Abstract:Immunotherapy with depigmented and glutaraldehyde-polymerized extract of Parietaria judaica pollen is safe and effective to treat patients with allergic rhinitis and clinical sensitivity to this pollen.
“…Larger studies are needed to make more definitive statements on safety. Similar favourable safety profiles were demonstrated for depigmented glutaraldehyde-polymerized allergen extracts in children and adults with allergic rhinoconjuncti-vitis and/or asthma due to HDMs and pollen [19,22,23,[36][37][38][39]. In two prospective, non-interventional studies including 175 and 766 patients who received a variety of different depigmented glutaraldehyde-polymerized allergen extracts, no grades-3 or -4 systemic reactions were reported [23,40].…”
SCIT with depigmented polymerized birch pollen extract significantly reduced symptom and medication scores when compared with the placebo, was well tolerated, and resulted in immunological changes comparable with those of native pollen extracts.
“…Larger studies are needed to make more definitive statements on safety. Similar favourable safety profiles were demonstrated for depigmented glutaraldehyde-polymerized allergen extracts in children and adults with allergic rhinoconjuncti-vitis and/or asthma due to HDMs and pollen [19,22,23,[36][37][38][39]. In two prospective, non-interventional studies including 175 and 766 patients who received a variety of different depigmented glutaraldehyde-polymerized allergen extracts, no grades-3 or -4 systemic reactions were reported [23,40].…”
SCIT with depigmented polymerized birch pollen extract significantly reduced symptom and medication scores when compared with the placebo, was well tolerated, and resulted in immunological changes comparable with those of native pollen extracts.
“…Although we did not compare the results in the different treatment arms with a pure placebo group, we were able to answer our original research question, which was to demonstrate the superiority of the combined treatment over SIT alone. Anyway, the superiority of these both treatment options over placebo has already been shown in previous reports [17–20, 31–33]. There are now several open‐label studies which have shown that SIT also lowers the onset of new sensitization and the progression from allergic rhinoconjunctivitis to bronchial asthma [34, 35].…”
Combination of omalizumab with SIT for treatment of patients with SAR and co-morbid SAA was safe and reduced the symptom load in a statistically significant and clinically meaningful manner.
“…Other possibilities, currently in use, include the modification of allergens with glutaraldehyde [22,23], which produces extracts with decreased IgE-binding capacity. Depigmented and polymerized allergen extracts have also been proven to be safe and clinically efficacious [6,[24][25][26][27][28][29][30], allowing for the administration of high doses in a short period of time. The safety of these vaccines has also been confirmed using a rush build-up phase in a large group of patients [31].…”
Specific immunotherapy using modified allergen vaccines is safe to treat allergic patients. The percentage of adverse reactions detected is lower than those reported in the literature with native-unmodified allergen extracts.
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