Cytotoxic T cells swarm by homotypic chemokine signalling

Author:

Galeano Niño Jorge Luis12,Pageon Sophie V12ORCID,Tay Szun S12ORCID,Colakoglu Feyza12,Kempe Daryan12,Hywood Jack3,Mazalo Jessica K12,Cremasco James12,Govendir Matt A12,Dagley Laura F45ORCID,Hsu Kenneth6,Rizzetto Simone27ORCID,Zieba Jerzy28,Rice Gregory9,Prior Victoria610ORCID,O'Neill Geraldine M610,Williams Richard J1112,Nisbet David R1113,Kramer Belinda6,Webb Andrew I45,Luciani Fabio27,Read Mark N14,Biro Maté12ORCID

Affiliation:

1. EMBL Australia, Single Molecule Science node, University of New South Wales, Sydney, Australia

2. School of Medical Sciences, Faculty of Medicine, University of New South Wales, Sydney, Australia

3. Sydney Medical School, The University of Sydney, Sydney, Australia

4. The Walter and Eliza Hall Institute of Medical Research, Melbourne, Australia

5. Department of Medical Biology, University of Melbourne, Melbourne, Australia

6. Children's Cancer Research Unit, The Children's Hospital at Westmead, Sydney, Australia

7. The Kirby Institute for Infection and Immunity in Society, UNSW, Sydney, Australia

8. Neuroscience Research Australia (NeuRA), Randwick, Australia

9. Department of Statistics and Actuarial Science, University of Waterloo, Waterloo, Canada

10. Discipline of Child and Adolescent Health, University of Sydney, Sydney, Australia

11. Biofab3D, St. Vincent’s Hospital, Melbourne, Australia

12. Institute for Innovation in Mental and Physical Health and Clinical Translation (iMPACT), School of Medicine, Deakin University, Victoria, Australia

13. Advanced Biomaterials Lab, Research School of Engineering, ANU, Canberra, Australia

14. School of Computer Science, Westmead Initiative, and Charles Perkins Centre, University of Sydney, Sydney, Australia

Abstract

Cytotoxic T lymphocytes (CTLs) are thought to arrive at target sites either via random search or following signals by other leukocytes. Here, we reveal independent emergent behaviour in CTL populations attacking tumour masses. Primary murine CTLs coordinate their migration in a process reminiscent of the swarming observed in neutrophils. CTLs engaging cognate targets accelerate the recruitment of distant T cells through long-range homotypic signalling, in part mediated via the diffusion of chemokines CCL3 and CCL4. Newly arriving CTLs augment the chemotactic signal, further accelerating mass recruitment in a positive feedback loop. Activated effector human T cells and chimeric antigen receptor (CAR) T cells similarly employ intra-population signalling to drive rapid convergence. Thus, CTLs recognising a cognate target can induce a localised mass response by amplifying the direct recruitment of additional T cells independently of other leukocytes.

Funder

NSERC

National Health and Medical Research Council

University of Sydney

EMBL Australia

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

Reference63 articles.

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