TY - JOUR
T1 - Generation of a human anti-tumor necrosis factor-α monoclonal antibody by in vitro immunization with a multiple antigen peptide
AU - Fujiki, Tsukasa
AU - Tsun, Atsuji
AU - Matsumoto, Shin Ei
AU - Yamashita, Makiko
AU - Teruya, Kiichiro
AU - Shirahata, Sanetaka
AU - Katakura, Yoshinori
PY - 2010
Y1 - 2010
N2 - We developed the in vitro immunization method to induce antigen-specific immune responses in human peripheral blood mononuclear cells (PBMCs). However, when we used a peptide as sensitizing antigen, the antigen-specific immune response was found to be weak, and hence, we could not effectively obtain the antigen-specific antibody gene. In the present study, we attempted to improve the in vitro immunization method by augmenting the immune response to the peptide antigen. We used a multiple antigen peptide for sensitization. In vitro immunization of the multivalent antigen elicited a strong antigen-specific immune response in the PBMCs, and we succeeded in obtaining antigen-specific antibody genes by the phage-display method. Further, by combining the variable-region genes and constant-region genes of human IgG, we obtained four independent human monoclonal antibodies specific for tumor necrosis factor-a. This might be a good strategy for generating antigen-specific human monoclonal antibodies using a peptide antigen.
AB - We developed the in vitro immunization method to induce antigen-specific immune responses in human peripheral blood mononuclear cells (PBMCs). However, when we used a peptide as sensitizing antigen, the antigen-specific immune response was found to be weak, and hence, we could not effectively obtain the antigen-specific antibody gene. In the present study, we attempted to improve the in vitro immunization method by augmenting the immune response to the peptide antigen. We used a multiple antigen peptide for sensitization. In vitro immunization of the multivalent antigen elicited a strong antigen-specific immune response in the PBMCs, and we succeeded in obtaining antigen-specific antibody genes by the phage-display method. Further, by combining the variable-region genes and constant-region genes of human IgG, we obtained four independent human monoclonal antibodies specific for tumor necrosis factor-a. This might be a good strategy for generating antigen-specific human monoclonal antibodies using a peptide antigen.
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U2 - 10.1271/bbb.100243
DO - 10.1271/bbb.100243
M3 - Article
C2 - 20834155
AN - SCOPUS:77957345197
VL - 74
SP - 1836
EP - 1840
JO - Bioscience, Biotechnology and Biochemistry
JF - Bioscience, Biotechnology and Biochemistry
SN - 0916-8451
IS - 9
ER -