H2020Individual fellowship2017–2018

ILTIS · Innate-Like T-Cells In Sepsis (ILTIS): Implications for Early Diagnosis and Rescue of Immune Suppression.

Horizon 2020 — Marie Skłodowska-Curie Actions

Duration
2017-09-01 → 2018-08-31
EU contribution
€97,727
Participants
1
Scheme
MSCA-IF-EF-ST

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Results in brief

Innate-Like T-Cells In Sepsis (ILTIS): Implications for Early Diagnosis and Rescue of Immune Suppression.

"Problematic: Research on infectious diseases has high priority for the scientific and medical communities worldwide, to tackle the alarming spread of multidrug resistant bacteria, to fight and prevent virus outbreaks, and to improve patient management in severe infections including sepsis. Sepsis is recognised as one of the biggest challenges in modern healthcare. It kills as many as 30% of affected patients and leaves a lasting legacy even in those that survive. Although effective antimicrobials can improve the outcome of sepsis, diagnosis of the underlying infection is difficult and possible only in less than 60% of cases. A better understanding of the cellular and molecular signatures in acute disease may pave the way to earlier and more accurate diagnosis, targeted and personalised treatments and thus better outcomes. Research in the host laboratory at Cardiff University (Division of Infection and Immunity, School of Medicine) has shown that microbes interact at various levels with the immune system and leave disease-specific ""immune fingerprints"" that discriminate between different groups of organisms and inform the design of novel tests for infection diagnosis. Among the major breakthroughs in the understanding of host innate immune responses is the characterization of innate-like or unconventional T cells such as γδ T cells and mucosal-associated invariant T (MAIT) cells in acute disease. The organisms sensed by one or both of these unconventional T cell subsets include the causative agents of global health threats like tuberculosis and most hospital-acquired infections. Objectives: The aim of the proposed project was to study the phenotype and function of innate immune cells during acute sepsis, with a particular focus on γδ T-cells and mucosal-associated invariant T (MAIT) cells. This translational research involved bed to bench-side approaches and addressed the potential of unconventional T cells to be exploited for novel diagnostics to predict the causative pathogen long before traditional culture results become available, and for novel therapies aimed at overcoming the detrimental immunosuppression frequently observed in sepsis and that is associated with poor clinical outcomes and elevated susceptibility to fatal second-hit infections. "

Data: CORDIS, © European Union

Project objective

Research on infectious diseases has high priority for the scientific and medical communities worldwide, to tackle the alarming spread of multidrug resistant bacteria and to fight and prevent virus outbreaks. On the French island of La Réunion, infections such as leptospirosis and chikungunya pose considerable threats for public health. My career aspiration is to establish myself as a clinical scientist in the field of immunology of microbial infections, especially in severe conditions such as septic shock and leptospirosis. I am also interested in deciphering the emerging role of host cell-derived factors (HSDF) in shaping the innate immune response. The immune response to pathogens and HSDF involves numerous cell types and soluble factors such as cytokines but remains ill-characterized. A better understanding of the cellular and molecular signatures in acute disease may pave the way to better and earlier diagnosis, targeted treatment and improved outcomes. The aim of the proposed study is to study the phenotype and function of innate immune cells during sepsis, with a particular focus on γδ T-cells, neutrophils and monocytes. This translational research involves bed to bench-side approaches (clinical investigations on septic shock during community-acquired pneumonia) and in vitro studies in cell culture, by analysing cell viability and activation as well as key cellular functions such as cytokine release, phagocytosis and antigen presentation in relation to the causative pathogen. I am keen to link this project with my previous studies on immune-mediated cell death during septic shock and on the early immune response to leptospirosis. The possibility to join the internationally renowned immunology teams at Cardiff University will be of great benefit to my research and will allow me to further my skills and expertise as well as create a network of productive collaborations for my future career when returning to Reunion.

Original text from CORDIS.

Participants

Links

Data: CORDIS, © European Union