Liver sinusoid constraints make random search of CD8 T cells for Plasmodium parasites efficient 2254515

Abstract Introduction A relatively small number of liver-localized CD8 T cells can provide sterilizing protection against exposure to Plasmodium sporozoites. Previously published mathematical model-based simulations of randomly searching for an infection T cells, assuming that T cells move in open space or on a regular lattice, suggested that some degree of attraction is needed for cells to find the infection. Yet, in our previous experiments we failed to find evidence of attraction towards the infection in most T cells. Because the movement of liver-localized T cells is confined to sinusoids, the blood vessels of the liver, T cells may in fact be attracted to the infection site via the sinusoids. Methods In new experiments we imaged Plasmodium-specific CD8 T cells, sporozoites, and liver sinusoids simultaneously. We also developed a new method to model imaged sinusoids as graphs and to simulate movement of T cells on graphs, and new tests to detect biased cell movement on graphs. Results As before, our previously published open space/3D-based metric suggested that few T cells are attracted to the infection site in presence of moderate cluster of T cells. However, with our new graph-based metric we could not detect attraction when constraining T cell movement to sinusoids. Surprisingly, simulations of T cells searching for an infection via liver sinusoids showed that a relatively small number of T cells (1 cell/imaging volume or < 10^5 cells/liver), moving without attraction at experimentally observed speeds, is sufficient to find the infection within 24 hours, well below the expected lifespan of the Plasmodium liver stage in mice. Conclusion Our results suggest that the constrained environment of the tissue structure makes a random search more effective, and that detecting T cell attraction towards specific areas may arise as an artifact of metrics designed for open space/3D. Our results thus call for a re-evaluation of the implicit assumption that attraction is necessary for T cells to find infections in tissues. Funding Source R01GM118553, R01AI158963 Topic Categories Vaccines and Immunotherapy (VAC)

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Publication Details

Journal
The Journal of Immunology
Published
2026-07-28
DOI
https://doi.org/10.1093/jimmun/vkag141.228
Primary Topic
Diffusion and Search Dynamics
Type
article
Field-Weighted Citation Impact
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article

Liver sinusoid constraints make random search of CD8 T cells for Plasmodium parasites efficient 2254515

Vitaly Ganusov, Michael Langston, Viktor Zenkov, Ian Cockburn
The Journal of Immunology
Diffusion and Search Dynamics
article

Liver sinusoid constraints make random search of CD8 T cells for Plasmodium parasites efficient 2254515

Vitaly Ganusov, Michael Langston, Viktor Zenkov, Ian Cockburn
article en

Abstract

Abstract Introduction A relatively small number of liver-localized CD8 T cells can provide sterilizing protection against exposure to Plasmodium sporozoites. Previously published mathematical model-based simulations of randomly searching for an infection T cells, assuming that T cells move in open space or on a regular lattice, suggested that some degree of attraction is needed for cells to find the infection. Yet, in our previous experiments we failed to find evidence of attraction towards the infection in most T cells. Because the movement of liver-localized T cells is confined to sinusoids, the blood vessels of the liver, T cells may in fact be attracted to the infection site via the sinusoids. Methods In new experiments we imaged Plasmodium-specific CD8 T cells, sporozoites, and liver sinusoids simultaneously. We also developed a new method to model imaged sinusoids as graphs and to simulate movement of T cells on graphs, and new tests to detect biased cell movement on graphs. Results As before, our previously published open space/3D-based metric suggested that few T cells are attracted to the infection site in presence of moderate cluster of T cells. However, with our new graph-based metric we could not detect attraction when constraining T cell movement to sinusoids. Surprisingly, simulations of T cells searching for an infection via liver sinusoids showed that a relatively small number of T cells (1 cell/imaging volume or < 10^5 cells/liver), moving without attraction at experimentally observed speeds, is sufficient to find the infection within 24 hours, well below the expected lifespan of the Plasmodium liver stage in mice. Conclusion Our results suggest that the constrained environment of the tissue structure makes a random search more effective, and that detecting T cell attraction towards specific areas may arise as an artifact of metrics designed for open space/3D. Our results thus call for a re-evaluation of the implicit assumption that attraction is necessary for T cells to find infections in tissues. Funding Source R01GM118553, R01AI158963 Topic Categories Vaccines and Immunotherapy (VAC)

The Journal of ImmunologyVol. 215(Supplement_1)
Australian National University (AU), Biomed Research Institute (US), University of Tennessee at Knoxville (US)
Openalex Percentile: Top 15%
Diffusion and Search Dynamics
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