Ruiter B, Trégoat V, M'rabet L, Garssen J, Bruijnzeel-Koomen C A F M, Knol E F, Hoffen E
Department of Dermatology/Allergology, University Medical Center, Utrecht, The Netherlands.
Clin Exp Allergy. 2006 Mar;36(3):303-10. doi: 10.1111/j.1365-2222.2006.02436.x.
One to two percent of infants suffer from IgE-mediated allergic reactions against cow's milk proteins. Most children develop clinical tolerance, but approximately 15% are still allergic by the age of 10 years. Little is known about the T cell epitopes in individual cow's milk protein in relation to allergy and tolerance.
To identify T cell epitopes in alphas1-casein, the most abundant milk protein, and to investigate T cell responses toward these epitopes in allergic, atopic and non-atopic children.
Allergen-specific T cell lines (TCLs) were derived from peripheral blood mononuclear cells of 11 cow's milk allergic, nine atopic and nine non-atopic children. T cell responses were measured to alphas1-casein and to overlapping peptides (18-mers), spanning the alphas1-casein molecule. Proliferation was determined by incorporation of (3)H-thymidine, and cytokine production (IL-10, IL-13 and IFN-gamma) was measured by ELISA.
Four main regions (amino acid (AA) residues 43-66, 73-96, 91-114 and 127-180) in the alphas1-casein molecule were immunogenic to T cells, among which the AA residues 133-156 spanned the immunodominant part. Only subtle differences were found in peptide recognition between the subject groups. Some of the peptides induced slightly Th1- or Th2-skewed cytokine responses. The increased levels of IL-10 in response to alphas1-casein observed in TCLs from atopic children appeared not to be linked to recognition of specific IL-10-inducing epitopes.
The immunodominant sequence in alphas1-casein is spanned by AA residues 133-156. Tolerance towards alphas1-casein in atopic children may be mediated by an overall induction of IL-10 and not by recognition of certain T cell epitopes. The identified T cell epitopes in children with cow's milk allergy may be useful targets in developing peptide immunotherapy.
1%至2%的婴儿会发生针对牛奶蛋白的IgE介导的过敏反应。大多数儿童会产生临床耐受性,但到10岁时仍有大约15%的儿童过敏。关于个别牛奶蛋白中的T细胞表位与过敏和耐受性的关系,人们了解甚少。
鉴定αs1-酪蛋白(最丰富的乳蛋白)中的T细胞表位,并研究过敏、特应性和非特应性儿童对这些表位的T细胞反应。
从11名牛奶过敏儿童、9名特应性儿童和9名非特应性儿童的外周血单个核细胞中获得过敏原特异性T细胞系(TCL)。检测TCL对αs1-酪蛋白和跨越αs1-酪蛋白分子的重叠肽(18肽)的T细胞反应。通过掺入³H-胸腺嘧啶核苷测定增殖,通过ELISA检测细胞因子产生(IL-10、IL-13和IFN-γ)。
αs1-酪蛋白分子中的四个主要区域(氨基酸(AA)残基43 - 66、73 - 96、91 - 114和127 - 180)对T细胞具有免疫原性,其中AA残基133 - 156跨越免疫显性部分。在各受试组之间,肽识别方面仅发现细微差异。一些肽诱导了轻微的Th1或Th2偏向的细胞因子反应。在特应性儿童的TCL中观察到的对αs1-酪蛋白反应中IL-10水平升高,似乎与特定IL-10诱导表位的识别无关。
αs1-酪蛋白中的免疫显性序列由AA残基133 - 156跨越。特应性儿童对αs1-酪蛋白的耐受性可能由IL-10的总体诱导介导,而非通过某些T细胞表位的识别。在牛奶过敏儿童中鉴定出的T细胞表位可能是开发肽免疫疗法的有用靶点。