Study How HIV-Driven Changes to Immunometabolism Impact Immune Response to TB and HBV

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NIAID will support research that helps define how HIV-driven alterations to immunometabolism affect immune responses and increase the risk for poor outcomes due to second, potentially long-term infections such as Mycobacterium tuberculosis (Mtb) or hepatitis B virus (HBV). Through two new notices of funding opportunities (NOFOs)—Elucidating Immunometabolic Responses to HIV Infection that Increase TB or HBV Risk (R01, Clinical Trial Not Allowed) and Elucidating Immunometabolic Responses to HIV Infection that Increase TB or HBV Risk (R21, Clinical Trial Not Allowed)—we aim to increase understanding of these mechanisms in order to identify candidate markers of disease progression as well as potential targets for immune-modulatory treatment to decrease TB and HBV risks in people living with HIV.  

While the R01 NOFO (PAR-25-315) supports well-developed applications that can extend up to 5 years, the R21 NOFO (PAR-25-316) calls for applications that support exploratory/developmental research activities that extend up to 2 years and apply to early and conceptual stages of research projects. 

Research Areas of Interest 

Research topics of interest on HIV immunometabolism and increased risk to either TB or HBV include, but are not limited to:  

  • Studies of alterations to immunometabolism due to HIV infection and the impact of such alterations on TB or HBV disease progression and/or pathogenesis of Mtb or HBV.
  • Defining the role of immunometabolism in cell-cell interactions in HIV co-infection with Mtb or HBV.
  • Dissection of multi-omic immune cell profiles and correlates of disease progression during co-infection (HIV with Mtb, HIV with HBV, or HIV with Mtb and HBV).
  • Discovery of immunometabolism-associated therapeutic targets or biomarkers of disease progression during co-infection. 

To better accomplish those scientific aims, we encourage applicants to: 

  • Form inter-disciplinary teams to leverage a range of strengths and expertise among multiple investigators.
  • Apply novel machine learning or artificial intelligence (AI) approaches.
  • Utilize existing clinical samples in conjunction with translational approaches including in vitro and in vivo model systems. 

NIAID will consider nonresponsive and will not review applications that propose the following: 

  • Elucidation of immunometabolic changes driven by causes other than HIV infection.
  • Exploration of immunometabolic effects of HIV infection without co-infection.
  • Clinical trials.

Keep in mind, peer reviewers will assess specifically the extent to which your proposed research addresses the fundamental understanding of biological mechanisms underlying HIV-induced immunometabolic alterations that affect immune cell regulation, cell-cell interactions, response to treatment, and, ultimately, TB and HBV disease progression. 

Application Deadlines and Budget  

Application deadlines follow NIH AIDS standard due dates, i.e., May 7, September 7, and January 7, by 5 p.m. local time of the applicant organization, through January 7, 2028. 

While application budgets for the R01 opportunity are not limited, they need to reflect the actual needs of the proposed project. For the R21 opportunity, the combined budget for direct costs for the 2-year project period may not exceed $275,000. No more than $200,000 in direct costs may be requested in any single year. 

Contact Information 

For questions, reach out to Dr. Josh Radke at 301-761-6525 or josh.radke@nih.gov.

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Measuring Innovation: Laboratory Infrastructure to Deliver Essential HIV Clinical Trial Results

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This blog is the fifth in a series about the future of NIAID's HIV clinical research enterprise. For more information, please visit the HIV Clinical Research Enterprise page.

The outcomes of HIV clinical trials are often determined by precisely and accurately measuring how specific interventions work biologically in people. Whether tracking immune responses to a preventive vaccine candidate, monitoring changes to the amount of virus in the body, or screening for certain adverse events after administering a novel therapeutic, study teams routinely interact with clinical trial participants to safely obtain, store, transport, and analyze tissue and bodily fluid samples to answer important scientific questions about the impact of an HIV intervention in a laboratory. High quality, reliable laboratory infrastructure is critical to the accuracy and validity of clinical trial results. 

More than 150 NIAID-supported laboratories in 20 countries are addressing the diverse scientific programs of the four clinical trials networks in the Institute’s HIV clinical research enterprise. Since the start of HIV clinical research, laboratory capacities have grown in scope to support an increasing number of global clinical trials, emerging complexities in study protocol design and laboratory testing demands and evolving regulatory requirements for research and licensure.

NIAID is engaging research partners, community representatives, and other public health stakeholders in a multidisciplinary evaluation of its HIV clinical trials networks’ progress toward short- and long-term scientific goals. This process assesses knowledge gained since the networks were last awarded in 2020 to identify an essential path forward based on the latest laboratory and clinical evidence. Future NIAID HIV clinical research investments build on the conclusions of these discussions. 

