Opportunity Information: Apply for RFA DK 19 008

This funding opportunity, RFA-DK-19-008, is a National Institutes of Health (NIH) discretionary grant announcement using the R01 mechanism, with clinical trials allowed but not required (clinical trial optional). It is focused on a growing health problem: obesity is becoming more common among people with HIV (PWH), and this rise in obesity is linked to a range of downstream complications. The announcement emphasizes that obesity in PWH may not be driven by the same biology as obesity in people without HIV, and that HIV infection itself, along with antiretroviral drugs used for HIV treatment or for pre-exposure prophylaxis (PrEP), may contribute to weight gain through distinct pathways. The overall intent is to support research that clarifies why obesity is increasing in this population and what is different at the level of fat cells and fat tissue.

The scientific emphasis is on adipogenesis (how new fat cells develop), adipocyte function (how fat cells behave metabolically and hormonally), and broader adipose tissue biology in the context of HIV infection and exposure to antiretroviral agents. The opportunity is specifically seeking studies that can elucidate mechanisms, meaning applicants are expected to move beyond describing associations and instead identify underlying biological processes and pathways. This includes understanding how HIV and/or antiretroviral drugs may alter adipose tissue in ways that promote obesity or change how adipose tissue regulates metabolism, inflammation, and other physiological processes. Because the funding is aligned with the mission of the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), the work is expected to connect these adipose-related changes to metabolic and physiological outcomes relevant to diabetes, endocrine and metabolic health, digestive diseases, nutrition, and kidney-related complications where applicable.

A key theme in the announcement is that adipocytes in overweight or obese PWH may be biologically different from adipocytes in overweight or obese individuals without HIV. This points to research opportunities comparing groups to pinpoint what HIV infection, chronic immune activation, viral reservoirs, antiretroviral exposure, or PrEP exposure might be doing to adipose tissue. Projects could reasonably involve mechanistic studies of fat distribution changes, adipose inflammation and immune cell composition, insulin sensitivity and glucose metabolism, lipid handling, mitochondrial function, endocrine signaling from adipose tissue (adipokines), or how specific antiretroviral drug classes might influence weight regulation pathways. Since clinical trials are optional, projects may range from basic and translational laboratory studies using human samples and model systems to clinical or clinical-translational studies in people, including interventional designs where appropriate.

Administratively, the grant is categorized under the Food and Nutrition and Health activity areas, and it is associated with CFDA number 93.847. The agency is NIH, with NIDDK as the institute framing the mission priorities described in the text. The source data lists an award ceiling of $500,000, signaling the maximum annual direct cost level typically allowed under this announcement (as presented in the listing). The original closing date shown is 2019-11-07, and the opportunity record was created on 2019-05-29, indicating this is a specific, time-bound solicitation from that period rather than an open-ended standing program announcement.

Eligibility is broad and includes many organization types commonly allowed under NIH research grants. Eligible applicants include state, county, city/township, and special district governments; independent school districts; public and state-controlled institutions of higher education; private institutions of higher education; federally recognized Native American tribal governments; Native American tribal organizations other than federally recognized tribal governments; public housing authorities/Indian housing authorities; nonprofits (both with and without 501(c)(3) status, excluding institutions of higher education in those categories as specified); for-profit organizations other than small businesses; small businesses; and other categories. The announcement also explicitly calls out additional eligible applicants such as Alaska Native and Native Hawaiian Serving Institutions, Asian American Native American Pacific Islander Serving Institutions (AANAPISIs), Hispanic-serving Institutions, Historically Black Colleges and Universities (HBCUs), Tribally Controlled Colleges and Universities (TCCUs), faith-based or community-based organizations, eligible federal agencies, regional organizations, U.S. territories or possessions, and non-U.S. entities (foreign organizations). This reflects an intent to encourage participation from a wide range of institutions, including those serving populations disproportionately affected by HIV and related metabolic complications, and to support research capacity across diverse settings.

In practical terms, the opportunity is aimed at generating actionable biological insight that can eventually inform prevention and treatment strategies for obesity and metabolic disease in the context of HIV and antiretroviral exposure. The research supported under this FOA is meant to clarify what is driving weight gain and adipose dysfunction in PWH and in people exposed to antiretrovirals for prevention, and to connect those adipose changes to clinically meaningful metabolic and physiological outcomes within NIDDK priorities.

  • The National Institutes of Health in the food and nutrition, health sector is offering a public funding opportunity titled "Adipogenesis, Adipocyte Function and Obesity Following HIV Infection, Antiretroviral Therapy, or Pre-Exposure Prophylaxis (R01 Clinical Trial Optional)" and is now available to receive applicants.
  • Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 93.847.
  • This funding opportunity was created on 2019-05-29.
  • Applicants must submit their applications by 2019-11-07. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
  • Each selected applicant is eligible to receive up to $500,000.00 in funding.
  • Eligible applicants include: State governments, County governments, City or township governments, Special district governments, Independent school districts, Public and State controlled institutions of higher education, Native American tribal governments (Federally recognized), Public housing authorities/Indian housing authorities, Native American tribal organizations (other than Federally recognized tribal governments), Nonprofits having a 501 (c) (3) status with the IRS, other than institutions of higher education, Nonprofits that do not have a 501 (c) (3) status with the IRS, other than institutions of higher education, Private institutions of higher education, For-profit organizations other than small businesses, Small businesses, Others.
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Frequently Asked Questions (FAQs) - RFA-DK-19-008

What is RFA-DK-19-008?

