Two sides of a cellular coin: CD4(+)CD3- cells regulate memory responses and lymph-node organization
Open accessAbstract
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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LTi cells are CD3−CD4+ and play a role in promoting the survival of T cells that support memory B cells within lymphoid tissue.
“These might represent a small subset of ILCs, called lymphoid tissue-inducer (LTi) cells, which are CD3−CD4+ and play a role in promoting the survival of T cells that support memory B cells within lymphoid tissue.38”
From Characterizing the cellular immune response to subretinal AAV gene therapy in the murine retina (2021) · cites this paper as [38]
The Abstract proposes that adult CD4+CD3− cells promote T-cell survival, and ‘T-cell help for memory antibody responses’ links their survival signals to memory T cells that help B cells. ‘Lymph-node organogenesis’ identifies inducer cells with a similar CD4+CD3− phenotype but says their relationship to the adult cells is contentious. The paper therefore supports the proposed function of adult cells, not an established survival role for LTi cells as such. (LLM, conf=0.84)
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- Authors
- Lane, P. J. L., Gaspal, F. M. C., & Kim, M.-Y.
- Affiliations
- University of Birmingham (GB)
- Corresponding author
- Lane, Peter J. L.
- Venue
- Nature Reviews Immunology
- Published
- 2005-07-20
- Volume
- 5
- Issue
- 8
- Pages
- 655-660
- ISSN
- 1474-1733 (ISSN-L)
- 1474-1741
- PMC
- PMC1351344
- OpenAlex
- W1528686575
- Cited by
- 76
- References
- 61
- Citations by year
- 2025: 3 · 2024: 1 · 2023: 2 · 2021: 1 · 2020: 2 · 2019: 1 · 2018: 2 · 2017: 2 · 2016: 1 · 2015: 1 · 2014: 2 · 2013: 7 · 2012: 6
- FWCI
- 0.58
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature reviews. Immunology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- University of Birmingham Research Portal (University of Birmingham) (submittedVersion)
- Funders
- Wellcome Trust (065695)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Virology › HIV Research and Treatment
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Keywords
- thymic stromal cells, lymphoid organogenesis, germinal center, B cell help, affinity maturation, memory B cells, HIV infection, CCR4, CD4, AIDS, immunosenescence
- MeSH terms
- Animals, HIV, Immunologic Memory, Lymph Nodes, CD4-Positive T-Lymphocytes, CD4 Antigens, CD3 Complex, Organogenesis, Mice
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