Hoyne G F, Callow M G, Kuo M C, Thomas W R
Division of Molecular Biology, Western Australian Research Institute for Child Health, Princess Margaret Hospital, Perth.
Immunology. 1994 Oct;83(2):190-5.
H-2b mice respond to the 222 residue allergen Der p I by producing T cells sensitized to the dominant epitopes encompassed in peptides 21-49, 78-100, 110-131 and 197-212. Immunization with the synthetic peptides 120-143 and 144-169, however, revealed cryptic epitopes which could sensitize T cells for responses to the respective peptides and, providing splenic adherent cells were added to lymph node cultures, to the whole allergen. It is shown that feeding recombinant fusion peptides can markedly inhibit the ability of the whole antigen to immunize mice, as measured by the in vitro interleukin-2 (IL-2) and granulocyte-macrophage colony-stimulating factor (GM-CSF)/IL-3 release on stimulation with protein or peptides, although inhibition measured by IL-2 release was more marked. The inhibition extended to epitopes other than those in the fusion peptides used for feeding. Thus feeding peptide 101-154 inhibited responses to 110-131 and 78-100. Fusion peptides 1-14 and 188-222 did not inhibit responses, although 188-222 did contain an epitope. Inhibition was also obtained when mice were fed a fusion containing the cryptic epitope 144-169. The ability of peptides containing the cryptic epitopes to inhibit responses has significant implications for peptide-based immunotherapy.
H-2b小鼠通过产生对包含在肽段21 - 49、78 - 100、110 - 131和197 - 212中的显性表位敏感的T细胞,对222个氨基酸残基的变应原Der p I产生反应。然而,用合成肽120 - 143和144 - 169进行免疫时,发现了隐蔽表位,这些表位可使T细胞对相应肽段敏感,并在将脾黏附细胞添加到淋巴结培养物中时,对整个变应原敏感。结果表明,喂食重组融合肽可显著抑制全抗原免疫小鼠的能力,这通过用蛋白质或肽刺激后体外白细胞介素-2(IL-2)和粒细胞-巨噬细胞集落刺激因子(GM-CSF)/IL-3的释放来衡量,尽管通过IL-2释放测量的抑制作用更为明显。这种抑制作用扩展到了除用于喂食的融合肽中的表位之外的其他表位。因此,喂食肽段101 - 154可抑制对110 - 131和78 - 100的反应。融合肽1 - 14和188 - 222没有抑制反应,尽管188 - 222确实包含一个表位。当给小鼠喂食含有隐蔽表位144 - 169的融合肽时,也获得了抑制作用。含有隐蔽表位的肽段抑制反应的能力对基于肽的免疫疗法具有重要意义。