Fine specificity of a proliferating T-cell clone activated by a conformational determinant of the I-E molecule
Immunogenetics, ISSN: 0093-7711, Vol: 15, Issue: 4, Page: 399-412
1982
- 12Citations
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations12
- Citation Indexes12
- CrossRef12
- 12
Article Description
We have examined the fine specificity of a stable Thy-1.2, Lyt-1.2, Lyt-2, and I-A anti-I-E proliferating T-cell clone isolated from an A.TH anti-A.TL secondary mixed lymphocyte culture. Spleen cells from various I-A, E strains induced either a strong (A.TL, OH, and CBA) or a weak (AKR and B10.BR) proliferative response, although such cells expressed at their surface similar amounts of I-E antigens. Analysis of H-2 recombinant strains indicated that this clone recognized a conformational determinant carried by the EEdimer, but not on the Ea chain per se. Among the Fl hybrid strains in which the combinatorial EEproduct was detected by cellular binding with monoclonal E-specific antibodies (mAb), some [(BIO.S(8R) × BlO.HTT) but not others (for example, B10.A(4R) × B10.A(5R)] were stimulatory. Seventeen anti-E mAb, regardless of the three spatially separated domains that they defined by antibody binding competition, completely inhibited the restimulation of this clone, whereas 15 other anti-A mAb failed to do so. This clone was not reactivated by stimulating cells from strains with the H-2 haplotypes p, j, v, b, r, and s but it proliferated strongly against cells from several H-2 or H-2 strains. Genetic evidence or blocking studies with selected mAb assigned these cross-reactive mixed lymphocyte reaction determinants to the A or A molecules, respectively. The data support the conclusion that alloreactive T cells may define a polymorphism of I-region coded products not detected by serological analyses and extend at the T-cell level the observations of serological cross-reactions between A and E molecules. © 1982 Springer-Verlag.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0020036099&origin=inward; http://dx.doi.org/10.1007/bf00364263; http://www.ncbi.nlm.nih.gov/pubmed/6176538; http://link.springer.com/10.1007/BF00364263; http://www.springerlink.com/index/10.1007/BF00364263; http://www.springerlink.com/index/pdf/10.1007/BF00364263; https://dx.doi.org/10.1007/bf00364263; https://link.springer.com/article/10.1007/BF00364263
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