Regulation of dendritic cell function by neutrophil-derived reactive oxygen species in pulmonary aspergillosis

Information

  • Research Project
  • 10439070
  • ApplicationId
    10439070
  • Core Project Number
    K08HL136903
  • Full Project Number
    3K08HL136903-05S1
  • Serial Number
    136903
  • FOA Number
    PA-20-272
  • Sub Project Id
  • Project Start Date
    5/3/2017 - 8 years ago
  • Project End Date
    3/9/2022 - 3 years ago
  • Program Officer Name
    MONGODIN, EMMANUEL FRANCK
  • Budget Start Date
    9/10/2021 - 3 years ago
  • Budget End Date
    3/9/2022 - 3 years ago
  • Fiscal Year
    2021
  • Support Year
    05
  • Suffix
    S1
  • Award Notice Date
    9/9/2021 - 3 years ago

Regulation of dendritic cell function by neutrophil-derived reactive oxygen species in pulmonary aspergillosis

PROJECT SUMMARY/ABSTRACT This proposal outlines a five-year training program for Dr. Cagnina to establish a career as an independent investigator in Pulmonary and Critical Care Medicine. Under the guidance of mentor Dr. Bruce Levy, the broad, long-term objective is for Dr. Cagnina to gain the knowledge and skills necessary to evolve into an independent physician-scientist, while making significant contributions to understanding the immune response to Aspergillus. Aspergillus species are ubiquitous molds that cause clinical disease in hosts with impaired immunity or abnormal mucosal defenses. Neutrophils play a key role in host defenses against this pathogen but little is known about the contribution of these cells in in this context beyond their direct microbicidal role. We have previously shown that, during host response to Aspergillus in the lung, neutropenia results in a defect in the traffic and maturation of inflammatory monocyte-derived dendritic cells. In the preliminary data for this proposal, we report that deficiency in neutrophil reactive oxygen species production is sufficient to induce this phenotype; that, in hosts unable to generate reactive oxygen species, both the inflammatory dendritic cell recruitment and lung injury are dependent on TNF; and that neutropenia impairs the development of protective immunity against the pathogen. We therefore seek to test the hypothesis that in response to Aspergillus, reactive oxygen species-dependent neutrophil signaling to inflammatory dendritic cells mediates (a) protection from acute lung injury and (b) generation of protective adaptive immunity against Aspergillus. We will test this under two specific aims: (1) To identify the mechanism by which neutrophil-derived ROS modulates dendritic cell function during the innate immune response to Aspergillus and (2) To define the role of neutrophil ROS in the development of protective adaptive immunity against Aspergillus. The proposed studies are relevant to public health by defining a new mechanism of host defense against an important human pathogen that should allow for future development of novel therapeutics or preventative strategies.

IC Name
NATIONAL HEART, LUNG, AND BLOOD INSTITUTE
  • Activity
    K08
  • Administering IC
    HL
  • Application Type
    3
  • Direct Cost Amount
    63900
  • Indirect Cost Amount
    5112
  • Total Cost
    69012
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    838
  • Ed Inst. Type
  • Funding ICs
    NHLBI:69012\
  • Funding Mechanism
    OTHER RESEARCH-RELATED
  • Study Section
  • Study Section Name
  • Organization Name
    BRIGHAM AND WOMEN'S HOSPITAL
  • Organization Department
  • Organization DUNS
    030811269
  • Organization City
    BOSTON
  • Organization State
    MA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    021156110
  • Organization District
    UNITED STATES