Granulocyte-macrophage Colony Stimulating Factor (GM-CSF) as an Immune-based Therapy in HIV Infection

The HIV/AIDS epidemic continues to spread despite more than 20 years of significant research and major advances in its treatment.

The introduction of HAART in recent years has significantly improved disease treatment with a dramatic impact in HIV/AIDS associated morbidity and mortality in countries which have access to this therapy.

Despite these advances, such therapies are imperfect and other therapeutic modalities, including immune-based therapies, are being actively sought.

Potential benefits of immune-based therapies include: 1) the improvement of HIV-specific immunity to enhance control of viral replication, 2) the improvement of other aspects of host immunity in order to prevent or delay the development of opportunistic infections and 3) the potential to purge virus from cellular reservoirs which are sustained despite the effects of potent antiretroviral therapy.

Granulocyte-macrophage colony-stimulating factor (GM-CSF) has been studied as one of these immune-based therapies.

Several randomized, controlled trials have demonstrated benefits of using GM-CSF as an adjunct to conventional anti-retroviral therapy, although such benefits have not been universally observed.

Individual studies have shown that GM-CSF increases CD4+ T cell counts and may be associated with decreased plasma HIV RNA levels.

There is limited evidence that GM-CSF may help prevent the emergence of antiretroviral drug resistant virus and that it may decrease the risk of infection in advanced HIV disease.

The authors conclude, “Despite its high costs and the need to be administered subcutaneously, encouraging results continue to emerge from further studies, suggesting that GM-CSF has the potential to become an effective agent in the treatment of HIV infection.”

06/08/05

Reference
P A Brown and J B Angel. Granulocyte-macrophage colony stimulating factor as an immune-based therapy in HIV infection. Journal of Immune Based Therapies and Vaccines 18;3(1): May 3, 2005 [Epub ahead of print]

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