Kurisaki J, Atassi H, Atassi M Z
Eur J Immunol. 1986 Mar;16(3):236-40. doi: 10.1002/eji.1830160305.
In the preceding report, we described the systematic localization of the full profile of the continuous antigenic sites on ragweed allergen, Ra3, with antibodies from three different host species using a comprehensive strategy, previously introduced by this laboratory. The strategy consists of studying the immunochemical activity of a series of consecutive synthetic overlapping peptides, of uniform size and overlaps, which encompass the entire protein chain. This study reports the localization of the continuous regions on Ra3 that are recognized by T cells from mice immunized with Ra3. The 10 overlapping peptides encompassing the entire Ra3 molecule were examined in vitro for their ability to stimulate lymph node cells from Ra3-primed BALB/c (H-2d), C3H/He (H-2k) SWR (H-2q) and SJL (H-2s) mice. Several regions of the molecule (T sites) were found to stimulate Ra3-primed lymph node cells. This strategy has enabled the localization of the full submolecular profile of T cell recognition of the Ra3 molecule by these mouse strains. Three of the regions recognized by T cells coincided with regions recognized by antibodies (i.e. B cells). It is noteworthy that in addition to sites recognized by both T and B cells the protein has at least one site which is recognized exclusively by T cells and to which no detectable antibody response is directed.
在之前的报告中,我们使用本实验室先前引入的综合策略,描述了用来自三种不同宿主物种的抗体对豚草过敏原Ra3上连续抗原位点的完整图谱进行系统定位。该策略包括研究一系列连续的、大小和重叠度均一的合成重叠肽的免疫化学活性,这些肽涵盖了整个蛋白质链。本研究报告了用Ra3免疫的小鼠的T细胞所识别的Ra3上的连续区域的定位。对包含整个Ra3分子的10个重叠肽进行了体外检测,以评估它们刺激来自经Ra3免疫的BALB/c(H-2d)、C3H/He(H-2k)、SWR(H-2q)和SJL(H-2s)小鼠的淋巴结细胞的能力。发现该分子的几个区域(T位点)能刺激经Ra3免疫的淋巴结细胞。这种策略使得能够定位这些小鼠品系对Ra3分子的T细胞识别的完整亚分子图谱。T细胞识别的三个区域与抗体(即B细胞)识别的区域一致。值得注意的是,除了T细胞和B细胞都识别的位点外,该蛋白质至少还有一个仅被T细胞识别的位点,并且没有可检测到的抗体反应针对该位点。