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Virus-associated apoptosis of blood neutrophils as a risk factor for invasive meningococcal disease
  1. Harry Smith1,
  2. Sharon L Rogers2,
  3. Helen V Smith3,
  4. David Gillis4,
  5. Victor Siskind5,
  6. Judith A Smith1
  1. 1Department of Paediatrics, University of Queensland, Royal Children's Hospital, Brisbane, Queensland, Australia
  2. 2Division of Haematology, Pathology Queensland, Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia
  3. 3Public Health Microbiology, Communicable Disease, Forensic and Scientific Services, Queensland Health, Brisbane, Queensland, Australia
  4. 4Division of Immunology, Pathology Queensland, Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia
  5. 5Cancer Epidemiology Unit, Queensland Institute of Medical Research, Brisbane, Queensland, Australia
  1. Correspondence to Dr Harry Smith, Department of Paediatrics, University of Queensland, Royal Children's Hospital, Herston Road, Brisbane, Queensland 4029, Australia; harry.smith{at}uq.edu.au

Abstract

Aims To quantify a range of haematological indicators of viral infection (leucocyte apoptosis, cytopenia of normal lymphocytes, reactive lymphocyte increase, neutropenia) in patients with recent onset invasive meningococcal disease (IMD), with a view to test the association of viral infection with IMD and identify possible haematological risk factors for its development.

Subjects and methods 88 patients with recent onset IMD, classified on clinical severity as fatal (n=14), septic shock survived (n=26) and no shock (n=48), and 50 healthy controls were studied. Blood film microscopy and leucocyte counts were used to quantify the virus-associated indicators. Cocci-containing neutrophils were also quantified.

Results All viral parameters were significantly more frequent or higher in patients than controls, with leucocyte apoptosis found only in the patients. A significant gradient in accord with clinical severity was found for neutrophil and lymphocyte apoptosis, neutropenia and cocci-containing neutrophils. Crucially, apoptotic neutrophils did not contain cocci, and cocci-containing neutrophils were not apoptotic.

Conclusions The correlation between magnitude of neutrophil apoptosis and severity of IMD suggests a cause–effect relationship. We propose that neutrophil apoptosis is more likely a facilitator rather than an effect of IMD for these reasons: (1) apoptotic neutrophils did not contain cocci and cocci-containing neutrophils were not apoptotic, (2) leucocyte apoptosis is a recognised viral effect and (3) Neisseria meningitidis is incapable of producing a Panton–Valentine type leucocidin. The lymphocyte apoptosis which accompanies neutrophil death may contribute to risk by impairing the generation of microbicidal antibody. Leucocyte apoptosis is a morphological expression of viral immunosuppression and, we suggest, is a likely contributor to a range of viral effects.

  • Apoptosis
  • Leucocytes
  • Virus

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