Background In recent years the prevalence of type I allergy to latex has co
ntinuously increased, in particular among healthcare workers, to about 10%.
While most forms of type I allergy caused by other environmental allergens
can be treated by pharmacotherapy or specific immunotherapy, minimizing ex
posure to latex proteins may represent an effective preventive measure for
latex allergy.
Objective To investigate whether it is possible to select by in vitro and i
n vivo testing low-allergen latex gloves for prevention of latex allergy.
Methods We obtained separate extracts by standard aqueous extraction from t
he inner and outer surfaces of 15 different commonly used (10 examination,
five surgical) glove brands. The extracts were analysed by quantitative (bi
cinchoninic protein assay, immunoglobulin [Ig] E-ELISA, ELISA competition)
and qualitative (SDS-PAGE, silver staining, IgE immunoblotting) methods for
their protein and allergen contents. In addition, the glove extracts were
analysed for their capacity to induce basophil histamine release and immedi
ate skin reactions.
Results Extracts from different glove brands contained cross-reactive IgE e
pitopes. However, IgE binding studies, basophil histamine release and skin
testing showed that different glove brands and their inner and outer surfac
es contained widely varying protein and allergen contents. While the determ
ination of total protein contents was not sufficient to identify low-allerg
en gloves, IgE measurements, basophil histamine release and skin testing we
re in good agreement and allowed to select low-allergen products.
Conclusion We suggest the use of low-allergen latex products identified by
IgE binding, basophil histamine release assays and skin testing as a feasib
le preventive measure for latex allergy.