The overall aim of the Clinical Core is to support the projects on three important sexually-transmitted organisms, Trichomonas vaginalis, group B streptococci, and Treponema pallidum. In addition to providing clinical specimens and providing an environment for education and training in sexually transmitted diseases, the Core has specific aims which are logical and important clinical extensions of the projects on T. vaginalis and group B streptococci. In the Core's aim on T. vaginalis, we will determine whether phenotype is related to several clinical measures of virulence (symptoms of infection, persistence or recurrence of infection, or infection in sexual partners). Similarly, in the Core's aim on group B streptococci, we will determine whether the lipoteichoic acid chain type is related to two measures of virulence (persistence of infection and in vitro attachment to vaginal epithelial cells. The clinical studies will be carried out in cohorts of culture positive women. Because these organisms exact a heavy burden, it is pertinent to determine these clinical correlates so that strategies for intervention and control may be advanced.

Project Start
Project End
Budget Start
Budget End
Support Year
5
Fiscal Year
1989
Total Cost
Indirect Cost
Name
University of Texas Health Science Center San Antonio
Department
Type
DUNS #
800772162
City
San Antonio
State
TX
Country
United States
Zip Code
78229
Williams, D M; Grubbs, B G; Park-Snyder, S et al. (1996) Activation of latent transforming growth factor beta during Chlamydia trachomatis-induced murine pneumonia. Res Microbiol 147:251-62
Magee, D M; Williams, D M; Smith, J G et al. (1995) Role of CD8 T cells in primary Chlamydia infection. Infect Immun 63:516-21
Williams, D M; Grubbs, B G; Schachter, J et al. (1993) Gamma interferon levels during Chlamydia trachomatis pneumonia in mice. Infect Immun 61:3556-8
Lohman, K L; Kieber-Emmons, T; Kennedy, R C (1993) Molecular characterization and structural modeling of immunoglobulin variable regions from murine monoclonal antibodies specific for hepatitis B virus surface antigen. Mol Immunol 30:1295-306
Cox, F; Taylor, L; Eskew, E K et al. (1993) Prevention of group B streptococcal colonization and bacteremia in neonatal mice with topical vaginal inhibitors. J Infect Dis 167:1118-22
Magee, D M; Igietseme, J U; Smith, J G et al. (1993) Chlamydia trachomatis pneumonia in the severe combined immunodeficiency (SCID) mouse. Reg Immunol 5:305-11
Anderson, S A; Ostberg, L G; Ehrlich, P H et al. (1992) Characterization of private and cross-reactive idiotypes associated with human antibodies to hepatitis B surface antigen. Int Immunol 4:135-45
Magee, D M; Smith, J G; Bleicker, C A et al. (1992) Chlamydia trachomatis pneumonia induces in vivo production of interleukin-1 and -6. Infect Immun 60:1217-20
Alderete, J F; Newton, E; Dennis, C et al. (1991) The vagina of women infected with Trichomonas vaginalis has numerous proteinases and antibody to trichomonad proteinases. Genitourin Med 67:469-74
Alderete, J F; Newton, E; Dennis, C et al. (1991) Antibody in sera of patients infected with Trichomonas vaginalis is to trichomonad proteinases. Genitourin Med 67:331-4

Showing the most recent 10 out of 46 publications