Abstract | BACKGROUND: OBJECTIVES: A randomized, double-blind, placebo-controlled trial was carried out to assess the efficacy of a vaccine made of keyhole lampet hemocyanin (KLH)-conjugated decapeptide from the Fc(epsilon4) domain of the IgE in cypress pollinosis. METHODS: Sixty patients with cypress pollen allergy were studied. They were included on a suggestive clinical history, positive skin tests and nasal challenge to cypress pollen extract. Three intramuscular injections of the vaccine (250 microg) or placebo were administered monthly with a booster injection 5 to 8 weeks later. The primary end-point criterion was the threshold dose inducing a positive nasal challenge. The secondary end-point was the symptom-medication scores measured when cypress pollen grains were over 50 grains/m3. RESULTS: Nasal challenge before treatment was non-significantly different between the placebo and vaccine groups. After treatment there was no significant difference between the two groups. Pollen counts were over 50 grains/m3 for 8 weeks during the trial. There was no significant difference in total symptom scores between the placebo and vaccine groups. The vaccine was safe. CONCLUSIONS:
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Authors | P Demoly, L Persi, H Dhivert, M Delire, J Bousquet |
Journal | Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology
(Clin Exp Allergy)
Vol. 32
Issue 7
Pg. 1071-6
(Jul 2002)
ISSN: 0954-7894 [Print] England |
PMID | 12100056
(Publication Type: Clinical Trial, Journal Article, Randomized Controlled Trial)
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Chemical References |
- Immunoglobulin G
- Oligopeptides
- Vaccines
- Immunoglobulin E
- Hemocyanins
- keyhole-limpet hemocyanin
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Topics |
- Adult
- Cupressus
(immunology)
- Double-Blind Method
- Female
- Hemocyanins
(immunology)
- Humans
- Hypersensitivity
(therapy)
- Immunoglobulin E
(blood)
- Immunoglobulin G
(blood)
- Male
- Middle Aged
- Oligopeptides
(immunology)
- Vaccines
(adverse effects, immunology)
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