Primary HIV-1 infection is a period of explosive viral growth in which critical lymphoid organs are seeded and in which the initial movement toward viral diversity is established. The mergence of a multifaceted humoral and cellular immune response is associated with a rapid decline in plasma levels of HIV-1 RNA but virus is not eliminated from the host. Initial events in the virus/host interactions clearly play a critical role in limiting viral replication and in determining the subsequent natural history f the illness. Viral and/or immunologic factors that permit the virus to evade elimination have not yet been delineated. Emerging data suggest that antiretroviral intervention during primary infection may have profound implications for the virus/host interaction. It has been suggested that this interval during which viral diversity is relatively limited and in which viral seeding of lymphoid organs is still incomplete may be a time during which potent antiretroviral chemotherapy might even eliminate virus from the host. We have assembled a group of laboratory-based and clinical investigators who wish to intensively characterize viral and immunologic events during primary infection in the context of therapeutic interventions with maximally active antiretroviral regimens. These investigations will provide additional insights into the immunopathogenesis of HIV-1 infection and will have important implications for designing antiretroviral chemotherapeutic strategies and for AIDS vaccine development.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project--Cooperative Agreements (U01)
Project #
3U01AI041536-04S2
Application #
6601024
Study Section
Special Emphasis Panel (ZAI1 (M1))
Program Officer
Matula, Margaret A
Project Start
1997-07-01
Project End
2005-06-30
Budget Start
2002-08-15
Budget End
2005-06-30
Support Year
4
Fiscal Year
2002
Total Cost
$669,191
Indirect Cost
Name
University of Colorado Denver
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
065391526
City
Aurora
State
CO
Country
United States
Zip Code
80045
Moore, Camille M; MaWhinney, Samantha; Forster, Jeri E et al. (2017) Accounting for dropout reason in longitudinal studies with nonignorable dropout. Stat Methods Med Res 26:1854-1866
Meditz, Amie L; Connick, Elizabeth; McCarter, Martin (2014) Safety of excisional inguinal lymph node biopsies performed for research purposes in HIV-1-infected women and men. Surg Infect (Larchmt) 15:399-403
Hecht, Frederick M; Wellman, Robert; Busch, Michael P et al. (2011) Identifying the early post-HIV antibody seroconversion period. J Infect Dis 204:526-33
Meditz, Amie L; MaWhinney, Samantha; Allshouse, Amanda et al. (2011) Sex, race, and geographic region influence clinical outcomes following primary HIV-1 infection. J Infect Dis 203:442-51
Apuzzo, Linda G; Vaida, Florin; Gallant, Joel E et al. (2009) Tolerability and efficacy of PI versus NNRTI-based regimens in subjects receiving HAART during acute or early HIV infection. J Acquir Immune Defic Syndr 50:267-75
Behbahani, Homira; Walther-Jallow, Lilian; Klareskog, Elin et al. (2007) Proinflammatory and type 1 cytokine expression in cervical mucosa during HIV-1 and human papillomavirus infection. J Acquir Immune Defic Syndr 45:9-19
Connick, Elizabeth; Mattila, Teresa; Folkvord, Joy M et al. (2007) CTL fail to accumulate at sites of HIV-1 replication in lymphoid tissue. J Immunol 178:6975-83
Al-Harthi, Lena; MaWhinney, Sam; Connick, Elizabeth et al. (2007) Immunophenotypic alterations in acute and early HIV infection. Clin Immunol 125:299-308
Hecht, Frederick M; Wang, Lei; Collier, Ann et al. (2006) A multicenter observational study of the potential benefits of initiating combination antiretroviral therapy during acute HIV infection. J Infect Dis 194:725-33
Folkvord, Joy M; McCarter, Martin D; Ryder, John et al. (2006) alpha-Defensins 1, 2, and 3 are expressed by granulocytes in lymphoid tissues of HIV-1-seropositive and -seronegative individuals. J Acquir Immune Defic Syndr 42:529-36

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