SBIR/STTR Research Award

High Resolution Multiplexed DNA reverse-SSO Typing Assay

Award identifier 006c943190a5a5b8f8820098aef35b99a12cab8e2c5ab1de35200688a254a6e6Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$0

Program and phase

SBIR · Phase I

Award year

2005

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
One Lambda, Inc.
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
Not reported
Topic code
Not reported

Research abstract

DESCRIPTION (provided by applicant): A multiplexed reverse-SSO hybridization assay will be developed to achieve high resolution DNA typing for improved matching of donor and recipient for bone marrow transplantation (BMT). The system has already been applied to low-resolution typing (e.g. for preliminary screening of bone marrow donors), and will be further developed to provide allele-level typing information that is important to improve the clinical outcome of BMT, particularly for the HLA-DRB1 locus (which affects the incidence of Graft vs. Host Disease (GvHD). Over the 3-year project period, HLA-A and -B group-specific typing assays will be added for resolution of serological ambiguities such as Bw4, Bw6, and high resolution typing of HLA-C following National Marrow Donor Program (NMDP) priorities. To complete product line capabilities for HLA typing, generic kits will also be developed for DPB1, DQA1, and DPA1 (DQB1 and DRB3,4,5 were already produced). Additional work will be aimed at rSSO typing of the KIR region genes, since recent evidence has shown a beneficial effect of mismatching for these genes in acute myeloid leukemia (AML) patients, where a Graft vs Leukemia (GvL) effect was noted to reduce the recurrence of leukemia. The application of a high throughput multiplexed assay to this clinical testing offers the advantage of both cost and labor savings, as well as enabling the resolution of many typing ambiguities observed with current methods such as sequence based typing. In particular, the use of proprietary gap-primers and gap-probes allows for fewer rounds of PCR amplification to achieve the desired rSSO typing. In addition, primers for KIR will be designed to allow for multiplex PCR of the various loci. Finally, analytical software will be developed, which will require new algorithms for assignment of KIR typing results, due to the multiple and variable number of alleles expressed for each individual. Following validation testing and regulatory clearance, a complete line of superior HLA and KIR typing products will be available to the NMDP and HLA laboratories.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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