In the next iteration of HIV clinical trials networks, laboratory functions will continue to evolve to align with scientific priorities and research approaches. Networks will support small early-phase trials, large registrational trials and implementation science research to examine preventive vaccine candidates and non-vaccine prevention interventions, antiviral treatments, HIV curative strategies, and therapies to improve the clinical outcomes of people affected by and living with HIV. Selected studies also will rely on high quality laboratory resources to examine interventions for tuberculosis, hepatitis, mpox and other infectious diseases. Clinical trial networks will need to employ a variety of laboratory types to achieve these objectives.  To increase flexibility and ensure the timeliness and the high quality standards the HIV field relies on for evidence that informs science, licensure and equitable practice, NIAID will have the ultimate authority for laboratory selection and approval.

Efficiency and Versatility 

Laboratory assays for HIV clinical trials continue to expand in quantity and complexity and require proportionate technical expertise and management. Future clinical research needs will include immunologic, microbiologic, and molecular testing, as well as standard chemistries and hematologic assays, with fluctuating volumes across a global collection of research sites. Balancing capacity, efficiency, scalability, and cost will require a mixed methods approach. These may include centralized laboratory testing where feasible and advantageous for protocol-specified tests; standardized processes for rapid assessment and approval of new network laboratories; and validated third-party outsourcing of routine assays to ensure timely turnaround when demands surge. 

Quality and Standardization

Ensuring consistent laboratory operations and high quality laboratory data will require continued compliance with the NIAID Division of AIDS Good Clinical Laboratory Practices and other applicable regulatory guidelines, ongoing external quality assurance monitoring, strong inventory management, importation and exportation expertise, and data and specimen management.

The research community plays an essential role in shaping NIAID’s scientific direction and research enterprise operations. We want to hear from you. Please share your questions and comments at NextNIAIDHIVNetworks@mail.nih.gov.

About NIAID’s HIV Clinical Trials Networks

The clinical trials networks are supported through grants from NIAID, with co-funding from and scientific partnerships with NIH’s National Institute of Mental Health, National Institute on Drug Abuse, National Institute on Aging, and other NIH institutes and centers. There are four networks—Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections, the HIV Vaccine Trials Network, the HIV Prevention Trials Network, and the International Maternal Pediatric Adolescent AIDS Clinical Trials Network.

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Contact the NIAID Media Team.

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niaidnews@niaid.nih.gov

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Help Develop Long-Acting and Simplified HIV Treatments

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Through the notice of funding opportunity (NOFO) Advancing Translation of Long-Acting Strategies for HIV and HIV-Associated Co-infections (AT LASt) (R61/R33 Clinical Trial Not Allowed), NIAID will support the development of safe and effective long-acting/sustained release (LA/SR) technologies to help prevent and treat HIV and related co-infections such as tuberculosis (TB), hepatitis B (HBV), and hepatitis C (HCV). LA/SR technologies not only maintain consistent and effective drug levels for extended periods of time but also provide effective drug concentrations at reduced drug dosing intervals—thereby simplifying dosing requirements and helping reduce the life-long burden that HIV prevention and treatment approaches can have on patients.  

Research Objectives and Research Plan Requirements 

In your application, you should show a strong rationale, competitive advantage, and effectiveness in appropriate nonclinical or animal models at intermittent dosing from either a single administration (such as injection, topical, oral administration) or continuous dosing regimen (such as an implant or transdermal patch) with a minimum dosing interval of once every 3 months for HIV treatment or prevention or a minimum of once-a-month treatment for TB, HBV, or HCV.  

Proposed LA/SR technologies may include small molecules, peptides, proteins, oligonucleotides, gene therapies, polymers, and contain a single or a combination of Active Pharmaceutical Ingredients or be used in combination with other agents, such as transporters, enzyme inhibitors, or immunomodulators, to improve their efficacy and prolong therapeutic effect. 

Applicants must include (1) a Target Product Profile to summarize long-acting drug product critical properties and targets for development, (2) a defined investigational new drug (IND)-directed product development strategy in concordance with FDA guidance that addresses all IND components, (3) description of ownership and intellectual property (IP) rights for the proposed product to ensure freedom to operate, (4) a plan for a pre-IND meeting with the FDA by the end of the fourth year of funding, and (5) a timeline. Applicants must also define critical points within the timeline and establish a set of benchmarks throughout the entire program to monitor progress and to stay focused on program objectives towards filing the IND application. 

