Imperial College London

DrNesrinaImami

Faculty of MedicineDepartment of Infectious Disease

Reader in Immunology
 
 
 
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Contact

 

+44 (0)20 3315 5987n.imami Website

 
 
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Location

 

I.2.8Chelsea and Westminster HospitalChelsea and Westminster Campus

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Summary

 

Publications

Citation

BibTex format

@article{Hardy:2002,
author = {Hardy, GA and Imami, N and Gotch, FM},
journal = {J HIV Ther},
pages = {40--45},
title = {Improving HIV-specific immune responses in HIV-infected patients.},
url = {https://www.ncbi.nlm.nih.gov/pubmed/12553687},
volume = {7},
year = {2002}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - Deficiencies in potentially highly protective HIV-1-specific immune responses have led to interventions with immunotherapeutic strategies such as post-exposure vaccination. The application of exogenous antigen to the HIV-infected individual by therapeutic vaccination might be expected to induce renewed virus-specific effector T-cell and neutralising-antibody responses. However, the nature of HIV-1 immunopathogenicity precludes this approach: high levels of viral turnover, persistent expression and presentation of HIV-1 antigen to the immune system, T-cell hyperactivation and exhaustion and clonal T-cell anergy all successfully counter any effect of exogenous antigen. Even with the use of highly active antiretroviral therapy (HAART), when HIV-1 activity is profoundly restricted, the induction of immune responses remains problematic. Different vaccine strategies are currently being tested, including a whole killed virus preparation (Remune), a yeast virus-like particle (p24 VLP), whole antigen preparations (VaxSyn), canarypox immunogens (ALVAC) and DNA plasmids. Therapeutic vaccine strategies currently in the earliest stages of development include adenovirus vectors and a topical DNA preparation, DermaVir.
AU - Hardy,GA
AU - Imami,N
AU - Gotch,FM
EP - 45
PY - 2002///
SN - 1462-0308
SP - 40
TI - Improving HIV-specific immune responses in HIV-infected patients.
T2 - J HIV Ther
UR - https://www.ncbi.nlm.nih.gov/pubmed/12553687
VL - 7
ER -