T cell receptor (TCR)mediated repertoire selection and loss of TCR vbeta diversity during the initiation of a CD4(+) T cell response

• Main Authors: Marcella Fassò, Niroshana An, Frances Crawford, C. Garrison Fathman, William M. Ridgway
• Other Authors: The Pennsylvania State University CiteSeerX Archives
• Format: Text
• Language: English
• Published: 2000
• Subjects: Sperm whale
• Online Access: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.282.2508

We recently described a novel way to isolate populations of antigen-reactive CD4 � T cells with a wide range of reactivity to a specific antigen, using immunization with a fixed dose of nominal antigen and FACS ® sorting by CD4 high expression. Phenotypic, FACS ® , functional, antibody inhibition, and major histocompatibility complex–peptide tetramer analyses, as well as T cell receptor V � sequence analyses, of the antigen-specific CD4 high T cell populations demonstrated that a diverse sperm whale myoglobin 110–121–reactive CD4 � T cell repertoire was activated at the beginning (day 3 after immunization) of the immune response. Within 6 d of immunization, lower affinity clones were lost from the responding population, leaving an expanded population of oligoclonal, intermediate affinity (and residual high affinity) T cells. This T cell subset persisted for at least 4 wk after immunization and dominated the secondary immune response. These data provide evidence that CD4 � T cell repertoire selection occurs early in the immune response in vivo and suggest that persistence and expansion of a population of oligoclonal, intermediate affinity T cells is involved in CD4 � T cell memory. Key words: T cells • clonal selection • T cell receptor • major histocompatibility complex class II tetramers • immune response