Document 0667 DOCN M9650667 TI Single-cell PCR analysis of TCR repertoires selected by antigen in vivo: a high magnitude CD8 response is comprised of very few clones. DT 9605 AU Maryanski JL; Jongeneel CV; Bucher P; Casanova JL; Walker PR; Ludwig Institute for Cancer Research, Swiss Institute for; Experimental Cancer Research, Epalinges, Switzerland. SO Immunity. 1996 Jan;4(1):47-55. Unique Identifier : AIDSLINE MED/96158750 AB Taking advantage of a potent MHC class I-restricted response that allows the identification of antigen-selected CD8 T cells directly ex vivo, we characterized the antigen-specific T cell repertoires that develop in individual mice by single-cell PCR analysis. Each of the immune mice displayed distinct yet structurally similar TCR repertoires. The overall repertoire size was estimated to be in the range of 15-20 for most mice. No major differences were observed between primary and secondary responses. Moreover, for a hyperimmunized mouse the antigen-specific TCR repertoire expressed 8 months after the initial immunization was very similar to that found at the peak of the primary response. Our results demonstrate that a high magnitude immune response may be composed of very few clones, and that at least in the system analyzed, the memory response largely reflects the repertoire selected by the peak of the primary response. DE Amino Acid Sequence Animal *Antigen Presentation Base Sequence Clone Cells/IMMUNOLOGY CD8-Positive T-Lymphocytes/*IMMUNOLOGY Immunity, Cellular Mice Mice, Inbred DBA Molecular Sequence Data Polymerase Chain Reaction Receptors, Antigen, T-Cell/*IMMUNOLOGY T-Lymphocyte Subsets/IMMUNOLOGY JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).