THE USE OF MAMMARY-TUMOR VIRUS (MTV)-NEGATIVE AND SINGLE-MTV MICE TO EVALUATE THE EFFECTS OF ENDOGENOUS VIRAL SUPERANTIGENS ON THE T-CELL REPERTOIRE

Citation
Mt. Scherer et al., THE USE OF MAMMARY-TUMOR VIRUS (MTV)-NEGATIVE AND SINGLE-MTV MICE TO EVALUATE THE EFFECTS OF ENDOGENOUS VIRAL SUPERANTIGENS ON THE T-CELL REPERTOIRE, The Journal of experimental medicine, 182(5), 1995, pp. 1493-1504
Citations number
59
Categorie Soggetti
Immunology,"Medicine, Research & Experimental
ISSN journal
00221007
Volume
182
Issue
5
Year of publication
1995
Pages
1493 - 1504
Database
ISI
SICI code
0022-1007(1995)182:5<1493:TUOMV(>2.0.ZU;2-I
Abstract
Most laboratory strains of mice have between two and eight endogenous superantigens. These viral superantigens (vSAGs) are coded by genes in the 3'long terminal repeats of endogenous mammary tumor viruses (Mtv' s). A line of Mtv-negative mice and several lines of mice containing s ingle Mtv's were created by inbreeding the F-2 progeny of CBA/CaJ and C58/J mice, which have no Mtv integrants in common. This allowed the T cell repertoire of H-2(k) mice, unaffected by Mtv superantigens, as w ell as the effects of vSAGs upon that repertoire, to be studied. Altho ugh each individual mouse had a different mix of C58/J and CBA/CaJ bac kground genes, the T cell repertoires of different Mtv-negative mice w ere very similar and were reproducible. Since the background genes did not affect the VP repertoire, there are no superantigens, other than those encoded by Mtv's, that differ between CBA/CaJ and C58/J. CD4 and CD8 T cells had quite different repertoires in the Mtv-negative mice because of the effects of class I and class II major histocompatibilit y complex molecules on positive and negative selection. vSAG3 was foun d to delete V beta 5 T cells, while vSAG8 deleted V beta 7 T cells, an d vSAG9 deleted V beta 13 T cells in addition to their previously repo rted specificities. vSAG17 deletes a small proportion of CD4(+) T cell s bearing V beta 11 and -12. VSAG14 and -30 have little effect on the T cell repertoire and are not expressed in thymocytes and splenocytes. An endogenous superantigen that has a low avidity for a particular VP may positively select thymocytes, leading to an increased frequency o f peripheral T cells bearing the relevant V beta s. We found evidence that vSAG11 may positively select T cells bearing V beta 8.2. Our data , which analyzed the effects of seven endogenous Mtv's, showed little evidence of positive selection by any other vSAGs on T cells bearing a ny VB tested, despite published reports to the contrary.