锁孔血蓝蛋白
抗原
抗体
免疫疗法
表位
免疫学
表皮生长因子受体
接种疫苗
癌症
免疫系统
生物
癌症研究
医学
内科学
作者
Robert J. Schmittling,Gary E. Archer,Duane A. Mitchell,Amy B. Heimberger,Charles N. Pegram,James E. Herndon,Henry S. Friedman,Darell D. Bigner,John H. Sampson
标识
DOI:10.1016/j.jim.2008.08.004
摘要
The epidermal growth factor receptor variant III (EGFRvIII) is a consistent tumor-specific mutation that is widely expressed in glioblastoma multiforme (GBM) and other neoplasms. As such it represents a truly tumor-specific target for antitumor immunotherapy. Although endogenous humoral responses to EGFRvIII have been reported in patients with EGFRvIII-expressing breast cancer, it is not known whether de novo responses can be generated or endogenous responses enhanced with an EGFRvIII-specific vaccine. To assess this in clinical trials, we have developed and validated an immunoassay to measure and isolate anti-EGFRvIII and anti-KLH antibodies from the serum of patients vaccinated with an EGFRvIII-specific peptide (PEPvIII) conjugated to keyhole limpet hemocyanin (KLH). Using magnetic beads with immobilized antigen we captured and detected anti-EGFRvIII and anti-KLH antibodies in serum from patients before and after vaccinations. Using this assay, we found that significant levels of antibody for tumor-specific antigen EGFRvIII (> 4 µg/mL) and KLH could be induced after vaccination with PEPvIII-KLH.
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