Standardized bronehial allergen provoeation was performed twiee in nineteen extrinsic, well defined, stable asthmatic patients, with an interval of median 15 days (range 14-19) to study the reproducibility of the bronchial response. Smoking and medications were withheld prior to the provocation after a rigid scheme. Ten-fold increasing concentrations of allergen solution 0 9 ml were inhaled by tidal volume breathing for 5 min with intervals of 10 min. The bronchial response to inhaled allergen was determined by forced expiratory volume in the first sec (FEV|) and by total resistance to breathing (R,) determined by an opening interrupter method. The provocation was continued until an allergen concentration causing at least 20% decrease ofthe postsaline FEVi or a 40% increase in Rt was reached. A PC20-FEV1 and a PC40-R1 was calculated by interpolation on the log-dose-response curve. The reproducibility of PC20-FEV1 allergen was high with a 95% confidence interval (CI) for a single determination being the observed value ±0 83, ten-fold concentration difference, the intraelass correlation (IC) was 0 99 and the coefiicient of variation 8 46%. Concerning PC40-R1 a 95% CI for a single determination was calculated being the observed value +0 58, ten-fold concentration difi'erence, IC was 0 99 and the coefiicient of variation was 5 79%. No significant correlation was found between difi"erences in pre-challenge FEV, and R, values and the corresponding PC20-FEV1 and PC40-R1 values. Least square regression between PC20-FEV: and PC40-R1 was performed for the first and the second provocation (/'<0 05). We conclude that bronchial allergen challenge performed in stable asthmatics is highly reproducible and as such a valuable test in the diagnosis of allergic asthma when connected with anamnesis, skin-prick test and the level of specific immunoglobulin E in peripheral blood.