Sadoulet Marie-Odile, Franceschi Cécile, Aubert Muriel, Silvy Françoise, Bernard Jean-Paul, Lombardo Dominique, Mas Eric
INSERM UMR-777, Faculté de Médecine-Timone, 27 Boulevard Jean Moulin, 13385 Marseille Cedex 05, France.
Glycobiology. 2007 Jun;17(6):620-30. doi: 10.1093/glycob/cwm028. Epub 2007 Mar 20.
In human pancreatic adenocarcinoma, alterations of glycosylation processes leads to the expression of tumor-associated carbohydrate antigens, representing potential targets for cancer immunotherapy. Among these pancreatic tumor-associated carbohydrate antigens, the J28 glycotope located within the O-glycosylated mucin-like C-terminal domain of the fetoacinar pancreatic protein (FAPP) and expressed at the surface of human tumoral tissues, can be a good target for anticancer therapeutic vaccines. However, the oncodevelopmental self character of the J28 glycotope associated with the low immunogenicity of tumor-associated carbohydrate antigens may be a major obstacle to effective anti-tumor vaccine therapy. In this study, we have investigated a method to increase the immunogenicity of the recombinant pancreatic oncofetal J28 glycotope by glycoengineering Galalpha1,3Galss1,4GlcNAc-R (alphaGal epitope) which may be recognized by natural anti-alphaGal antibody present in humans. For this purpose, we have developed a stable Chinese hamster ovary cell clone expressing the alphaGal epitope by transfecting the cDNA encoding the alpha1,3galactosyltransferase. These cells have been previously equipped to produce the recombinant O-glycosylated C-terminal domain of FAPP carrying the J28 glycotope. As a consequence, the C-terminal domain of FAPP produced by these cells carries the alphaGal epitope on oligosaccharide structures associated with the J28 glycotope. Furthermore, we show that this recombinant "alpha1,3galactosyl and J28 glycotope" may not only be targeted by human natural anti-alphaGal antibodies but also by the mAbJ28, suggesting that the J28 glycotope remains accessible to the immune system as vaccinating agent. This approach may be used for many identified tumor-associated carbohydrate antigens which can be glycoengineered to carry a alphaGal epitope to increase their immunogenicity and to develop therapeutic vaccines.
在人类胰腺腺癌中,糖基化过程的改变会导致肿瘤相关碳水化合物抗原的表达,这些抗原是癌症免疫治疗的潜在靶点。在这些胰腺肿瘤相关碳水化合物抗原中,位于胎儿胰腺蛋白(FAPP)的O-糖基化粘蛋白样C末端结构域内且在人类肿瘤组织表面表达的J28糖表位,可能是抗癌治疗性疫苗的良好靶点。然而,J28糖表位的肿瘤发生性自身特性与肿瘤相关碳水化合物抗原的低免疫原性相关,这可能是有效抗肿瘤疫苗治疗的主要障碍。在本研究中,我们研究了一种通过糖工程化Galα1,3Galβ1,4GlcNAc-R(αGal表位)来提高重组胰腺癌胚J28糖表位免疫原性的方法,αGal表位可被人类中存在的天然抗αGal抗体识别。为此,我们通过转染编码α1,3-半乳糖基转移酶的cDNA,开发了一个稳定表达αGal表位的中国仓鼠卵巢细胞克隆。这些细胞之前已具备产生携带J28糖表位的重组O-糖基化FAPP C末端结构域的能力。因此,这些细胞产生的FAPP C末端结构域在与J28糖表位相关的寡糖结构上携带αGal表位。此外,我们表明这种重组的“α1,3-半乳糖基和J28糖表位”不仅可被人类天然抗αGal抗体靶向,还可被单克隆抗体J28靶向,这表明J28糖表位作为疫苗接种剂时对免疫系统仍然是可及的。这种方法可用于许多已确定的肿瘤相关碳水化合物抗原,这些抗原可通过糖工程化携带αGal表位来提高其免疫原性并开发治疗性疫苗。