Amino acid sequence identity between these tropomyosins ranges from 73% to 74%, and some regions predicted as IgE-binding epitopes in shrimp tropomyosin Selleckchem Smoothened Agonist were found to be identical in these molecules. We also found that IgE antibodies to rAsc l 3 represent a high proportion (∼50%) of the total IgE response to an unfractionated parasite extract, and there was allergenic equivalence between rAsc l 3 and the native counterpart in the A. lumbricoides extract. Moreover, the anti-tropomyosin

IgE antibodies of sensitized subjects reacted against A. lumbricoides tropomyosin and induced mediator release in effector cells, both in vivo and in vitro. The clinical impact of these findings relies on the particular environmental conditions of the tropics (especially urbanized areas of low income), BGB324 concentration where perennial exposure to high concentrations of mite allergens and intermittent infections with A. lumbricoides are common. In this setting, allergenic stimulation by cross-reacting tropomyosins may provide signals for sustaining IgE synthesis and perpetuate the allergic inflammation.

Supporting this hypothesis, our mite-allergic patients with asthma are more frequently and more strongly sensitized to rAsc l 3 than controls, both groups being sensitized to the Ascaris extract (Figure 3). Because the main risk factor for asthma in the tropics is specific IgE to mites, it is possible that this pattern of reactivity is attributable to the exposure to cross-reactive tropomyosins (144). This mechanism may also explain, at a population level, why in tropical

environments from Africa and South America, tropomyosins from mite and other invertebrates (e.g. cockroaches) constitute very important allergens, with sensitization frequencies above 50% (145,146), while PI-1840 in developed regions among mite-sensitized patients, tropomyosin is a minor allergen (5–16%) (130,147,148), probably because of the low concentrations of this allergen in the mite body. These findings suggest that Asc l 3 influences the patterns of IgE responses to mite tropomyosins and may not be restricted to this allergen because Ascaris extract has at least 7 IgE cross-reactive components (200, 116, 77, 58, 40, 33 and 23 kDa) that may exert similar enhancer effects (24). Conventionally, the diagnosis of Ascaris infection is achieved by the identification of parasite eggs in stool samples. However, the evaluation of A. suum infection in pigs shows that egg counts in faeces greatly underestimate the proportion of exposed individuals compared with anti-Ascaris IgG titration by ELISA (149). Similar findings were obtained in humans, where serodiagnosis of ascariasis, as detected by Ascaris-positive IgE, is three times the positive egg prevalence (150,151).