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Updated: Jun 5, 2026

Engineering Antiviral Agents via Surface Plasmon Resonance
Published on: June 14, 2022
Mannose-binding lectin in HIV infection
Sarah Eisen1, Agnieszka Dzwonek, Nigel J Klein
1Department of Infectious Diseases & Microbiology, Institute of Child Health, University College London, 30 Guilford Street, London, WC1N 1EH, UK, Tel.: +44 207 905 2215; ; s.eisen@ich.ucl.ac.uk.
Abstract:
Infection with HIV represents a significant global health problem, with high infection rates and high mortality worldwide. Treatment with antiretroviral therapy is inaccessible to many patients and efficacy is limited by development of resistance and side effects. The interactions of HIV with the human immune system, both innate and humoral, are complex and complicated by the profound ability of the virus to disable the host immune response. Mannose-binding lectin, a component of the innate immune system, has been demonstrated to play a role in host-virus interactions. This protein may have a key role in determining host susceptibility to infection, pathogenesis and progression of disease, and may contribute to the extensive variability of host response to infection. Further understanding and manipulation of the mannose-binding lectin response may represent a target for immunomodulation in HIV infection, which may, in conjunction with highly active antiretroviral therapy, allow development of a novel therapeutic approach to HIV infection.
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