In addition, applicants are required to identify an industry partner or translational advisor with an established record in product development as well as potential collaborators or consultants with specialized expertise.  

If you propose the following research in your application, NIAID will consider it nonresponsive and not review it:  

  • Discovery and early product development work. 
  • LA/SR technologies for HIV and HIV-associated co-infections that do not meet the minimum dosing interval requirements as defined in the NOFO. 
  • Development of broadly neutralizing antibodies (bnAbs), non-neutralizing antibodies, bispecific or trispecific antibodies, or other engineered antibody-based approaches (e.g., molecules combining antibody domains with other non-antibody domains, such as CD4) as long-acting agents. 
  • Single agent prevention modalities that include advancement of Tenofovir or cabotegravir, including pro-drugs. 
  • Strategies for HIV, TB, HBV, or HCV vaccines for treatment or prevention, or PrEP strategies coupled to a vaccine. 
  • Clinical trials are not allowed, but use of samples from clinical trials supported elsewhere is allowed. 
  • Applications lacking the following components: 
    • Target Product Profile (TPP) 
    • Defined IND-directed product development strategy 
    • Description of ownership and IP rights for the proposed product 
    • Timeline and/or Gantt Chart 
    • Inclusion of an industry partner or translational advisor 
    • Plans for an External Advisory Board  
    • Milestones for the R61 Phase 
    • Clearly articulated plans for a pre-IND meeting 

Due to the high-risk, high-impact nature of the research and the milestone-driven preclinical development activities, this funding opportunity will use the R61/R33 Exploratory/Developmental Phased award with investigator-provided milestones. Proposed milestones will be reviewed and negotiated prior to award.  

Note that applications without milestones will not be reviewed.  

Application Deadlines and Budget 

Application budgets are not expected to exceed $700,000 in direct costs less consortium indirect (facilities & administrative) costs per year during the R61 Phase and $1,000,000 in direct costs less consortium indirect costs per year during the R33 Phase. Applicants may request up to 2 years of support for the R61 phase, and up to 3 years of support for the R33 Phase. It is expected that approximately half of the projects supported during the R61 Phase will continue into the R33 Phase.  

The maximum project period for an application submitted in response to this NOFO cannot exceed 5 years total. 

NIAID intends to fund three to five awards in fiscal year 2026. 

Applications are due March 13, 2025, at 5 p.m. local time of the applicant organization. Send an optional letter of intent 30 days prior to the due date. 

Contacts 

For application questions please contact the following: HIV prevention contact Dr. Kristen A. Porter at kristen.porter@nih.gov or 301-761-7022 and for treatment of HIV, TB, HBV, HCV contact Dr. Marina Protopopova at marina.protopopova@nih.gov or 301-761-7653. Reach out to Dr. Shiv A. Prasad with peer review questions at shiv.prasad@nih.gov or 240-627-3219.

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Study Challenges Assumptions About How Tuberculosis Bacteria Grow

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Establishing Preclinical Animal Models to Study Post-TB Lung Disease Development

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NIAID invites research applications to better understand the pathophysiology of long-term lung damage resulting from Mycobacterium tuberculosis (Mtb) and the role of the immune response during tuberculosis treatment through Notice of Special interest (NOSI): Establishing and Utilizing Preclinical Animal Models to Study Post-TB Lung Disease Development

Mtb is a significant global health challenge that produces a spectrum of clinical states and disease in humans during both active disease and latent infection. Clinicians will base a treatment’s success or failure primarily on microbiological outcomes defined by sputum culture. 

However, some cured patients are afflicted with irreversible lung damage and debilitating chronic lung function impairment that has come to be known as Post-TB Lung Disease (PTLD). While most of our understanding of PTLD comes from long-term human cohorts, using animal models for PTLD development could help address difficult mechanistic questions when relying solely on human studies. To prevent the long-term impact of active TB on patients’ lung health, a better understanding of the mechanisms involved in the development of PTLD at all stages of TB treatment is needed.

Research Objectives and Scope

The purpose of this NOSI is to invite applications for basic and translational research establishing and utilizing animals to model the development of PTLD. This NOSI supports the establishment and usage of preclinical animal models that strive to better understand the pathophysiology of long-term lung damage resulting from pulmonary TB. Validating results with animal models using clinical samples is allowed, but clinical trials and clinical research will not be supported under this NOSI. 