RFA-DK-19-008 is a National Institutes of Health (NIH) discretionary funding opportunity announcement that uses the R01 research project grant mechanism. It focuses on understanding why obesity is increasing among people with HIV (PWH), with a particular emphasis on fat cell development and fat tissue biology.

Which NIH institute is most closely aligned with this opportunity?

The opportunity is aligned with the mission priorities of the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), especially where adipose tissue changes connect to metabolic and physiological outcomes relevant to diabetes, endocrine and metabolic health, digestive diseases, nutrition, and kidney-related complications (where applicable).

What is the main health problem this funding opportunity is trying to address?

The announcement targets a growing problem: obesity is becoming more common in people with HIV, and this increase is linked to downstream complications. The FOA emphasizes that obesity in PWH may involve different biology than obesity in people without HIV.

Why does the FOA suggest obesity in people with HIV may be biologically different?

The FOA highlights that HIV infection itself, chronic immune activation, viral reservoirs, and exposure to antiretroviral drugs (used for HIV treatment or for pre-exposure prophylaxis, PrEP) may contribute to weight gain through distinct biological pathways. This creates a need to identify what is different in adipocytes and adipose tissue in PWH compared to individuals without HIV.

What types of science are emphasized in this announcement?

The scientific emphasis is on adipogenesis (how new fat cells develop), adipocyte function (how fat cells behave metabolically and hormonally), and broader adipose tissue biology in the context of HIV infection and exposure to antiretroviral agents.

Does this opportunity prioritize mechanistic research or observational associations?

This opportunity specifically seeks studies that elucidate mechanisms. Applicants are expected to move beyond describing associations and instead identify underlying biological processes and pathways that help explain obesity and adipose dysfunction in the context of HIV and antiretroviral exposure.

How does antiretroviral therapy or PrEP fit into the research scope?

The FOA states that antiretroviral drugs used for HIV treatment or for PrEP may contribute to weight gain through distinct pathways. Projects may examine how exposure to these agents alters adipose tissue in ways that promote obesity or change metabolic, inflammatory, or endocrine functions.

What kinds of biological topics or mechanisms could a project focus on?

Based on the FOA description, relevant mechanistic topics may include changes in fat distribution, adipose inflammation and immune cell composition, insulin sensitivity and glucose metabolism, lipid handling, mitochondrial function, endocrine signaling from adipose tissue (including adipokines), and how specific antiretroviral drug classes might influence weight regulation pathways.

Is comparative research between people with HIV and people without HIV within scope?

Yes. A key theme is that adipocytes in overweight or obese PWH may differ from adipocytes in overweight or obese individuals without HIV. Studies comparing these groups to pinpoint HIV-related or antiretroviral-related effects on adipose tissue are consistent with the FOA’s emphasis.

Are clinical trials required under this FOA?

No. Clinical trials are allowed but not required. The FOA is described as clinical trial optional.

What study types are allowed (basic, translational, clinical)?

The FOA supports a range of approaches, from basic and translational laboratory studies using human samples and model systems to clinical or clinical-translational studies in people. Interventional designs may be appropriate when relevant, but they are not mandatory.

What does the R01 mechanism imply for this opportunity?

This FOA uses the NIH R01 mechanism, which supports discrete, specified research projects. The FOA framing emphasizes generating actionable biological insight into obesity-related adipose changes in the context of HIV and antiretroviral exposure.

What are the activity areas associated with this funding opportunity?

The opportunity is categorized under the Food and Nutrition and Health activity areas.

What is the CFDA number listed for this opportunity?

The CFDA number associated with this opportunity is 93.847.

What is the maximum award amount listed?

The source listing shows an award ceiling of $500,000, described as the maximum annual direct cost level typically allowed under this announcement (as presented in the listing).

When was this opportunity created and what is the closing date shown?

The opportunity record was created on 2019-05-29, and the original closing date shown is 2019-11-07. This indicates it was a time-bound solicitation from that period rather than an open-ended standing program announcement.

Who is eligible to apply?

Eligibility is broad and includes many organization types commonly allowed under NIH research grants. Eligible applicants include various levels of government (state, county, city/township, special district), independent school districts, public and state-controlled institutions of higher education, private institutions of higher education, federally recognized Native American tribal governments, tribal organizations other than federally recognized tribal governments, public housing authorities/Indian housing authorities, nonprofits (with or without 501(c)(3) status, excluding institutions of higher education in those nonprofit categories as specified), for-profit organizations other than small businesses, small businesses, and other categories.

Are minority-serving institutions and community-based organizations eligible?

Yes. The FOA explicitly calls out additional eligible applicants such as Alaska Native and Native Hawaiian Serving Institutions, AANAPISIs, Hispanic-serving Institutions, HBCUs, TCCUs, and faith-based or community-based organizations.

Are federal agencies and U.S. territories eligible?

Yes. The FOA explicitly includes eligible federal agencies, regional organizations, and U.S. territories or possessions among eligible applicants.

Are non-U.S. (foreign) organizations eligible to apply?

Yes. The eligibility list explicitly includes non-U.S. entities (foreign organizations).

What outcomes or impact is this research expected to support?

In practical terms, the FOA aims to generate actionable biological insight that can eventually inform prevention and treatment strategies for obesity and metabolic disease in the context of HIV and antiretroviral exposure. It expects projects to connect adipose changes to clinically meaningful metabolic and physiological outcomes within NIDDK priority areas.

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