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抗原特异性辅助因子诱导细胞毒性淋巴细胞反应。

Induction of cytotoxic lymphocyte responses by antigen-specific helper factors.

作者信息

Krowka J F, Shiozawa C, Diener E, Paetkau V, Pilarski L M

出版信息

J Immunol. 1984 Oct;133(4):2018-24.

PMID:6206146
Abstract

Antigen-specific helper factors (ASHF) were purified by antigen-affinity chromatography from supernatants of long-term helper T lymphocyte (TH) lines. We have modified an established helper-dependent assay system to demonstrate the antigen specificity and H-2 restriction properties of ASHF in the induction of cytotoxic T lymphocyte precursors (CTLp). Antigen specificity is demonstrated by the binding of ASHF molecules only to nominal antigen, both during purification and in tests of functional activity. Our ASHF preparations do not contain any interleukin 2 (IL 2) activity. The ASHF, purified by antigen-affinity chromatography in the presence of Ca++, is defined as Ca++-sufficient ASHF, whereas ASHF purified on antigen-affinity columns in the absence of Ca++ is defined to be Ca++ deficient. Ca++-sufficient ASHF is not H-2 restricted (as defined by the phenotype of the ASHF-producing cells) in the recognition of nominal antigen or in its interactions with CTLp or adherent stimulator cells. In contrast, when the "complete" (Ca++-sufficient) ASHF is functionally dissociated into subunits by removal of Ca++, the "incomplete" antigen-specific subunit of ASHF (Ca++-deficient ASHF) is still H-2-unrestricted in its ability to bind nominal antigen, but requires products from syngeneic adherent cells to trigger CTLp. When adherent cells that are H-2 identical to the ASHF are provided in culture, the "incomplete" ASHF is able to trigger either syngeneic or allogeneic CTLp in an antigen-specific manner. We interpret the results of our experiments to suggest that an H-2-restricted molecular interaction occurs in CTLp induction by ASHF. An antigen-specific, TH-derived receptor appears to require association with Ca++ and self major histocompatibility complex (MHC)-encoded molecules to form a "complete" ASHF that is able to trigger CTLp in an apparently H-2-unrestricted manner.

摘要

通过抗原亲和层析从长期辅助性T淋巴细胞(TH)系的上清液中纯化出抗原特异性辅助因子(ASHF)。我们改进了一个已建立的依赖辅助因子的检测系统,以证明ASHF在诱导细胞毒性T淋巴细胞前体(CTLp)过程中的抗原特异性和H-2限制性特性。在纯化过程和功能活性测试中,ASHF分子仅与名义抗原结合,从而证明了抗原特异性。我们的ASHF制剂不包含任何白细胞介素2(IL 2)活性。在Ca++存在下通过抗原亲和层析纯化的ASHF被定义为Ca++充足的ASHF,而在无Ca++的情况下在抗原亲和柱上纯化的ASHF被定义为Ca++缺乏的。Ca++充足的ASHF在识别名义抗原或与CTLp或贴壁刺激细胞相互作用时不受H-2限制(由产生ASHF的细胞表型定义)。相反,当通过去除Ca++将“完整的”(Ca++充足的)ASHF功能上解离成亚基时,ASHF的“不完整的”抗原特异性亚基(Ca++缺乏的ASHF)在结合名义抗原的能力上仍然不受H-2限制,但需要同基因贴壁细胞的产物来触发CTLp。当在培养中提供与ASHF H-2相同的贴壁细胞时,“不完整的”ASHF能够以抗原特异性方式触发同基因或异基因CTLp。我们解释我们的实验结果表明,在ASHF诱导CTLp的过程中发生了H-2限制性分子相互作用。一种抗原特异性的、源自TH的受体似乎需要与Ca++和自身主要组织相容性复合体(MHC)编码的分子结合,以形成一个“完整的”ASHF,该ASHF能够以明显不受H-2限制的方式触发CTLp。

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