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NZB脾细胞对Qa-1b相关抗原决定簇的原发性体外细胞毒性反应。

Primary in vitro cytotoxic response of NZB spleen cells to Qa-1b-associated antigenic determinants.

作者信息

Rich R R, Sedberry D A, Kastner D L, Chu L

出版信息

J Exp Med. 1979 Dec 1;150(6):1555-60. doi: 10.1084/jem.150.6.1555.

Abstract

We have shown that cytotoxic lymphocytes generated in primary cultures of NZB spleen cells with H-2-identical BALB/c or B10.D2 stimulator cells exhibit specificity for Qa-1b-associated antigenic determinants. This unidirectional cytotoxicity constitutes the initial demonstration of a primary in vitro response to antigens of the Qa-Tla system. Such responses do not require H-2 homology between effector and target cells in the assay system. In fact, when H-2Dd homologous target cells were employed there was little, if any, evidence for development of primary H-2-restricted responses to minor locus histocompatibility antigens or viral antigens. In view of the recently defined role of Qa-1+, Ly-1,2,3+ cells as regulators of antibody responses, and of the deficiency of such cells in NZB mice, the observation of hyperreactivity for determinants of this system may be relevant to the development of autoimmunity in these animals.

摘要

我们已经表明,在具有H-2相同的BALB/c或B10.D2刺激细胞的NZB脾细胞原代培养物中产生的细胞毒性淋巴细胞对与Qa-1b相关的抗原决定簇具有特异性。这种单向细胞毒性构成了对Qa-Tla系统抗原的初次体外反应的初步证明。此类反应在检测系统中并不要求效应细胞和靶细胞之间具有H-2同源性。事实上,当使用H-2Dd同源靶细胞时,几乎没有证据表明对次要组织相容性抗原或病毒抗原产生了初次H-2限制性反应。鉴于最近确定的Qa-1+、Ly-1,2,3+细胞作为抗体反应调节因子的作用,以及NZB小鼠中此类细胞的缺乏,对该系统决定簇的高反应性观察可能与这些动物自身免疫的发展有关。

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