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Combinatorial Tim‐3 and PD‐1 activity sustains antigen‐specific Th1 cell numbers during blood‐stage malaria

Parasite Immunology, vol. 42, pp. e12723

Abstract

AIMS: Co-inhibitory receptors play a major role in controlling the Th1 response during blood-stage malaria. Whilst PD-1 is viewed as the dominant co-inhibitory receptor restricting T cell responses, the roles of other such receptors in coordinating Th1 cell activity during malaria are poorly understood. METHODS AND RESULTS: (Th1) OT-II cells transiently during the early stage of infection with transgenic Plasmodium yoelii NL parasites expressing ovalbumin (P yoelii NL-OVA). We reveal that co-blockade of Tim-3 and PD-L1 during the acute phase of P yoelii NL infection did not improve the Th1 cell response but instead led to a specific reduction in the numbers of splenic Th1 OT-II cells. Combined blockade of Tim-3 and PD-L1 did elevate anti-parasite IgG antibody responses. Nevertheless, co-blockade of Tim-3 and PD-L1 did not affect IFN-γ production by OT-II cells and did not influence parasite control during P yoelii NL-OVA infection. CONCLUSION: Thus, our results show that Tim-3 plays an unexpected combinatorial role with PD-1 in promoting and/ or sustaining a Th1 cell response during the early phase of blood-stage P. yoelii NL infection but combined blockade does not dramatically influence anti-parasite immunity.

Authors 9

  1. University of Manchester

    Affiliation as printed

    Faculty of Biology, Medicine and Health The Lydia Becker Institute of Immunology and Inflammation University of Manchester Manchester UK

    Faculty of Biology, Medicine and Health, The Lydia Becker Institute of Immunology and Inflammation, University of Manchester, Manchester, UK

  2. University of Manchester

    Affiliation as printed

    Faculty of Biology, Medicine and Health The Lydia Becker Institute of Immunology and Inflammation University of Manchester Manchester UK

    Faculty of Biology, Medicine and Health, The Lydia Becker Institute of Immunology and Inflammation, University of Manchester, Manchester, UK

  3. Leiden University Medical Center

    Affiliation as printed

    Leiden malaria group Department of Parasitology Leiden University Medical Center Leiden The Netherlands

    Leiden malaria group, Department of Parasitology, Leiden University Medical Center, Leiden, The Netherlands

  4. University of Oxford · Jenner Institute

    Affiliation as printed

    The Jenner Institute University of Oxford Oxford UK

    The Jenner Institute, University of Oxford, Oxford, UK

  5. University of Oxford · Jenner Institute

    Affiliation as printed

    The Jenner Institute University of Oxford Oxford UK

    The Jenner Institute, University of Oxford, Oxford, UK

  6. Leiden University Medical Center

    Affiliation as printed

    Leiden malaria group Department of Parasitology Leiden University Medical Center Leiden The Netherlands

    Leiden malaria group, Department of Parasitology, Leiden University Medical Center, Leiden, The Netherlands

  7. Leiden University Medical Center

    Affiliation as printed

    Leiden malaria group Department of Parasitology Leiden University Medical Center Leiden The Netherlands

    Leiden malaria group, Department of Parasitology, Leiden University Medical Center, Leiden, The Netherlands

  8. University of Manchester

    Affiliation as printed

    Faculty of Biology, Medicine and Health The Lydia Becker Institute of Immunology and Inflammation University of Manchester Manchester UK

    Faculty of Biology, Medicine and Health, The Lydia Becker Institute of Immunology and Inflammation, University of Manchester, Manchester, UK

  9. Kevin N. Couper corresponding

    University of Manchester

    Affiliation as printed

    Faculty of Biology, Medicine and Health The Lydia Becker Institute of Immunology and Inflammation University of Manchester Manchester UK

    Faculty of Biology, Medicine and Health, The Lydia Becker Institute of Immunology and Inflammation, University of Manchester, Manchester, UK

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References 47