Cytokine Profiles during Invasive Nontyphoidal Salmonella Disease Predict Outcome in African Children

Author:

Gilchrist James J.12,Heath Jennifer N.3,Msefula Chisomo L.456,Gondwe Esther N.3456,Naranbhai Vivek1,Mandala Wilson46,MacLennan Jenny M.47,Molyneux Elizabeth M.8,Graham Stephen M.489,Drayson Mark T.3,Molyneux Malcolm E.4610,MacLennan Calman A.341112

Affiliation:

1. Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom

2. Department of Paediatrics, University of Oxford, Oxford, United Kingdom

3. School of Immunity and Infection, College of Medicine and Dental Sciences, University of Birmingham, Birmingham, United Kingdom

4. Malawi-Liverpool-Wellcome Trust Clinical Research Programme, College of Medicine, University of Malawi, Blantyre, Malawi

5. Department of Microbiology, College of Medicine, University of Malawi, Blantyre, Malawi

6. Liverpool School of Tropical Medicine, Pembroke Place, Liverpool, United Kingdom

7. Department of Zoology, University of Oxford, Oxford, United Kingdom

8. Department of Paediatrics, College of Medicine, University of Malawi, Blantyre, Malawi

9. Centre for International Child Health, University of Melbourne and Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Australia

10. Department of Medicine, College of Medicine, University of Malawi, Blantyre, Malawi

11. Jenner Institute, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom

12. Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom

Abstract

ABSTRACT Nontyphoidal Salmonella is a leading cause of sepsis in African children. Cytokine responses are central to the pathophysiology of sepsis and predict sepsis outcome in other settings. In this study, we investigated cytokine responses to invasive nontyphoidal Salmonella (iNTS) disease in Malawian children. We determined serum concentrations of 48 cytokines with multiplexed immunoassays in Malawian children during acute iNTS disease ( n = 111) and in convalescence ( n = 77). Principal component analysis and logistic regression were used to identify cytokine signatures of acute iNTS disease. We further investigated whether these responses are altered by HIV coinfection or severe malnutrition and whether cytokine responses predict inpatient mortality. Cytokine changes in acute iNTS disease were associated with two distinct cytokine signatures. The first is characterized by increased concentrations of mediators known to be associated with macrophage function, and the second is characterized by raised pro- and anti-inflammatory cytokines typical of responses reported in sepsis secondary to diverse pathogens. These cytokine responses were largely unaltered by either severe malnutrition or HIV coinfection. Children with fatal disease had a distinctive cytokine profile, characterized by raised mediators known to be associated with neutrophil function. In conclusion, cytokine responses to acute iNTS infection in Malawian children are reflective of both the cytokine storm typical of sepsis secondary to diverse pathogens and the intramacrophage replicative niche of NTS. The cytokine profile predictive of fatal disease supports a key role of neutrophils in the pathogenesis of NTS sepsis.

Publisher

American Society for Microbiology

Subject

Microbiology (medical),Clinical Biochemistry,Immunology,Immunology and Allergy

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