Long-term effects of omalizumab on peripheral blood cells and C-reactive protein levels in patients with chronic spontaneous urticaria

被引:12
作者
Akdogan, Neslihan [1 ]
Ogut, Neslihan Demirel [1 ]
Dogan, Sibel [1 ]
Atakan, Nilgun [1 ]
机构
[1] Hacettepe Univ, Sch Med, Dept Dermatol & Venereol, TR-06100 Ankara, Turkey
关键词
therapy-systemic; urticaria; CRP; EPIDEMIOLOGY; EFFICACY;
D O I
10.1111/dth.12966
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Omalizumab's mechanism of action is not well-understood yet despite its strong therapeutic efficacy in chronic spontaneous urticaria (CSU). To determine the overall effect of omalizumab on peripheral blood cell counts and serum C-reactive protein levels (sCRP) during a 1-year follow-up in patients with CSU. Data of 74 patients (male/female: 20/54) were reviewed from medical charts. Leucocyte counts, percentages of peripheral blood cells(lymphocyte, monocyte, neutrophil [PPBN], eosinophil, basophil [PPBB]) and sCRP were recorded at baseline, 3rd, 6th, 12th months of omalizumab treatment. Although a dramatic increase in the mean PPBB (+/- SD) was observed at the 3rd month, PPBB (%) gradually decreased after the 3rd month (PPBB: 0.38 +/- 0.21 [baseline] vs. 0.59 +/- 0.3 [3rd month], p = .002). However, 12th month PPBB remained higher than baseline (PPBB:0.38 +/- 0.21 [baseline] vs. 0.46 +/- 0.27 [12th month], p = .03). A dramatic decrease in the mean PPBN (%) was noticed within the first 3 months (PPBN:62.85 +/- 8.97 [baseline] vs. 58.37 +/- 9.07 [3rd month], p = .04), and 12th month PPBN remained lower than baseline values (PPBN: 62.85 +/- 8.97 [baseline] vs. 60.31 +/- 8.02 [12th month], p = .045).Mean sCRP (mg/dL) decreased rapidly within the first 3 months (sCRP: 1.09 +/- 1.53 [baseline] vs. 0.56 +/- 0.45 [3rd month], p = .17) and 12th month sCRP still remained lower than baseline levels (sCRP: 1.09 +/- 1.53 [baseline] vs. 0.83 +/- 1.06 [12th month], p = .01). Omalizumab substantially increases PPBB,and reduces PPBN accompanied by a reduction in sCRP especially in the first 3 months; however, these effects may continue in the long-term. The alterations in peripheral blood cell ratios and sCRP may contribute to the therapeutic effect of omalizumab in CSU.
引用
收藏
页数:6
相关论文
共 19 条
[1]  
Acer E, 2018, CUTAN OCUL TOXICOL, V10, P1, DOI [10.1080/15569527.2018.1495227, DOI 10.1080/15569527.2018.1495227]
[2]   The potential pharmacologic mechanisms of omalizumab in patients with chronic spontaneous urticaria [J].
Chang, Tse Wen ;
Chen, Christina ;
Lin, Chien-Jen ;
Metz, Martin ;
Church, Martin K. ;
Maurer, Marcus .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2015, 135 (02) :337-+
[3]   Blood basophil numbers in chronic ordinary urticaria and healthy controls: diurnal variation, influence of loratadine and prednisolone and relationship to disease activity [J].
Grattan, CEH ;
Dawn, G ;
Gibbs, S ;
Francis, DM .
CLINICAL AND EXPERIMENTAL ALLERGY, 2003, 33 (03) :337-341
[4]  
Jackson JM, 2018, DERMATOLOGY, P2242
[5]   Mechanisms of action that contribute to efficacy of omalizumab in chronic spontaneous urticaria [J].
Kaplan, A. P. ;
Gimenez-Arnau, A. M. ;
Saini, S. S. .
ALLERGY, 2017, 72 (04) :519-533
[6]   Pathogenesis of chronic urticaria [J].
Kaplan, A. P. ;
Greaves, M. .
CLINICAL AND EXPERIMENTAL ALLERGY, 2009, 39 (06) :777-787
[7]   C-reactive protein is linked to disease activity, impact, and response to treatment in patients with chronic spontaneous urticaria [J].
Kolkhir, P. ;
Altrichter, S. ;
Hawro, T. ;
Maurer, M. .
ALLERGY, 2018, 73 (04) :940-948
[8]  
Kolkhir P, 2017, EUR ANN ALLERGY CLIN, V49, P189, DOI 10.23822/EurAnnACI.1764-1489.05
[9]   Epidemiology of chronic spontaneous urticaria: results from a nationwide, population-based study in Italy [J].
Lapi, F. ;
Cassano, N. ;
Pegoraro, V. ;
Cataldo, N. ;
Heiman, F. ;
Cricelli, I. ;
Levi, M. ;
Colombo, D. ;
Zagni, E. ;
Cricelli, C. ;
Vena, G. A. .
BRITISH JOURNAL OF DERMATOLOGY, 2016, 174 (05) :996-1004
[10]   CRP relevance in clinical assessment of chronic spontaneous urticaria Tunisian patients [J].
Maouia, A. ;
Youssef, M. ;
Leban, N. ;
Ben Chibani, J. ;
Helal, A. N. ;
Kassab, A. .
CUTANEOUS AND OCULAR TOXICOLOGY, 2017, 36 (04) :387-392