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Published on: September 26, 2013
Microbial parasitism cross-reactive with host antigen: implications concerning loss of "self" tolerance and
Abstract:
The implications of inserting eukaryotic genetic material coding for human "self" antigens into prokaryotic microbe vectors that parasitize humans are discussed against the background of contemporary concepts of immunologic tolerance to "self" constituents and the types of host autoreactive immune responses that might occur. The injurious potential of autoreactive immune responses elicited by infecting microbes which share antigenic constituents with host "self" antigens is carefully weighed. The risk of similar cross-reacting microbial vectors arising as a consequence of ongoing recombinant DNA technology and experimentation and posing public health concerns for humans is examined. On balance, the risk would appear to be extraordinarily low.
Insights
Inserting human self antigen genes into microbes could trigger autoimmune responses. However, the risk of such engineered microbes causing public health issues is exceptionally low.
Area of Science:
- Immunology
- Microbiology
- Genetic Engineering
Background:
- Contemporary understanding of immunologic tolerance to self antigens.
- Potential for autoreactive immune responses to microbial antigens.
- Role of microbial vectors in human parasitism.
Purpose of the Study:
- To discuss implications of inserting eukaryotic DNA into prokaryotic vectors.
- To analyze potential host autoreactive immune responses.
- To assess public health risks associated with recombinant DNA technology.
Main Methods:
- Review of immunologic tolerance concepts.
- Analysis of potential cross-reactivity between microbial and self antigens.
- Examination of risks posed by engineered microbial vectors.
Main Results:
- Eukaryotic genetic material in prokaryotic vectors may elicit autoreactive immune responses.
- Microbes sharing antigenic constituents with host self antigens pose a risk.
- Ongoing recombinant DNA technology could create similar vectors.
Conclusions:
- The overall risk to public health from such engineered microbial vectors is considered extraordinarily low.
- Careful consideration of antigenic similarities is crucial.
- Further research into host-microbe interactions is warranted.
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