My question is prompted by the recent fungal contamination of a
long-term human CTL line. I recently moved from the murine realm where
lymphoid cells abound into human T cell work and employ (precious and
limited) PBL as culture material.
Any comments on how a supplement like amphotericin-B/fungizone impacts
the yield/effector function (i.e. cytolytic activity, cytokine release)
of peptide-stimulated PBL cultures would be appreciated.
I don't anticipate fungal contamination becoming a real problem, but to
loose any long-term cultures significantly impact my work.
Thanks in advance.
Geff Cole
