# IMPACT OF RBC-DERIVED DAMPS ON INNATE IMMUNITY IN PEDIATRIC SEPSIS (RBC-DAMPS)

> **NIH NIH K08** · WASHINGTON UNIVERSITY · 2020 · $178,169

## Abstract

PROJECT SUMMARY
This proposal comprises a 4-year plan to prepare Kenneth E. Remy, MD, MHSc. for independence as a
physician-scientist studying the influence of dysregulated plasma heme metabolism upon alterations to host
immunity and to develop mechanistic therapies for this problem. Dr. Remy’s previous work at the National
Institutes of Health and currently at Washington University serve as the basis for this proposal. Washington
University School of Medicine is an exemplary location for Dr. Remy to develop his research platform in
hematology-immunology, as there is a longstanding history of NIH funded research and breadth of resources
available. Additionally, there is significant crosstalk among departments (Dr. Remy’s mentors across two different
departments) and with other institutions including the NIH, Harvard University, and Columbia University (Dr.
Remy’s proposed advisory panel).
Dr. Remy’s immediate goal is to fulfill the aims outlined in this proposal. Sepsis is an invasive infectious disease
associated with dysregulated systemic inflammation and more than 4 million deaths worldwide per annum.
Specific targeted therapies are lacking. Many of these patients (~50%) receive a red blood cell (RBC) transfusion
as supportive therapy. Recent evidence indicates that RBC transfusions may further disrupt a patient’s immune
system and lead to worse outcomes. This disruption may be causally linked to release of free heme from the
RBC transfusion, by altering evolution of host immune phenotype in response to infection. This project will focus
on pediatric sepsis with the following three specific aims:
 Aim 1: Determine the effect of RBC transfusion during sepsis on heme processing in plasma.
 Aim 2: Characterize the effect of plasma heme on monocyte immune phenotype.
 Aim 3: Elucidate the effect of plasma heme on toll-like receptor 4 (TLR4) - and HO-1-based
 monocyte signaling.
The knowledge gained from successfully achieving these aims will help define the impacts and clinical
consequences of RBC transfusion on plasma heme metabolism and immune function in sepsis and, more
generally, in other critical illnesses. This knowledge is crucial so that Dr. Remy’s laboratory can translate these
to development of mechanistic therapies that may improve sepsis outcomes.

## Key facts

- **NIH application ID:** 9978894
- **Project number:** 5K08GM129763-03
- **Recipient organization:** WASHINGTON UNIVERSITY
- **Principal Investigator:** Kenneth Eugene Remy
- **Activity code:** K08 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2020
- **Award amount:** $178,169
- **Award type:** 5
- **Project period:** 2018-08-01 → 2022-07-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/9978894

## Citation

> US National Institutes of Health, RePORTER application 9978894, IMPACT OF RBC-DERIVED DAMPS ON INNATE IMMUNITY IN PEDIATRIC SEPSIS (RBC-DAMPS) (5K08GM129763-03). Retrieved via AI Analytics 2026-05-24 from https://api.ai-analytics.org/grant/nih/9978894. Licensed CC0.

---

*[NIH grants dataset](/datasets/nih-grants) · CC0 1.0*