Atopy and Response to Omalizumab Treatment in Chronic Spontaneous Urticaria

被引:3
作者
Costa, Celia [1 ,2 ]
Caldeira, Leonor Esteves [1 ]
Paulino, Marisa [1 ]
Santos, Diana F. [3 ]
Silva, Susana L. [1 ,2 ]
机构
[1] Ctr Hosp Univ Lisboa Norte, Hosp Santa Maria, Serv Imunoalergol, Lisbon, Portugal
[2] Ctr Acad Med Lisboa, Clin Univ Imunoalergol, Fac Med Lisboa, Lisbon, Portugal
[3] Univ Lisbon, Fac Med, Inst Med Mol Joao Lobo Antunes, Lisbon, Portugal
关键词
Atopy; Chronic spontaneous urticaria; Omalizumab response; Sensitization patterns; UCARE; MECHANICAL CHARACTERIZATION; AEROALLERGEN SENSITIZATION; CHILDREN; TISSUE; IGE;
D O I
10.1159/000535414
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Introduction: The possible influence of sensitization to aeroallergens on omalizumab response in chronic spontaneous urticaria (CSU) has been insufficiently investigated. This study's aim was to investigate atopy's influence on omalizumab response in CSU patients. Method: Retrospective study of CSU patients followed at a Portuguese Urticaria Center of Reference and Excellence (UCARE), treated with omalizumab for at least 6 months, between 2015 and 2022. At T0, all patients underwent quantification of specific immunoglobulin E (IgE) for total extract of most prevalent aeroallergens (ImmunoCAP Thermo Fisher Scientific (R)) and were divided in 2 groups, according to their response to omalizumab during the first 16 weeks of treatment: responders (R) (UAS7 <7) versus partial (PR) (UAS7 = 7-15) and nonresponders (UAS7 >15). R were further classified as fast (FR) (4-6 weeks) and slow responders (SR) (12-16 weeks). Total serum IgE, circulating eosinophil, and basophil counts were compared between groups at T0. p < 0.05 was considered statistically significant (SPSS (R) v25.0). Results: Ninety-six patients (80% female) were studied, mean age 49 +/- 14 years. Median CSU duration pre-omalizumab was 3 (0.6-20) years and mean omalizumab treatment duration was 3.7 +/- 2.3 years. 38 (40%) had concomitant chronic inducible urticaria and 72 (75%) angioedema. Based on positive results of the specific IgE assay, 35 patients (36%) were considered atopic. Most patients (n = 30; 86%) were sensitized to house dust mites (HDM) (Dermatophagoides farinae = 28, Dermatophagoides pteronyssinus = 27, Blomia tropicalis = 19, Lepidoglyphus destructor = 17), followed by pollens (n = 12; 34%) (mixture of grasses = 10, Olea europaea = 7, Parietaria officinalis = 6), epithelia (n = 9; 26%) (dog = 8, cat = 7), and fungi (Alternaria alternata = 4; 11%). Eight patients (23%) were monosensitized to HDM and 4 (11%) to pollens. No significant association was found between aeroallergen sensitization and CSU duration, concomitant chronic inducible urticaria, or angioedema. Atopic patients featured significantly higher levels of baseline total serum IgE than nonatopic (469 vs. 94 U/mL, respectively; p = 0.0009). Mean baseline counts of eosinophils and basophils were not significantly different between atopic and non-atopic, respectively: eosinophils (128 vs. 121/mm(3)) and basophils (26 vs. 28/mm(3)). Regarding response to omalizumab, most patients (58; 60%) were responders: FR - 46 (79%); SR - 12 (21%). There was no significant association between aeroallergen sensitization and omalizumab response or speed of response. Conclusions: As far as we know, this is the first study exploring the influence of atopy sensitization pattern on omalizumab response in CSU. According to our results, presence of atopy/sensitization pattern does not influence omalizumab response in CSU patients.
引用
收藏
页码:260 / 266
页数:7
相关论文
共 43 条
[1]   The role of eosinophils in chronic spontaneous urticaria [J].
Altrichter, Sabine ;
Frischbutter, Stefan ;
Fok, Jie Shen ;
Kolkhir, Pavel ;
Jiao, Qingqing ;
Skov, Per Stahl ;
Metz, Martin ;
Church, Martin K. ;
Maurer, Marcus .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2020, 145 (06) :1510-1516
[2]   Therapeutic Strategy According to Differences in Response to Omalizumab in Patients With Chronic Spontaneous Urticaria [J].
Arnau A M, Gimenez ;
Santiago A, Valero ;
Tomas J, Bartra ;
Presa I, Jauregui ;
Labrador-Horrillo, M. ;
Miquel F J, Miquel ;
de Frutos J, Ortiz ;
Sastre, J. ;
Salvador J F, Silvestre ;
Puga M, Ferrer .
JOURNAL OF INVESTIGATIONAL ALLERGOLOGY AND CLINICAL IMMUNOLOGY, 2019, 29 (05) :338-348
[3]   Tissue mechanics regulate brain development, homeostasis and disease [J].
Barnes, J. Matthew ;
Przybyla, Laralynne ;
Weaver, Valerie M. .
JOURNAL OF CELL SCIENCE, 2017, 130 (01) :71-82
[4]  
Bernardino A., 2023, J ALLERGY CLIN IMMUN
[5]   Malformations of cortical development and epilepsies: neuropathological findings with emphasis on focal cortical dysplasia [J].
Bluemcke, Ingmar ;
Vinters, Harry V. ;
Armstrong, Dawna ;
Aronica, Eleonora ;
Thom, Maria ;
Spreafico, Roberto .
EPILEPTIC DISORDERS, 2009, 11 (03) :181-193
[6]   Stochastic nanoroughness modulates neuron-astrocyte interactions and function via mechanosensing cation channels [J].
Blumenthal, Nils R. ;
Hermanson, Ola ;
Heimrich, Bernd ;
Shastri, V. Prasad .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2014, 111 (45) :16124-16129
[7]   Anti-TPO IgG/Total IgE Ratio: Biomarker for Omalizumab Response Prediction in Chronic Spontaneous Urticaria [J].
Bras, Rita ;
Caldeira, Leonor Esteves ;
Bernardino, Ana ;
Costa, Celia .
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 2023, 184 (09) :866-869
[8]   Omalizumab in Chronic Spontaneous Urticaria (CSU): Real-Life Experience in Dose/Interval Adjustments and Treatment Discontinuation [J].
Bras, Rita ;
Costa, Celia ;
Limao, Rita ;
Caldeira, Leonor Esteves ;
Paulino, Marisa ;
Pedro, Elisa .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE, 2023, 11 (08) :2392-2402
[9]   Rheological characterization of human brain tissue [J].
Budday, S. ;
Sommer, G. ;
Haybaeck, J. ;
Steinmann, P. ;
Holzapfel, G. A. ;
Kuhl, E. .
ACTA BIOMATERIALIA, 2017, 60 :315-329
[10]   Mechanical characterization of human brain tissue [J].
Budday, S. ;
Sommer, G. ;
Birkl, C. ;
Langkammer, C. ;
Haybaeck, J. ;
Kohnert, J. ;
Bauer, M. ;
Paulsen, F. ;
Steinmann, P. ;
Kuhl, E. ;
Holzapfel, G. A. .
ACTA BIOMATERIALIA, 2017, 48 :319-340