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The emerging role of CD40 ligand in HIV infection.
Kornbluth, R S.
Afiliación
  • Kornbluth RS; Department of Medicine, University of California San Diego and the VA San Diego Healthcare System, La Jolla 92093, USA.
J Leukoc Biol ; 68(3): 373-82, 2000 Sep.
Article en En | MEDLINE | ID: mdl-10985254
CD40 ligand (also called CD40L, CD154, or TNFSF5) is a membrane protein expressed mainly by activated CD4+ T cells, which interacts with its receptor, CD40, on a variety of cells. The crucial importance of the CD40L-CD40 system for many immune responses has been extensively described. This review focuses on the multiple roles that this system may play in HIV infection. In early HIV infection, CD40L expression contributes to the immunological control of viral replication by inducing HIV-suppressive chemokines and supporting the production of anti-HIV antibodies and cytotoxic T cells. However, by activating antigen-presenting cells, such as dendritic cells and macrophages, CD40L can also lead to increased CD4+ T cell activation, which promotes the replication of HIV in these lymphocytes. Later, with the development of AIDS, CD40L-expressing CD4+ T cells become selectively depleted, perhaps as a result of a gp120-induced signal through CD4 that down-regulates CD40L expression. This acquired CD40L deficiency may explain the similarity between the types of opportunistic infections that occur in AIDS and in congenital CD40L deficiency. Vaccines or other strategies that promote the growth of CD4+ T cells capable of expressing CD40L may help to sustain host immunity against HIV and prevent AIDS-defining opportunistic infections.
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Glicoproteínas de Membrana / Infecciones por VIH / VIH Límite: Animals / Humans Idioma: En Revista: J Leukoc Biol Año: 2000 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Glicoproteínas de Membrana / Infecciones por VIH / VIH Límite: Animals / Humans Idioma: En Revista: J Leukoc Biol Año: 2000 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido