IL-10 augments antibody production in in vitro immunized lymphocytes by inducing a Th2-type response and B cell maturation

An in vitro immunization (IVI) protocol enables antigen specific antibody production from L-Leucyl-L Leudse methyl ester (LLME)-treated human peripheral blood lymphocytes (PBL) upon antigen stimulation In the presence of IL-2, IL-4, and muramyl dipeptide. In the course of our studies, we have found...

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Published inBioscience, biotechnology, and biochemistry Vol. 68; no. 11; pp. 2279 - 2284
Main Authors Xu, Q. (Kyushu Univ., Fukuoka (Japan). Faculty of Agriculture), Katakura, Y, Yamashita, M, Fang, S, Tamura, T, Matsumoto, S, Aiba, Y, Teruya, K, Osada, K, Nishikawa, R, Shirahata, S
Format Journal Article
LanguageEnglish
Published Tokyo Japan Society for Bioscience, Biotechnology, and Agrochemistry 01.11.2004
Japan Society for Bioscience Biotechnology and Agrochemistry
Oxford University Press
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Summary:An in vitro immunization (IVI) protocol enables antigen specific antibody production from L-Leucyl-L Leudse methyl ester (LLME)-treated human peripheral blood lymphocytes (PBL) upon antigen stimulation In the presence of IL-2, IL-4, and muramyl dipeptide. In the course of our studies, we have found that IL-10 added at the antigen sensitization significantly augmented antibody production level from the LLME-treated PBL. In the present study, we tried to demonstrate the role of IL-10 In the augmentation of antibody production in an IV[ protocol by clarifying the cytokine expression profiles In CD4+ and CD8+ T cells. The results showed that IL-10 skewed the Th1/Th2 balance to Th2-type responses by suppressing Thl-type cytokine production and augmenting Th2-type cytokine production In CD4+ and CD8+ T cells, as well as in CD19+ B cells Furthermore, IL-10 augmented the expression of CD3g, an antigen marker of plasma cells, on B cells, which clearly Indicates that IL-10 promoted differentiation and maturation of B cells In an WI protocol. These results Indicate that IL-10 plays an important role in setting the cellular milieu to produce antibodies In an IVI protocol.
Bibliography:2005004556
U30
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ISSN:0916-8451
1347-6947
DOI:10.1271/bbb.68.2279