4.7 Article

Association of Human Antibodies to Arabinomannan With Enhanced Mycobacterial Opsonophagocytosis and Intracellular Growth Reduction

Journal

JOURNAL OF INFECTIOUS DISEASES
Volume 214, Issue 2, Pages 300-310

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/infdis/jiw141

Keywords

tuberculosis; Mycobacterium tuberculosis; Mycobacterium bovis BCG; immunoglobulin; human antibodies; antibody-mediated immunity; immune response; polysaccharide; oligosaccharide; bacterial capsule

Funding

  1. Food and Drug Administration [1U18 FD004012/01]
  2. Aeras TB Vaccine Foundation
  3. Bill and Melinda Gates Foundation
  4. Alberta Glycomics Centre
  5. Canadian Institutes for Health Research
  6. National Institutes of Health (NIH) National Institute of Allergy and Infectious Diseases [AI105684]
  7. Wellcome Trust
  8. National Center for Advancing Translational Sciences [UL1 TR001073, TL1 TR001072]
  9. NIH National Cancer Institute [P30CA013330]

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Background. The relevance of antibodies ( Abs) in the defense against Mycobacterium tuberculosis infection remains uncertain. We investigated the role of Abs to the mycobacterial capsular polysaccharide arabinomannan ( AM) and its oligosaccharide ( OS) fragments in humans. Methods. Sera obtained from 29 healthy adults before and after primary or secondary bacillus Calmette- Guerin ( BCG) vaccination were assessed for Ab responses to AM via enzyme- linked immunosorbent assays, and to AM OS epitopes via novel glycan microarrays. Effects of prevaccination and postvaccination sera on BCG phagocytosis and intracellular survival were assessed in human macrophages. Results. Immunoglobulin G ( IgG) responses to AM increased significantly 4- 8 weeks after vaccination ( P <.01), and sera were able to opsonize BCG and M. tuberculosis grown in both the absence and the presence of detergent. Phagocytosis and intracellular growth inhibition were significantly enhanced when BCG was opsonized with postvaccination sera ( P <.01), and these enhancements correlated significantly with IgG titers to AM ( P <.05), particularly with reactivity to 3 AM OS epitopes ( P <.05). Furthermore, increased phagolysosomal fusion was observed with postvaccination sera. Conclusions. Our results provide further evidence for a role of Ab- mediated immunity to tuberculosis and suggest that IgG to AM, especially to some of its OS epitopes, could contribute to the defense against mycobacterial infection in humans.

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