Project Grant R43AI172555
- This Project Grant award of $240,300 from the National Institute of Allergy and Infectious Diseases (NIAID) under the Allergy and Infectious Diseases Research program (CFDA 93.855) aims to develop bispecific antibodies (bAbs) that can efficiently penetrate the blood-brain barrier and deliver neutralizing antibodies against Eastern Equine Encephalitis Virus (EEEV) to the brain. The project will evaluate the therapeutic effectiveness of the bAbs compared to alternative antibody delivery methods...
- This Project Grant award, totaling $155,454, was provided by the National Institute of Allergy and Infectious Diseases (NIAID) under the Allergy and Infectious Diseases Research program (CFDA 93.855) to The Washington University in Missouri. The award supports research to identify alternative receptors and improve therapeutic decoy molecules for Venezuelan Equine Encephalitis Virus (VEEV), a mosquito-borne virus that causes severe neurological symptoms. The key products and services to be...
- This $452,769 federal Project Grant award from the National Institute of Allergy and Infectious Diseases (NIAID) under the Allergy and Infectious Diseases Research program (CFDA 93.855) supports research to evaluate the impact of the BDGR-49 compound on preventing long-term neurological sequelae caused by Venezuelan equine encephalitis virus (VEEV) infection. The research, conducted by Virginia Polytechnic Institute & State University, aims to determine if BDGR-49 can reduce VEEV replication...
- The Flavivirus and Alphavirus REVAMPP (FLARE) Center, funded by a $46,715,173 Cooperative Agreement award from the National Institute of Allergy and Infectious Diseases (CFDA 93.855 Allergy and Infectious Diseases Research), is developing and optimizing protein nanoparticle, virion-based, and mRNA vaccine platforms, as well as monoclonal antibody-based treatments to rapidly respond to emerging flaviviruses and alphaviruses with pandemic potential. The Center integrates the work of multiple...
- This Project Grant award from the National Institute of Allergy and Infectious Diseases (NIAID), under the Allergy and Infectious Diseases Research Federal Grant Program (CFDA 93.855), provides $281,786 to L2 Diagnostics LLC for the development of a safe and effective viral vector-based vaccine to induce both humoral and cellular immune protection against Powassan virus. The goal is to leverage the Modified Vaccinia Ankara vector platform to stimulate robust antibody and T cell responses that...
- The University of Missouri System, under a $650,000 project grant from the USDA National Institute of Food and Agriculture (NIFA) Agriculture and Food Research Initiative (AFRI) program, is developing safe and effective live attenuated swine influenza vaccines using Newcastle disease virus (NDV) as the vector. The project aims to address the challenges with current swine influenza vaccines, which often fail to provide cross-protection against diverse virus strains. The key products and...
- The federal Cooperative Agreement award, funded by the Advanced Research Projects Agency for Health (ARPA-H) under CFDA 93.384, aims to develop a broad vaccine that can protect against multiple emergent alphavirus infections. The $62,534,750 award to Vanderbilt University will leverage advanced computational biology, structural biology, vaccinology, virology, and immunology techniques to design and test novel vaccine candidates. The project's key objectives are to: Create hetero-nanoparticle...
- The National Institute of Allergy and Infectious Diseases (NIAID) awarded a $299,968 Project Grant under the Allergy and Infectious Diseases Research (CFDA 93.855) program to Viva Viral Vaccines, Inc. to develop a broad-spectrum, multivalent vaccine platform for pandemic and seasonal influenza. The platform leverages innovations in the production of influenza neuraminidase (NA) proteins in mammalian cells, enabling the development of VLP-based vaccines that can provide broad heterologous...
- The National Institute of Allergy and Infectious Diseases (NIAID) awarded a $781,718 Project Grant through its Allergy and Infectious Diseases Research program (CFDA 93.855) to Loyola University of Chicago to develop a novel T cell-based vaccine to prevent Dengue and Zika virus infections. The 5-year project aims to create a vaccine that induces cytotoxic T cells targeting the Zika virus non-structural protein 3, without causing antibody-dependent enhancement observed with vaccines targeting the...
- This Project Grant award of $847,000, provided by the National Institute of Allergy and Infectious Diseases (CFDA 93.855 - Allergy and Infectious Diseases Research) on July 15, 2025, will be used to assess the ferret model for evaluating the efficacy of antivirals against Venezuelan Equine Encephalitis Virus (VEEV). The objectives are to evaluate the virology and pathogenesis of the ferret model for the VEEV-INH strain (Aim 1) and to use this model to assess the toxicity, prophylactic, and...
