The candidate is a mid-career Ph.D. epidemiologist interested in an academic research career. She seeks training and research experience in collaborative immunoepidemiologic methods. Helicobacter pylori, intestinal helminths and Mycobacterium tuberculosis are three of the most common chronic infections of the developing world. We hypothesize that combined infection with two or more of these agents alters host responses to individual infections resulting in different clinical outcomes. The objectives of this study are to (1) identify asymptomatic adults in San Francisco South Bay communities who have combinations of infections with Helicobacter pylori, intestinal helminths and/or Mycobacterium tuberculosis; (2) to conduct immunologic studies evaluating differential patterns of host immune response to chronic co-infection in untreated subjects; and (3) to evaluate immune and clinical responses post-treatment in a pilot sample of subjects with known sequence of eradication therapy. As part of an ongoing prospective study of H. pylori transmission in the South Bay Area, approximately 1000 adults (ages 18-45) will be screened for latent TB infection [LTBI], Helicobacter pylori (CagA+) and intestinal helminth infection using established screening tests. Based on these results, approximately 200 subjects with combinations of single and multiple infection, including a sample without target infections, will be selected for specialized immunologic studies. In this group, additional assessments will include medical history, testing for other major infections, and in a subset, gastric cytokine expression. We will compare baseline measures of cellular and humoral immunity, including Th-1 and Th-2 associated cytokine production, delayed-type hypersensitivity, species-specific antibody subclass responses and measures of gastric inflammation pre- and post-treatment of these agents, and assess intra- and inter-subject variabilities in time. Secondary aims of the study include characterization of regulatory T-cell activity associated with co-infection. We will also store specimens with linked epidemiologic data for possible use in future studies to assess variations in PBMC gene expression patterns. Studies characterizing the immuno-modulatory effects of co-infection with these organisms have implications for treatment intervention and vaccine development of great relevance to the health needs of U.S. foreign born and the developing world.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Mentored Patient-Oriented Research Career Development Award (K23)
Project #
1K23AI054443-01A1
Application #
6733859
Study Section
Microbiology and Infectious Diseases B Subcommittee (MID)
Program Officer
Van de Verg, Lillian L
Project Start
2004-07-01
Project End
2009-03-31
Budget Start
2004-07-01
Budget End
2005-03-31
Support Year
1
Fiscal Year
2004
Total Cost
$131,490
Indirect Cost
Name
Stanford University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
009214214
City
Stanford
State
CA
Country
United States
Zip Code
94305
Chang, Alicia H; Perry, Sharon; Du, Jenny N T et al. (2013) Decreasing intestinal parasites in recent Northern California refugees. Am J Trop Med Hyg 88:191-7
Perry, S; Hussain, R; Parsonnet, J (2011) The impact of mucosal infections on acquisition and progression of tuberculosis. Mucosal Immunol 4:246-51
Perry, Sharon; de Jong, Bouke C; Solnick, Jay V et al. (2010) Infection with Helicobacter pylori is associated with protection against tuberculosis. PLoS One 5:e8804
Perry, Sharon; Sanchez, Luz; Yang, Shufang et al. (2008) Reproducibility of QuantiFERON-TB gold in-tube assay. Clin Vaccine Immunol 15:425-32