IMMUNE REACTIVITY OF COW-ASTHMATIC DAIRY FARMERS TO THE MAJOR ALLERGEN OF COW (BDA20) AND TO OTHER COW-DERIVED PROTEINS - THE USE OF PURIFIED BDA20 INCREASES THE PERFORMANCE OF DIAGNOSTIC-TESTS IN RESPIRATORY COW ALLERGY
T. Virtanen et al., IMMUNE REACTIVITY OF COW-ASTHMATIC DAIRY FARMERS TO THE MAJOR ALLERGEN OF COW (BDA20) AND TO OTHER COW-DERIVED PROTEINS - THE USE OF PURIFIED BDA20 INCREASES THE PERFORMANCE OF DIAGNOSTIC-TESTS IN RESPIRATORY COW ALLERGY, Clinical and experimental allergy, 26(2), 1996, pp. 188-196
Background Cow dust is one of the most important inducers of occupatio
nal allergic diseases in Finland. For example, in 1991 it accounted fo
r almost 40% of the new occupational asthma cases. Objective This stud
y compares the performance of the purified major cow allergen (BDA20)
and crude bovine epithelial extract (BEA) in diagnostic tests and exam
ines the role of milk allergy-associated bovine proteins (bovine serum
albumin, alpha-lactalbumin, beta-lactoglobulin, casein) in respirator
y cow allergy. Methods The humoral responses of cow-asthmatic and heal
thy farmers to the various components of BEA were analysed with sodium
dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and imm
unoblotting. The levels of specific IgE and IgG antibodies were quanti
ficated with enzyme-linked immunosorbent assays (ELISAs). The cellular
responses were analysed with antigen-specific lymphocyte proliferatio
n tests. Results The specific anti-BDA20 IgE measurement was found to
be best in distinguishing between the asthmatic farmers and their heal
thy colleagues. It proved possible to determine a cut-off value that g
ave the analysis a specificity and sensitivity of 100%; the distinctio
n between the two groups was highly significant (P < 0.0001). In the l
ymphocyte proliferation analysis, cow asthma was more closely associat
ed with reactivity to BDA20 than to BEA. In the measurement of anti-BD
A20 and anti-BEA IgG antibody levels, considerable overlap between the
groups was observed, suggesting that these antibodies are not directl
y involved in cow allergy. When proteins associated with milk allergy
were used as test reagents, no statistically significant differences c
ould be observed between the groups, except for anti-casein IEE antibo
dies the level of which, however, overlapped considerably between the
farmer groups. Conclusion These findings suggest that purified BDA20 i
s better than BEA for diagnosing cow asthma and that proteins associat
ed with milk allergy are of only marginal significance in this disease
.