DEVELOPMENT OF A CROSS-PROTECTIVE NEW WORLD ENCEPHALITIC ALPHAVIRUS SUBUNIT VACCINE - 7. PROJECT SUMMARY/ABSTRACT THE ENCEPHALITIC NEW WORLD ALPHAVIRUSES (NWAVS), CONSISTING OF EASTERN, VENEZUELAN AND WESTERN EQUINE ENCEPHALITIS VIRUSES (EEEV, VEEV AND WEEV, RESPECTIVELY), ARE TRANSMITTED BY MOSQUITOES THROUGH RODENT OR BIRD HOSTS AND HAVE CAUSED SIGNIFICANT PERIODIC EPIZOOTIC OUTBREAKS IN EQUINES AND HUMANS IN THE AMERICAS. NWAVS CAN CAUSE SEVERE NEUROLOGICAL DISEASE, WITH FATAL ENCEPHALITIS IN UP TO 70% OF CASES, AND SIGNIFICANT LONG-TERM SEQUELAE IN SURVIVORS. WITH RECENT CLIMATE CHANGES, GEOLOGICAL REDISTRIBUTION OF MOSQUITOES CARRYING NWAVS FURTHER ENHANCES THE POTENTIAL FOR FUTURE OUTBREAKS. MOREOVER, CONCERN OVER THEIR POTENTIAL USE AS BIOWEAPONS IS WELL-FOUNDED DUE TO THEIR EASE OF PRODUCTION, HIGH INFECTIVITY, ABILITY FOR AEROSOLIZATION, AND CAPACITY TO INDUCE DISEASE, RESULTING IN SELECT AGENT CLASSIFICATION FOR E/VEEV. DESPITE AWARENESS OF THESE VIRUSES FOR NEARLY 100 YEARS, LICENSED HUMAN VACCINES AGAINST E/V/WEEV REMAIN UNAVAILABLE FOR GENERAL USE. THE DEVELOPMENT OF NEXT-GENERATION VACCINES THAT CAN SAFELY AND EFFECTIVELY PROTECT HUMANS AGAINST THESE PATHOGENIC ALPHAVIRUS INFECTIONS ARE URGENTLY NEEDED. THIS PROJECT SEEKS TO DEVELOP A CROSS-PROTECTIVE RECOMBINANT SUBUNIT E/V/WEEV VACCINE BASED ON THE LINKED ECTODOMAIN PORTIONS OF ENVELOPE 2 (E2) AND E1 PROTEINS OF EACH NWAV ADJUVANTED WITH SLA-LSQ, A NOVEL TLR4 AGONIST COMBINED WITH THE SAPONIN QS-21 IN A LIPOSOMAL FORMULATION. THE PROPOSED APPROACH PROVIDES A MEANS TO DELIVER A SAFE AND STABLE VACCINE TO PROTECT AGAINST INFECTION BY ALL THREE NWAVS USING A SCALABLE MANUFACTURING PLATFORM THAT, IN COMBINATION WITH A PROVEN TH1/TH2 BALANCED ADJUVANT, ELICITS A ROBUST, EFFICACIOUS AND DURABLE IMMUNE RESPONSE THROUGH BOTH NEUTRALIZING AND NON-NEUTRALIZING MEANS. THE PROPOSED NWAV VACCINE IS BASED ON OUR HIGHLY IMMUNOGENIC AND FULLY PROTECTIVE PRE-CLINICAL E2/E1 CANDIDATE VACCINE FOR THE CLOSELY RELATED CHIKUNGUNYA VIRUS (CHIKV). NEW PRELIMINARY DATA DEMONSTRATES THAT MICE IMMUNIZED WITH THE NWAV E2/E1 SUBUNITS GENERATE HIGH NAB TITERS TO NON-SELECT AGENT STRAINS OF E/V/WEEV. THE SPECIFIC AIMS OF THIS PROJECT ARE: 1) EVALUATE THE IMMUNOGENICITY AND OPTIMIZE FORMULATIONS OF INDIVIDUAL AND COMBINED RECOMBINANT E/V/WEEV SUBUNIT PROTEINS WITH SLA-LSQ ADJUVANT; 2) DEMONSTRATE THE ABILITY OF THE CANDIDATE VACCINE TO INDUCE A DURABLE IMMUNE RESPONSE IN MICE; AND 3) DEMONSTRATE THE CROSS-PROTECTIVE EFFICACY OF THE CANDIDATE VACCINE IN MICE UPON NWAV CHALLENGE. HAWAII BIOTECH AND THE BAYLOR COLLEGE OF MEDICINE WILL COLLABORATE TO DEVELOP, EVALUATE AND ADVANCE THIS NOVEL TRIVALENT NWAV VACCINE CANDIDATE. THE DEVELOPMENT OF A CROSS-PROTECTIVE RECOMBINANT SUBUNIT VACCINE TO PROTECT AGAINST ALL THREE PATHOGENIC NWAVS WOULD PROVIDE A VALUABLE MEDICAL COUNTERMEASURE TO SAFEGUARD AGAINST THE CONSIDERABLE THREAT POSED BY THESE ENCEPHALITIC ALPHAVIRUSES.
Mod # | Description | ReasonForModification | Federal Obligation | Date |
|---|---|---|---|---|
| Not listed | $203.3k | 2/16/24 | ||
| Not listed | $0 | 7/14/23 | ||
| Not listed | $0 | 7/14/23 | ||
| Not listed | $204.3k | 3/7/23 | ||
| Not listed | $204.3k | 3/7/23 |