Abstract
In a double blind 3-yr prospective study 40 grass pollen allergic patients were allocated to specific immunotherapy (hyposensitization) with 2 timothy [P. pratense] major allergens, 19, 25 or partially purified timothy extract. The extracts were biologically standardized and coupled to Al(OH)3) for treatment. Efficacy of hyposensitization was evaluated by titrated nasal provocations and skin prick tests with the 2 treatment extracts and a 5-grass mixture. The threshold dose for skin prick test (skin thresholds) produced reactions identical to histamine chloride 5.43 mmol/l, and the threshold dose for nasal provocations (nasal thresholds) produced 2 of the 3 reactions: at least 0.5 ml of nasal secretion, at least 5 sneezes, and/or at least a 20% fall in nasal peak flow. Nasal thresholds showed highest efficacy from partially purified timothy extract but equal protection against timothy and the 5-grass mixture. Nasal thresholds of 14 untreated patients corresponded to treatment with the 2 major allergens. Changes in skin and nasal thresholds after 12 and after 64 wk of treatment predicted the severity of hay fever. Increase in nasal thresholds coincided with a marked effect on asthma. Nasal thresholds below 1 HEP before treatment predicted major systemic side effects.