There is increasing evidence that T cells are able to control
tumor growth and survival in
cancer patients, both in early and late stages of the disease. However,
tumor-specific T-cell responses are difficult to mount and sustain in
cancer patients, and are limited by numerous immune escape mechanisms of
tumor cells selected during immunoediting. An alternative approach to engage T cells for
cancer therapy are
antibodies, which are bispecific for a surface target
antigen on
cancer cells, and for CD3 on T cells. These are capable of connecting any kind of cytotoxic T cell to a
cancer cell, independently of T-cell receptor specificity, costimulation, or
peptide antigen presentation. Here, we review the principle of a new class of
bispecific antibodies called
BiTE (for "bispecific T-cell engager")
antibodies. Recent results from clinical studies with a CD19/CD3-bispecific
BiTE antibody suggest that this therapeutic paradigm is finally showing promise for treatment of both bulky and
minimal residual disease.