Induction of CD4 T cell memory by local cellular collectivity

Author:

Polonsky Michal1ORCID,Rimer Jacob1,Kern-Perets Amos1,Zaretsky Irina1,Miller Stav1,Bornstein Chamutal1,David Eyal1ORCID,Kopelman Naama Meira2,Stelzer Gil2,Porat Ziv2ORCID,Chain Benjamin3ORCID,Friedman Nir1ORCID

Affiliation:

1. Department of Immunology, Weizmann Institute of Science, Rehovot, Israel.

2. Life Sciences Core Facilities, Weizmann Institute of Science, Rehovot, Israel.

3. Division of Infection and Immunity, University College London, London, UK.

Abstract

Modeling memory differentiation in T cells The balance between effector and central memory T cells shifts toward the latter as the number of T cells participating in immune responses increases. Polonsky et al. determined the mechanisms by which T cell quorum sensing affects memory differentiation by using live-cell imaging to track cell proliferation and differentiation. They found that the rate of memory CD4 + T cell differentiation is determined by cell number. This rate substantially increases above a threshold number of locally interacting cells. Mathematical modeling suggests that the number of initially seeded cells and the number of cell divisions are not critical. Instead, the instantaneous number of interacting cells continuously modulates the differentiation rate. This is partly fueled by increased sensitivity to the cytokines interleukin-2 (IL-2) and IL-6, independent of any effects on cell proliferation. Science , this issue p. eaaj1853

Funder

Israel Science Foundation

Ministry of Science, Technology and Space of the State of Israel and the German Cancer Research Center (DKFZ).

WeizmannUK

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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