Toward a general model of CD4 + T cell subset specification and memory cell formation
Immunity, ISSN: 1074-7613, Vol: 56, Issue: 3, Page: 475-484
2023
- 18Citations
- 62Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations18
- Citation Indexes18
- 18
- CrossRef10
- Captures62
- Readers62
- 62
Review Description
In the past few decades, a number of transformative discoveries have been made regarding memory CD8 + T cell biology; meanwhile, the CD4 + T cell field has lagged behind this progress. This perspective focuses on CD4 + helper T (Th) cell subset specification and memory cell formation. Here, we argue that the sheer number of Th effector and memory cell subsets and a focus on their differences have been a barrier to a general model of CD4 + memory T cell formation that applies to all immune responses. We highlight a bifurcation model that relies on an IL-2 signal-dependent switch as an explanation for the balanced production of diverse Th memory cells that participate in cell-mediated or humoral immunity in most contexts.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S1074761323000845; http://dx.doi.org/10.1016/j.immuni.2023.02.010; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85150315611&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/36921574; https://linkinghub.elsevier.com/retrieve/pii/S1074761323000845; https://dx.doi.org/10.1016/j.immuni.2023.02.010
Elsevier BV
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