In vitro infection of epidermal Langerhans cells with human immunodeficiency virus type 1 (HTLV-IIIB isolate)
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Ex Vivo Infection of Murine Epidermis with Herpes Simplex Virus Type 1
Published on: August 24, 2015
P Delorme1, C Dezutter-Dambuyant, A Ebersold
1INSERM U346, Peau humaine et Immunité, Hôpital Edouard-Herriot, Lyon, France.
Insights
Human epidermal Langerhans cells (LC) can be infected by human immunodeficiency virus type 1 (HIV-1) in vitro. Electron microscopy revealed viral budding from LC membranes, indicating successful HIV-1 replication in these cells.
Area of Science:
- Immunology
- Virology
- Dermatology
Background:
- Human epidermal Langerhans cells (LC) play a crucial role in skin immunity.
- The interaction between Langerhans cells and human immunodeficiency virus type 1 (HIV-1) is not fully understood.
- Investigating HIV-1 permissivity in LC is important for understanding viral transmission and pathogenesis.
Purpose of the Study:
- To investigate the permissivity of human epidermal Langerhans cells (LC) for in vitro infection with human immunodeficiency virus type 1 (HIV-1).
- To observe the early stages of HIV-1 infection and replication within LC.
- To assess the effect of specific treatments on viral production in infected LC.
Main Methods:
- Isolation of human epidermal Langerhans cells (LC) from normal skin via trypsinization.
- Co-culture of isolated LC with HIV-1-carrying promonocytic cells (U937).
- Observation of viral budding and release using electron microscopy.
- Treatment of infected LC with phorbol esters/bacterial lipopolysaccharide or tumor necrosis factor alpha.
Main Results:
- Electron microscopy confirmed retroviral-type budding from the LC membrane as an early sign of HIV-1 infection.
- Various stages of viral budding and release into the extracellular space were visualized.
- Treatment with phorbol esters/bacterial lipopolysaccharide or tumor necrosis factor alpha did not significantly increase viral production.
Conclusions:
- Human epidermal Langerhans cells (LC) are permissive to in vitro infection by human immunodeficiency virus type 1 (HIV-1).
- The study visualized the process of HIV-1 budding from LC membranes.
- Further research is needed to determine if infected LC can transmit the virus and how infection affects their antigen-presenting function.
Abstract:
Human epidermal Langerhans cells (LC) isolated from normal skin were infected in vitro with human immunodeficiency virus type 1 (HIV1). To control the permissivity of LC for HIV1, cells isolated from the epidermal sheet of normal skin by trypsinization were cocultured with HIV1-carrying promonocytic cells (U937) and observed by electron microscopy. An early sign of infection occurring in the coculture was the formation of retroviral type buds from LC membrane. Different steps in the process of viral budding up to virus release into the extracellular space were observed by electron microscopy. Treatment with either coupled phorbol esters/bacterial lipopolysaccharide or a recombinant cytokine (tumour necrosis factor alpha) did not significantly enhance viral production. The ability of in vitro infected LC to transmit virus to other haematopoietic cells and the consequences of such an infection on antigen-presenting function of LC remain to be elucidated.
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