Research Topics of Interest 

NIAID is interested in research topics that establish preclinical animal models of PTLD development that could enhance studies such as:

  • Lung repair mechanisms during and after TB treatment, including interactions among lung resident and circulating immune cells that contribute to tissue destruction and repair.
  • Intrinsic host factors predisposing to the development of or protection against PTLD.
  • Mechanisms of resolution of lung tissue damaging inflammatory response, including host immune effector and cell death processes.
  • Potential effect of HIV including the impact of CD4+ T cell counts, antiretroviral therapy (ART) status and regimen, and viral suppression.

Extensive studies of the effect of HIV have not been conducted to determine whether ART, the level of viral suppression, or immune reconstitution have roles in PTLD development.

Nonresponsive Areas of Research

Review the list below for research areas that will be considered nonresponsive and will not be reviewed.

  • Applications proposing clinical research, or the use of clinical samples outside of validating results from animal models.
  • Applications exclusively focusing on modeling established PTLD.
  • Applications involving TB reactivation in animal models.
  • Applications on therapeutics focused on treatment shortening or improving Mtb killing unrelated to long-term lung health.

Application and Submission Information

This notice applies to due dates on or after February 5, 2025, and subsequent receipt dates through January 7, 2028. Apply for this initiative using one of the following notices of funding opportunities (NOFOs) or any subsequent reissueances of these NOFOs through the expiration date of this NOSI.

You should follow all instructions in the SF 424 (R&R) Application Guide and the NOFO through which you submit. Additionally, you must include “NOT-AI-24-082” (without quotation marks) in the Agency Routing Identifier field (box 4B) of the SF 424 R&R form to be considered for funding in response to this initiative. NIAID will not consider applications that do not have this information in box 4B.

Contact Information

Direct any inquiries to NIAID’s scientific/research contact, Dr. Robert Mahon at robert.mahon@nih.gov or 240-669-5427.

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Reviving Immune Responsiveness after Tuberculosis

NIH Awards UAMS $3.7 Million in Quest for More Effective Tuberculosis Vaccine

Shaping the Next Era of HIV Therapeutics and Care

NIAID Now |

This blog is the fourth in a series about the future of NIAID's HIV clinical research enterprise. For more information, please visit the HIV Clinical Research Enterprise page.

The development of HIV therapy is one of the great success stories in modern infectious disease research, marked by rapid advances that scientists in the field could only dream of in the 1980s and 1990s. Once a handful of daily pills that only partially suppressed the virus and caused systemic adverse events, today’s antiretroviral therapy (ART) consists of highly effective, well-tolerated medications that can be taken in a single daily dose or a long-acting injection. ART not only offers individual benefits, but also suppresses viral replication to prevent onward transmission. The understanding that undetectable = untransmittable, also known as “U=U,” is based on the foundational NIAID-funded discovery that an undetectable HIV viral load makes it impossible to transmit the virus to sexual partners.

Today’s high standard of HIV care is possible because of the enduring effort of advocates and policymakers who insist that HIV science be sufficiently funded to address key evidence gaps and public health needs, as well as the research teams that propel a constant stream of discovery and the clinical trial participants who allow their lived experience to become evidence for a population-level benefit. This progress is extraordinary, but more advances are still needed to assure the long-term health and quality of life of all people with HIV. Among many persisting challenges, we must address HIV-related complications and conditions that share health determinants with HIV, including tuberculosis (TB), viral hepatitis and mpox.

NIAID supports four research networks as part of its HIV clinical research enterprise. Every seven years, the Institute engages research partners, community representatives, and other public health stakeholders in a multidisciplinary evaluation of network progress toward short- and long-term scientific goals. This process takes stock of knowledge gained since the networks were last awarded and identifies essential course corrections based on the latest laboratory and clinical evidence. Subsequent NIAID HIV research investments build on the conclusions of these discussions.

These investments are paying off. Recent scientific advances include:

  • Basic and translational research that illuminated HIV’s structure, contributing to the development of the first drug in the capsid inhibitor class of antiretroviral drugs; 
  • A U.S. clinical trial showing that long-acting injectable ART can support viral suppression in people who experience barriers to daily pill-taking;
  • A global trial that found daily statin use reduces the risk of major adverse cardiovascular events in people with HIV;
  • A large international clinical trial that found a one-month course of rifapentine and isoniazid was as safe and effective as a nine-month course of isoniazid for preventing active tuberculosis in people with HIV;
  • Promising results from a hepatitis B virus (HBV) vaccine candidate for people with HIV who do not mount an immune response to current HBV vaccines;
  • Evidence that sustained virological response to direct-acting antiviral therapy for hepatitis C virus (HCV) is possible with minimal clinical monitoring—a strategy that could be crucial to the global HCV elimination agenda; and
  • Rapid engagement by the ACTG clinical trials network to examine antivirals for COVID-19 and mpox, demonstrating the essential role networks can—and should—play in pandemic preparedness and response.

