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Timothy grass pollen therapeutic vaccine: optimal dose for subcutaneous immunotherapy.
Sola, Javier; da Silva Ferreira, José Alberto; Dionicio Elera, Javier; Plácido, José Luís; Pereira, Celso; Fonseca, João; Panizo, Carmen; Inácio, Luís Filipe; Cancelleire, Nataly; Zubeldia Ortuño, José Manuel; Landeta, Araitz; Madariaga, Begoña; Martínez, Alberto.
Afiliação
  • Sola J; Allergy Service, Hospital Universitario Ramón y Cajal, Madrid, Spain.
  • da Silva Ferreira JA; Imuno-Allergology Department, Centro Hospitalar Vila Nova de Gaia/Espinho, Portugal.
  • Dionicio Elera J; Allergy Service, Hospital Puerta de Hierro Majadahonda, Madrid, Spain.
  • Plácido JL; Imuno-Allergology Service, Centro Hospitalar de S. João, Porto, Portugal.
  • Pereira C; Imuno-Allergology Service, Hospital da Universidade de Coimbra, Portugal.
  • Fonseca J; Imuno-Allergology Service, CUF Porto Instituto e Hospital, Universidade do Porto, Portugal.
  • Panizo C; Allergy Service, Hospital Nuestra Señora del Prado, Talavera de la Reina, Spain.
  • Inácio LF; Imuno-Allergology Service, Centro Hospitalar de Setúbal, Portugal.
  • Cancelleire N; Department of Allergy, Hospital Universitario La Paz, Madrid, Spain.
  • Zubeldia Ortuño JM; Allergy Service, Hospital General Universitario Gregorio Marañón, Madrid, Spain CIBERER (U-761).
  • Landeta A; Bial Industrial Farmacéutica S.A., Zamudio, Spain.
  • Madariaga B; Bial Industrial Farmacéutica S.A., Zamudio, Spain.
  • Martínez A; Bial Industrial Farmacéutica S.A., Zamudio, Spain.
Immunotherapy ; 8(3): 251-63, 2016.
Article em En | MEDLINE | ID: mdl-26760111
AIMS: To establish the optimal dose of Phleum pratense subcutaneous immunotherapy (SCIT) in patients with allergic rhinoconjunctivitis with/without asthma. MATERIALS & METHODS: One hundred and fifty-one patients were randomized to receive SCIT 0.25, 0.5, 1.0, 2.0 or 4.0 skin-prick test units (SPT) or placebo. The primary end point was the variation in the concentration of Phleum pratense extract needed to produce a positive nasal provocation test from baseline (V0) to final visit (FV). RESULTS: After 17 weeks, a dose-dependent trend was apparent in the concentration of P. pratense extract needed to produce a positive nasal provocation response. Systemic adverse reactions occurred with 3.2% of administered doses. Grade III (n = 2) and IV (n = 2) events were observed only at the two highest doses. CONCLUSION: P. pratense depot SCIT showed signs of clinical and immunological efficacy by dose-dependently decreasing the allergen sensitization rate. Risk-benefit favored doses below 1.0 SPT units for confirmatory trials.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Asma / Conjuntivite Alérgica / Alérgenos / Rinite Alérgica Sazonal / Dessensibilização Imunológica / Phleum / Antígenos de Plantas / Rinite Alérgica Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies Limite: Adult / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Asma / Conjuntivite Alérgica / Alérgenos / Rinite Alérgica Sazonal / Dessensibilização Imunológica / Phleum / Antígenos de Plantas / Rinite Alérgica Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies Limite: Adult / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Ano de publicação: 2016 Tipo de documento: Article