Opportunity Information: Apply for RFA MH 18 301
The grant opportunity titled "Role of Myeloid Cells in Persistence and Eradication of HIV-1 Reservoirs from the Brain (R21)" (Funding Opportunity Number RFA-MH-18-301) is a National Institutes of Health (NIH) discretionary research grant focused on understanding and ultimately disrupting HIV-1 persistence within the central nervous system (CNS). The core idea behind the announcement is that, even when HIV is well controlled in the blood with antiretroviral therapy, the virus can remain in long-lived cellular reservoirs. This FOA emphasizes myeloid cells as a particularly important and challenging reservoir in the brain, and it encourages projects that clarify how HIV persists in these cells and how that persistence might be targeted to reduce or eliminate the brain reservoir.
This FOA is designed to support both basic science and translational research. On the basic side, applicants are encouraged to investigate the underlying mechanisms that allow HIV-1 to persist in CNS-associated myeloid populations, such as macrophages and microglia, including viral and host factors that promote latency, low-level replication, immune evasion, or survival of infected cells. On the translational side, the announcement is looking for strategies that could feasibly move the field toward interventions, meaning approaches that help identify, target, or clear infected myeloid cells in the brain or otherwise reduce the reservoir. The FOA explicitly notes that studies can be conducted in domestic or international settings, signaling that research involving global cohorts, unique clinical populations, or specialized international collaborations is welcome when scientifically justified.
The "R21" mechanism is an important part of what this opportunity is trying to accomplish. RFA-MH-18-301 uses the NIH Exploratory/Developmental Grant (R21), which is typically meant for early-stage, innovative, or high-risk/high-reward ideas that may not yet have extensive preliminary data. The announcement even highlights that projects lacking preliminary data or projects that make strong use of existing datasets may be especially appropriate for the R21. In contrast, a companion FOA (RFA-MH-18-300) uses the R01 mechanism, which is generally better suited for more mature projects backed by substantial preliminary results. In practical terms, this means the R21 is meant to help researchers test novel hypotheses, pilot emerging methods, or open up new lines of inquiry related to HIV persistence in brain myeloid cells without needing to present the same depth of prior evidence often expected for an R01.
From an administrative standpoint, this is a grant (Funding Instrument Type: Grant) and falls under education and health-related federal activity categories. The CFDA numbers associated with the opportunity are 93.242, 93.279, and 93.853. The FOA was created on May 1, 2017, and lists an original closing date of September 6, 2017. The listed award ceiling is $200,000, which frames the scale of work expected under this R21 call (often meaning a smaller, focused project aimed at generating key proof-of-concept results).
Eligibility is broad and intentionally inclusive. In addition to standard applicants like public and private institutions of higher education, nonprofits, for-profits (other than small businesses), and small businesses, the FOA allows applications from many government entities (state, county, city/township, special districts), independent school districts, and public housing authorities/Indian housing authorities. It also includes federally recognized Native American tribal governments and tribal organizations (including those not federally recognized). The FOA explicitly calls out additional eligible applicant categories such as Historically Black Colleges and Universities (HBCUs), Hispanic-serving institutions, Tribally Controlled Colleges and Universities (TCCUs), Alaska Native and Native Hawaiian Serving Institutions, and Asian American Native American Pacific Islander Serving Institutions (AANAPISIs). It also welcomes faith-based and community-based organizations, eligible federal agencies, regional organizations, U.S. territories or possessions, and non-U.S. entities (foreign organizations). Taken together, the eligibility language signals a strong interest in encouraging diverse institutional participation and enabling research that may require specialized community ties, clinical access, or international infrastructure.
Collaboration is encouraged but not mandatory. The FOA notes that multidisciplinary teams and collaborative alliances are welcome, which fits the complexity of studying HIV persistence in the brain, where progress often depends on combining virology, immunology, neuroscience, imaging, neuropathology, clinical research, bioinformatics, and therapeutic development. At the same time, the announcement leaves room for smaller groups with a strong, focused idea to compete, which aligns well with the exploratory nature of an R21.
Overall, this opportunity is aimed at pushing the field toward a clearer, mechanistic understanding of how HIV-1 survives in CNS myeloid cells and toward credible strategies for targeting that reservoir. It is positioned as a catalyst for innovative, potentially transformative projects that can generate the kinds of insights and feasibility data needed to support larger future studies, including subsequent R01-level efforts focused on HIV reservoir eradication in the brain.Apply for RFA MH 18 301
- The National Institutes of Health in the education, health sector is offering a public funding opportunity titled "Role of Myeloid Cells in Persistence and Eradication of HIV-1 Reservoirs from the Brain (R21)" and is now available to receive applicants.
- Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 93.242, 93.279, 93.853.
- This funding opportunity was created on 2017-05-01.
- Applicants must submit their applications by 2017-09-06. (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 $200,000.00 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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FAQs: Role of Myeloid Cells in Persistence and Eradication of HIV-1 Reservoirs from the Brain (R21)
What is the official title of this grant opportunity?
The opportunity is titled "Role of Myeloid Cells in Persistence and Eradication of HIV-1 Reservoirs from the Brain (R21)."
What is the Funding Opportunity Number (FOA number)?
The Funding Opportunity Number is RFA-MH-18-301.
Which agency is offering this opportunity?
This is a National Institutes of Health (NIH) discretionary research grant opportunity.
What is the main scientific focus of this FOA?
