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New Monoclonal Antibodies That Define Multiple Epitopes and a Human‐Specific Marker on the Interleukin 2 Receptor Molecules of Primates
Author(s) -
Tanaka Yuetsu,
Inoi Takeshi,
Tozawa Hideki,
Sugamura Kazuo,
Hinuma Yorio
Publication year - 1986
Publication title -
microbiology and immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.664
H-Index - 70
eISSN - 1348-0421
pISSN - 0385-5600
DOI - 10.1111/j.1348-0421.1986.tb00954.x
Subject(s) - monoclonal antibody , epitope , antibody , microbiology and biotechnology , biology , immunoprecipitation , cell culture , virology , immunology , genetics
Twelve hybridoma cell lines producing monoclonal antibodies to the human interleukin 2 (IL‐2) receptor (IL‐2R) molecule were prepared. These antibodies were characterized by competitive antibody‐binding assay and sequential immunoprecipitation assay with four known monoclonal antibodies to the human IL‐2R molecule. The twelve new monoclonal antibodies were divided among the four known antibody types, the HIEI‐, H‐A26‐, H‐31‐, and anti‐Tac‐type, and an additional new type, the H‐48‐type. The H‐48 antibody did not compete with any other antibodies in the competitive binding assay. The binding of 125 I‐IL‐2 to MT‐2 cells and the IL‐2‐dependent growth of normal activated T‐cells were both strongly inhibited by all the H‐31‐ and anti‐Tac‐type antibodies, and partially or slightly inhibited by HIEI‐ and H‐A26‐type antibodies, but were not inhibited by the H‐48 antibody. Thus, the same type of monoclonal antibodies had a similar effect on the function of IL‐2R. These results suggest that epitopes for the same type of antibodies could be single identical epitopes or epitopes closely associated with each other. On the other hand, these antibodies also reacted variously with a panel of various human and simian lymphoid cell lines immortalized with human T‐cell leukemia virus type‐I (HTLV‐I): the H‐45 antibody reacted only with the human cell lines, the H‐Cl and H‐44 and H‐47 antibodies reacted with human and ape cell lines, and the other antibodies reacted with cell lines of humans, apes and Old and New World monkeys. These differences in the reactivity of the antibodies with the primate cell lines suggest that the antigenic structure of the IL‐2R molecule changed during evolutionary divergence of the primates.