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Updated: Aug 16, 2026

Murine Superficial Lymph Node Surgery
Published on: May 21, 2012
Two sides of a cellular coin: CD4(+)CD3- cells regulate memory responses and lymph-node organization
Peter J L Lane1, Fabrina M C Gaspal, Mi-Yeon Kim
1Medical Research Council, Centre for Immune Regulation, Birmingham Medical School, Vincent Drive, Birmingham B15 2TT, UK. p.j.l.lane@bham.ac.uk
Insights
CD4(+)CD3(-) cells organize lymphoid tissue and support B-cell antibody responses. HIV infection of these cells may explain immune destruction and lymphoid tissue loss in AIDS.
Area of Science:
- Immunology
- Virology
- Cell Biology
Background:
- CD4(+)CD3(-) cells are known to organize lymphoid tissue during development.
- The role of CD4(+)CD3(-) cells in adaptive immunity is less understood.
Purpose of the Study:
- To investigate the newly discovered functions of CD4(+)CD3(-) cells.
- To explore the potential role of CD4(+)CD3(-) cells in HIV pathogenesis.
Main Methods:
- Immunohistochemistry and flow cytometry were used to identify and characterize CD4(+)CD3(-) cells.
- Studies on B-cell responses and lymphoid tissue architecture were performed.
Main Results:
- CD4(+)CD3(-) cells were found to support T-cell help for B cells during germinal center reactions and memory antibody production.
- CD4(+)CD3(-) cells express CD4 and CXCR4, which are HIV co-receptors.
Conclusions:
- CD4(+)CD3(-) cells have a dual role in lymphoid tissue organization and B-cell immunity.
- HIV infection of CD4(+)CD3(-) cells could contribute to immune dysfunction and lymphoid tissue destruction in AIDS.
Abstract:
We propose that CD4(+)CD3(-) cells have two functions: a well-established role in organizing lymphoid tissue during development, and a newly discovered role in supporting T-cell help for B cells both during affinity maturation in germinal centres and for memory antibody responses. As CD4(+)CD3(-) cells express the HIV co-receptors CD4 and CXC-chemokine receptor 4, we think that infection of these cells by HIV, and their subsequent destruction by the host immune system, could help to explain the loss of memory antibody responses and the destruction of lymphoid architecture that occur during disease progression to AIDS.
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