Where there were sequences associated with two or more isotypes in a set, averages sequences were generated for each isotype. To investigate the role of antigen selection in the evolution of patterns of mutation within the IgE sequences, the proportion

of replacement mutations within the CDR1 and CDR2 of each sequence was calculated. Broad definitions of CDR1 and CDR2 were used, incorporating the CDR regions of both Kabat [22] and IMGT [23], and analysis was made with reference to a random model of mutations as previously described [13]. In this model, the probability that a random mutation would introduce a replacement mutation in the CDR was estimated to be 0.26, based upon patterns of mutation

and hotspots in a data set of non-productive sequences [13]. Analysis showed that this estimate was appropriate for all IGHV sequences, BMS-777607 manufacturer for there is little variation in the mutability of different IGHV genes (data not shown). Using the binomial distribution, the estimate was then used to establish 95% confidence limits for the proportion of the total mutations that would be replacement mutations in the CDR (RCDR), if the mutation process targeted hotspots, but if these mutations were not subject to antigen selection pressure. Proportions were calculated for varying numbers of total IGHV mutations (Mv). The upper limit (97.5%) was used to distinguish sequences that

showed evidence of antigen selection from sequences that lacked such selleck screening library evidence. Total serum immunoglobulin concentrations were determined for all PNG samples, and the results are summarized in Table 2. Concentrations of serum IgE antibodies were all above the laboratory Reverse transcriptase reference range for healthy Sydney adults, and the mean IgE concentration of the serum samples was 2465 kU/l. IgG subclass concentrations are also shown in Table 2. IgG1 and IgG4 concentrations were particularly high. Nine of the 14 PNG individuals had IgG1 concentrations above the laboratory reference range for healthy Sydney adults, while all but one of the individuals studied had serum IgG4 concentrations that were above the Laboratory Reference Range. In Western populations, IgG4 is typically the least abundant IgG subclass, but IgG4 in these PNG samples was seen at substantially higher concentrations than IgG3. Sequences were aligned against the germline IGHV, IGHD and IGHJ gene repertoires using the iHMMune-align program, while IGHG gene identity was confirmed by blast. PCR error rates were determined by analysis of errors within the IGHG constant region genes and were shown to vary from 0.9‰ (IgG2) to 1.2‰ (IgG4). The amplified constant region of the IgE sequences was too short for such a calculation.