Source:http://linkedlifedata.com/resource/pubmed/id/15992849
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2005-8-5
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pubmed:abstractText |
Two HIV-1 isolates (CM4 and CM9) able to use alternate HIV-1 coreceptors on transfected cell lines were tested for their sensitivity to inhibitors of HIV-1 entry on primary cells. CM4 was able to use CCR5 and Bob/GPR15 efficiently in transfected cells. The R5 isolate grew in Delta32/Delta32 CCR5 PBMC in the absence or presence of AMD3100, a CXCR4-specific inhibitor, indicating that it uses a receptor other than CCR5 or CXCR4 on primary cells. It was insensitive to the CCR5 entry inhibitors RANTES and PRO140, but was partially inhibited by vMIP-1, a chemokine that binds CCR3, CCR8, GPR15 and CXCR6. The coreceptor used by this isolate on primary cells is currently unknown. CM9 used CCR5, CXCR4, Bob/GPR15, CXCR6, CCR3, and CCR8 on transfected cells and was able to replicate in the absence or presence of AMD3100 in Delta32/Delta32 CCR5 PBMC. It was insensitive to eotaxin, vMIP-1 and I309 when tested individually, but was inhibited completely when vMIP-1 or I309 was combined with AMD3100. Both I309 and vMIP-1 bind CCR8, strongly suggesting that this isolate can use CCR8 on primary cells. Collectively, these data suggest that some HIV-1 isolates can use alternate coreceptors on primary cells, which may have implications for strategies that aim to block viral entry.
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pubmed:grant |
http://linkedlifedata.com/resource/pubmed/grant/AI062514,
http://linkedlifedata.com/resource/pubmed/grant/MH 64408,
http://linkedlifedata.com/resource/pubmed/grant/P01 AI52048,
http://linkedlifedata.com/resource/pubmed/grant/R01 AI084133-03,
http://linkedlifedata.com/resource/pubmed/grant/R01 AI41420
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0042-6822
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pubmed:author |
pubmed-author:CilliersTonieT,
pubmed-author:ClaphamPaulP,
pubmed-author:CoetzerMiaM,
pubmed-author:MooreJohn PJP,
pubmed-author:MorrisLynnL,
pubmed-author:PapathanasopoulosMariaM,
pubmed-author:PatienceTrudyT,
pubmed-author:PugachPavelP,
pubmed-author:SullivanW MathewWM,
pubmed-author:TrkolaAlexandraA,
pubmed-author:WilleySamanthaS
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pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
339
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
136-44
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pubmed:dateRevised |
2011-8-1
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pubmed:meshHeading |
pubmed-meshheading:15992849-Adult,
pubmed-meshheading:15992849-Amino Acid Sequence,
pubmed-meshheading:15992849-Cell Line,
pubmed-meshheading:15992849-Female,
pubmed-meshheading:15992849-HIV Envelope Protein gp120,
pubmed-meshheading:15992849-HIV Infections,
pubmed-meshheading:15992849-HIV-1,
pubmed-meshheading:15992849-Humans,
pubmed-meshheading:15992849-Male,
pubmed-meshheading:15992849-Molecular Sequence Data,
pubmed-meshheading:15992849-Receptors, Chemokine,
pubmed-meshheading:15992849-Receptors, HIV,
pubmed-meshheading:15992849-Virus Replication
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pubmed:year |
2005
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pubmed:articleTitle |
Use of alternate coreceptors on primary cells by two HIV-1 isolates.
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pubmed:affiliation |
AIDS Virus Research Unit, National Institute for Communicable Diseases, Private Bag X4, Sandringham 2131, Johannesburg, South Africa.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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