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Serologic identification of the human secondary B cell antigens. Correlations between function, genetics, and
The Journal of Experimental Medicine
|September 1, 1982
Summary
Researchers identified secondary B cell (SB) antigens using the ILR1 antibody, linking them to Ia-like molecules and a new HLA subregion. This discovery advances understanding of human immune system genetics and T cell recognition.
Area of Science:
- Immunogenetics
- Molecular Immunology
- Human Leukocyte Antigen (HLA) System
Background:
- Secondary B cell (SB) antigens are polymorphic, HLA-linked determinants found on B cells and macrophages.
- These antigens are recognized by primed T cells and are genetically distinct from HLA-DR, MB, and MT antigens.
Purpose of the Study:
- To serologically identify the SB molecule using the monoclonal antibody ILR1.
- To correlate SB antigen function in T cell recognition with molecular structure and genetic location.
- To characterize the genetic locus of SB antigens within the HLA system.
Main Methods:
- Utilized the monoclonal antibody ILR1 for serologic identification of SB antigens.
- Assessed T cell proliferative responses to SB2 and SB3 antigens.
- Examined ILR1 reactivity in a panel of HLA-deletion mutant lymphoblastoid cell lines.
Main Results:
- The ILR1 antibody specifically identifies an epitope on certain SB gene alleles.
- ILR1 reactivity correlated with SB2 and SB3 polymorphism and inhibited T cell responses.
- Serologic studies revealed two HLA regions centromeric to HLA-B controlling Ia-like molecule expression, including SB antigens.
Conclusions:
- SB antigens are associated with Ia-like molecules, indicating their role in immune recognition.
- The genetic locus for SB antigens represents a new HLA subregion.
- These findings provide a molecular and genetic basis for understanding SB antigen function in T cell responses.