Extracellular pH affects the proliferation of cultured human T cells and their expression of the interleukin-2 receptor

被引:22
作者
Carswell, KS [1 ]
Papoutsakis, ET [1 ]
机构
[1] Northwestern Univ, Dept Chem Engn, Evanston, IL 60208 USA
来源
JOURNAL OF IMMUNOTHERAPY | 2000年 / 23卷 / 06期
关键词
pH; T cells; Ex vivo expansion; interleukin-2; receptor; apoptosis;
D O I
10.1097/00002371-200011000-00008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Ex vivo expansion of T cells is an important aspect of many cellular immunotherapy protocols, and the effects of the culture environment on the cells must be understood to produce large numbers of functional cells. Extracellular pH is a Fundamental parameter that has many different effects on cultured cells. In this study, peripheral blood mononuclear cells were stimulated with phytohemagglutinin and cultured at pH values of 7.0, 7.2, or 7.4. The effects of pH on the cells were studied during the 2 to 3 weeks of proliferation resulting from phytohemagglutinin stimulation, in order to examine the culture kinetics over realistic lime scales for ex vivo expansion. The proliferation capacity of the T cells increased more than three-fold for the pH 7.0 and 7.2 cultures compared with the pH 7.4 cultures. The culture pH also affected the kinetics of the interleukin-2 receptor down-regulation process. The faster receptor down-regulation in both the pH 7.2 and 7.4 cultures resulted in a more than twofold greater fraction of interleukin-2 receptor(+) cells in the pH 7.0 cultures. Although the fraction of apoptotic cells (using the Annexin V flow-cytometric method) remained less than 10%, we observed 27% more apoptosis in the pH 7.4 cultures than in the 7.2 cultures and 49% more apoptosis in the pH 7.4 cultures than in the 7.0 cultures. These effects on interleukin-2 receptor expression and cellular apoptosis may partially explain the observed effects of pH on T-cell proliferation.
引用
收藏
页码:669 / 674
页数:6
相关论文
共 25 条
[21]   EFFECT OF AMMONIUM ION AND EXTRACELLULAR PH ON HYBRIDOMA CELL-METABOLISM AND ANTIBODY-PRODUCTION [J].
MCQUEEN, A ;
BAILEY, JE .
BIOTECHNOLOGY AND BIOENGINEERING, 1990, 35 (11) :1067-1077
[22]  
MILLER WM, 1988, BIOTECHNOL BIOENG, V32, P965
[23]   NUTRIENT AND METABOLITE GRADIENTS IN MAMMALIAN-CELL HOLLOW FIBER BIOREACTORS [J].
PIRET, JM ;
DEVENS, DA ;
COONEY, CL .
CANADIAN JOURNAL OF CHEMICAL ENGINEERING, 1991, 69 (02) :421-428
[24]   Systemic T cell adoptive immunotherapy of malignant gliomas [J].
Plautz, GE ;
Barnett, GH ;
Miller, DW ;
Cohen, BH ;
Prayson, RA ;
Krauss, JC ;
Luciano, M ;
Kangisser, DB ;
Shu, SY .
JOURNAL OF NEUROSURGERY, 1998, 89 (01) :42-51
[25]   Infusion of cytotoxic T cells for the prevention and treatment of Epstein-Barr virus-induced lymphoma in allogeneic transplant recipients [J].
Rooney, CM ;
Smith, CA ;
Ng, CYC ;
Loftin, SK ;
Sixbey, JW ;
Gan, YJ ;
Srivastava, DK ;
Bowman, LC ;
Krance, RA ;
Brenner, MK ;
Heslop, HE .
BLOOD, 1998, 92 (05) :1549-1555