A comparison of serum-free media for the support of in vitro mitogen-induced blastogenic expansion of cytolytic lymphocytes

• Published in: Cytotechnology (Dordrecht) Vol. 6; no. 2; pp. 105 - 113
• Main Authors: MCVICAR, D. W, FEI LI, MCCRADY, C. W, MERCHANT, R. E
• Format: Journal Article
• Language: English
• Published: Dordrecht Springer 01-06-1991
• Subjects: Animal cells; Biological and medical sciences; Biotechnology; Blood; Cells, Cultured; Culture Media; Establishment of new cell lines, improvement of cultural methods, mass cultures; Eukaryotic cell cultures; Fundamental and applied biological sciences. Psychology; Humans; Ionomycin - pharmacology; Killer Cells, Lymphokine-Activated - immunology; Lymphocyte Activation; Lymphocytes - immunology; Methods. Procedures. Technologies; Mitogens - pharmacology; Phorbol 12,13-Dibutyrate - pharmacology; Phytohemagglutinins - pharmacology; Cell proliferation; Cell culture; Cytolysis; Serum free medium; Signal transduction; Induction; Animal; Cytotoxicity; Stimulation; Mitogen; Phytohemagglutinin; Lymphocyte
• ISSN: 0920-9069; 1573-0778
• DOI: 10.1007/BF00373027

The high cost and potential dangers of including human AB serum in incubation media used to expand lymphocyte populations in vitro for adoptive immunotherapy have stimulated efforts to develop defined media which can support both the expansion and induction of lymphocytes with tumor cytolytic activity in the absence of serum. Lymphocyte proliferation following exposure to either PHA or the combination of phorbol 12,13-dibutyrate (PDBu) and the calcium ionophore, ionomycin, was evaluated. Although the media tested, X-Vivo 10, HB-104, AIM V, and HL-1, supported the generation of comparable levels of LAK activity after 3-5 days incubation with 10(3) U human recombinant interleukin-2 (rIL-2)/ml, there were striking differences in the ability of each medium to support mitogenically stimulated lymphocytes in the absence of serum, with cells in AIM V and X-Vivo 10 showing the highest levels of DNA synthesis. In long-term cultures (17 days) of blood MNC stimulated by PDBu and ionomycin, X-Vivo 10 and HB-104 yielded the greatest numbers of cells. The addition of 2% AB serum greatly enhanced the ability of each medium to support cell proliferation to equivalent maximum levels. The results indicate that while all four serum-free media were suitable for lymphocyte culture and support the development of LAK activity, they differ in their capacity to support expansion of lymphocyte populations in response to polyclonal mitogenic activation. This latter characteristic should be considered before choosing a particular serum-free formulation as its constituents may affect mechanistic interpretations regarding signal transduction events.