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1.
Acta Derm Venereol ; 102: adv00689, 2022 Apr 07.
Article in English | MEDLINE | ID: mdl-35166853

ABSTRACT

The AWARE (A World-wide Antihistamine-Refractory chronic urticaria patient Evaluation) study investigated outcomes in patients with chronic urticaria refractory to H1-antihistamine. The objective of the current study was to analyse the effects of treatment on patients' symptoms and quality of life for a period of up to 2 years. Over the 2 years, there was clear improvement in the high rates of disease burden from baseline, as evidenced by lower scores for disease severity scales, better quality of life, and a decreasing rate of medical resource utilization. However, this is the result of treatment adherence to the guidelines in highly specialized Scandinavian urticaria centres, and has its basis in the relatively low treatment intensity and control at enrolment. There is a need for greater adherence to the treatment guidelines and better management of antihistamine-refractory chronic urticaria.


Subject(s)
Chronic Urticaria , Urticaria , Chronic Disease , Chronic Urticaria/diagnosis , Chronic Urticaria/drug therapy , Follow-Up Studies , Histamine H1 Antagonists/adverse effects , Humans , Quality of Life , Urticaria/chemically induced , Urticaria/diagnosis , Urticaria/drug therapy
2.
Acta Derm Venereol ; 99(2): 158-163, 2019 Feb 01.
Article in English | MEDLINE | ID: mdl-30250961

ABSTRACT

Psoriasis is a stigmatizing chronic skin condition in which impairment of quality of life is associated with visibility of skin lesions, disease activity and severity. The ultimate goal of treatment is complete clearance of skin symptoms. The worldwide "Clear About Psoriasis" survey explored patients' perspectives on clear/almost clear skin and the impact of psoriasis on daily life. We report here results from the Nordic countries (n = 609). Of respondents, 44% achieved clear/almost clear skin with their current treatment, of which 71% were comfortable discussing this expectation with their physician, compared with only 46% of patients who had not achieved clear/almost clear skin. Of patients who achieved clear/almost clear skin, 85% reported treatment satisfaction vs. 39% who had not. Psoriasis profoundly affected daily life, with 88% of respondents reporting discrimination/humiliation and 61% reporting an impact on their professional life. This report highlights stigmatization among Nordic patients with psoriasis and the potential to improve physician-patient communication.


Subject(s)
Patient Satisfaction , Psoriasis/therapy , Skin/pathology , Adult , Cost of Illness , Female , Humans , Male , Middle Aged , Prejudice , Psoriasis/epidemiology , Psoriasis/pathology , Psoriasis/psychology , Quality of Life , Remission Induction , Scandinavian and Nordic Countries/epidemiology , Severity of Illness Index , Stereotyping , Treatment Outcome
3.
Immunology ; 132(1): 144-54, 2011 Jan.
Article in English | MEDLINE | ID: mdl-20875077

ABSTRACT

Emerging evidence suggests that haematopoietic CD34(+) progenitor cells migrate from bone marrow (BM) to sites of allergen exposure where they can undergo further proliferation and final maturation, potentially augmenting the degree of tissue inflammation. In the current study we used a well-characterized mouse model of allergen-induced airway inflammation to determine the role of CCR3 receptor-ligand interactions in the migration and function of CD34(+) cells. Allergen exposure significantly increased BM, blood and airway CD34(+) CCR3(+) cells as well as airway CD34(+) CCR3(+) stem cell antigen-1-positive (Sca-1(+) ) and CD34(+) CD45(+) interleukin-5 receptor-α-positive (IL-5Rα(+) ) cells. A portion of the newly produced CD34(+) CCR3(+), Sca-1(+) CCR3(+) and IL-5Ralpha(+) lung cells showed a significant proliferative capacity in response to allergen when compared with saline-treated animals. In addition, in vitro colony formation of lung CD34(+) cells was increased by IL-5 or eotaxin-2 whereas eotaxin-2 had no effect on BM CD34(+) cells. Furthermore, both eotaxin-1 and eotaxin-2 induced migration of BM and blood CD34(+) CCR3(+) cells in vitro. These data suggest that the CCR3/eotaxin pathway is involved in the regulation of allergen-driven in situ haematopoiesis and the accumulation/mobilization of eosinophil-lineage-committed progenitor cells in the lung. Hence, targeting both IL-5 and CCR3-mediated signalling pathways may be required to control the inflammation associated with allergen-induced asthma.


Subject(s)
Antigens, CD34/immunology , Cell Lineage/immunology , Eosinophils/cytology , Lung/cytology , Mesenchymal Stem Cells/immunology , Receptors, CCR3/immunology , Animals , Antibodies, Monoclonal/immunology , Cell Proliferation , Eosinophils/immunology , Interleukin-5 Receptor alpha Subunit/immunology , Lung/immunology , Male , Mesenchymal Stem Cells/pathology , Mice , Mice, Inbred BALB C , Mice, Transgenic , Ovalbumin/administration & dosage
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