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Page 36

Infectious Diseases Congress 2019

Journal of Bacteriology and Infectious Diseases | Volume 3

June 12-13, 2019 | Bangkok, Thailand

OF EXCELLENCE

IN INTERNATIONAL

MEETINGS

alliedacademies.com

YEARS

BACTERIOLOGY AND INFECTIOUS DISEASES

2

nd

Global Congress on

J Bacteriol Infec Dis 2019, Volume 3

IMMUNOPROFILING OF NON-TUBERCULOUS MYCOBACTERIAL INFECTION PATIENTS

REVEAL GLOBAL T CELL DYSFUNCTION AND INDIVIDUALS AT RISK

John J Miles

1, 2, 3, 5

, Viviana P Lutzky

1

, Champa N Ratnatunga

1, 2, 3

, Daniel J Smith

1, 4

, Andreas Kupz

2

,

Denise L Doolan

1, 2

, DavidW Reid

1, 4

, Rachel MThomson

3, 4

and

Scott C Bell

1, 3, 4

1

QIMR Berghofer Medical Research Institute, Australia

2

AITHM-James Cook University, Australia

3

University of Queensland, Australia

4

The Prince Charles Hospital, Australia

5

Cardiff University School of Medicine, United Kingdom

T

he increasing global incidence of non-tuberculous mycobacterial (NTM) infection is of growing concern. New

evidence of person-to-person transmission of multidrug-resistant NTM adds to the global alarm. The reasons

why certain individuals are at risk of these infections is unknown. Using high definition flow cytometry author

studied the immune profiles of two groups of at risk NTM patients and matched controls. The first group was

cystic fibrosis (CF) patients and the second group was elderly individuals. CF patients with active NTM infection or

a history of NTM infection exhibited a unique surface T cell phenotype with a marked global deficiency in TNFα

production. Immune-based biomarkers were determined that could identify CF individuals at risk of NTM infection

with a regression model of AUC=1. In contrast, elderly individuals with NTM infection exhibited a separate T cell

phenotype underlined by the high prevalence of exhaustion markers and dysregulation in type I cytokine release.

Collectively, these data will be of significant diagnostic and prognostic value for NTM patient management and

could be used to identify new therapeutic pathways and new targets to correct T cell dysfunction.