Table 1

Myeloid lineage cell types and their potential roles and proposed mechanisms in HIV-1 latency

Cell types
Primary Locations
Cellular markers
Potential role in HIV latency and proposed mechanisms
References

Monocytes
Peripheral blood
CD14++
or CD16+CD14+
YES, but possibly mainly in CD16+ cells
• Restricted HIV-1 replication at different steps of viral life-cycle
• Low molecular weight APOBEC3G (CD16+ only)
• Low level or undetectable Cyclin T1
• Impaired phosphorylation of CDK9
[10-12,87-92,94]

Macrophages
Mucosal surface/tissues
CD14-
EMR1+
CD68+
NO
• High level Cyclin T1
• Phosphorylation of CDK9 and active P-TEFb
[14,18,94,97]

Myeloid DCs
Peripheral blood (immature)
Lymph node (mature)
CD11c+
CD123-
BDCA1+
YES
• Low level virus replication
• Lymph node biopsies reveal presence
• Unknown mechanism
[101,107,112]

Plasmacytoid DCs
Peripheral blood (immature)
Lymph node (mature)
CD11c-
CD123+
BDCA2+
BDCA4+
Unlikely
• Inhibiting HIV-1 replication through the secretion of IFNα and an unidentified small molecule
• Unknown mechanism
[49,50,101]

Langerhans cells
Mucosal surface and epidermal tissue
CD1a+
Langerin+
Unlikely
• Langerin inhibits virus transmission and enhances virus take-up and degradation
• May act differently in co-infections
[40,41,113]

EMR1, epidermal growth factor module-containing mucin-like receptor 1 (a G-protein coupled receptor); BDCA, blood DC antigen.

Coleman and Wu Retrovirology 2009 6:51   doi:10.1186/1742-4690-6-51

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