Monoclonal Antibodies for the Depletion of Specific Subpopulations of Lymphocytes
Herman Waldmann, Steve Cobbold, Shixin Qin, Richard J. Benjamin, Tony Nash, Jane Welsh, Georgia Tarnesby
Abstract
Herman Waldmann, Steve Cobbold, Shixin Qin, Richard J. Benjamin, Tony Nash, Jane Welsh, Georgia Tarnesby
Abstract
A number of rat monoclonal antibodies of the IgG2b subclass have been used to deplete mice of T lymphocyte subsets. It has been possible to produce long-term depletion where antibodies are administered to mice thymectomized in their adult life, or short-term depletion in euthymic animals. It is therefore feasible to ablate a T lymphocyte subpopulation at any stage in the course of an immune response and to examine in detail the role of a particular subset in the induction or effector phases of that response. We have used such ablative procedures to define the T cell subsets which participate in graft rejection, graft-versus-host disease, antigenic competition and antiviral and anti-self immunity and have attempted to exploit such knowledge to establish immunological tolerance in an adult animal.
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A number of rat monoclonal antibodies of the IgG2b subclass have been used to deplete mice of T lymphocyte subsets. It has been possible to produce long-term depletion where antibodies are administered to mice thymectomized in their adult life, or short-term depletion in euthymic animals. It is therefore feasible to ablate a T lymphocyte subpopulation at any stage in the course of an immune response and to examine in detail the role of a particular subset in the induction or effector phases of that response. We have used such ablative procedures to define the T cell subsets which participate in graft rejection, graft-versus-host disease, antigenic competition and antiviral and anti-self immunity and have attempted to exploit such knowledge to establish immunological tolerance in an adult animal.
Key concepts: Monoclonal antibody, Immunology, Lymphocyte subsets, Effector, Immune system, Subclass, Antibody, Biology