# New Approaches to Pathogenesis and Diagnosis of Heparin-Induced

> **NIH NIH K08** · MAYO CLINIC ROCHESTER · 2021 · $158,760

## Abstract

PROJECT SUMMARY/ABSTRACT
This research is aimed at gaining a better understanding of the pathophysiology of heparin-induced
thrombocytopenia/thrombosis (HIT), a common and sometimes life-threatening complication of heparin
treatment, and developing better tools for early diagnosis and management.
The candidate, Anand Padmanabhan M.D., Ph.D, is a junior faculty member at the BloodCenter of Wisconsin (BCW).
BCW has made a firm commitment to protect the applicant's research time at the 75% level and to provide necessary
space and personnel support. The applicant will be mentored by a highly experienced physician-investigator, Dr. Richard
Aster, MD aided by Dr. Demin Wang, PhD and Dr. Jian Liu, PhD, recognized authorities in immunology and
glycobiology, respectively. An ambitious career development plan is described that includes basic training in
glycobiology, statistics and clinical immunology and will facilitate Dr. Padmanabhan's professional growth into an
independent investigator. The research plan is based on Dr. Padmanabhan's recent finding that heparin-induced, platelet-
activating (“pathogenic”) antibodies bind to platelets pre-treated with platelet factor 4 (PF4) in the absence of heparin,
whereas non-activating (“benign”) antibodies do not. Dr. Padmanabhan hypothesizes that the distinction between the two
types of antibodies is that pathogenic antibodies preferentially recognize subtle structural changes induced in PF4 when it
reacts with chondroitin sulfate (CS) linked to an unidentified core protein that makes up the dominant platelet surface
proteoglycan (PG). He anticipates that a better understanding at biochemical, structural and functional levels of the
process by which PF4 “primes” platelets for pathogenic antibody binding and of the antibodies themselves will lead to
new understanding of HIT pathogenesis and to improved diagnostic tools for early identification of patients at risk for
HIT and its thrombotic complications. In support of this concept, he has developed a novel assay, the PF4-dependent p-
selectin expression assay (PEA), which in preliminary testing was found to be more accurate and less technically
demanding than the gold standard serotonin release assay (SRA). Dr. Padmanabhan will further assess the diagnostic
utility and treatment impact of the PEA in a rigorously-designed prospective study in patients suspected of HIT. Dr.
Padmanabhan is a promising junior physician-investigator in a supportive and scientifically-rich environment proposing a
well defined and challenging project that has important clinical implications. The K08 award will enable him to focus the
majority of his time on this promising research while expanding his scientific capabilities through formal training as
outlined in his application. The program described will provide Dr. Padmanabhan ideal preparation for a career as an
independent investigator in hematology/transfusion medicine.

## Key facts

- **NIH application ID:** 10143277
- **Project number:** 5K08HL133479-05
- **Recipient organization:** MAYO CLINIC ROCHESTER
- **Principal Investigator:** Anand Padmanabhan
- **Activity code:** K08 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2021
- **Award amount:** $158,760
- **Award type:** 5
- **Project period:** 2017-04-01 → 2022-03-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10143277

## Citation

> US National Institutes of Health, RePORTER application 10143277, New Approaches to Pathogenesis and Diagnosis of Heparin-Induced (5K08HL133479-05). Retrieved via AI Analytics 2026-05-23 from https://api.ai-analytics.org/grant/nih/10143277. Licensed CC0.

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