Tree pollen allergens

2020 ◽  
pp. 141-154
Author(s):  
Rosa Codina ◽  
Fernando Pineda ◽  
Ricardo Palacios
Keyword(s):  
2014 ◽  
pp. 113-132
Author(s):  
Katharina Marth ◽  
Tetiana Garmatiuk ◽  
Ines Swoboda ◽  
Rudolf Valenta
Keyword(s):  

1999 ◽  
Vol 113 (5) ◽  
pp. 830-837 ◽  
Author(s):  
Susanne Heiss ◽  
Rudolf Valenta ◽  
Vera Mahler ◽  
Renate Steiner ◽  
Susanne Spitzauer ◽  
...  

2020 ◽  
Vol 145 (2) ◽  
pp. AB72
Author(s):  
Laura Victorio Puche ◽  
Maria Somoza Alvarez ◽  
Jose Damian Lopez Sanchez ◽  
Maria Garrido-Arandia ◽  
Laura Martín-Pedraza ◽  
...  

1991 ◽  
Vol 28 (8) ◽  
pp. 897-906 ◽  
Author(s):  
Madeleine Rohac ◽  
Thomas Birkner ◽  
Ingrid Reimitzer ◽  
Barbara Bohle ◽  
Renate Steiner ◽  
...  

2004 ◽  
Vol 4 (5) ◽  
pp. 384-390 ◽  
Author(s):  
Nadine Mothes ◽  
Rudolf Valenta
Keyword(s):  

2014 ◽  
Vol 2014 ◽  
pp. 1-5 ◽  
Author(s):  
Andrzej Bozek ◽  
Krzysztof Kolodziejczyk ◽  
Jerzy Jarzab

Background. Specific immunotherapy (SIT) with an ultrarush administration schedule with Purethal for tree pollen allergens has been evaluated to assess its efficacy and safety.Methods. The study group consisted of 22 patients with symptoms of allergic rhinitis and confirmed allergy to tree pollens. Patients were randomized and given an administration schedule of either ultrarush therapy or conventional preseasonal SIT. Treatment was performed during three consecutive years.Results. After three years of treatment, a similar reduction in nasal symptoms was observed; according to the visual analog scale, there was a decrease from 3.991 ± 0.804 points to 1.634 ± 0.540 in the ultrarush group and from 3.845 ± 0.265 to 1.501 ± 0.418 in the group desensitized using the conventional method (P>0.05). There was also a comparable reduction in the use of relief drugs during pollen season and an increase in the serum concentration of IgG4 to tree pollens. No significant differences in the safety profile were observed.Conclusion. An administration schedule of ultrarush SIT with Purethal Trees is a safe treatment in preliminary observations. This therapy is comparable with conventional administration of SIT in the field of efficacy and safety.


1986 ◽  
Vol 80 (1) ◽  
pp. 26-32 ◽  
Author(s):  
E. Florvaag ◽  
S. Elsayed ◽  
A.S.E. Hammer

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