Project 2: Genomics of allogeneic transplantation. The goal of this project is to identify and characterize the genomic and transcriptional variants that provide long-term, relapse-free survival to AML patients after allogeneic hematopoietic cell transplantation (alloHCT). Relapse after alloHCT remains common and challenging to resolve. Donor T-cell responses to minor histocompatibility antigens (mHAs) presented on the surface of recipient cells are important drivers of the beneficial graft-versus-leukemia (GVL) effect and harmful graft-versus-host disease (GVHD) pathology following major histocompatibility complex (MHC)-matched alloHCT. mHAs are a diverse collection of peptides that are bound by the MHC and are derived from polymorphic proteins that differ between the donor and recipient. In this proposal, we will utilize state-of-the-art genome and transcriptome sequencing to study the role of mHAs in alloHCT as follows:
Specific Aim 1 : We will define human mHAs that provide strong GVL activity, but not GVHD. We will evaluate 60 AML patients who have maintained a morphologic complete remission for at least 24 months after MHC-matched sibling alloHCT. To segregate the ?therapeutic? mHAs providing a GVL response, from the ?pathogenic? targets of GVHD, we will evaluate equal numbers of AML patients who did (n=30) or did not (n=30) develop grade II-IV acute or chronic GVHD after transplantation. All mHA disparities that are expressed within each donor-recipient pair in the graft-versus-host direction (i.e., variant present in the recipient but not donor) will be defined by enhanced whole genome (eWGS) and transcriptome sequencing. Candidate mHAs will be predicted using in silico peptide binding prediction algorithms and validated using immunological assays, mass spectrometry, and correlative studies with recipient samples collected post-alloHCT.
Specific Aim 2 : We will define the genetic and epigenetic changes that contribute to AML relapse after allogeneic ?selection? in mice and humans. Our hypothesis is that relapse after alloHCT is mediated via downregulation or loss of immunogenic mHAs and/or selection of rare cells that lacked expression of the immunogenic mHAs. In humans, we will evaluate patients who have relapsed after undergoing an MHC- matched sibling alloHCT. RNA-seq (bulk and single cell), coupled with eWGS will be performed on primary and post-alloHCT relapse AML sample pairs, as well as the donor?s blood mononuclear cells, to identify mHAs and evaluate the events that make subclones progress after an alloHCT. In mice we will use novel C57Bl/6 (B6)- derived Dnmt3a R878H/FLT3-ITD AML tumors and apply allogeneic immunological pressure using MHC- mismatched mice (BALB/c) or MHC-matched mice that differ from B6 mice at multiple mHAs (C3H.SW and 129Sv/J). We will characterize the allogeneic-resistant AML cells by WGS and RNA-seq to identify mechanisms that contribute to immunologic ?escape?. Taken together, these studies may provide T cell targets (immunogenic mHAs) with which to develop novel immunotherapies for use before, during, or after alloHCT.

Public Health Relevance

Although allogeneic hematopoietic cell transplantation (alloHCT) is the only potentially curative therapy for many patients with Acute Myeloid Leukemia (AML), relapse after alloHCT remains a major cause of treatment failure. Disparities in minor histocompatibility antigens underlie the beneficial grant-versus-leukemia (GVL) effect and life threatening graft-versus-host disease (GVHD) pathology that arises in the HLA-matched alloHCT setting. We will use state-of-the-art genome sequencing techniques and a novel mouse model of AML to identify minor histocompatibility antigens that are associated with strong GVL activity in the absence of GVHD, to better define the events that contribute to relapse after alloHCT.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA101937-17
Application #
10067515
Study Section
Special Emphasis Panel (ZCA1)
Program Officer
Jhappan, Chamelli
Project Start
Project End
Budget Start
2020-12-01
Budget End
2021-11-30
Support Year
17
Fiscal Year
2021
Total Cost
Indirect Cost
Name
Washington University
Department
Type
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
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