunotherapy (SLIT) for the treatment of AR and asthma may be associated with inhibition of IL-17 expression and also agreed with Sakashita et al , 31 who showed that long-term SLIT reduced the serum levels of IL-17. So, the serum level of IL-17A might prove useful as a biologic parameter to ascertain the effectiveness of SLIT.…”
Section: Discussionsupporting
confidence: 91%
“…Furthermore, no clear relationship between serum cytokines and clinical outcome of AIT has been demonstrated. Besides addressing interleukins, numerous studies during AIT investigated chemokines CCR3 (unchanged) and CCR4 (increased) and other original serum markers, like adiponectin (unchanged), apolipoprotein A‐IV (increased), beta thromboglobulin (unchanged), complement factors C3a and 5a (decreased), C4a (increased), ECP (unchanged), eotaxin (increased/decreased), soluble HLA molecules (unchanged), leptin (unchanged or increased), signalling lymphocytic activation molecule (increased), thymus and activation‐regulated chemokine (TARC) (increased), TRAIL (reduced), transthyretin (increased) to tryptase (unchanged). Importantly, none of these markers showed any correlation with the clinical response.…”
Section: Resultsmentioning
confidence: 99%
“…It is therefore possible that the JCPspecific IgE level might decrease if the trial period were extended. Serum IL-17A, SCCA2, periostin, saliva, and pathogenic Th2 cells have been reported as potentially useful clinical biomarkers for evaluating the efficacy of SLIT for JCP [17][18][19]. Periostin is highly expressed in chronic inflammatory diseases like asthma, chronic rhinosinusitis, atopic dermatitis, and allergic conjunctivitis [20], and has emerged as a useful biomarker of allergic diseases.…”
Section: Discussionmentioning
confidence: 99%