TY - JOUR
T1 - Therapeutic application of antibody fragments in autoimmune diseases
T2 - current state and prospects
AU - Fernandes, João C.
N1 - Funding Information:
This work was supported by National Funds from FCT – Fundação para a Ciência e a Tecnologia through project UID/Multi/50016/2013.
Funding Information:
This work was supported by National Funds from FCT ? Funda??o para a Ci?ncia e a Tecnologia through project UID/Multi/50016/2013.
Publisher Copyright:
© 2018 Elsevier Ltd
PY - 2018/12
Y1 - 2018/12
N2 - Over the past decades, conventional antibodies have been dissected through different strategies into smaller antigen-binding fragments. Therapeutic solutions built on such fragments can offer several advantages, including the capacity to access challenging epitopes, reduced immunogenicity, lower production costs, and higher stability. Although the development of antibody fragments for cancer therapy has received more attention than any other potential therapeutic application, the development of pharmacological tools based on these molecules for the treatment of autoimmune diseases (AIDs) has been growing at a fast pace. Here, I provide an in-depth characterization of the various formats for the treatment of autoimmune diseases in development across the industry, including antigen-binding fragments (Fab), single-chain variable fragments (scFv), and single variable-domain fragments, as well as multimeric antibody fragments and antibody–drug conjugates.
AB - Over the past decades, conventional antibodies have been dissected through different strategies into smaller antigen-binding fragments. Therapeutic solutions built on such fragments can offer several advantages, including the capacity to access challenging epitopes, reduced immunogenicity, lower production costs, and higher stability. Although the development of antibody fragments for cancer therapy has received more attention than any other potential therapeutic application, the development of pharmacological tools based on these molecules for the treatment of autoimmune diseases (AIDs) has been growing at a fast pace. Here, I provide an in-depth characterization of the various formats for the treatment of autoimmune diseases in development across the industry, including antigen-binding fragments (Fab), single-chain variable fragments (scFv), and single variable-domain fragments, as well as multimeric antibody fragments and antibody–drug conjugates.
UR - http://www.scopus.com/inward/record.url?scp=85048582382&partnerID=8YFLogxK
U2 - 10.1016/j.drudis.2018.06.003
DO - 10.1016/j.drudis.2018.06.003
M3 - Review article
C2 - 29890227
AN - SCOPUS:85048582382
SN - 1359-6446
VL - 23
SP - 1996
EP - 2002
JO - Drug Discovery Today
JF - Drug Discovery Today
IS - 12
ER -