Disparate Individual Fates Compose Robust CD8 + T Cell Immunity

Author:

Buchholz Veit R.1,Flossdorf Michael23,Hensel Inge1,Kretschmer Lorenz1,Weissbrich Bianca1,Gräf Patricia1,Verschoor Admar1,Schiemann Matthias14,Höfer Thomas23,Busch Dirk H.1456

Affiliation:

1. Institute for Medical Microbiology, Immunology and Hygiene, Technische Universität München (TUM), Munich 81675, Germany.

2. Division of Theoretical Systems Biology, German Cancer Research Center (DKFZ), Heidelberg 69120, Germany.

3. BioQuant Center, University of Heidelberg, Heidelberg 69120, Germany.

4. Clinical Cooperation Groups “Antigen-specific Immunotherapy” and “Immune-Monitoring,” Helmholtz Center Munich (Neuherberg), TUM, Munich 81675, Germany.

5. Focus Group “Clinical Cell Processing and Purification,” Institute for Advanced Study, TUM, Munich 81675, Germany.

6. National Centre for Infection Research (DZIF), Munich 81675, Germany.

Abstract

Dynamic Protection During an immune response, CD8 + T cells are recruited to provide protection. Most cells differentiate into short-lived effectors that help to clear the pathogen, whereas others form long-lived memory cells to protect against reinfection. Gerlach et al. (p. 635 , published online 14 March) and Buchholz et al. (p. 630 , published online 14 March) used in vivo fate mapping of mouse T cells with a defined specificity during a bacterial infection to show that the dynamics of the single-cell response are not uniform. The response of a particular T cell population is the average of a small number of clones that expand greatly (“large clones”) and many clones that only proliferate at low amounts (“small clones”). The memory pool arises largely from small clones whereas effectors are primarily made up of large clones.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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