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Cell Culture conditions determine the enhancement of specific monoclonal antibody productivity of calcium alginate‐entrapped S3H5/γ2bA2 hybridoma cells
Author(s) -
Lee Gyun Min,
Chuck Alice S.,
Palsson Bernhard O.
Publication year - 1993
Publication title -
biotechnology and bioengineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.136
H-Index - 189
eISSN - 1097-0290
pISSN - 0006-3592
DOI - 10.1002/bit.260410307
Subject(s) - monoclonal antibody , calcium alginate , chemistry , calcium , cell culture , productivity , antibody , microbiology and biotechnology , biochemistry , immunology , biology , genetics , organic chemistry , macroeconomics , economics
Immobilization offers several intrinsic advantages over free suspension cultures for the production of monoclonal antibodies. An important advantage of immobilization is the improved specific monoclonal antibody (MAb) productivity (q MAb ) that can be obtained. However, there are conflicting reports in the literature on the enhancement of the q MAb with immobilization. The discrepancies between these reports can be attributed to the different to either the cultivation methods used for immobilized cell or to difference between the cell lines used in the various studies. We show that these differences may be attributed to the different cultivation methods used for one model hybridoma cell line. S3H5/ϒ2bA2 hybridoma cells entrapped in different sizes of calcium alginate beads were cultivated in both T‐ and spinner flasks in order to determine whether cultivation methods (T‐ and spinner flasks) and bead size influence the q MAb Free‐suspended cell cultures inoculated with cells recovered from alginate beads were also carried out in order to determine whether changes in the q Mab of the entrapped cells are reversible. The cultivation methods was found to influence significantly the q MAb of the entrapped cells. When the entrapped cells in 1‐mn diameter beads were cultivated in T‐flasks, the q MAb was not increased by 200% as previously observed in an entrapped cell culture using 1‐mm‐diameter alginate beads in spinner flasks. The q MAb of the entrapped cell was approximately 58% higher than that of the free‐suspended cells in a control experiment. Unlike the cultivation method, the bead size in the range of 1‐ to 3‐mm diameter did not significantly influence the q MAb , regardless of cultivations methods. The changes in q MAb of an entrapped cells were reversible. When the free‐suspended cells recovered from the T‐ and spinner flasks were sub‐cultured in T‐ and spinner flasks enhanced q MAb of the entrapped cells in both cases decreased to the level of the free‐suspended cell in a control experiments. Taken together, these results shows that the method of cultivation of hybridoma cells immobilized in alginate beads determines the extent of enhancement of the q MAb . © 1993 John Wiley & Sons, Inc.