PMID- 19740315 OWN - NLM STAT- MEDLINE DCOM- 20100125 LR - 20220331 IS - 1365-2567 (Electronic) IS - 0019-2805 (Print) IS - 0019-2805 (Linking) VI - 128 IP - 1 Suppl DP - 2009 Sep TI - Balance between early life tolerance and sensitization in allergy: dependence on the timing and intensity of prenatal and postnatal allergen exposure of the mother. PG - e541-50 LID - 10.1111/j.1365-2567.2008.03028.x [doi] AB - Allergens can be maternally transferred to the fetus or neonate, though it is uncertain how this initial allergen exposure may impact the development of allergy responses. To evaluate the roles of timing and level of maternal allergen exposure in the early life sensitization of progeny, female BALB/c mice were given ovalbumin (OVA) orally during pregnancy, lactation or weekly at each stage to investigate the immunoglobulin E (IgE) antibody production and cellular responsiveness of their offspring. Exposure to OVA during pregnancy was also evaluated in OVA-specific T-cell receptor (TCR) transgenic (DO11.10) mice. The effect of prenatal antigen exposure on offspring sensitization was dependent on antigen intake, with low-dose OVA inducing tolerance followed by neonatal immunization that was sustained even when pups were immunized when 3 weeks old. These offspring received high levels of transforming growth factor-beta via breastfeeding. High-dose exposure during the first week of pregnancy or perinatal period induced transient inhibition of IgE production following neonatal immunization; although for later immunization IgE production was enhanced in these offspring. Postnatal maternal antigen exposure provided OVA transference via breastfeeding, which consequently induced increased offspring susceptibility to IgE antibody production according to week post-birth. The effect of low-dose maternal exposure during pregnancy was further evaluated using OVA transgenic TCR dams as a model. These progeny presented pronounced entry of CD4(+) T cells into the S phase of the cell cycle with a skewed T helper type 2 response early in life, revealing the occurrence of allergen priming in utero. The balance between tolerance and sensitization depended on the amount and timing of maternal allergen intake during pregnancy. FAU - Fusaro, Ana Elisa AU - Fusaro AE AD - Laboratory of Dermatology and Immunodeficiencies, School of Medicine, University of Sao Paulo, Sao Paulo, Brazil. FAU - de Brito, Cyro Alves AU - de Brito CA FAU - Taniguchi, Eliana Futata AU - Taniguchi EF FAU - Muniz, Bruno Pacola AU - Muniz BP FAU - Victor, Jefferson Russo AU - Victor JR FAU - Orii, Noemia Mie AU - Orii NM FAU - Duarte, Alberto Jose da Silva AU - Duarte AJ FAU - Sato, Maria Notomi AU - Sato MN LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20081218 PL - England TA - Immunology JT - Immunology JID - 0374672 RN - 0 (Allergens) RN - 0 (Cytokines) RN - 0 (Receptors, Antigen, T-Cell) RN - 0 (Transforming Growth Factor beta) RN - 37341-29-0 (Immunoglobulin E) RN - 9006-59-1 (Ovalbumin) SB - IM MH - Administration, Oral MH - Allergens/*immunology MH - Animals MH - CD4-Positive T-Lymphocytes/immunology MH - Cytokines/biosynthesis/*immunology MH - Female MH - Hypersensitivity/*immunology MH - *Immune Tolerance MH - Immunoglobulin E/blood MH - Male MH - *Maternal Exposure MH - Maternal-Fetal Exchange/*immunology MH - Mice MH - Mice, Inbred BALB C MH - Mice, Transgenic MH - Ovalbumin/immunology MH - Pregnancy MH - Receptors, Antigen, T-Cell/metabolism MH - Transforming Growth Factor beta/metabolism PMC - PMC2753947 EDAT- 2009/09/25 06:00 MHDA- 2010/01/26 06:00 PMCR- 2010/09/01 CRDT- 2009/09/11 06:00 PHST- 2009/09/11 06:00 [entrez] PHST- 2009/09/25 06:00 [pubmed] PHST- 2010/01/26 06:00 [medline] PHST- 2010/09/01 00:00 [pmc-release] AID - IMM3028 [pii] AID - 10.1111/j.1365-2567.2008.03028.x [doi] PST - ppublish SO - Immunology. 2009 Sep;128(1 Suppl):e541-50. doi: 10.1111/j.1365-2567.2008.03028.x. Epub 2008 Dec 18.