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The QA2 subregion controls the expression of two antigens recognized by H-2- unrestricted cytotoxic T cells

B6.KI mice were immunized with spleen cells from B6.K2, a Qa2-subregion congenic strain. Cytotoxic T cells were generated that recognize two target antigens controlled by this region. One of the target antigens is Qa-2. This was demonstrated by the findings that pretreatment of target cells with mon...

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Detalles Bibliográficos
Autores principales: Forman, J, Trial, J, Tonkonogy, S, Flaherty, L
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1982
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2186634/
https://www.ncbi.nlm.nih.gov/pubmed/6174664
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author Forman, J
Trial, J
Tonkonogy, S
Flaherty, L
author_facet Forman, J
Trial, J
Tonkonogy, S
Flaherty, L
author_sort Forman, J
collection PubMed
description B6.KI mice were immunized with spleen cells from B6.K2, a Qa2-subregion congenic strain. Cytotoxic T cells were generated that recognize two target antigens controlled by this region. One of the target antigens is Qa-2. This was demonstrated by the findings that pretreatment of target cells with monoclonal anti-Qa-2 antibody blocked lysis of target cells, and Qa-2 target antigens and serological determinants had a concordant distribution on a panel of B10.W (wild) mice. The gene controlling the Qa-2 target antigen is not polymorphic because B6.K2 and three strains of Qa-2(+) B10.W mice express the same antigens, as determined by a CTL cold target competition assay. Anti-Qa-2 CTL were H-2 unrestricted because effector cells lysed Qa-2(+) targets irrespective of their H-2 haplotype, including five B 10.W strains, and lysis was not inhibited by pretreating target cells with anti-H-2 sera. The Qa2 subregion does not act as a restricting locus for anti-minor-H antigen CTL. A second target antigen was detected that was associated with the expression of the Qa-5 determinant. However, CTL activity could not be blocked by pretreating target cells with monoclonal anti-Qa-5. Therefore, the CTL target antigen may be expressed on a Qa-5(-) molecule. Although the Qa-5 associated CTL specificity is only detected on H-2D(b) strains, it is unlikely that CTL recognition is H-2 restricted because anti-H-2(b) sera has no effect in blocking this reactivity. Qa-2 and H-2 class I antigens share a similar structure and serve as target antigens for unrestricted CTL. However, unlike class I H-2 genes, Qa-2 neither restricts antigen-specific CTL nor is polymorphie. Therefore, it is likely that Qa-2 and H-2 are derived from a common ancestral gene and have evolved to serve different functions.
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spelling pubmed-21866342008-04-17 The QA2 subregion controls the expression of two antigens recognized by H-2- unrestricted cytotoxic T cells Forman, J Trial, J Tonkonogy, S Flaherty, L J Exp Med Articles B6.KI mice were immunized with spleen cells from B6.K2, a Qa2-subregion congenic strain. Cytotoxic T cells were generated that recognize two target antigens controlled by this region. One of the target antigens is Qa-2. This was demonstrated by the findings that pretreatment of target cells with monoclonal anti-Qa-2 antibody blocked lysis of target cells, and Qa-2 target antigens and serological determinants had a concordant distribution on a panel of B10.W (wild) mice. The gene controlling the Qa-2 target antigen is not polymorphic because B6.K2 and three strains of Qa-2(+) B10.W mice express the same antigens, as determined by a CTL cold target competition assay. Anti-Qa-2 CTL were H-2 unrestricted because effector cells lysed Qa-2(+) targets irrespective of their H-2 haplotype, including five B 10.W strains, and lysis was not inhibited by pretreating target cells with anti-H-2 sera. The Qa2 subregion does not act as a restricting locus for anti-minor-H antigen CTL. A second target antigen was detected that was associated with the expression of the Qa-5 determinant. However, CTL activity could not be blocked by pretreating target cells with monoclonal anti-Qa-5. Therefore, the CTL target antigen may be expressed on a Qa-5(-) molecule. Although the Qa-5 associated CTL specificity is only detected on H-2D(b) strains, it is unlikely that CTL recognition is H-2 restricted because anti-H-2(b) sera has no effect in blocking this reactivity. Qa-2 and H-2 class I antigens share a similar structure and serve as target antigens for unrestricted CTL. However, unlike class I H-2 genes, Qa-2 neither restricts antigen-specific CTL nor is polymorphie. Therefore, it is likely that Qa-2 and H-2 are derived from a common ancestral gene and have evolved to serve different functions. The Rockefeller University Press 1982-03-01 /pmc/articles/PMC2186634/ /pubmed/6174664 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Forman, J
Trial, J
Tonkonogy, S
Flaherty, L
The QA2 subregion controls the expression of two antigens recognized by H-2- unrestricted cytotoxic T cells
title The QA2 subregion controls the expression of two antigens recognized by H-2- unrestricted cytotoxic T cells
title_full The QA2 subregion controls the expression of two antigens recognized by H-2- unrestricted cytotoxic T cells
title_fullStr The QA2 subregion controls the expression of two antigens recognized by H-2- unrestricted cytotoxic T cells
title_full_unstemmed The QA2 subregion controls the expression of two antigens recognized by H-2- unrestricted cytotoxic T cells
title_short The QA2 subregion controls the expression of two antigens recognized by H-2- unrestricted cytotoxic T cells
title_sort qa2 subregion controls the expression of two antigens recognized by h-2- unrestricted cytotoxic t cells
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2186634/
https://www.ncbi.nlm.nih.gov/pubmed/6174664
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