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Dale R. Taylor

Researcher at University of Birmingham

Publications -  11
Citations -  2151

Dale R. Taylor is an academic researcher from University of Birmingham. The author has contributed to research in topics: Germinal center & Antigen. The author has an hindex of 9, co-authored 11 publications receiving 2085 citations.

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Haemopoietic colony stimulating factors promote cell survival by suppressing apoptosis

TL;DR: It is shown that the death of haemopoietic precursor cells on withdrawal of the relevant CSF is due to active cell death5, or apoptosis, indicating that CSFs promote cell survival by suppression of the process of apoptosis.
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Intrinsic constraint on plasmablast growth and extrinsic limits of plasma cell survival

TL;DR: Immunoglobulin variable region gene sequencing, and 5-bromo-2′-deoxyuridine pulse–chase studies indicate that long-lived splenic plasma cells are a mixture of cells derived from the extrafollicular and germinal center responses and cellsderived from virgin and memory B cells.
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T Helper 1 (Th1) and Th2 Characteristics Start to Develop During T Cell Priming and Are Associated with an Immediate Ability to Induce Immunoglobulin Class Switching

TL;DR: It is shown that a Th2 response to hapten–protein can proceed in a node where there is substantial Th1 activity, indicating that the Th1 or Th2 profile is at least partially established at the time of the first cognate T cell interaction with B cells in the T zone.
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Immunoglobulin switch transcript production in vivo related to the site and time of antigen-specific B cell activation.

TL;DR: It is argued that Ig class switching at this time, which is associated with cognate T cell-B cell interaction in the T zone, has a major impact on the class and subclasses of Ig produced during the response.
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Low-level Hypermutation in T Cell–independent Germinal Centers Compared with High Mutation Rates Associated with T Cell–dependent Germinal Centers

TL;DR: It is concluded that efficient activation of hypermutation depends on interaction with T cells, but some hypermutations may be induced without such signals, even outside germinal centers.