Chronic Infection by Mucoid Pseudomonas aeruginosa Associated with Dysregulation in T-Cell Immunity to Outer Membrane Porin F.

TitleChronic Infection by Mucoid Pseudomonas aeruginosa Associated with Dysregulation in T-Cell Immunity to Outer Membrane Porin F.
Publication TypeJournal Article
Year of Publication2015
AuthorsQuigley KJ, Reynolds CJ, Goudet A, Raynsford EJ, Sergeant R, Quigley A, Worgall S, Bilton D, Wilson R, Loebinger MR, Maillere B, Altmann DM, Boyton RJ
JournalAm J Respir Crit Care Med
Volume191
Issue11
Pagination1250-64
Date Published2015 Jun 01
ISSN1535-4970
KeywordsAdult, Aged, Animals, Female, Humans, Longitudinal Studies, Lung, Male, Mice, Middle Aged, Porins, Pseudomonas aeruginosa, Pseudomonas Infections, Sputum, T-Lymphocytes, Young Adult
Abstract

RATIONALE: Pseudomonas aeruginosa (PA) is an environmental pathogen that commonly infects individuals with cystic fibrosis (CF) and non-CF bronchiectasis, impacting morbidity and mortality. To understand the pathobiology of interactions between the bacterium and host adaptive immunity and to inform rational vaccine design, it is important to understand the adaptive immune correlates of disease.

OBJECTIVES: To characterize T-cell immunity to the PA antigen outer membrane porin F (OprF) by analyzing immunodominant epitopes in relation to infection status.

METHODS: Patients with non-CF bronchiectasis were stratified by frequency of PA isolation. T-cell IFN-γ immunity to OprF and its immunodominant epitopes was characterized. Patterns of human leukocyte antigen (HLA) restriction of immunodominant epitopes were defined using HLA class II transgenic mice. Immunity was characterized with respect to cytokine and chemokine secretion, antibody response, and T-cell activation transcripts.

MEASUREMENTS AND MAIN RESULTS: Patients were stratified according to whether PA was never, sometimes (<50%), or frequently (≥50%) isolated from sputum. Patients with frequent PA sputum-positive isolates were more likely to be infected by mucoid PA, and they showed a narrow T-cell epitope response and a relative reduction in Th1 polarizing transcription factors but enhanced immunity with respect to antibody production, innate cytokines, and chemokines.

CONCLUSIONS: We have defined the immunodominant, HLA-restricted T-cell epitopes of OprF. Our observation that chronic infection is associated with a response of narrowed specificity, despite strong innate and antibody immunity, may help to explain susceptibility in these individuals and pave the way for better vaccine design to achieve protective immunity.

DOI10.1164/rccm.201411-1995OC
Custom 1

https://www.ncbi.nlm.nih.gov/pubmed/25789411?dopt=Abstract

Alternate JournalAm. J. Respir. Crit. Care Med.
PubMed ID25789411
PubMed Central IDPMC4476516
Grant List272200900046C / / PHS HHS / United States
/ / Medical Research Council / United Kingdom
HHSN272200900046C / AI / NIAID NIH HHS / United States
R01 AI103341-01 / AI / NIAID NIH HHS / United States
R01 AI103341 / AI / NIAID NIH HHS / United States

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