The overall objective of Project 1 is to define the role of sex hormones in regulating the innate immune system of the FRT. Epithelial cells within the fallopian tube, uterus, cervix and vagina are the first line of defense against potentially pathogenic microbes and are individually responsive to estradiol and progesterone. In studies proposed in this application, we will test the hypothesis that epithelial cells represent the front line of the innate immune system throughout the human FRT and that innate immune protection by these cells is precisely regulated by female sex hormones. These studies will define the mechanisms whereby sex hormones influence phenotype, innate function, and communication between the innate and adaptive immune systems. We postulate that the innate immune responses of epithelial cells are under hormone control and that, in addition to conferring protection, these cells are capable of initiating an adaptive immune response. More specifically, we will: 1) Define the processes by which sex hormones modulate anti-bacterial activity, defensins and Secretory Leukocyte Protease Inhibitor (SLPI) produced by epithelial cells throughout the FRT; 2) Determine if exposure to specific PAMP (antigens) enhances or limits continued expression/production of anti-bacterial activity, defensins and SLPI in a way which is mediated through TLRs, and is precisely controlled by sex hormones; 3) Examine the role of sex hormones in regulating cytokine expression by reproductive tract epithelial cells in the presence and/or absence of PAMP; and 4) Define the role of sex hormone environment in modulating the interactions between reproductive tract epithelial cells and immune cells and determine if sex hormones directly influence links between the innate and adaptive immune systems. Understanding how the immune system in the reproductive tract can respond to bacterial and viral challenges requires that we understand the unique characteristics of the immune system in the female reproductive tract and the ways in which the innate and adaptive immune system are either enhanced and/or suppressed at particular times in a woman?s life. These studies should provide the basis of knowledge essential for understanding the role of hormones in autoimmune diseases such as Multiple Sclerosis, the prevention of local infection in the genital mucosa, and the management of sexually transmitted diseases as well as the treatment of gynecological cancers and endometriosis.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program Projects (P01)
Project #
1P01AI051877-01
Application #
6509007
Study Section
Special Emphasis Panel (ZAI1)
Project Start
2002-04-01
Project End
2007-03-31
Budget Start
Budget End
Support Year
1
Fiscal Year
2002
Total Cost
Indirect Cost
Name
Dartmouth College
Department
Type
DUNS #
041027822
City
Hanover
State
NH
Country
United States
Zip Code
03755
Wira, Charles R; Fahey, John V; Rodriguez-Garcia, Marta et al. (2014) Regulation of mucosal immunity in the female reproductive tract: the role of sex hormones in immune protection against sexually transmitted pathogens. Am J Reprod Immunol 72:236-58
Ghosh, Mimi; Rodriguez-Garcia, Marta; Wira, Charles R (2014) The immune system in menopause: pros and cons of hormone therapy. J Steroid Biochem Mol Biol 142:171-5
Spear, Paul; Barber, Amorette; Sentman, Charles L (2013) Collaboration of chimeric antigen receptor (CAR)-expressing T cells and host T cells for optimal elimination of established ovarian tumors. Oncoimmunology 2:e23564
Ghosh, Mimi; Shen, Zheng; Fahey, John V et al. (2013) Pathogen recognition in the human female reproductive tract: expression of intracellular cytosolic sensors NOD1, NOD2, RIG-1, and MDA5 and response to HIV-1 and Neisseria gonorrhea. Am J Reprod Immunol 69:41-51
Ghosh, Mimi; Rodriguez-Garcia, Marta; Wira, Charles R (2013) Immunobiology of genital tract trauma: endocrine regulation of HIV acquisition in women following sexual assault or genital tract mutilation. Am J Reprod Immunol 69 Suppl 1:51-60
Patel, Mickey V; Ghosh, Mimi; Fahey, John V et al. (2012) Uterine epithelial cells specifically induce interferon-stimulated genes in response to polyinosinic-polycytidylic acid independently of estradiol. PLoS One 7:e35654
Coleman, Kimberly D; Ghosh, Mimi; Crist, Sarah G et al. (2012) Modulation of hepatocyte growth factor secretion in human female reproductive tract stromal fibroblasts by poly (I:C) and estradiol. Am J Reprod Immunol 67:44-53
Ochiel, Daniel O; Rossoll, Richard M; Schaefer, Todd M et al. (2012) Effect of oestradiol and pathogen-associated molecular patterns on class II-mediated antigen presentation and immunomodulatory molecule expression in the mouse female reproductive tract. Immunology 135:51-62
Fahey, John V; Bodwell, Jack E; Hickey, Danica K et al. (2011) New approaches to making the microenvironment of the female reproductive tract hostile to HIV. Am J Reprod Immunol 65:334-43
Kopcow, H D; Eriksson, M; Mselle, T F et al. (2010) Human decidual NK cells from gravid uteri and NK cells from cycling endometrium are distinct NK cell subsets. Placenta 31:334-8

Showing the most recent 10 out of 28 publications