TY - CHAP
T1 - Antibody-Based Cancer Therapy
T2 - Successful Agents and Novel Approaches
AU - Hendriks, D
AU - Choi, G
AU - de Bruyn, M
AU - Wiersma, V R
AU - Bremer, E
N1 - © 2017 Elsevier Inc. All rights reserved.
PY - 2017
Y1 - 2017
N2 - Since their discovery, antibodies have been viewed as ideal candidates or "magic bullets" for use in targeted therapy in the fields of cancer, autoimmunity, and chronic inflammatory disorders. A wave of antibody-dedicated research followed, which resulted in the clinical approval of a first generation of monoclonal antibodies for cancer therapy such as rituximab (1997) and cetuximab (2004), and infliximab (2002) for the treatment of autoimmune diseases. More recently, the development of antibodies that prevent checkpoint-mediated inhibition of T cell responses invigorated the field of cancer immunotherapy. Such antibodies induced unprecedented long-term remissions in patients with advanced stage malignancies, most notably melanoma and lung cancer, that do not respond to conventional therapies. In this review, we will recapitulate the development of antibody-based therapy, and detail recent advances and new functions, particularly in the field of cancer immunotherapy. With the advent of recombinant DNA engineering, a number of rationally designed molecular formats of antibodies and antibody-derived agents have become available, and we will discuss various molecular formats including antibodies with improved effector functions, bispecific antibodies, antibody-drug conjugates, antibody-cytokine fusion proteins, and T cells genetically modified with chimeric antigen receptors. With these exciting advances, new antibody-based treatment options will likely enter clinical practice and pave the way toward more successful control of malignant diseases.
AB - Since their discovery, antibodies have been viewed as ideal candidates or "magic bullets" for use in targeted therapy in the fields of cancer, autoimmunity, and chronic inflammatory disorders. A wave of antibody-dedicated research followed, which resulted in the clinical approval of a first generation of monoclonal antibodies for cancer therapy such as rituximab (1997) and cetuximab (2004), and infliximab (2002) for the treatment of autoimmune diseases. More recently, the development of antibodies that prevent checkpoint-mediated inhibition of T cell responses invigorated the field of cancer immunotherapy. Such antibodies induced unprecedented long-term remissions in patients with advanced stage malignancies, most notably melanoma and lung cancer, that do not respond to conventional therapies. In this review, we will recapitulate the development of antibody-based therapy, and detail recent advances and new functions, particularly in the field of cancer immunotherapy. With the advent of recombinant DNA engineering, a number of rationally designed molecular formats of antibodies and antibody-derived agents have become available, and we will discuss various molecular formats including antibodies with improved effector functions, bispecific antibodies, antibody-drug conjugates, antibody-cytokine fusion proteins, and T cells genetically modified with chimeric antigen receptors. With these exciting advances, new antibody-based treatment options will likely enter clinical practice and pave the way toward more successful control of malignant diseases.
KW - CHIMERIC ANTIGEN RECEPTOR
KW - APOPTOSIS-INDUCING LIGAND
KW - ACUTE MYELOID-LEUKEMIA
KW - NON-HODGKINS-LYMPHOMA
KW - CHRONIC LYMPHOCYTIC-LEUKEMIA
KW - TRAIL FUSION PROTEIN
KW - B-CELL MALIGNANCIES
KW - RICIN-A-CHAIN
KW - CAR-T-CELLS
KW - METASTATIC BREAST-CANCER
U2 - 10.1016/bs.ircmb.2016.10.002
DO - 10.1016/bs.ircmb.2016.10.002
M3 - Chapter
C2 - 28325214
SN - 978-0-12-812469-7
VL - 331
T3 - International Review of Cell and Molecular Biology
SP - 289
EP - 383
BT - International Review of Cell and Molecular Biology
A2 - Galluzi, Lorenzo
A2 - Vitale, Ilio
PB - Elsevier
ER -