ToxSci Advance Access published online on September 29, 2004
Toxicological Sciences, doi:10.1093/toxsci/kfh287
Toxicological Sciences © Society of Toxicology 2004; all rights reserved
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1 Division of Environmental Medicine, Norwegian Institute of Public Health, P.O.Box 4404 Nydalen, NO-0403 Oslo, Norway
* To whom correspondence should be addressed. E-mail: unni.cecilie.nygaard{at}fhi.no.
Particle exposure has traditionally been monitored as mass concentration of PM10 (particles with an aerodynamic diameter less than 10 µm), more recently also as PM2.5. The mass concentration is strongly influenced by the large particles. Therefore, particle mass is a poor measure for characterizing the amount of the small, possibly more biologically potent particles. We used polystyrene particles (PSP) ranging in diameter from 0.0588 to 11.14 µm, carbon black (CB) and diesel exhaust particles (DEP), to study the adjuvant effect of particles on the immune response to the allergen ovalbumin (OVA) after subcutaneous injection into the footpad of BALB/cA mice. At a given mass dose, the small particles (0.0588 and 0.202 µm PSP, CB and DEP) increased the allergen-specific IgE serum levels to a substantially higher degree than the larger particles (1.053, 4.64 and 11.14 µm PSP). Further, in the draining lymph node during the primary response, the fine particles (0.202 µm) with OVA increased cell numbers, expression of surface markers (CD19, MHC class II, CD86 and CD23) and ex vivo production of IL-4 and IL-10, whereas the largest (11.14 µm) particles did not. Linear regression analyses indicated that the IgE response was not predicted by particle mass (R2=0.06), but was predicted by the total particle surface (R2=0.64), number of particles (R2=0.62) and particle diameter (R2=0.58). In conclusion, we found that fine particles exerted stronger adjuvant effects on allergic responses than larger particles at equal mass doses. Consequently, the dose described as total particle surface area or particle number predict the adjuvant effect of particles better than the currently used particle mass.
Accepted September 22, 2004
Immunotoxiocology
The Capacity of Particles to Increase Allergic Sensitization is Predicted by Particle Number and Surface Area, Not by Particle Mass
2 Division of Infectious Disease Control, Norwegian Institute of Public Health, P.O.Box 4404 Nydalen, NO-0403 Oslo, Norway
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