2014, Number 3
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Rev Cubana Hematol Inmunol Hemoter 2014; 30 (3)
Obtention of cell culture supernatant for erythrocyte agglutination of blood group B antigen
Miranda AA, Justiz LAC, Mures DYL, Romaguera FY
Language: Spanish
References: 13
Page: 248-256
PDF size: 137.20 Kb.
ABSTRACT
Introduction: The obtention of monoclonal antibodies in ascite fluid has been
declining gradually due to the appearance of alternative
in vitro production that
achieve higher volumes and a more precise monitoring of the production process,
which increases the reproducibility of processes and the quality of products.
Objective: To evaluate two methods to make cell culture supernatant rich in
murine monoclonal IgG2b type, with agglutinating activity against human red cell of
blood group antigen B (ABO system), which is secreted by murine hybridoma C6G4.
Methods: Two methods were evaluated for antibody production in cell culture
supernatant using as model a CELLine bioreactor for the production of monoclonal
antibodies in high cell density culture. Both methods essentially differed in the
seeding cell density in the bioreactor and the fermentation period between seeding
and harvesting of the culture broth rich in antibodies. The specific antibody
concentration and potency of agglutination was determined in the obtained
supernatant and also the cell density and cell viability of the culture reached at the
time of harvest.
Results: Both methods generated culture supernatants with similar agglutination
strength despite differences found in the rest of the variables measured. Even when
one of the methods produced a higher antibody concentration in the supernatants,
no differences in potency of the supernatants agglutination obtained by both
alternatives were observed.
Conclusions: Both methods generated supernatant anti-B with different
concentrations of antibodies but similar potency of agglutination. The main
difference was that with one of the methods the same volume of the product was
obtained in a considerably minor time.
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