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小鼠对同种异体细胞的迟发型超敏反应。III. 对主要组织相容性复合体及其他基因编码的细胞表面抗原的敏感性。

Delayed-type hypersensitivity to allogeneic cells in mice. III. Sensitivity to cell-surface antigens coded by the major histocompatibility complex and by other genes.

作者信息

Smith F I, Miller J F

出版信息

J Exp Med. 1979 Oct 1;150(4):965-76. doi: 10.1084/jem.150.4.965.

Abstract

DTH could be induced to cell-surface antigens coded by either H-2 or non-H-2 genes. Sensitivity was more readily induced across I region than across K- or D-region differences. The presence of an I-region difference during sensitization did not significantly increase the DTH response to K- or D-region-coded antigens. Macrophage processing appeared to be the major route of sensitization to background antigens. Thus, high levels of sensitivity were achieved equally well using viable or disrupted cells, the response was independent of the H-2 haplotype of the allogeneic cells, and transfer was restricted to the K end of the host H-2 complex. Although sensitization to H-2 antigens was obtained with disrupted cells, transfer of sensitivity against viable cells was unrestricted. This suggests a minor role for macrophage processing in sensitization to H-2 antigens.

摘要

迟发型超敏反应(DTH)可由H-2或非H-2基因编码的细胞表面抗原诱导产生。相较于跨越K或D区域差异,跨越I区域更容易诱导出敏感性。致敏过程中I区域差异的存在,并未显著增加对K或D区域编码抗原的DTH反应。巨噬细胞处理似乎是对背景抗原致敏的主要途径。因此,使用活细胞或破碎细胞均可同样良好地实现高敏感性水平,该反应与同种异体细胞的H-2单倍型无关,且转移仅限于宿主H-2复合体的K端。尽管用破碎细胞可获得对H-2抗原的致敏,但对活细胞的敏感性转移不受限制。这表明巨噬细胞处理在对H-2抗原致敏中起次要作用。

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