HIV-1 Infection Detection Assay for Seroconverted HIV-1 Vaccine Recipients

Description:
Available for licensing and commercial distribution is a serological test specifically designed to distinguish between antibodies generated in HIV vaccine recipients and those generated in a natural HIV infection. The method is useful in HIV vaccine development and clinical studies as it can readily detect early breakthrough infections in seroconverted vaccine recipients, thus providing the information required to determine vaccine efficacy. The test kit includes diagnostic peptide fragments derived from human immunodeficiency virus-1 (HIV-1). The peptide epitopes are primarily derived from the GAG-p6 and gp41 genes. These epitopes are broadly reactive with early sera from HIV infected individuals, but do not illicit protective antibodies, or immunologic cytotoxicity, and thus can readily be excluded from current and future HIV-1 vaccine candidates.
Patent Information:
For Information, Contact:
William Ronnenberg
Alternate TDC - FDA Special Volunteer
NIH Technology Transfer
240-402-4561
wronnenberg@mail.nih.gov
Inventors:
Surender Khurana
Hana Golding
Keywords:
assay
DA4AXX
DA4XXX
DAXXXX
Detectiion
Detection
Diagnosis
DXXXXX
EARLY
HIV
HIV-1
Hyper IgM syndrome
Immunodeficiency 2
Immunodeficiency 4
Immunodeficiency-3
Infection
Novel
Patent Category - Biotechnology
Peptides
Recipients
seroconverted
Severe combined immunodeficiency, x-linked
Vaccine
Wiskott Aldrich syndrome
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