New Lab Test to Detect Persistent HIV Strains in Africa May Aid Search for Cure

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Weill Cornell Medicine
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New Lab Test to Detect Persistent HIV Strains in Africa May Aid Search for Cure
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Exploratory Analysis Associates HIV Drug Abacavir with Elevated Cardiovascular Disease Risk in Large Global Trial

Current or previous use of the antiretroviral drug (ARV) abacavir was associated with an elevated risk of major adverse cardiovascular events (MACE) in people with HIV, according to an exploratory analysis from a large international clinical trial primarily funded by the National Institutes of Health (NIH). There was no elevated MACE risk for the other antiretroviral drugs included in the analysis. The findings will be presented at the 2024 International AIDS Conference (AIDS 2024) in Munich, Germany.

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Long-Acting Injectable Cabotegravir for HIV Prevention Is Safe in Pregnancy

Long-acting injectable cabotegravir (CAB-LA) was safe and well tolerated as HIV pre-exposure prophylaxis (PrEP) before and during pregnancy in the follow-up phase of a global study among cisgender women. The analysis of outcomes from more than 300 pregnancies and infants will be presented at the 2024 International AIDS Conference (AIDS 2024) in Munich, Germany. 

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An Isolated Viral Load Test May Generate False Positive Results for People Using Long-Acting PrEP

A single laboratory-based HIV viral load test used by U.S. clinicians who provide people with long-acting, injectable cabotegravir (CAB-LA) HIV pre-exposure prophylaxis (PrEP) did not reliably detect HIV in a multi-country study. In the study, a single positive viral load test was frequently found to be a false positive result. However, a second viral load test with a new blood sample was able to distinguish true positive results from false positive results for all participants whose initial viral load test was positive.

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Help Strengthen the Pipeline of Antiviral Drugs for the Next Pandemic

Funding News Editions:
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Through Notice of Special Interest (NOSI): Discovery and Development of Oral Small-Molecule Direct-Acting Antivirals Targeting Viruses of Pandemic Potential, NIAID invites research project grant applications to advance candidate antiviral drugs suitable for widespread use in the community in future outbreaks or pandemics. 

Specifically, the NOSI encourages discovery and development of small molecule compounds (molecular weight less than 2 kilodaltons) with activity against viral targets that could be administered orally as monotherapy or in combination with other drugs to treat infections caused by viruses of pandemic potential. Such research may range from early discovery and lead series optimization to late-stage preclinical development and investigational new drug-enabling profiling.  

Example project activities include, but are not limited to: 

  • Structure-based design and medicinal chemistry 
  • Biochemical screening 
  • In vitro efficacy 
  • In vivo efficacy 
  • Mechanism of action studies 
  • Pharmacology and toxicology 

We strongly encourage applicants to collaborate with pharmaceutical organizations to access chemical starting points and critical medicinal chemistry, as well as regulatory and drug development expertise. 

Incorporating multidisciplinary activities may also be appropriate, depending on the project’s stage of candidate discovery and development. 

As for what viruses to target, the NOSI considers viral pathogens from the following RNA virus families within scope: 

  • Coronaviruses (activity against multiple coronaviruses, ‘pan-CoV,’ required) 
  • Paramyxoviruses 
  • Bunyaviruses (Bunyavirales order) 
  • Togaviruses 
  • Filoviruses 
  • Picornaviruses 
  • Flaviviruses 
  • Orthomyxoviruses 

You must not focus on other virus families or we will consider your application nonresponsive under this NOSI. Likewise, the NOSI will not support the following: 

  • Approaches that target the host and not the virus. 
  • Therapeutics that will require intravenous, intranasal, or other non-oral delivery routes. 
  • Antibody or other non-small molecule approaches in which the candidate’s molecular weight exceeds 2 kilodaltons. 
  • Efforts to repurpose or reformulate marketed drugs. 

How to Apply 

For standard due dates on or after October 5, 2024, through July 16, 2027, you may apply using the following parent notices of funding opportunities (NOFOs) or their subsequent reissues: 

Remember, you must list “NOT-AI-24-053” in the Agency Routing Identifier field (Box 4B) of the SF 424 R&R form.  

To determine your project’s maximum project period, budget limits, and specific submission deadline, refer to the NOFO through which you choose to apply.   

Direct questions about the NOSI to our scientific/research contacts for the initiative: Dr. Mindy Davis at mindy.davis@nih.gov or 301-761-6689 and Dr. Dipanwita Basu at dipanwita.basu@nih.gov or 240-627-3469.

Contact Us

Email us at deaweb@niaid.nih.gov for help navigating NIAID’s grant and contract policies and procedures.

Features of H5N1 Influenza Viruses in Dairy Cows May Facilitate Infection, Transmission in Mammals

A series of experiments with highly pathogenic H5N1 avian influenza (HPAI H5N1) viruses circulating in infected U.S. dairy cattle found that viruses derived from lactating dairy cattle induced severe disease in mice and ferrets when administered via intranasal inoculation. The virus from the H5N1-infected cows bound to both avian (bird) and human-type cellular receptors, but, importantly, did not transmit efficiently among ferrets exposed via respiratory droplets.

Contact

Submit a Media Request

Contact the NIAID News & Science Writing Branch.

301-402-1663
niaidnews@niaid.nih.gov
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