Background: We have previously reported that simple and well-characterised
particles, such as polystyrene particles (PSP), have an IgE adjuvant effect
in mice. The purpose of this study was to explore the importance of geneti
c background concerning the adjuvant effect of PSP in different strains of
mice. Methods: Inbred NIH/Ola, BALB/c and C3H/HeJ mice were given two intra
peritoneal injections with either PSP plus OVA or OVA alone, and then an in
traperitoneal challenge with OVA alone. NIH/Ola mice were also pre-sensitis
ed to develop a weak or strong IgE response to OVA, and then given an intra
peritoneal challenge with PSP plus OVA or OVA alone. Serum levels of total
and allergen-specific IgE and IgG2a were measured. Results: PSP had a speci
fic IgE and IgG2a adjuvant effect in NIH/Ola mice but not in C3H/HeJ and BA
LB/c mice. Weakly pre-sensitised NIH/Ola mice showed the same response patt
ern as the naive NIH/Ola mice. In contrast, strongly pre-sensitised mice sh
owed an antibody response pattern similar to that of high-responder BALB/c
mice. Conclusion: Our results indicate that the allergen responder status,
either genetic or induced, is of importance for the adjuvant effect from pa
rticles. The IgE and IgG2a adjuvant effect may depend on the genetically de
termined susceptibility of an individual to be influenced by exposure to th
e adjuvant. Therefore, the allergy-enhancing effect from particle pollution
may differ between individuals. Copyright (C) 2000 S. Karger AG. Basel.