OMRF Awarded $6.4 Million for Lupus Study, Seeks Study Volunteers

Abby Overacre-Delgoffe Earned an Award from the National Institute of Allergy and Infectious Diseases

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University of Pittsburgh School of Medicine
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Abby Overacre-Delgoffe Earned an Award from the National Institute of Allergy and Infectious Diseases
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Clinical Study Examining Biological, Molecular Signals of Vitiligo Underway at UMass Chan Medical School

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UMass Chan Medical School
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Clinical Study Examining Biological, Molecular Signals of Vitiligo Underway at UMass Chan Medical School
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Severe COVID-19 May Lead to Long-Term Innate Immune System Changes

Severe COVID-19 may cause long-lasting alterations to the innate immune system, the first line of defense against pathogens, according to a small study funded by the National Institute of Allergy and Infectious Diseases, part of the National Institutes of Health. These changes may help explain why the disease can damage so many different organs and why some people with long COVID have high levels of inflammation throughout the body. The findings were published online today in the journal Cell

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Trethera Receives Grant from National Institute of Allergy and Infectious Diseases for the Advancement of TRE-515 in Lupus

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Trethera Corporation
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Trethera Receives Grant from National Institute of Allergy and Infectious Diseases for the Advancement of TRE-515 in Lupus
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Alternative Cellular "Fuels" Boost Immunity

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Van Andel Institute
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Alternative Cellular "Fuels" Boost Immunity
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This Disease Can Be Caused by a Food Allergy and Prevent Children from Eating. A New Study May Show How to Treat It

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Tulane University
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This Disease Can Be Caused by a Food Allergy and Prevent Children from Eating
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Resources to Advance Pediatrics and HIV Prevention Science (RAPPS)

NIAID maintains contracts to support the development of emerging HIV therapeutics, vaccines, and non-vaccine biomedical prevention (nBP) candidates. As promising adult and pediatric formulations emerge for the treatment and prevention of HIV and co-infections, there is a critical need to move these candidates rapidly and efficiently into clinical testing.

Icahn School of Medicine at Mount Sinai Researchers Awarded $15.1 Million Grant to Explore Immune Rejection of Transplanted Organs

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Icahn School of Medicine at Mount Sinai
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Icahn School of Medicine at Mount Sinai Researchers Awarded $15.1 Million Grant to Explore Immune Rejection of Transplanted Organs
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Propose Research on Mucosal Immunity Against Enteric Eukaryotic Pathogens

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There are no vaccines or other immune-mediated interventions available for treatment or prevention of diseases caused by parasites like Cryptosporidium spp. (e.g., Cryptosporidium parvum and Cryptosporidium hominis), Giardia duodenalis (i.e., Giardia lamblia)and Entamoeba histolytica. Through our Notice of Special Interest (NOSI): Understanding Mucosal Immunity Against Enteric Eukaryotic Pathogens to Advance Discovery of New Interventions, we invite studies to better understand host-pathogen interactions and pathogen-specific immunity at mucosal sites, including infection-induced mucosal immunity at the site of infection, host target identification, antigen or immunogen discovery, and design and testing of vaccines, monoclonal antibodies (mAbs), or host-directed therapies.

As a baseline, you should aim to build on recent breakthroughs in biology of mucosal systems, biology and immunology of mucosal infection, and microbiome research. Leverage emerging technologies such as transfection and molecular genetics, in vitro culture and natural mouse models, imaging or organoid culture, novel vaccinology platforms, mAb or mAb-related approaches, and other host-directed therapy modalities.

Address public health issues associated with the aforementioned group of human pathogens: Cryptosporidium spp., Giardia duodenalis, and Entamoeba histolytica.

Specific research topics could include:

  • Parasite biology and host-parasite interaction at mucosal sites.
  • Impact of mucosal biology, immunology, nervous system, and microbiome on pathogen pathogenesis and clearance.
  • Pathogen-specific immunity, including correlates of protection.
  • Establishing biological assays for functional evaluation.
  • Developing models that mimic pathophysiology of human disease, e.g., organoids, animals (including nonhuman primates).
  • Host target discovery, immunogen design, mAb identification.
  • Vaccines, mAb product candidates or mAb-related interventions, or host-directed therapies, especially those using novel platforms.

To apply for this NOSI, submit an application through either the parent R01 or R21 notice of funding opportunity (NOFO):

You must write “NOT-AI-23-045” in the Agency Routing Identifier field (box 4B) of the SF 424 R&R form.

Follow the budget and project period constraints listed in the NOFO through which you apply. Refer to NIH’s Standard Due Dates for application deadlines.

If you have any questions, contact one of NIAID’s scientific/research contacts for the initiative: Dr. Annie Mo at moa@niaid.nih.gov or 240-627-3320; Dr. John Pesce at john.pesce@nih.gov or 240-627-3343; or Dr. Glen McGugan at gmcgugan@niaid.nih.gov or 240-627-3314.

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