The goal of this Collaborative Mucosal Immunology Program is to provide basic information concerning immunological defense mechanisms in the human male urogenital tract (UGT) that will lead to improved efficacy of anti-HIV vaccines in preventing the sexual transmission of HIV-1. Our research addresses a series of fundamental questions: What is the best approach for monitoring male UGT antibody and cellular immune response? Do male UGT immunological parameters reflect those at other sites that are easier to monitor (ie: blood, saliva)? Is male UGT immunity influenced by HIV infection or antiviral therapy? Do male UG anti-HIV antibody and cellular immune responses correlates with each other? Do seronegative men with a history of high risk sexual behavior have protective cellular or antibody anti-HIV UGT immunity? Is male UGT immunity influenced by HIV vaccination? Do HIV vaccines affect levels of infectious HIV-1 in semen via lacerations in local immunity? Do male UGT anti-HIV anti-HIV antibody and cellular immune responses correlate with each other? Our aims are: 1) To optimize methods for detecting anti-HIV antibody and cellular immune responses in the male UGT and to characterize UGT immunological parameters as a function of HIV disease stage and antiviral therapy, and in relation to immunological parameters measured in blood and other mucosal secretions; 2) To characterize HIV-specific antibody and/or cellular responses (if any) in the UGT of HIV-1 seronegative men that engage in high risk sexual activity with HIV-1 infected partners; 3) To monitor antibody and cellular UGT response following vaccination with HIV vaccines; 4) To use the cholera toxin mucosal vaccine as a model to determine if the male UGT IgA response is a component of the common mucosal immune network, and whether it is affected by HIV-1 infection; 5) To determine if HIV vaccination affects levels of HIV-1 in UGT secretions. This study is designed to provide novel methods for measuring anti-HIV immune defense mechanisms in the male urogenital tract; and fundamental information to promote the development of vaccines that provide safe and effective mucosal protection of uninfected men against HIV-1 infection and reduce the frequency of transmission of HIV from infected men to sexual partners.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI035564-04
Application #
2004082
Study Section
Special Emphasis Panel (SRC (82))
Project Start
1993-11-01
Project End
1998-03-14
Budget Start
1996-11-01
Budget End
1998-03-14
Support Year
4
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Brigham and Women's Hospital
Department
Type
DUNS #
071723621
City
Boston
State
MA
Country
United States
Zip Code
02115
Pudney, Jeffrey; Anderson, Deborah (2011) Innate and acquired immunity in the human penile urethra. J Reprod Immunol 88:219-27
Anderson, Deborah; Politch, Joseph A; Pudney, Jeffrey (2011) HIV infection and immune defense of the penis. Am J Reprod Immunol 65:220-9
Politch, Joseph A; Mayer, Kenneth H; Anderson, Deborah J (2009) Depletion of CD4+ T cells in semen during HIV infection and their restoration following antiretroviral therapy. J Acquir Immune Defic Syndr 50:283-9
Bezold, Guntram; Politch, Joseph A; Kiviat, Nancy B et al. (2007) Prevalence of sexually transmissible pathogens in semen from asymptomatic male infertility patients with and without leukocytospermia. Fertil Steril 87:1087-97
Anderson, D J; Politch, J A; Tucker, L D et al. (1998) Quantitation of mediators of inflammation and immunity in genital tract secretions and their relevance to HIV type 1 transmission. AIDS Res Hum Retroviruses 14 Suppl 1:S43-9
Quayle, A J; Xu, C; Tucker, L et al. (1998) The case against an association between HIV-1 and sperm: molecular evidence. J Reprod Immunol 41:127-36
Quayle, A J; Coston, W M; Trocha, A K et al. (1998) Detection of HIV-1-specific CTLs in the semen of HIV-infected individuals. J Immunol 161:4406-10
Quayle, A J; Xu, C; Mayer, K H et al. (1997) T lymphocytes and macrophages, but not motile spermatozoa, are a significant source of human immunodeficiency virus in semen. J Infect Dis 176:960-8
Haimovici, F; Mayer, K H; Anderson, D J (1997) Quantitation of HIV-1-specific IgG, IgA, and IgM antibodies in human genital tract secretions. J Acquir Immune Defic Syndr Hum Retrovirol 15:185-91
Anderson, D J (1996) The importance of mucosal immunology to problems in human reproduction. J Reprod Immunol 31:3-19