Chianese-Bullock Kimberly A, Lewis Sarah T, Sherman Nicholas E, Shannon John D, Slingluff Craig L
Department of Surgery/Division of Surgical Oncology/Human Immune Therapy Center, University of Virginia, Charlottesville, VA 22908, United States.
Vaccine. 2009 Mar 10;27(11):1764-70. doi: 10.1016/j.vaccine.2009.01.018. Epub 2009 Feb 8.
To date, most peptide-based vaccines evaluated for the treatment of cancer have consisted of one or few peptides. However, as a greater number of peptide antigens become available for use in experimental therapies, it is important to establish the feasibility of combining multi-peptide reagents as individual peptide mixtures. We have found that mixtures of up to 12 peptides can be analyzed accurately for identity, purity, and stability (for at least 5 years) using a combination of high-performance liquid chromatography (HPLC) and mass spectrometry and these complex peptide mixtures have been acceptable for use in human clinical trials. We have also identified some specific concerns for degradation products that should be considered in multi-peptide vaccine preparation and follow-up quality assurance studies. Results from these analyses have implications for changing the way peptide-based vaccines are manufactured and demonstrate that multi-peptide vaccines are reliable reagents for use in peptide-based immune therapies.
迄今为止,大多数用于癌症治疗评估的肽基疫苗都由一种或几种肽组成。然而,随着越来越多的肽抗原可用于实验性治疗,确定将多种肽试剂作为单个肽混合物组合使用的可行性变得很重要。我们发现,使用高效液相色谱(HPLC)和质谱联用技术,可以准确分析多达12种肽的混合物的同一性、纯度和稳定性(至少5年),并且这些复杂的肽混合物已被批准用于人体临床试验。我们还确定了一些关于降解产物的具体问题,这些问题在多肽疫苗制备和后续质量保证研究中应予以考虑。这些分析结果对改变肽基疫苗的生产方式具有启示意义,并表明多肽疫苗是用于肽基免疫治疗的可靠试剂。