Wang Z G, Williams L J, Zhang X F, Zatorski A, Kudryashov V, Ragupathi G, Spassova M, Bornmann W, Slovin S F, Scher H I, Livingston P O, Lloyd K O, Danishefsky S J
Division of Genitourinary Oncology, Department of Medicine, and Laboratory of Bio-organic Chemistry, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.
Proc Natl Acad Sci U S A. 2000 Mar 14;97(6):2719-24. doi: 10.1073/pnas.97.6.2719.
We have previously reported on a carbohydrate-based vaccine program for immunotherapy in cancer patients. One such vaccine, based on the globo H antigen conjugated to the protein keyhole limpet hemocyanin (KLH), has been in clinical evaluation. Although this and other carbohydrate vaccines have been shown to induce antibody responses, there are currently no quantitative data on the antibody levels achieved in immunized patients by these or other anti-cancer vaccines. We report herein an efficient route to complex synthetic oligosaccharides attached to an affinity matrix for identifying and isolating antibodies elicited against such a carbohydrate-based vaccine in humans. Pre- and postvaccination profiles from serum samples of patients immunized with globo H-KLH were compared. All anti-globo H antibody activity was efficiently separated from other serum constituents. The isolated antibodies were readily quantified, and their specificities were analyzed. Since no comparable data were available on antibodies resulting from the vaccination of other cancer patients, we compared the observed levels with those quoted in studies with bacterial polysaccharide vaccines that had been quantified. Remarkably, cancer patients immunized with globo H-KLH produce anti-globo H antibody levels often exceeding those formed by immunization with bacterial polysaccharides. In addition, substantial quantities of both IgG and IgM antibodies were elicited, clearly indicating a class switch to IgG. Taken together, these analyses serve to clarify several aspects of the immune response to the vaccine and give several new insights to the carbohydrate-based vaccination strategy. Furthermore, antibodies so isolated could well have applications in clinical therapy.
我们之前报道过一项针对癌症患者免疫治疗的基于碳水化合物的疫苗计划。其中一种疫苗,是基于与钥孔血蓝蛋白(KLH)偶联的球 H 抗原,目前正在进行临床评估。尽管这种以及其他碳水化合物疫苗已被证明能诱导抗体反应,但目前尚无关于这些或其他抗癌疫苗在免疫患者体内所达到的抗体水平的定量数据。我们在此报告一种有效的方法,用于合成与亲和基质相连的复杂寡糖,以识别和分离人类针对这种基于碳水化合物的疫苗产生的抗体。比较了接种球 H-KLH 的患者血清样本接种前和接种后的情况。所有抗球 H 抗体活性都能有效地与其他血清成分分离。分离出的抗体易于定量,并对其特异性进行了分析。由于没有其他癌症患者接种疫苗后产生抗体的可比数据,我们将观察到的水平与已定量的细菌多糖疫苗研究中引用的水平进行了比较。值得注意的是,接种球 H-KLH 的癌症患者产生的抗球 H 抗体水平常常超过接种细菌多糖所形成的水平。此外,还诱导产生了大量的 IgG 和 IgM 抗体,这清楚地表明发生了向 IgG 的类别转换。综上所述,这些分析有助于阐明对该疫苗免疫反应的几个方面,并为基于碳水化合物的疫苗接种策略提供了一些新的见解。此外,如此分离出的抗体很可能在临床治疗中具有应用价值。