A Therapeutic Antibody for Cancer, Derived from Single Human B Cells
Author(s) -
Ryan T. Bushey,
M. Anthony Moody,
Nathan L. Nicely,
Barton F. Haynes,
S. Munir Alam,
Stephen T. Keir,
Rex C. Bentley,
Kingshuk Roy Choudhury,
Elizabeth B. Gottlin,
Michael J. Campa,
HuaXin Liao,
Edward F. Patz
Publication year - 2016
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2016.04.038
Subject(s) - antibody , lytic cycle , anaphylatoxin , complement system , cancer research , cancer , cancer cell , phage display , biology , cytotoxicity , autoantibody , immunology , chemistry , in vitro , virus , biochemistry , genetics
Some patients with cancer never develop metastasis, and their host response might provide cues for innovative treatment strategies. We previously reported an association between autoantibodies against complement factor H (CFH) and early-stage lung cancer. CFH prevents complement-mediated cytotoxicity (CDC) by inhibiting formation of cell-lytic membrane attack complexes on self-surfaces. In an effort to translate these findings into a biologic therapy for cancer, we isolated and expressed DNA sequences encoding high-affinity human CFH antibodies directly from single, sorted B cells obtained from patients with the antibody. The co-crystal structure of a CFH antibody-target complex shows a conformational change in the target relative to the native structure. This recombinant CFH antibody causes complement activation and release of anaphylatoxins, promotes CDC of tumor cell lines, and inhibits tumor growth in vivo. The isolation of anti-tumor antibodies derived from single human B cells represents an alternative paradigm in antibody drug discovery.
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