The overall goal of this proposal is to provide the principal investigator (PI) with the experiences and skills necessary to become an independent researcher, with the focus on studying immune cell trafficking mechanisms. My long-term career goal is to establish a comprehensive and independent research program dedicated to dissect the trafficking mechanism of immune cells in inflammatory and infectious corneal disease, leading to new therapeutic targets. Corneal antigen-presenting cells (APC) have a critical role in maintaining the clarity of the cornea and preserving vision. APC-mediated immune responses require contact-dependent information exchange between APC and T cells. Ag presentation by mature DC to naive T cells induces T cell activation and proliferation into effector T cells, which is in turn thought to be controlled by several mechanisms, including the action of regulatory T cells (Treg). Career decisions taken by APC are regulated molecules on the surface of APC and T cells. Despite their unique position in the immune system, the signals APC need to enter the cornea, and the clues they require to leave the cornea, are still largely unexplored. In preliminary work for this project, we have developed a new multiphoton intravital microscopy (MP-IVM) model to study APC in intact corneas of anesthetized mice. This imaging approach uses transgenic mice, in which APC subsets expresses distinct genetically encoded fluorescent tags, and produces 3D time-lapse movies of APC at subcellular resolution, interacting with surrounding cells. These cells will be studied to investigate the traffic signals that guide them to normal and inflamed corneas and will be used to address the following three specific aims: 1.) To dissect the molecular mechanisms by which APC travel to normal and inflamed corneas;2.) To analyze the mechanisms involved in migration of APC from the cornea to local lymph nodes under normal conditions and during inflammation;and 3) examine the spatial, temporal and behavioral characteristics of donor and host APC after corneal transplantation and their interaction with T cells in lymph nodes.
This aim will also analyze how effector T cells or Tregs enter the cornea. The proposed experiments will generate a comprehensive, mechanism-oriented survey of the behavioral similarities and differences between distinct APC subsets under normal condition and inflammation.

Public Health Relevance

Identification of critical pathways of immune cell migration to and from the cornea from the proposed studies, will provide new molecular targets for pharmacological intervention in inflammatory, infectious, and autoimmune corneal diseases, as well as in corneal transplantation. These targets may lead to novel and highly specific strategies for immunotherapy, through modulation of immune cell trafficking.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Clinical Investigator Award (CIA) (K08)
Project #
5K08EY020575-03
Application #
8292172
Study Section
Special Emphasis Panel (ZEY1-VSN (10))
Program Officer
Agarwal, Neeraj
Project Start
2010-05-01
Project End
2014-04-30
Budget Start
2012-05-01
Budget End
2013-04-30
Support Year
3
Fiscal Year
2012
Total Cost
$238,142
Indirect Cost
$16,862
Name
Massachusetts Eye and Ear Infirmary
Department
Type
DUNS #
073825945
City
Boston
State
MA
Country
United States
Zip Code
02114
Cavalcanti, Bernardo M; Cruzat, Andrea; Sahin, Afsun et al. (2018) In vivo confocal microscopy detects bilateral changes of corneal immune cells and nerves in unilateral herpes zoster ophthalmicus. Ocul Surf 16:101-111
Harris, Deshea L; Yamaguchi, Takefumi; Hamrah, Pedram (2018) A Novel Murine Model of Radiation Keratopathy. Invest Ophthalmol Vis Sci 59:3889-3896
Moein, Hamid-Reza; Kheirkhah, Ahmad; Muller, Rodrigo T et al. (2018) Corneal nerve regeneration after herpes simplex keratitis: A longitudinal in vivo confocal microscopy study. Ocul Surf 16:218-225
Lopez, Maria J; Seyed-Razavi, Yashar; Jamali, Arsia et al. (2018) The Chemokine Receptor CXCR4 Mediates Recruitment of CD11c+ Conventional Dendritic Cells Into the Inflamed Murine Cornea. Invest Ophthalmol Vis Sci 59:5671-5681
Cruzat, Andrea; Qazi, Yureeda; Hamrah, Pedram (2017) In Vivo Confocal Microscopy of Corneal Nerves in Health and Disease. Ocul Surf 15:15-47
Cruzat, Andrea; Hamrah, Pedram; Cavalcanti, Bernardo M et al. (2016) Corneal Reinnervation and Sensation Recovery in Patients With Herpes Zoster Ophthalmicus: An In Vivo and Ex Vivo Study of Corneal Nerves. Cornea 35:619-25
Qazi, Yureeda; Hurwitz, Shelley; Khan, Sarosh et al. (2016) Validity and Reliability of a Novel Ocular Pain Assessment Survey (OPAS) in Quantifying and Monitoring Corneal and Ocular Surface Pain. Ophthalmology 123:1458-68
Dohlman, Thomas H; Di Zazzo, Antonio; Omoto, Masahiro et al. (2016) E-Selectin Mediates Immune Cell Trafficking in Corneal Transplantation. Transplantation 100:772-80
Müller, Rodrigo T; Pourmirzaie, Roxanna; Pavan-Langston, Deborah et al. (2015) In Vivo Confocal Microscopy Demonstrates Bilateral Loss of Endothelial Cells in Unilateral Herpes Simplex Keratitis. Invest Ophthalmol Vis Sci 56:4899-906
Müller, Rodrigo T; Abedi, Farshad; Cruzat, Andrea et al. (2015) Degeneration and Regeneration of Subbasal Corneal Nerves after Infectious Keratitis: A Longitudinal In Vivo Confocal Microscopy Study. Ophthalmology 122:2200-9

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