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Coisogenic All-Plus-One Immunization: A Model for Identifying Missing Proteins in Null-Mutant Conditions. Antibodies to Dystrophin in mdx Mouse After Transplantation of Muscle from Normal Coisogenic Donor

Authors: Harald Höger; Berthold Streubel; T. Voit; Sigrid Shorny; Gabriele Schaden; Reginald E. Bittner;

Coisogenic All-Plus-One Immunization: A Model for Identifying Missing Proteins in Null-Mutant Conditions. Antibodies to Dystrophin in mdx Mouse After Transplantation of Muscle from Normal Coisogenic Donor

Abstract

Specific antibody response against an alien protein is one of the basic immunologic mechanisms in immunecompetent organisms. They can be used as a first step in various approaches leading to the identification of proteins or even an antigen-encoding gene. Accordingly, we wanted to find out whether a null-mutant immunecompetent organism would produce specific antibodies against the missing gene product. We chose the mouse mutant mdx (X-linked muscular dystrophy) which represents a null-mutant condition for the gene product of the Duchenne muscular dystrophy (DMD) gene, dystrophin. When dystrophin-deficient mdx mice received dystrophin-containing muscle grafts from coisogenic normal mice, high titres of antibodies specific for dystrophin were detected in the transplanted animals' sera. Because dystrophin-containing muscle grafts were not rejected but have properly regenerated even in the presence of high titre antibodies against dystrophin, these findings have important bearings on all therapeutical strategies based on dystrophin supplementation. Using the mdx mouse as null-mutant model we showed that there was no immune tolerance for the missing protein but specific antibodies were produced when the organism came in contact with this protein. This simple approach may serve as a shortcut for identifying missing proteins presumably not only in neuromuscular disorders but in a wide range of diseases where null-mutant animal models and corresponding coisogenic inbred strains exist.

Keywords

Male, Blotting, Western, Muscular Dystrophy, Animal, Antibodies, Muscular Dystrophies, Dystrophin, Mice, Inbred C57BL, Mice, Transplantation, Isogeneic, Antibody Specificity, Mutation, Immune Tolerance, Mice, Inbred mdx, Animals, Humans, Chromosome Deletion, Child, Muscle, Skeletal

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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
5
Average
Average
Average