The Center for HIV/AIDS Vaccine Immunology (CHAVI) will be an extramural HIV/AIDS vaccine center consortium whose overall mission is to address key immunological roadblocks to HIV-1 vaccine development and to design, develop, and test novel immunogens and adjuvants. The CHAVI consortium will be comprised of the Principal Investigator (B. Haynes, Duke), Senior Leadership Group members (N. Letvin, Harvard; J. Sodroski, Harvard; G. Shaw, UAB; A. McMichael, Oxford), and Core Leaders (S. Harrison, Harvard; R. Dolin, Harvard; D.Goldstein, Duke; and M. Cohen, UNC). Overall goals of the CHAVI consortium will be: 1) To elucidate early viral and immunological events and host genetic factors associated with HIV-1 transmission, establishment of infection, and (partial) containment of virus replication; 2) To determine correlates of SIV immune protection in primates; 3) To design, develop, and test novel immunogens and adjuvants that elicit persistent mucosal and/or systemic immune responses to HIV-1 and SIV in humans and primates; and 4) To evaluate HIV-1 vaccine candidates in early phase clinical trials. The centerpiece of the CHAVI research agenda is the principal investigator's R01 project, which has four aims: 1) characterization of transmitted HIV-1; 2) ontogeny of cellular immune responses in acute and early HIV-1 infection; 3) ontogeny of humoral immune responses in acute and early HIV-1 infection; and 4) host genetic factors influencing HIV-1 infection and early progression.
These aims, in turn, are closely linked to senior leadership group research projects: Neutralization properties of transmitted HIV-1 (Shaw); Viral, immunological, and host genetic factors in HIV-1 exposed-uninfected individuals (McMichael); Correlates of immune protection in SIV vaccinated macaques (Letvin); and Structure of transmitted HIV-1 envelope trimers (Sodroski). A major strength of the CHAVI is the breadth and depth of vaccine-related research that it will undertake, the opportunities for unique synergies among its participants, and the demonstrated abilities of the principal investigator in leading a large basic and clinical research enterprise. The CHAVI Consortium will be an integral component of the Global HIV-1 Vaccine Enterprise. It will address critical gaps in scientific knowledge and will contribute in a direct and meaningful fashion to the successful development of an efficacious and globally applicable HIV-1 vaccine.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program--Cooperative Agreements (U19)
Project #
5U19AI067854-07
Application #
8331717
Study Section
Special Emphasis Panel (ZAI1-CL-A (M1))
Project Start
2011-07-01
Project End
2013-06-30
Budget Start
2011-07-01
Budget End
2013-06-30
Support Year
7
Fiscal Year
2011
Total Cost
$608,264
Indirect Cost
Name
Duke University
Department
Type
DUNS #
044387793
City
Durham
State
NC
Country
United States
Zip Code
27705
Song, Hongshuo; Giorgi, Elena E; Ganusov, Vitaly V et al. (2018) Tracking HIV-1 recombination to resolve its contribution to HIV-1 evolution in natural infection. Nat Commun 9:1928
Boelen, Lies; Debebe, Bisrat; Silveira, Marcos et al. (2018) Inhibitory killer cell immunoglobulin-like receptors strengthen CD8+ T cell-mediated control of HIV-1, HCV, and HTLV-1. Sci Immunol 3:
Winawer, Melodie R; Griffin, Nicole G; Samanamud, Jorge et al. (2018) Somatic SLC35A2 variants in the brain are associated with intractable neocortical epilepsy. Ann Neurol 83:1133-1146
Roohi, Jasmin; Crowe, Jennifer; Loredan, Denis et al. (2017) New diagnosis of atypical ataxia-telangiectasia in a 17-year-old boy with T-cell acute lymphoblastic leukemia and a novel ATM mutation. J Hum Genet 62:581-584
Epi4K Consortium; EuroEPINOMICS-RES Consortium; Epilepsy Phenome Genome Project (2017) Application of rare variant transmission disequilibrium tests to epileptic encephalopathy trio sequence data. Eur J Hum Genet 25:894-899
Liu, Donglai; Wang, Chu; Hora, Bhavna et al. (2017) A strongly selected mutation in the HIV-1 genome is independent of T cell responses and neutralizing antibodies. Retrovirology 14:46
Pacheco, Beatriz; Alsahafi, Nirmin; Debbeche, Olfa et al. (2017) Residues in the gp41 Ectodomain Regulate HIV-1 Envelope Glycoprotein Conformational Transitions Induced by gp120-Directed Inhibitors. J Virol 91:
Fouda, Genevieve G; Eudailey, Joshua; Kunz, Erika L et al. (2017) Systemic administration of an HIV-1 broadly neutralizing dimeric IgA yields mucosal secretory IgA and virus neutralization. Mucosal Immunol 10:228-237
Shen, Xiaoying; Bogers, Willy M; Yates, Nicole L et al. (2017) Cross-Linking of a CD4-Mimetic Miniprotein with HIV-1 Env gp140 Alters Kinetics and Specificities of Antibody Responses against HIV-1 Env in Macaques. J Virol 91:
Fischetti, Lucia; Zhong, Ziyun; Pinder, Christopher L et al. (2017) The synergistic effects of combining TLR ligand based adjuvants on the cytokine response are dependent upon p38/JNK signalling. Cytokine 99:287-296

Showing the most recent 10 out of 395 publications