Innate immune defenses in HIV-1 infection: prospects for a novel immune therapy

ABSTRACT: HIV-1 infection leads to a severe decrease of CD4+ T lymphocytes, dysregulation of several leukocyte subpopulations and generalized immune activation, with the subsequent development of opportunistic infections and malignancies. Administration of highly active antiretroviral therapy (HAART...

Full description

Autores:
Montoya Guarín, Carlos Julio
Rugeles López, María Teresa
Landay, Alan L
Tipo de recurso:
Article of investigation
Fecha de publicación:
2006
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/37251
Acceso en línea:
https://hdl.handle.net/10495/37251
Palabra clave:
Fármacos Anti-VIH - uso terapéutico
Anti-HIV Agents - therapeutic use
Infecciones por VIH - tratamiento farmacológico
HIV Infections - drug therapy
Infecciones por VIH - inmunología
HIV Infections - immunology
VIH-1
HIV-1
Inmunidad Innata
Immunity, Innate
Receptores Toll-Like
Toll-Like Receptors
Reconstitución Inmune
Immune Reconstitution
Terapia Antirretroviral Altamente Activa
Antiretroviral Therapy, Highly Active
Rights
openAccess
License
http://creativecommons.org/licenses/by-nc-nd/2.5/co/
Description
Summary:ABSTRACT: HIV-1 infection leads to a severe decrease of CD4+ T lymphocytes, dysregulation of several leukocyte subpopulations and generalized immune activation, with the subsequent development of opportunistic infections and malignancies. Administration of highly active antiretroviral therapy (HAART) has been successful in reducing HIV-1 plasma viremia; however, the ability of HAART to restore immunocompetence appears incomplete, particularly in patients with chronic and advanced disease. Several components of the innate immune system have direct anti-HIV-1 effects, and studies to analyze the benefits of enhancing the function of the innate response during HIV-1 infection are increasing. Development of any complementary therapeutic approaches to HIV-1 infection, particularly those able to compensate for the limitations of HAART, and enhance the anti-HIV-1 innate immune activity would be of interest. The stimulation of innate immune responses using Toll-like receptor agonists, such as monophosphoryl lipid A and oligodeoxynucleotides with CpG motifs, are currently being investigated and their benefit in HIV-1-infected patients are under evaluation.