Monocytes and macrophages (M?) sense the presence of pathogens, tissue damage, and host-derived mediators in their environment and respond by differentiating into distinct functional phenotypes that mediate host innate immune responses. The process of M? differentiation has often been described in terms of ?plastic- ity,? implying that these cells modulate their functions through rapidly reversible differentiation steps in re- sponse to environmental changes in the host. For example, ?classically activated? M? (CAM; M1) are highly microbicidal, yet their production of inflammatory cytokines and nitric oxide may also damage host tissue. At the other end of the functional spectrum, ?alternatively activated? M? (AAM or M2), induced by IL-4 and IL-13, mediate ?wound healing? through elimination of damaged tissue and other anti-inflammatory mechanisms. Dur- ing the past three decades, the PI has undertaken research designed to dissect the complex molecular under- pinnings of M? differentiation and how this impacts host defenses and disease outcome. In the proposed stud- ies, the central hypothesis to be tested is that activation of specific intracellular signaling pathways distal to en- gagement of TLR4 and/or other signaling receptors by influenza-induced PAMPs and DAMPs serve to pro- gram expression of discrete cassettes of pro- and anti-inflammatory genes that control the manner in which the host M? responds to infection.
Two Specific Aims are proposed to test this hypothesis in vitro and in vivo, with the ultimate goal of identifying novel therapeutic interventions for diseases where M? are required for contain- ing the invading pathogen and/or resolving tissue damage caused by pathogens or the host inflammatory re- sponse to infection. Both male and female mice (because of the availability of genetically engineered strains), and cotton rats (that are uniquely susceptible to human non-adapted isolates of influenza) will be utilized as models of primary (1o) influenza infection and 1o influenza infection followed by secondary (2o) bacterial infec- tion. The proposed innovative experimental approaches are designed to: (1) identify TLR4-interacting signaling receptors (i.e., PAR2, RAGE, CD11b/CD18) and delineate the contributions of these interactions to regulation of M? differentiation/susceptibility to influenza infection; and, (2) identify influenza-triggered, epigenetic and/or M? differentiative mechanisms that mediate susceptibility to 2o Gram-positive bacterial infection. At the conclu- sion of these comprehensive studies, key processes that govern interactions of TLR agonists that lead to changes in M? activation will have been defined that, in turn, can be expected to translate into reasonable and practical therapeutic approaches for controlling invading pathogens or counteracting inflammatory damage to tissues induced by pathogens, ultimately providing evidence-based therapies to treat infectious diseases.

Public Health Relevance

Macrophages are white blood cells that function as the front line of defense against many infectious microbes. An in-depth understanding of how macrophages sense and respond to invading pathogens is the goal of this project. Our research findings can be expected to lead to development of new drugs and treatments that will increase the capacity of macrophages to kill bacteria and viruses more effectively or to prevent or repair damage to tissues caused by bacterial or viral infection, and thereby promote survival of infected people.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI123371-03
Application #
9598331
Study Section
Immunity and Host Defense (IHD)
Program Officer
Jiang, Chao
Project Start
2016-12-05
Project End
2021-11-30
Budget Start
2018-12-01
Budget End
2019-11-30
Support Year
3
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Maryland Baltimore
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
188435911
City
Baltimore
State
MD
Country
United States
Zip Code
21201
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