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Generation of multivirus-specific T cells by a single stimulation of peripheral blood mononuclear cells with a peptide mixture using serum-free medium

机译:通过使用无血清培养基的肽混合物的外周血单核细胞的单核单核细胞进行多种毒素特异性T细胞的产生

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Background: Restoration of virus-specific immunity by virus specific T cells (VSTs) offers an attractive alternative to conventional drugs, and can be highly effective in immunocompromised patients, including hematopoietic stem cell transplant (HSCT) recipients. However, conventional VSTs manufacture requires preparation of specialized antigen-presenting cells (APCs), prolonged ex vivo culture in serum-containing medium and antigen re-stimulation with viruses or viral vectors to provide viral antigens for presentation on APCs. Methods: To simplify this complex process, we developed a method to generate multiple VSTs by direct stimulation of peripheral blood mononuclear cells (PBMCs) with overlapping peptide libraries in serum-free medium. Results: We generated VSTs that targeted seven viruses (cytomegalovirus [CMV], Epstein-Barr virus [EBV], adenovirus [AdV], human herpesvirus 6 [HHV-6], BK virus [BKV], JC virus [JCV] and Varicella Zoster virus [VZV]) in a single line. The phenotype, growth and specificity of multiple VSTs produced in serum-free medium were equivalent to those generated in conventional serum-containing medium. Discussion: The use of serum-free medium allows this approach to be readily introduced to clinical practice with lower cost, greater reproducibility due to the absence of batch-to batch variability in serum and without concerns for infectious agents in the serum used. This simplified approach will now be tested in recipients of Human Leukocyte Antigen (HLA) matched sibling HSCT.
机译:背景:病毒特异性T细胞(VSTS)恢复病毒特异性免疫(VST)为常规药物提供有吸引力的替代品,并且可以在免疫功能性患者中具有高度效果,包括造血干细胞移植(HSCT)接受者。然而,常规Vsts制造需要制备专用抗原呈递细胞(APC),延长含血清培养基的离体培养和用病毒或病毒载体的抗原再刺激,以提供病毒抗原以呈现APC呈递。方法:为了简化这种复杂的方法,我们开发了一种通过直接刺激无血清培养基中的重叠肽文库的外周血单核细胞(PBMC)产生多VST的方法。结果:我们生成了患有七种病毒的VSTS(CytomeGalovirus [CMV],Epstein-Barr病毒[EBV],腺病毒[ADV],人疱疹病毒6 [HHV-6],BK病毒[BKV],JC病毒[JCV]和水痘在单线中扎带病毒[VZV])。在无血清培养基中产生的多个Vsts的表型,生长和特异性与常规含血清培养基产生的那些相同。讨论:使用无血清培养基允许这种方法能够以较低的成本,由于血清中没有分批变异性而较低的成本,更高的再现性,并且不担心使用的血清中的感染剂的缺陷剂。现在将在人白细胞抗原(HLA)匹配的兄弟HSCT的接受者中测试这种简化的方法。

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