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通过免疫特惠部位诱导的鼠 CD8 抑制性 T 细胞的免疫放大:功能定量抑制性 T 细胞。

Immune amplification of murine CD8 suppressor T cells induced via an immune-privileged site: quantifying suppressor T cells functionally.

机构信息

Department of Immunology, University of Connecticut Health Center, Farmington, Connecticut, United States of America.

出版信息

PLoS One. 2011;6(8):e22496. doi: 10.1371/journal.pone.0022496. Epub 2011 Aug 2.

Abstract

BACKGROUND

CD8(+) suppressor T cells exert antigen-specific suppression of the expression of hypersensitivity by activated T cells. Therefore, CD8(+) suppressor T cells serve a major regulatory role for the control of active immunity. Accordingly, the number and/or activity of CD8(+) suppressor T cells should be influenced by an immune response to the antigen. To test this hypothesis we used an adoptive transfer assay that measures the suppression of the expression of delayed-type hypersensitivity (DTH) by CD8(+) suppressor T cells to quantify the antigen-specific suppression of DTH by these suppressor T cells.

METHODS

Suppressor T cells were induced in the spleens of mice by the injection of antigen into the anterior chamber of an eye. Following this injection, the mice were immunized by the same antigen injected into the anterior chamber. Spleen cells recovered from these mice (AC-SPL cells) were titrated in an adoptive transfer assay to determine the number of AC-SPL cells required to effect a 50% reduction of antigen-induced swelling (Sw50) in the footpad of immunized mice challenged by antigen.

RESULTS

Suppression of the expression of DTH is proportional to the number of AC-SPL cells injected into the site challenged by antigen. The number of AC-SPL cells required for a 50% reduction in DTH-induced swelling is reduced by injecting a cell population enriched for CD8(+) AC-SPL cells. Immunizing the mice receiving intracameral antigen to the same antigen decreases the RSw50 of AC-SPL cells required to inhibit the expression of DTH.

CONCLUSIONS

The results provide the first quantitative demonstration that the numbers of antigen-specific splenic CD8(+) suppressor T cells are specifically amplified by antigen during an immune response.

摘要

背景

CD8(+) 抑制性 T 细胞通过激活的 T 细胞特异性抑制过敏反应的表达。因此,CD8(+) 抑制性 T 细胞在主动免疫的控制中发挥主要的调节作用。因此,CD8(+) 抑制性 T 细胞的数量和/或活性应该受到对该抗原的免疫反应的影响。为了检验这一假说,我们使用了一种过继转移测定,该测定通过 CD8(+) 抑制性 T 细胞对迟发型超敏反应(DTH)表达的抑制作用来定量这些抑制性 T 细胞对 DTH 的抗原特异性抑制作用。

方法

在眼部前房注射抗原诱导小鼠脾脏中的抑制性 T 细胞,然后用相同的抗原在前房内免疫。从这些小鼠中回收的脾细胞(AC-SPL 细胞)在过继转移测定中进行滴定,以确定在接受抗原挑战的免疫小鼠的足垫中使抗原诱导的肿胀(Sw50)减少 50%所需的 AC-SPL 细胞数。

结果

DTH 表达的抑制与注入抗原刺激部位的 AC-SPL 细胞数成正比。用富含 CD8(+) AC-SPL 细胞的细胞群注射可减少抑制 DTH 诱导肿胀所需的 AC-SPL 细胞数。用相同的抗原免疫接受前房内抗原的小鼠可降低抑制 DTH 表达所需的抑制性 AC-SPL 细胞的 RSw50。

结论

这些结果首次定量证明了在免疫反应中,特异性抗原的脾脏 CD8(+) 抑制性 T 细胞的数量是特异性扩增的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daa5/3149055/16298d2c0923/pone.0022496.g001.jpg

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