Single Naive CD4+ T Cells from a Diverse Repertoire Produce Different Effector Cell Types during Infection
Author(s) -
Noah J. Tubo,
Antonio J. Pagán,
Justin J. Taylor,
Ryan Nelson,
Jonathan L. Linehan,
James M. Ertelt,
Eric S. Huseby,
Sing Sing Way,
Marc K. Jenkins
Publication year - 2013
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2013.04.007
Subject(s) - biology , effector , t cell receptor , population , t cell , naive t cell , microbiology and biotechnology , major histocompatibility complex , immunology , antigen presenting cell , streptamer , antigen , immune system , demography , sociology
A naive CD4(+) T cell population specific for a microbial peptide:major histocompatibility complex II ligand (p:MHCII) typically consists of about 100 cells, each with a different T cell receptor (TCR). Following infection, this population produces a consistent ratio of effector cells that activate microbicidal functions of macrophages or help B cells make antibodies. We studied the mechanism that underlies this division of labor by tracking the progeny of single naive T cells. Different naive cells produced distinct ratios of macrophage and B cell helpers but yielded the characteristic ratio when averaged together. The effector cell pattern produced by a given naive cell correlated with the TCR-p:MHCII dwell time or the amount of p:MHCII. Thus, the consistent production of effector cell subsets by a polyclonal population of naive cells results from averaging the diverse behaviors of individual clones, which are instructed in part by the strength of TCR signaling.
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