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DEVELOPMENT AND OPTIMIZATION OF ANIMAL ORIGIN-FREE, SERUM-FREE MEDIA FOR HUMAN TREG MANUFACTURING

机译:无人血清制造的无动物源,无血清培养基的开发和优化

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Regulatory T cells (Treg) constitute a small subset of immunosuppressive CD4+ T cells. Studies have shown that imbalanced or aberrant Treg function can result in autoimmune disorders. The importance of Tregs in dampening immune responses has been described in multiple studies and Treg immunotherapies are being explored to develop personalized therapies for various autoimmune diseases. Scalable commercial development of Treg therapies suffers similar challenges as other T cell immunotherapies: biosafety and supply chain concerns of human serum and limitations regarding bioprocess development due to serum variability. Additionally, there a challenges regarding Treg isolation for both magnetically isolated (blockade of CD25+ epitope may affect function and low purity) and flow cytometry sorted Tregs (low numbers and viability). In addition, the starting population and purity (measured by FOXP3 expression) can be low, resulting in small cell numbers post expansion which can impact dose escalation studies. To address these challenges, we are developing a serum-free, animal origin component - free, defined medium and Treg optimized Dynabeads~(TM). Our strategy was to exploit metabolic differences between Tregs and conventional Tcells as well as optimizing the level of activation ligands to develop a defined Treg manufacturing system. Using design of experiment (DOE) approaches we explored factors described in the literature to be associated with Treg development. DOE studies were followed by testing in combination with Treg Dynabeads~(TM) in development. Feasibility was evaluated with positively selected Tregs (CD4+CD25+CD127lo, n=5). Tregs cultured in our system achieve higher FOXP3+ frequencies (>60% FOXP3+) outperforming control containing 10% human serum (~30% FOXP3+). In summary, our results suggest that serum can be eliminated from Treg workflows to generate highly suppressive enriched FOXP3+ Treg immunotherapy product. We believe that our defined serum-free medium and Dynabeads~(TM) Treg system will enable the development of better immunotherapies for autoimmunity.
机译:调节性T细胞(Treg)构成了免疫抑制CD4 + T细胞的一小部分。研究表明,Treg功能失衡或异常可能导致自身免疫性疾病。在多项研究中已经描述了Treg在抑制免疫反应中的重要性,并且正在探索Treg免疫疗法来开发针对各种自身免疫疾病的个性化疗法。 Treg疗法的可扩展的商业开发面临着与其他T细胞免疫疗法类似的挑战:人血清的生物安全性和供应链问题以及由于血清变异性而对生物过程发展的限制。另外,对于磁性分离的Treg分离(CD25 +表位的阻断可能影响功能和低纯度)和流式细胞仪分选的Treg(低数量和生存力)都存在挑战。此外,起始种群和纯度(通过FOXP3表达测量)可能很低,导致扩增后的细胞数量少,这可能会影响剂量递增研究。为解决这些挑战,我们正在开发无血清,动物来源的成分-无定义的培养基和Treg优化的Dynabeads〜(TM)。我们的策略是利用Treg和传统Tcell之间的代谢差异,以及优化激活配体的水平来开发确定的Treg制造系统。使用实验设计(DOE)方法,我们探索了文献中描述的与Treg发育相关的因素。在DOE研究之后,与开发中的Treg Dynabeads〜(TM)组合进行了测试。用阳性选择的Tregs(CD4 + CD25 + CD127lo,n = 5)评估可行性。在我们的系统中培养的Treg可以达到更高的FOXP3 +频率(> 60%FOXP3 +),胜过包含10%人血清(〜30%FOXP3 +)的对照。总而言之,我们的结果表明可以从Treg工作流程中消除血清,以产生高度抑制性的富FOXP3 + Treg免疫疗法产品。我们相信,我们定义的无血清培养基和DynabeadsT​​M Treg系统将能够为自身免疫开发更好的免疫疗法。

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