Innate immunity is present from birth and represents the inherited resistance to infection. Microbial infection is detected by pattern-recognition receptors (PRRs) through recognition of microbe-associated molecular patterns (MAMPs). Since MAMPs are conserved in a wide range of pathogenic or commensal organisms, it is not clear how PRR-MAMP interactions per se lead to differential host responses to pathogens and commensals. This application proposes that pathogens exploit selective pattern recognition pathways in ways that perturb the otherwise homeostatic PRR-MAMP interactions, leading to chronic persistence of the pathogen and nonproductive inflammation. This outcome is detrimental especially to the elderly host due to age-related alterations in pattern-recognition mechanisms. In this regard, it is proposed that pathway-specific alterations in innate recognition render the aging innate immune system more amenable to exploitation by pathogens than its younger counterpart. Taking advantage of the accessibility and relevance of the oral cavity in host-microbial interactions, these concepts will be investigated in the context of periodontitis and the model pathogen Porphyromonas gingivalis. P. gingivalis interacts via its surface fimbriae with the CD14/Toll-like receptor 2 recognition complex and induces phosphatidylinositol-3-kinase signaling for activating the adhesive capacity of CR3, a monocytic beta2 integrin with PRR capabilities. Although this proadhesive pathway promotes the migratory activity of monocytes, it has surprisingly been co-opted by P. gingivalis for exploiting CR3. By means of immunological, genetic, and biophysical techniques, as well as a mouse periodontitis model, these studies will test the hypothesis that the interaction of P. gingivalis with activated CR3 leads to pathogen internalization, suppression of normal defense clearing mechanisms, inhibition of apoptosis, and promotion of intracellular persistence. Moreover, it is hypothesized that the inducibility of this co-opted pathway becomes higher with age leading to enhanced immune evasion by P. gingivalis and potentially increased periodontal disease activity. This study has been designed not only for answering fundamental questions in innate immunity, but also for facilitating the development of novel immunomodulatory concepts at a translational level. Indeed, only by knowing how the innate response is deregulated by pathogens, could effective immunomodulatory strategies be implemented for redirecting the oral mucosal immune defense to the benefit of the elderly host. While the proposed experimental model focuses on a periodontal pathogen, the fundamental concept of immune evasion by corruption of PRR function and how this process changes with advancing age may be applicable to infections of less accessible mucosal tracts such as the respiratory, gastrointestinal, and genitourinary tracts.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Project (R01)
Project #
7R01DE018292-06
Application #
8388428
Study Section
Special Emphasis Panel (ZDE1-YL (20))
Program Officer
Burgoon, Penny W
Project Start
2007-03-06
Project End
2013-02-28
Budget Start
2012-01-01
Budget End
2013-02-28
Support Year
6
Fiscal Year
2011
Total Cost
$238,622
Indirect Cost
Name
University of Pennsylvania
Department
Microbiology/Immun/Virology
Type
Schools of Dentistry
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Hajishengallis, George; Chavakis, Triantafyllos (2013) Endogenous modulators of inflammatory cell recruitment. Trends Immunol 34:1-6
Hajishengallis, George; Lambris, John D (2013) Complement-targeted therapeutics in periodontitis. Adv Exp Med Biol 735:197-206
Hajishengallis, George; Lambris, John D (2012) Complement and dysbiosis in periodontal disease. Immunobiology 217:1111-6
Hajishengallis, G; Lamont, R J (2012) Beyond the red complex and into more complexity: the polymicrobial synergy and dysbiosis (PSD) model of periodontal disease etiology. Mol Oral Microbiol 27:409-19
McIntosh, M L; Hajishengallis, G (2012) Inhibition of Porphyromonas gingivalis-induced periodontal bone loss by CXCR4 antagonist treatment. Mol Oral Microbiol 27:449-57
Eskan, Mehmet A; Jotwani, Ravi; Abe, Toshiharu et al. (2012) The leukocyte integrin antagonist Del-1 inhibits IL-17-mediated inflammatory bone loss. Nat Immunol 13:465-73
Darveau, R P; Hajishengallis, G; Curtis, M A (2012) Porphyromonas gingivalis as a potential community activist for disease. J Dent Res 91:816-20
Hajishengallis, George; Krauss, Jennifer L; Liang, Shuang et al. (2012) Pathogenic microbes and community service through manipulation of innate immunity. Adv Exp Med Biol 946:69-85
Hajishengallis, George; Darveau, Richard P; Curtis, Michael A (2012) The keystone-pathogen hypothesis. Nat Rev Microbiol 10:717-25
Liang, Shuang; Krauss, Jennifer L; Domon, Hisanori et al. (2011) The C5a receptor impairs IL-12-dependent clearance of Porphyromonas gingivalis and is required for induction of periodontal bone loss. J Immunol 186:869-77

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