Neutrophil-mediated innate immune resistance to mycobacteria

Adrian R. Martineau(Imperial College London), Sandra M. Newton(Wellcome Trust), Katalin A. Wilkinson(University of Cape Town), Beate Kampmann(University of Cape Town), Bridget Hall(Queen Mary University of London), Niga Nawroly(Imperial College London), Geoffrey E. Packe(Newham University Hospital), Robert N. Davidson(Northwick Park Hospital), Chris Griffiths(Queen Mary University of London), Robert J. Wilkinson(University of Cape Town)
Journal of Clinical Investigation
July 2, 2007
Cited by 389Open Access
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Abstract

Neutrophils contain antimicrobial peptides with antituberculous activity, but their contribution to immune resistance to tuberculosis (TB) infection has not been previously investigated to our knowledge. We determined differential white cell counts in peripheral blood of 189 adults who had come into contact with patients diagnosed with active TB in London, United Kingdom, and evaluated them for evidence of TB infection and capacity to restrict mycobacterial growth in whole-blood assays. Risk of TB infection was inversely and independently associated with peripheral blood neutrophil count in contacts of patients diagnosed with pulmonary TB. The ability of whole blood to restrict growth of Mycobacterium bovis bacille Calmette Guérin and Mycobacterium tuberculosis was impaired 7.3- and 3.1-fold, respectively, by neutrophil depletion. In microbiological media, human neutrophil peptides (HNPs) 1-3 killed M. tuberculosis. The neutrophil peptides cathelicidin LL-37 and lipocalin 2 restricted growth of the organism, the latter in an iron-dependent manner. Black African participants had lower neutrophil counts and lower circulating concentrations of HNP1-3 and lipocalin 2 than south Asian and white participants. Neutrophils contribute substantially to innate resistance to TB infection, an activity associated with their antimicrobial peptides. Elucidation of the regulation of neutrophil antimicrobial peptides could facilitate prevention and treatment of TB.


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