T cell studies in a peptide-induced model of systemic lupus erythematosus

M Khalil, K Inaba, R Steinman, J Ravetch… - The Journal of …, 2001 - journals.aai.org
M Khalil, K Inaba, R Steinman, J Ravetch, B Diamond
The Journal of Immunology, 2001journals.aai.org
We have previously reported that immunization with a peptide mimetope of dsDNA on a
branched polylysine backbone (DWEYSVWLSN-MAP) induces a systemic lupus
erythematosus-like syndrome in the nonautoimmune BALB/c mouse strain. To understand
the mechanism underlying this breakdown in self tolerance, we examined the role of T cells
in the response. Our results show that the anti-foreign and anti-self response induced by
immunization is T cell dependent and is mediated by IE d-restricted CD4+ T cells of the Th1 …
Abstract
We have previously reported that immunization with a peptide mimetope of dsDNA on a branched polylysine backbone (DWEYSVWLSN-MAP) induces a systemic lupus erythematosus-like syndrome in the nonautoimmune BALB/c mouse strain. To understand the mechanism underlying this breakdown in self tolerance, we examined the role of T cells in the response. Our results show that the anti-foreign and anti-self response induced by immunization is T cell dependent and is mediated by IE d-restricted CD4+ T cells of the Th1 subset. In addition, generation of the critical T cell epitope requires processing by APCs and depends on the presence of both DWEYSVWLSN and the MAP backbone. The breakdown in self tolerance does not occur through cross-reactivity between the T cell epitope of DWEYSVWLSN-MAP and epitopes derived from nuclear Ags. In this induced-model of SLE, therefore, autoreactivity results from the activation of T cells specific for foreign Ag and of cross-reactive anti-foreign, anti-self B cells. Despite the fact that tissue injury is mediated by Ab, the critical initiating T cell response is Th1.
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