dc.contributor.author |
Brinkley, Christie |
|
dc.contributor.author |
Busch, Michael P |
|
dc.contributor.author |
Chen, Y |
|
dc.contributor.author |
Demarco, C Todd |
|
dc.contributor.author |
Denny, Thomas Norton |
|
dc.contributor.author |
Gao, Feng |
|
dc.contributor.author |
Hora, Bhavna |
|
dc.contributor.author |
Keating, S |
|
dc.contributor.author |
Keinonen, Sarah |
|
dc.contributor.author |
Sanchez, Ana M |
|
dc.contributor.author |
Schito, M |
|
dc.contributor.author |
Stone, M |
|
dc.contributor.author |
Tobler, L |
|
dc.date.accessioned |
2017-06-01T20:11:05Z |
|
dc.date.available |
2017-06-01T20:11:05Z |
|
dc.date.issued |
2014-01-01 |
|
dc.identifier.issn |
0022-1759 |
|
dc.identifier.uri |
https://hdl.handle.net/10161/14716 |
|
dc.description.abstract |
The significant diversity among HIV-1 variants poses serious challenges for vaccine
development and for developing sensitive assays for screening, surveillance, diagnosis,
and clinical management. Recognizing a need to develop a panel of HIV representing
the current genetic and geographic diversity NIH/NIAID contracted the External Quality
Assurance Program Oversight Laboratory (EQAPOL) to isolate, characterize and establish
panels of HIV-1 strains representing global diverse subtypes and circulating recombinant
forms (CRFs), and to make them available to the research community. HIV-positive plasma
specimens and previously established isolates were collected through a variety of
collaborations with a preference for samples from acutely/recently infected persons.
Source specimens were cultured to high-titer/high-volume using well-characterized
cryopreserved PBMCs from National y donors. Panel samples were stored as neat culture
supernatant or diluted into defibrinated plasma. Characterization for the final expanded
virus stocks included viral load, p24 antigen, infectivity (TCID), sterility, coreceptor
usage, and near full-length genome sequencing. Viruses are made available to approved,
interested laboratories using an online ordering application. The current EQAPOL Viral
Diversity panel includes 100 viral specimens representing 6 subtypes (A, B, C, D,
F, and G), 2 sub-subtypes (F1 and F2), 7 CRFs (01, 02, 04, 14, 22, 24, and 47), 19
URFs and 3 group O viruses from 22 countries. The EQAPOL Viral Diversity panel is
an invaluable collection of well-characterized reagents that are available to the
scientific community, including researchers, epidemiologists, and commercial manufacturers
of diagnostics and pharmaceuticals to support HIV research, as well as diagnostic
and vaccine development. © 2014 Elsevier B.V.
|
|
dc.relation.ispartof |
Journal of Immunological Methods |
|
dc.relation.isversionof |
10.1016/j.jim.2014.01.004 |
|
dc.title |
Development of a contemporary globally diverse HIV viral panel by the EQAPOL program |
|
dc.type |
Journal article |
|
pubs.begin-page |
117 |
|
pubs.end-page |
130 |
|
pubs.organisational-group |
Clinical Science Departments |
|
pubs.organisational-group |
Duke |
|
pubs.organisational-group |
Duke Human Vaccine Institute |
|
pubs.organisational-group |
Institutes and Centers |
|
pubs.organisational-group |
Medicine |
|
pubs.organisational-group |
Medicine, Duke Human Vaccine Institute |
|
pubs.organisational-group |
Medicine, Infectious Diseases |
|
pubs.organisational-group |
School of Medicine |
|
pubs.publication-status |
Published |
|
pubs.volume |
409 |
|
dc.identifier.eissn |
1872-7905 |
|