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Human T cell differentiation antigens characterizing a cytotoxic/suppressor T cell subset
Hybridoma
|January 1, 1981
Summary
Two monoclonal antibodies, T411 and T811, were developed against T cells. T811 identified a T cell subset crucial for allo-antigen responses and B cell differentiation suppression.
Area of Science:
- Immunology
- Cell Biology
Background:
- Chronic lymphocytic leukemia (CLL) is a heterogeneous lymphoid malignancy.
- T cell subsets play distinct roles in immune responses and regulation.
Purpose of the Study:
- To develop and characterize novel monoclonal antibodies targeting T cell surface markers.
- To investigate the functional roles of T cell subsets defined by these antibodies.
Main Methods:
- Generation of monoclonal antibodies against T cells from a CLL patient.
- Indirect immunofluorescence for antibody reactivity and cell surface expression analysis.
- Functional assays including allo-antigen response and B cell differentiation studies.
Main Results:
- Antibodies T411 and T811 specifically recognized T cell lineage markers.
- T411 identified a molecule on most peripheral T cells; T811 identified a molecule on thymocytes and a subset of T cells.
- The T811+ T cell subset mediated allo-antigen responses and suppressed B cell differentiation, while the T811- subset supported B cell differentiation.
Conclusions:
- Monoclonal antibodies T411 and T811 define distinct T cell subsets with unique functional properties.
- The T811+ T cell subset is involved in adaptive immunity and immune regulation.
- These antibodies provide tools for further research into T cell subsets and their roles in health and disease.