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Conditioned immune response to interferon-gamma in humans
D L Longo1, P L Duffey, W C Kopp
1Biological Response Modifiers Program, National Cancer Institute-Frederick Cancer Research and Development Center, Frederick, Maryland, 21702-1201, USA.
Clinical Immunology (Orlando, Fla.)
|March 18, 1999
Summary
Classical conditioning with recombinant human interferon-gamma (rhIFN-gamma) and propylene glycol (PG) demonstrated that PG alone could prolong immune responses. This study shows potential for conditioning immune reactions in humans.
Area of Science:
- Immunology
- Neuroscience
- Behavioral Science
Background:
- Classical conditioning is a learning process where a neutral stimulus elicits a response after being associated with a stimulus that naturally elicits a response.
- Recombinant human interferon-gamma (rhIFN-gamma) is a cytokine known to stimulate immune responses.
- Propylene glycol (PG) is typically an immune-neutral substance.
Purpose of the Study:
- To investigate if classical conditioning can be used to elicit immunologic responses in humans.
- To determine if an immune-neutral stimulus (PG) can elicit an immune response after being paired with rhIFN-gamma.
Main Methods:
- A placebo-controlled, double-blind study was conducted with 31 healthy volunteers.
- Subjects were divided into three groups: rhIFN-gamma with PG, saline with PG, and rhIFN-gamma alone.
- Immune activation was assessed by measuring serum quinolinic acid (QUIN), neopterin, and Fc receptor (CD64) expression on peripheral blood mononuclear cells.
Main Results:
- rhIFN-gamma injections significantly altered immune parameters (QUIN, neopterin, CD64).
- Subjects receiving rhIFN-gamma and PG showed higher QUIN levels compared to rhIFN-gamma alone.
- The decline in neopterin levels was blunted in the rhIFN-gamma and PG group, and CD64 expression decline was also blunted.
Conclusions:
- Pairing rhIFN-gamma with PG allowed PG alone to prolong the cytokine-induced immune response.
- Classical conditioning may be a viable method to modulate immune responses in humans.
- This suggests a potential for using learned associations to influence physiological immune reactions.
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