期刊
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
卷 111, 期 41, 页码 14852-14857出版社
NATL ACAD SCIENCES
DOI: 10.1073/pnas.1403271111
关键词
follicular helper; infection; lymphocytes
资金
- Swiss National Science Foundation [PP00P3_144883, PDFMP3_137128]
- Swiss Vaccine Research Institute
- Swiss National Science Foundation (SNF) [PDFMP3_137128, PP00P3_144883] Funding Source: Swiss National Science Foundation (SNF)
Cumulative T-cell receptor signal strength and ensuing T-cell responses are affected by both antigen affinity and antigen dose. Here we examined the distinct contributions of these parameters to CD4 T-cell differentiation during infection. We found that high antigen affinity positively correlates with T helper (Th)1 differentiation at both high and low doses of antigen. In contrast, follicular helper T cell (T-FH) effectors are generated after priming with high, intermediate, and low affinity ligand. Unexpectedly, memory T cells generated after priming with very low affinity antigen remain impaired in their ability to generate secondary Th1 effectors, despite being recalled with high affinity antigen. These data challenge the view that only strongly stimulated CD4 T cells are capable of differentiating into the TFH and memory T-cell compartments and reveal that differential strength of stimulation during primary T-cell activation imprints unique and long lasting T-cell differentiation programs.
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