The growth of T cells ex vivo for the purpose of T cell therapies is a rate-limiting step in the overall process for cancer patients to achieve remission. Growing T cells is a fiscally-, time-, and resource-intensive process. Cytokines have been shown to accelerate the growth of T cells, specifically IL-2, IL-7, and IL-15. Here a design of experiments was conducted to optimize the growth rate of different naïve and memory T cell subsets using combinations of cytokines. Mathematical models were developed to study the impact of IL-2, IL-7, and IL-15 on the growth of T cells. The results show that CD and CD naïve T cells grew effectively using moderate IL-2 and IL-7 in combination, and IL-7, respectively. CD and CD memory cells favored moderate IL-2 and IL-15 in combination and moderate IL-7 and IL-15 in combination, respectively. A statistically significant interaction was observed between IL-2 and IL-7 in the growth data of CD naïve T cells, while the interaction between IL-7 and IL-15 was found for CD naïve T cells. The important genes and related signaling pathways and metabolic reactions were identified from the RNA sequencing data for each of the four subsets stimulated by each of the three cytokines. This systematic investigation lays the groundwork for studying other T cell subsets.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9139303PMC
http://dx.doi.org/10.3390/cells11101701DOI Listing

Publication Analysis

Top Keywords

il-2 il-7
20
il-7 il-15
20
growth cells
12
naïve cells
12
cells
9
naïve memory
8
memory cells
8
il-7
8
il-15 growth
8
cell subsets
8

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!