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Murine transfer factor. IV. Studies with genetically regulated immune responses
S J Rozzo1, C F Merryman, C H Kirkpatrick
1Conrad D. Stephenson Laboratory, National Jewish Center for Immunology and Respiratory Medicine, Denver, Colorado 80206.
Cellular Immunology
|August 1, 1988
Summary
Transfer factor administration can convert low-responder mice into high responders, effectively transferring the high responder phenotype. This immune transfer is regulated by Ir genes but not restricted by MHC or Igh loci.
Area of Science:
- Immunology
- Genetics
Background:
- Delayed hypersensitivity is a crucial immune response.
- Genetic factors influence an individual's immune response capabilities.
- Transfer factor is a molecule implicated in immune modulation.
Purpose of the Study:
- To investigate the role of transfer factor in modulating immune responsiveness.
- To determine if transfer factor can transfer a high-responder phenotype to low-responder recipients.
- To explore the genetic regulation and limitations of transfer factor activity.
Main Methods:
- Preparation of transfer factor-containing dialysates from high and low responder mouse strains.
- Assaying dialysates for their ability to transfer delayed hypersensitivity.
- Testing transfer efficacy in both high and low responder murine recipients.
- Analyzing the influence of MHC and Igh loci disparities on transfer.
Main Results:
- Dialysates from high responders successfully transferred delayed hypersensitivity to both high and low responder recipients.
- Transfer factor activity was largely absent in dialysates from low responders.
- Immune transfer was effective irrespective of MHC or Igh locus differences.
- Low responder recipients gained the high responder phenotype after transfer factor administration.
Conclusions:
- Transfer factor administration effectively transfers the high responder phenotype to low responder recipients.
- The production of transfer factor appears to be regulated by Ir genes.
- The immunologic activities mediated by transfer factor are not restricted by MHC or Igh loci.