±õ³¾³¾³Ü²Ô´Ç°ä³Ü±ô³Ùâ„¢-³Ý¹ó
cGMP, serum-free, and xeno-free medium for the expansion of human T cells
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Overview
±õ³¾³¾³Ü²Ô´Ç°ä³Ü±ô³Ùâ„¢-³Ý¹ó can be used individually or in combination with ImmunoCultâ„¢ Human CD3/CD28 T Cell Activator or ImmunoCultâ„¢ Human CD3/CD28/CD2 T Cell Activator for a gentle, bead-free activation of T cells. For more information on the expansion of T cells with ImmunoCultâ„¢, please explore the Product Information Sheet.
Data Figures

Figure 1. ±õ³¾³¾³Ü²Ô´Ç°ä³Ü±ô³Ùâ„¢-³Ý¹ó Supports Equivalent or Faster T Cell Expansion Compared to Commercial Alternatives
T cells were isolated from human leukopaks using EasySepâ„¢ Human T Cell Isolation Kit (Catalog #17951), stimulated with ImmunoCultâ„¢ Human CD3/CD28/CD2 T Cell Activator (Catalog #10970), and cultured in either ±õ³¾³¾³Ü²Ô´Ç°ä³Ü±ô³Ùâ„¢-³Ý¹ó medium supplemented with human recombinant IL-2 (rhIL-2) or other commercially available media. All commercial alternatives were prepared according to their respective manufacturer recommendations and supplemented with human AB serum or a serum derivative. The cells were analyzed at different time points for fold expansion relative to initial cell seeding density. ±õ³¾³¾³Ü²Ô´Ç°ä³Ü±ô³Ùâ„¢-³Ý¹ó supported equal or higher expansion of total T cells compared to all commercial alternatives tested. T cells cultured in ±õ³¾³¾³Ü²Ô´Ç°ä³Ü±ô³Ùâ„¢-³Ý¹ó underwent an average of 13-, 106-, and 876-fold expansion on days 5, 7, and 10, respectively. Data shown are mean ± SEM (n = 3 - 7 donors).

Figure 2. ±õ³¾³¾³Ü²Ô´Ç°ä³Ü±ô³Ùâ„¢-³Ý¹ó Supports Equivalent or Greater T Cell Expansion than Other Commercial Alternatives
T cells were isolated from human leukopaks using EasySepâ„¢ Human T Cell Isolation Kit, stimulated with ImmunoCultâ„¢ Human CD3/CD28/CD2 T Cell Activator, and cultured in either ±õ³¾³¾³Ü²Ô´Ç°ä³Ü±ô³Ùâ„¢-³Ý¹ó medium supplemented with rhIL-2 or commercially available media. All commercial alternatives were prepared according to their respective manufacturer recommendations and supplemented with human AB serum or a serum derivative. T cells were analyzed on day 10 for fold expansion relative to the initial cell seeding density and culture viability. Compared to all commercial alternatives tested, ±õ³¾³¾³Ü²Ô´Ç°ä³Ü±ô³Ùâ„¢-³Ý¹ó showed similar or significantly higher expansion of total T cells (shown in bars) while supporting high viability (shown by data points) (> 95% viable on day 10). Data shown are mean + SEM (n = 3 - 7 donors). *p < 0.05, **p < 0.01 as determined by ANOVA using Dunnett's Multiple Comparison post-hoc test.

Figure 3. T Cells Expanded in ±õ³¾³¾³Ü²Ô´Ç°ä³Ü±ô³Ùâ„¢-³Ý¹ó Maintain Similar Proportions of CD4+ and CD8+ Cells Following 10 Days of Culture Expansion
CD3+ T cells were isolated from human leukopaks using EasySepâ„¢ Human T Cell Isolation Kit, stimulated with ImmunoCultâ„¢ Human CD3/CD28/CD2 T Cell Activator, and cultured in ±õ³¾³¾³Ü²Ô´Ç°ä³Ü±ô³Ùâ„¢-³Ý¹ó medium supplemented with rhIL-2. T cells were harvested on days (A) 0 and (B) 10 and analyzed by flow cytometry for the proportions of viable cells expressing CD4 and CD8. Data shown are from one representative donor; similar results were observed for the other 3 donors tested.

Figure 4. T Cells Expanded in ±õ³¾³¾³Ü²Ô´Ç°ä³Ü±ô³Ùâ„¢-³Ý¹ó Express Intracellular IFN-Æ”, TNF-α, and IL-4
T cells were isolated from human leukopaks using EasySepâ„¢ Human T Cell Isolation Kit, stimulated with ImmunoCultâ„¢ Human CD3/CD28/CD2 T Cell Activator, and cultured in ±õ³¾³¾³Ü²Ô´Ç°ä³Ü±ô³Ùâ„¢-³Ý¹ó medium supplemented with rhIL-2. On day 10, T cells were harvested and analyzed for intracellular IFN-Æ”, TNF-α, and IL-4 after stimulation with PMA and ionomycin for 4 hours, with Brefeldin A added after 2 hours. (A - C) IFN-Æ”, TNF-α, and IL-4 production in CD4+ cells after stimulation; (D and E) IFN-Æ” and TNF-α production in CD8+ cells after stimulation. Data shown are from one representative donor; similar results were observed for the other 3 donors tested. Unstimulated controls had < 0.5% IFN-Æ” and TNF-α expression, or < 5% IL-4 expression (data not shown).
Protocols and Documentation
Find supporting information and directions for use in the Product Information Sheet or explore additional protocols below.
Applications
This product is designed for use in the following research area(s) as part of the highlighted workflow stage(s). Explore these workflows to learn more about the other products we offer to support each research area.
Resources and Publications
Educational Materials (13)
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