Advances in the knowledge of the cellular and molecular basis of immunity have led to a thorough understanding of the immunologic features that characterize an allergic response. All humans can mount an IgE antibody (Ab) response to a parasite, but some genetically predisposed or atopic individuals mount this response to common antigens to which they are exposed either by inhalation, ingestion or by contact with the skin [1]. These non-parasitic antigens, called allergens, induce persistently elevated levels of specific IgE Ab and stimulate a Type-I immediate hypersensitivity [2, 3]. Common allergens include dust, plant and tree pollens, pet dander and food. Although a specific sample of pollen or house dust contains numerous antigens, only a few of them induce a specific IgE Ab response and are considered allergens. The epitope structure will determine if an antigen is an allergen [2–7].
Some, but not all antigens have epitopes that stimulate a Th2-like response, which induces an IgE Ab response [6]. Several factors contribute to the immune response to the allergens including the amount and the route of antigen exposure [4, 5, 7], the type of antigen-presenting cell [1, 8, 9], and the cytokine milieu. IFN- g will promote a Th1-like immune response, whereas IL-4 will promote a Th2-like response. Other factors to consider are the host immune response genes and environmental cofactors, such as adjuvants. These may bias the immune response to allergens towards a Th2-type response.
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Mohapatra, S.S., Shirley, S.A. (2009). Recombinant Allergens for Therapy and Prevention: Molecular Design and Delivery of Allergy Vaccines. In: Pawankar, R., Holgate, S.T., Rosenwasser, L.J. (eds) Allergy Frontiers: Therapy and Prevention. Allergy Frontiers, vol 5. Springer, Tokyo. https://doi.org/10.1007/978-4-431-99362-9_26
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