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1.
Ann Allergy Asthma Immunol ; 107(5): 441-7, 2011 Nov.
Article in English | MEDLINE | ID: mdl-22018617

ABSTRACT

BACKGROUND: Subcutaneous allergen-specific immunotherapy is a proven, highly effective treatment for immunoglobulin E-mediated diseases. Despite its proven benefits, only a small percentage of patients with allergic disease use immunotherapy, in part because of the inconvenience associated with treatment. Cluster allergen immunotherapy may offer patients a more convenient treatment option but is prescribed infrequently because of the perception that accelerated immunotherapy buildup leads a higher rate of systemic reactions. OBJECTIVE: To examine the safety of cluster immunotherapy and identify risk factors for systemic reactions during cluster buildup. METHODS: A retrospective, observational review in a large, multicenter allergy practice group was conducted for patients receiving cluster immunotherapy between May 2008 and October 2010. RESULTS: Data from 441 patients receiving cluster immunotherapy were collected. Forty-eight patients (10.9%) experienced systemic reactions. Based on the World Allergy Organization Subcutaneous Immunotherapy Systemic Reaction Grading System, 18 grade 1 reactions (38.3%), 23 grade 2 reactions (48.9%), 5 grade 3 reactions (10.6%), 1 grade 4 reaction (2.1%), and no grade 5 reactions were seen. Risk factors for a systemic reaction included: female sex, physician diagnosis of asthma, age 21 to 40 years, and inclusion of certain allergens in the immunotherapy vaccine. CONCLUSIONS: Cluster immunotherapy allows patients to reach their immunotherapy maintenance dose more rapidly and may lead to more rapid symptomatic improvement. However, the cluster buildup may lead to a higher rate of systemic reactions. Identifying risk factors for systemic reactions will help improve the safety of cluster immunotherapy.


Subject(s)
Air Pollutants/adverse effects , Allergens/adverse effects , Desensitization, Immunologic , Respiratory Hypersensitivity/drug therapy , Respiratory Hypersensitivity/immunology , Adult , Age Factors , Allergens/administration & dosage , Clinical Protocols , Female , Humans , Male , Middle Aged , Practice Guidelines as Topic , Pruritus/etiology , Respiratory Hypersensitivity/epidemiology , Retrospective Studies , Risk Factors , Severity of Illness Index , Sex Factors , Urticaria/etiology
2.
Am J Respir Crit Care Med ; 170(2): 175-80, 2004 Jul 15.
Article in English | MEDLINE | ID: mdl-15087299

ABSTRACT

Daycare attendance and siblings are associated with viral-induced wheezing in children. Preexisting immunologic factors may influence the expression of viral infections in infancy, and in turn, recurrent infections may influence the development of immune responses. A total of 285 children were enrolled in the Childhood Origins of Asthma Project at birth and followed for at least 1 year. Cord blood and 1-year mononuclear cells were stimulated with phytohemagglutinin, and cytokine-response profiles were measured by enzyme-linked immunosorbent assay. Nasal lavage was performed for moderate to severe respiratory illnesses. Daycare attendance and/or siblings significantly increased the likelihood of contracting respiratory syncytial virus (1.5-1.6-fold increase) and rhinovirus (1.8-2.1-fold increase), and increased the risk of rhinovirus-induced wheezing (14-18% vs. 2%, p = 0.011). Cord blood IFN-gamma responses were inversely related to the frequency of viral respiratory infections (r(s) = -0.11, p = 0.05), and more significant for subjects with high exposure to other children (r(s) = -0.27, p = 0.028). The interval change in infantile IFN-gamma responses correlated positively with the frequency of viral infections in infancy (r(s) = 0.12, p = 0.047). These data suggest that neonatal IFN-gamma responses may influence antiviral activity, or may represent a marker of antiviral immunity maturation. Conversely, the frequency of viral infections in infancy can influence IFN-gamma responses.


Subject(s)
Child Day Care Centers/statistics & numerical data , Cytokines/blood , Environmental Monitoring/statistics & numerical data , Respiratory Tract Infections/epidemiology , Respiratory Tract Infections/immunology , Virus Diseases/epidemiology , Virus Diseases/immunology , Child Development , Cohort Studies , Epidemiological Monitoring , Fetal Blood/immunology , Humans , Infant , Infant Care/statistics & numerical data , Infant, Newborn , Nasal Cavity/virology , Pediatrics/statistics & numerical data , Prospective Studies , Respiratory Sounds , Respiratory Tract Infections/virology , Siblings , Therapeutic Irrigation , Virus Diseases/virology , Wisconsin/epidemiology
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