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Endogenous Droops [modify] Minor lymphocyte stimulating (Mls) exotoxins were originally discovered in the thymic stromal cells of mice. These contaminants are encoded by SAg genes that were included into the mouse genome from the mouse mammary tumour infection (MMTV). The existence of these genes in the mouse genome enables the mouse to express the antigen in the thymus as a method of adversely selecting for lymphocytes with a variable Beta region that is prone to stimulation by the viral Droop.
Similar endogenous SAg-dependent choice has yet to be recognized in the human genome, but endogenous SAgs have been discovered and are suspected of playing an important function in viral infection. Infection by the Epstein, Barr virus, for example, is known to cause production of a Droop in infected cells, yet no gene for the contaminant has actually been discovered on the genome of the infection.

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Similar outcomes have been discovered with rabies, cytomegalovirus, and HIV. desmoplastic small round cell tumor pathology outlines [edit] Llewelyn M, Cohen J (March 2002). "Superantigens: microbial agents that corrupt immunity". Lancet Infect Dis. 2 (3 ): 15662. doi:10. 1016/S1473 -3099( 02 )00222-0. PMID 11944185. Li H., Llera A., Malchiodi E.L., Mariuzza R.A. The structural basis of T cell activation by superantigens.
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PDF] Manipulation of Innate and Adaptive Immunity by Staphylococcal Superantigens - Semantic Scholar
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