T cell help controls the speed of the cell cycle in germinal center B cells

Author:

Gitlin Alexander D.1,Mayer Christian T.1,Oliveira Thiago Y.1,Shulman Ziv1,Jones Mathew J. K.2,Koren Amnon3,Nussenzweig Michel C.14

Affiliation:

1. Laboratory of Molecular Immunology, The Rockefeller University, New York, NY 10065, USA.

2. Molecular Biology Program, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10065, USA.

3. Department of Genetics, Harvard Medical School, Boston, MA 02115, USA.

4. Howard Hughes Medical Institute (HHMI), The Rockefeller University, New York, NY 10065, USA.

Abstract

B cells have a need for speed High-affinity antibodies provide long-lasting protective immunity against many infections. Generating such antibodies requires help, in the form of T cells, which interact with antibody-producing B cells. As B cells proliferate and mutate their antibody genes, T cells select the cells producing high-affinity antibodies. Gitlin et al. show in mice that B cells that receive T cell help transit through the cell cycle more quickly by increasing the speed at which replication forks progress. Such a rapid cell cycle transition gives high-affinity B cells a selective advantage. Science , this issue p. 643

Funder

NIH

National Institute of Allergy and Infectious Diseases

NIH Medical Scientist Training Program

NIH Center for HIV/AIDS Vaccine Immunology and Immunogen Discovery (CHAVI-ID)

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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