Levels of natural antibodies to endotoxin in bronchial asthma patients undergoing allergen specific immunotherapy (SIT)

2003 ◽  
Vol 111 (2) ◽  
pp. S71 ◽  
Author(s):  
V.A. Beloglazov ◽  
A.I. Gordienko ◽  
A.A. Bakova ◽  
L.N. Znamenskaya ◽  
A.V. Rozovenko ◽  
...  
2008 ◽  
Vol 121 (2) ◽  
pp. S75-S75
Author(s):  
V BELOGLAZOV ◽  
L ZNAMENSKAYA ◽  
K BYELOGLAZOVA ◽  
A GORDIENKO ◽  
I DUBUSKE ◽  
...  

2004 ◽  
Vol 93 (1) ◽  
pp. 68-75 ◽  
Author(s):  
Krzysztof Kowal ◽  
Joanna Osada ◽  
Sebastian Zukowski ◽  
Milena Dabrowska ◽  
Lawrence DuBuske ◽  
...  

2021 ◽  
Vol 19 (3) ◽  
pp. 156-165
Author(s):  
Nazan TÖKMECI ◽  
Ali DEMIRHAN ◽  
Merve TURKEGUN SENGUL ◽  
Burcu CAGLAR YUKSEK ◽  
Aylin KONT ÖZHAN ◽  
...  

Objective: Allergen-specific immunotherapy (allergen-SIT) is a treatment method with variable efficacy in allergic diseases. This study aimed to investigate the effectiveness of allergen immunotherapy, frequency of LRs and SRs and variables affecting these parameters in patients who underwent allergen-SIT. Materials and Methods: In this study, the recorded data of 81 patients, who received subcutaneous (SCIT) or sublingual (SLIT) allergen immunotherapy for respiratory allergic diseases between 2014 and 2019, were analyzed. In asthma and/or allergic rhinoconjunctivitis (ARC) patients, the effectiveness of treatment was evaluated by analysing the change rates in disease symptom, medication and combined scores (symptom + medication) and visual analog score (VAS). Treatment success was defined by the degree of decrease in scores as; high response above 50%; low response between 20-50%; and failure <20%.Results: The mean age of allergen-SIT initiation was 11.4± 3.1 years. Diagnostic distributions of the patients were asthma (± ARC) in 64.2%, and ARC (without asthma) in 35.8%. The mode of allergen-SIT was SCIT in 77.8% (65% asthma and 35% ARC) and SLIT in 22.2% (61.1% asthma and 38.9% ARC). The main allergens used in allergen-SIT were mite (79%), grass-grain pollen (33.3%), alternaria (9.9%) and olea (8.6%). There was a significant decrease in symptoms, medication, combined and VAS scores in the asthma and ARC groups (p <0.0001), when end-SCIT values were compared to baseline. SLIT also resulted in significant decreases in these scores except asthma medication score. Among the asthma patients the rate of high-responders was 88.8% by SCIT and 50% by SLIT, according to combined asthma score. Among the ARC (without asthma) patients the rate of high-responders was 100% for both SCIT and SLIT. SCIT resulted in local (LR) and systemic side effects (SR) in 18% and 0.6% (all Grade I and Grade II) of the total injections performed. A high number of total injections was significantly associated with higher LR and SR rates. While LR was observed in 16.6% of the patients who underwent SLIT, no systemic reaction was found in any of the patients. Conclusion: SCIT was highly successful in the treatment of asthma and ARC in terms of the degree of therapeutic response. SLIT resulted in a high rate of good response in ARC patients, but a lower response degree in asthmatic patients. Systemic side effects were very low as a result of close risk monitoring and the dose adjustments performed. Keywords: Allergen-specific immunotherapy, SCIT, SLIT, efficacy, symptom score, medication score, visual analog score, side effects


2021 ◽  
Vol 19 (2) ◽  
pp. 202-206
Author(s):  
A. V. Sidarenka ◽  
◽  
L. R. Vykhristsenka ◽  

Background. Allergen-specific immunotherapy (ASIT) affects the immune response and the clinical course of bronchial asthma (BA). Objective. To evaluate the clinical efficacy of sublingual-oral low-dose ASIT in asthma based on the results of 5-year follow-up. Material and Methods. ASIT was carried out with a mixture of household allergens in 51 patients aged 18-60 years old. The patient's opinion, the number and severity of BA exacerbations, the duration of post-immunotherapeutic remission and the factors influencing it, adherence to treatment, and the safety of treatment were taken into account. Results. The effectiveness of ASIT according to the patient’s opinion: 45.1% - excellent, 49% - good result. In allergic asthma, remission after ASIT was significantly higher than in mixed asthma. Full adherence to treatment (3 courses of ASIT) - in 76.5% (39/51) of patients. There were no adverse reactions during the entire observation period. The mixed BA phenotype, contact with the allergen in everyday life, and smoking had a negative effect. Positive - high compliance to therapy. Conclusions. Sublingual-oral ASIT is an effective and safe method of treating allergic and mixed asthma. The duration of post-immunotherapeutic remission of BA for 3 years was observed after 3 courses of ASIT.


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