Abstract
Experimental evidence presented in this paper suggests that the T cell hyperreactivity of NZB mice against H-2 identical target cells is a true primary response and not the consequence of an in vivo T cell autoimmune priming event. Based on additional data, we believe an elevated potential of T cell help to be present in NZB mice, which facilitates the observed hyperreactivity F1 hybrids of NZB and normal strains of mice inherited the capacity to hyperreact against H-2 identical cells in an H-2-unrestricted fashion. Because the hybrids tested possess both Qa-1 alleles--Qa-1b and Qa-1a--our experiments either indicate the existence of heterogeneity within the Qa-1b system or of an H-2-unrestricted response against additional target antigens. The T cell hyperreactivity might prove to be a valuable tool in further investigations of the pathomechanism of autoimmune disease.
MeSH Terms
Animals
Autoantibodies/immunology
Cell Line
Cytotoxicity, Immunologic
H-2 Antigens/genetics,immunology
Hybridization, Genetic
Immunization
Leukemia, Experimental/immunology
Mice
Mice, Inbred NZB/immunology
T-Lymphocytes/immunology
Chemicals
Autoantibodies
H-2 Antigens
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Stockinger B
Botzenhardt U
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