# High-throughput proteomics using submicroliter amounts of plasma for comprehensive assessment of the immune status

> **NIH NIH U24** · BOSTON CHILDREN'S HOSPITAL · 2021 · $434,412

## Abstract

Summary
The SARS-CoV-2 pandemic of 2020 vastly affected normal clinical and research operations. The negative impact
is particularly severe on studies involving older adults given the high risk for severe COVID-19 disease, where
the mean/median age of deceased COVID-19 patients is >80 years of age. Due to these unique circumstances,
the years `20 and `21 will result in `lost years' for many longitudinal studies that involve older adults as it is too
risky for participants to leave the safe environment of their home for e.g. a blood draw.
A loss of two years of sampling is particularly damaging for longitudinal studies involving older adults including
the NIA-funded BIOCARD Study started in 1995 which has prospectively followed >300 cognitively normal
middle-aged participants in an effort to understand the pathogenesis of Alzheimer's disease (AD) and its
relationship with aging. This well characterized cohort undergoes detailed annual neuropsychologic testing and
blood collection with biannual MRI, PET and CSF collection for understanding the molecular basis of AD. The
challenge is to ensure the safety of these subjects without compromising data collection. One possibility is to
use NoviPlex cards for the safe at home collection of blood samples. However, only 2.5ul of plasma can be
collected – with current proteomics methods, this amount of plasma cannot yield a deep quantitative data set.
We hypothesize that integrating at home sample collection strategies using the NoviPlex cards and state-of-the-
art sample-sparing analyses strategies being developed by the Steen Lab (U24AI152179: High-throughput
proteomics using submicroliter amounts of plasma for comprehensive assessment of the immune status) will
allow the safe collection of samples and data from vulnerable patients during the current COVID-19 pandemic.
We propose that our platform will facilitate high quality data acquisition on small plasma volumes collected at
home in a quick and easy manner. Such an integrated sample-sparing collection and analysis strategy will allow
researchers to continue collecting useful plasma samples from participants of the BIOCARD study despite the
ongoing COVID-19 pandemic during this critical phase of BIOCARD where a substantive portion of the
participants are manifesting cognitive symptoms of AD given their advanced age. To test our hypothesis, we will
compare the proteome of venous vs. microcapillary (i.e. NoviPlex card) plasma (Specific Aim 1) and collect
microcapillary plasma remotely from active participants in the longitudinal BIOCARD study (Specific Aim 2).
This proposal for an administrative supplement will add an AD focus on the existing U24 from Dr. Steen, which
currently focuses on sample sparing plasma proteomic assays. The requested supplement will allow us to
establish an innovative approach facilitating remote collection of microcapillary plasma and high-quality data in
2021 from high-risk participants of the unique BIOCARD study. Furthermore, ...

## Key facts

- **NIH application ID:** 10287684
- **Project number:** 3U24AI152179-02S1
- **Recipient organization:** BOSTON CHILDREN'S HOSPITAL
- **Principal Investigator:** Hanno Steen
- **Activity code:** U24 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2021
- **Award amount:** $434,412
- **Award type:** 3
- **Project period:** 2020-04-09 → 2025-03-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10287684

## Citation

> US National Institutes of Health, RePORTER application 10287684, High-throughput proteomics using submicroliter amounts of plasma for comprehensive assessment of the immune status (3U24AI152179-02S1). Retrieved via AI Analytics 2026-05-25 from https://api.ai-analytics.org/grant/nih/10287684. Licensed CC0.

---

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