Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2022 Apr;15(4):542-550.
doi: 10.1038/s41385-022-00492-0. Epub 2022 Feb 16.

HIV transmitting mononuclear phagocytes; integrating the old and new

Affiliations
Review

HIV transmitting mononuclear phagocytes; integrating the old and new

Erica E Vine et al. Mucosal Immunol. 2022 Apr.

Abstract

In tissue, mononuclear phagocytes (MNP) are comprised of Langerhans cells, dendritic cells, macrophages and monocyte-derived cells. They are the first immune cells to encounter HIV during transmission and transmit the virus to CD4 T cells as a consequence of their antigen presenting cell function. To understand the role these cells play in transmission, their phenotypic and functional characterisation is important. With advancements in high parameter single cell technologies, new MNPs subsets are continuously being discovered and their definition and classification is in a state of flux. This has important implications for our knowledge of HIV transmission, which requires a deeper understanding to design effective vaccines and better blocking strategies. Here we review the historical research of the role MNPs play in HIV transmission up to the present day and revaluate these studies in the context of our most recent understandings of the MNP system.

PubMed Disclaimer

Conflict of interest statement

The authors declare no competing interests.

Figures

Fig. 1
Fig. 1. Current mononuclear phagocyte subsets represented in existing HIV literature.
A selection of existing literature describing HIV interactions with transmission site mononuclear phagocytes were selected for re-examination. Based on the phenotypic data that was presented (left column lists the publications that were assessed, the tissue studied, and the defining phenotypic characteristics presented by the authors), key HIV transmitting mononuclear phagocytes from each study were categorised into the current mononuclear subsets (the columns on the right). This does not consider the proportional contribution that each subset represents, only whether each described mononuclear phagocyte matches the phenotypic profile of the current subset.

References

    1. Andrade, V. M. & Stevenson, M. Host and Viral Factors Influencing Interplay between the Macrophage and HIV-1. J. Neuroimmune. Pharm. 1–11 (2018). 10.1007/s11481-018-9795-4 - PMC - PubMed
    1. King HL, et al. Pre-Exposure Prophylaxis Accessibility Research and Evaluation (PrEPARE Study) Aids Behav. 2014;18:1722–1725. doi: 10.1007/s10461-014-0845-5. - DOI - PMC - PubMed
    1. Schueler, K. et al. Pre-exposure Prophylaxis (PrEP) Awareness and Use Within High HIV Transmission Networks. Aids Behav. 1–11 (2019). 10.1007/s10461-019-02411-0 - PMC - PubMed
    1. Hladik F, Doncel GF. Preventing mucosal HIV transmission with topical microbicides: challenges and opportunities. Antivir. Res. 2010;88:S3–S9. doi: 10.1016/j.antiviral.2010.09.011. - DOI - PMC - PubMed
    1. Nunes R, Sarmento B, Neves Jdas. Formulation and delivery of anti-HIV rectal microbicides: advances and challenges. J. Control Release. 2014;194:278–294. doi: 10.1016/j.jconrel.2014.09.013. - DOI - PubMed