We look forward to continuing to address the barriers that separate us from truly optimized HIV care. Our goals include fostering the next generation of discoveries that will open up possibilities for people with HIV—including people who have taken ART for decades—to experience a typical lifespan with high life quality, free from a chronic medication burden; reducing the incidence of concurrent TB and hepatitis; and ensuring scientific advances can feasibly be scaled to all who stand to benefit. 

Beyond Lifelong ART

Current therapeutic regimens are suppressive at best, meaning that if a person experiences an interruption in treatment, HIV replication will typically resume and continue to damage the immune system. Long-acting formulations are transforming quality of life for people who could not take daily ART, but their durability is measured in months, not years. While substantially extending the durability of ART is feasible, we will reach the limit of what long-acting molecules can do. Beyond the horizon of ART, we are exploring several strategies including gene therapy, administration of broadly neutralizing antibodies, and therapeutic vaccines that could either halt HIV replication for years or life or clear all HIV from the body—efforts collectively grouped under cure research. The design and development of cure strategies must advance technologies that could be implemented at scale, especially in resource-limited settings where HIV prevalence is high.

Non-HIV Pathogens 

Even when HIV replication is well-controlled with current therapy, the residual effects of infection can hamper a person’s immune responses and increase their likelihood of experiencing clinical disease from other pathogens. Several infectious diseases also share health determinants with HIV, and require researchers to consider the full constellation of biological, social, and structural factors that can threaten the health of people with HIV. Through collaboration with NIAID’s Division of Microbiology and Infectious Diseases and other NIH Institutes and Centers, we will ensure that we avoid resolving one health condition at the expense of another. We also need to ensure that interventions for non-HIV health conditions will work for people with HIV. Scientific priorities include developing shorter, safer, and more effective treatment regimens for all forms of TB, a preventive TB vaccine, and a hepatitis B cure. 

Quality of life

Conditions associated with aging can have greater impact on people with HIV, including (but not limited to) cardiovascular disease, diabetes, perimenopause, and dementia. HIV care models and tools are no longer sufficient if they only support viral suppression. Critical research is underway to define the ways that treated HIV exacerbates or accelerates other chronic conditions seen in older people. In partnership with other NIH Institutes and Centers, we will continue working to improve the quality of life for people with HIV by supporting research to prevent and treat HIV-related coinfections, complications and comorbidities through the lifespan. Furthermore, we will ensure that person-centered HIV care incorporates health-related quality of life metrics alongside standard HIV monitoring and management in our clinical trials. 

Equitable progress

Equity remains central to NIAID’s research and development decision-making. ART, once in short supply, is now globally available to most people living with HIV, and long-acting formulations herald a future of easier adherence schedules without the constant reminder of the burden of HIV. While our science has always focused on prioritizing concepts that could be rolled out to all populations who could benefit, we must provide an evidence base to support a faster translation of discovery to equitable health care service delivery. Implementation science and social science research including behavioral research, together with medical advances, can accelerate progress toward health equity. We seek to maintain a continuous feedback channel with implementers, so that our priorities are aligned with their most pressing challenges.

The research community plays an essential role in shaping NIAID’s scientific direction and research enterprise operations. We want to hear from you. Please share your questions and comments at NextNIAIDHIVNetworks@mail.nih.gov.

About NIAID’s HIV Clinical Trials Networks

Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections is a global clinical trials network that conducts research to improve the management of HIV and its comorbidities; develop a cure for HIV; and innovate treatments for tuberculosis, hepatitis B, and emerging infectious diseases. The Network is supported through grants from NIAID, with co-funding and scientific partnership from the NIH National Institute of Mental Health, the NIH National Institute on Drug Abuse, the NIH National Institute on Aging, and other NIH Institutes and centers. Three other networks—the HIV Vaccine Trials Network, the HIV Prevention Trials Network, and the International Maternal Pediatric Adolescent AIDS Clinical Trials Network—generate complementary evidence on the scientific areas within their respective scopes.

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Pharmacokinetic Properties of Antiretroviral and Anti-Tuberculosis Drugs During Pregnancy and Postpartum

The purpose of this study is to evaluate the pharmacokinetic (PK) properties of antiretroviral (ARV) and anti-tuberculosis (TB) drugs administered during pregnancy and postpartum.

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Office/Contact: Jane Cabison
Phone: 323-865-1585
Email: janequan@usc.edu