The FOA focuses on understanding HIV-1 persistence in the central nervous system (CNS), particularly within long-lived cellular reservoirs in the brain, and on generating knowledge and approaches that could help disrupt, reduce, or eliminate those reservoirs.
Why does this FOA emphasize myeloid cells in the brain?
The announcement highlights CNS-associated myeloid cells as a particularly important and challenging HIV reservoir. Even when HIV is well controlled in blood using antiretroviral therapy, the virus can persist in long-lived reservoirs, and myeloid cells in the brain are emphasized as a key area where persistence may occur.
Which CNS myeloid cell types are specifically mentioned?
The FOA specifically mentions macrophages and microglia as CNS-associated myeloid populations of interest.
What kinds of research does the FOA support: basic, translational, or both?
The FOA is designed to support both basic science and translational research related to HIV-1 persistence in CNS myeloid cells.
What basic science topics does the FOA encourage?
On the basic side, the FOA encourages studies of mechanisms enabling HIV-1 persistence in CNS-associated myeloid populations, including viral and host factors that may promote latency, low-level replication, immune evasion, or survival of infected cells.
What translational topics does the FOA encourage?
On the translational side, the FOA encourages strategies that could move toward interventions, including approaches to identify, target, or clear infected myeloid cells in the brain, or otherwise reduce the CNS reservoir.
Can studies use existing datasets or do they need new data collection?
The FOA notes that projects making strong use of existing datasets may be especially appropriate for this mechanism.
Is preliminary data required for an R21 under this FOA?
The FOA indicates that projects lacking preliminary data may be especially appropriate for the R21 exploratory/developmental mechanism.
What grant mechanism is used for this opportunity?
This opportunity uses the NIH Exploratory/Developmental Grant mechanism (R21).
What is the purpose of the R21 mechanism in the context of this FOA?
Within this FOA, the R21 is positioned to support early-stage, innovative, or high-risk/high-reward ideas that may not yet have extensive preliminary evidence, including novel hypotheses, pilot studies, emerging methods, or new lines of inquiry focused on HIV persistence in brain myeloid cells.
Is there a related FOA for more mature projects?
Yes. The FOA notes a companion opportunity (RFA-MH-18-300) that uses the R01 mechanism, which is generally more appropriate for mature projects supported by substantial preliminary results.
What is the funding instrument type?
The funding instrument type is a grant.
What is the award ceiling listed for this FOA?
The listed award ceiling is $200,000.
What is the expected scale of work given the award ceiling and R21 mechanism?
Based on the R21 mechanism and the $200,000 award ceiling, the FOA frames a smaller, focused project intended to generate key proof-of-concept results or feasibility data rather than support a large, multi-year program of work.
When was this FOA created?
The FOA was created on May 1, 2017.
What is the original closing date listed for this opportunity?
The original closing date listed is September 6, 2017.
Where can the research be conducted (domestic vs. international)?
The FOA explicitly notes that studies may be conducted in domestic or international settings, including scientifically justified work involving global cohorts, unique clinical populations, or specialized international collaborations.
Who is eligible to apply?
Eligibility is broad. Eligible applicants include public and private institutions of higher education, nonprofits, for-profits (other than small businesses), small businesses, and many government entities (state, county, city/township, special districts), as well as independent school districts and public housing authorities/Indian housing authorities.
Are tribal governments and tribal organizations eligible?
Yes. The FOA includes federally recognized Native American tribal governments and tribal organizations, including tribal organizations that are not federally recognized.
Are minority-serving institutions (MSIs) specifically encouraged or included in eligibility?
Yes. The FOA explicitly lists multiple MSI categories as eligible, including Historically Black Colleges and Universities (HBCUs), Hispanic-serving institutions, Tribally Controlled Colleges and Universities (TCCUs), Alaska Native and Native Hawaiian Serving Institutions, and Asian American Native American Pacific Islander Serving Institutions (AANAPISIs).
Are faith-based or community-based organizations eligible?
Yes. The FOA states that faith-based and community-based organizations are included among eligible applicants.
Are U.S. territories or possessions eligible?
Yes. The FOA includes U.S. territories or possessions among eligible applicants.
Are non-U.S. (foreign) organizations eligible to apply?
Yes. The FOA includes non-U.S. entities (foreign organizations) as eligible applicants.
Does the FOA allow eligible federal agencies to apply?
Yes. The FOA includes eligible federal agencies in its eligibility language.
Is collaboration required?
No. Collaboration is encouraged but not required. The FOA welcomes multidisciplinary teams and collaborative alliances while still allowing smaller groups with strong, focused ideas to compete.
What kinds of expertise or disciplines fit the FOA?
The FOA notes that multidisciplinary approaches are welcome, aligning with the complexity of studying HIV persistence in the brain. The announcement references the need to combine areas such as virology, immunology, neuroscience, imaging, neuropathology, clinical research, bioinformatics, and therapeutic development.
What federal activity categories are associated with this opportunity?
The FOA is described as falling under education and health-related federal activity categories.
What CFDA numbers are associated with this FOA?
The CFDA numbers listed are 93.242, 93.279, and 93.853.
What is the overall goal or intended impact of this FOA?
The FOA aims to push the field toward a clearer mechanistic understanding of how HIV-1 survives in CNS myeloid cells and toward credible strategies for targeting the CNS reservoir, serving as a catalyst for innovative projects that can generate insights and feasibility data for larger future studies (including later R01-level efforts).
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