TY - JOUR
T1 - CD4+ T cells that help B cells – a proposal for uniform nomenclature
AU - Eisenbarth, Stephanie C.
AU - Baumjohann, Dirk
AU - Craft, Joe
AU - Fazilleau, Nicolas
AU - Ma, Cindy S.
AU - Tangye, Stuart G.
AU - Vinuesa, Carola G.
AU - Linterman, Michelle A.
N1 - Publisher Copyright:
© 2021 Elsevier Ltd
PY - 2021/8
Y1 - 2021/8
N2 - T follicular helper (Tfh) cells cognately guide differentiation of antigen-primed B cells in secondary lymphoid tissues. ‘Tfh-like’ populations not expressing the canonical Tfh cell transcription factor BCL6 have also been described, which can aid particular aspects of B cell differentiation. Tfh and Tfh-like cells are essential for protective and pathological humoral immunity. These CD4+ T cells that help B cells are polarized to produce diverse combinations of cytokines and chemokine receptors and can be grouped into distinct subsets that promote antibodies of different isotype, affinity, and duration, according to the nature of immune challenge. However, unified nomenclature to describe the distinct functional Tfh and Tfh-like cells does not exist. While explicitly acknowledging cellular plasticity, we propose categorizing these cell states into three groups based on phenotype and function, paired with their anatomical site of action.
AB - T follicular helper (Tfh) cells cognately guide differentiation of antigen-primed B cells in secondary lymphoid tissues. ‘Tfh-like’ populations not expressing the canonical Tfh cell transcription factor BCL6 have also been described, which can aid particular aspects of B cell differentiation. Tfh and Tfh-like cells are essential for protective and pathological humoral immunity. These CD4+ T cells that help B cells are polarized to produce diverse combinations of cytokines and chemokine receptors and can be grouped into distinct subsets that promote antibodies of different isotype, affinity, and duration, according to the nature of immune challenge. However, unified nomenclature to describe the distinct functional Tfh and Tfh-like cells does not exist. While explicitly acknowledging cellular plasticity, we propose categorizing these cell states into three groups based on phenotype and function, paired with their anatomical site of action.
UR - http://www.scopus.com/inward/record.url?scp=85109453575&partnerID=8YFLogxK
U2 - 10.1016/j.it.2021.06.003
DO - 10.1016/j.it.2021.06.003
M3 - Review article
SN - 1471-4906
VL - 42
SP - 658
EP - 669
JO - Trends in Immunology
JF - Trends in Immunology
IS - 8
ER -