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来自BALB/c-H-2dm2小鼠的细胞溶解性T淋巴细胞可识别水疱性口炎病毒糖蛋白,并受II类主要组织相容性复合体抗原的限制。

Cytolytic T lymphocytes from the BALB/c-H-2dm2 mouse recognize the vesicular stomatitis virus glycoprotein and are restricted by class II MHC antigens.

作者信息

Browning M J, Huang A S, Reiss C S

机构信息

Division of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA 02115.

出版信息

J Immunol. 1990 Aug 1;145(3):985-94.

PMID:1695651
Abstract

BALB/c-H-2dm2 mice (H-2KdI-AdI-EdDd), a congenic strain of BALB/c mice, have a deletion of the class I MHC Ag, H-2Ld. This gene encodes the exclusive class I MHC-restricting gene product for vesicular stomatitis virus-specific cytolytic T lymphocytes. When dm2 mice were immunized with infectious vesicular stomatitis virus, a specific CTL response was generated. These CTL lysed VSV-infected targets that expressed Iad gene products, but not VSV-infected Iad- targets. The CTL were used initially as long term cytolytic lines; 13 CTL clones were derived by limit dilution. All of the clones expressed the phenotype CD3+, CD4+, CD8-; some clones expressed TCR that are members of the V beta 8 family, others did not. The clones were restricted by class II MHC Ag, both I-Ad and I-Ed serving as restricting elements for individual clones of the panel. All of the clones derived from dm2 mice were specific for the immunizing serotype, Indiana, of VSV and did not lyse syngeneic cells infected with VSV of the New Jersey serotype. Studies using defective interfering virus particles, UV light-inactivated virus, and purified micelles of the viral glycoprotein indicated that infectious virus was not required for sensitization of target cells for immune recognition by the class II MHC-restricted CTL clones. Additional studies using recombinant vaccinia virus vectors to sensitize targets confirmed the specificity of the clones for the viral glycoprotein. These studies also demonstrated a cryptic population of class II-restricted CTL in BALB/c lines specific for VSV G. Naturally occurring variant viruses and mutant viruses, selected for escape from neutralization by mAb, were used in an effort to map the determinant(s) recognized; on the basis of patterns of target cell lysis, three groups of epitopes recognized by the clones were defined. Therefore, in the absence of the class I MHC Ag required for a CTL response to VSV, dm2 mice generated CTL with the CD4+ phenotype that recognized different epitopes on the viral glycoprotein, and lysed cells in a class II-MHC restricted, Ag-specific manner.

摘要

BALB/c-H-2dm2小鼠(H-2KdI-AdI-EdDd)是BALB/c小鼠的一个同源近交系,其I类主要组织相容性复合体(MHC)抗原H-2Ld缺失。该基因编码水疱性口炎病毒特异性细胞毒性T淋巴细胞唯一的I类MHC限制性基因产物。用感染性水疱性口炎病毒免疫dm2小鼠时,会产生特异性细胞毒性T淋巴细胞(CTL)反应。这些CTL可裂解表达Iad基因产物的水疱性口炎病毒感染的靶细胞,但不能裂解水疱性口炎病毒感染的Iad阴性靶细胞。最初将CTL用作长期细胞溶解系;通过有限稀释法获得了13个CTL克隆。所有克隆均表达CD3+、CD4+、CD8-表型;一些克隆表达属于Vβ8家族的T细胞受体(TCR),另一些则不表达。这些克隆受II类MHC抗原限制,I-Ad和I-Ed均可作为该组单个克隆的限制元件。所有源自dm2小鼠的克隆均对免疫所用的水疱性口炎病毒印第安纳血清型具有特异性,不能裂解感染新泽西血清型水疱性口炎病毒的同基因细胞。使用缺陷干扰病毒颗粒、紫外线灭活病毒以及病毒糖蛋白纯化微球进行的研究表明,靶细胞致敏以被II类MHC限制性CTL克隆进行免疫识别并不需要感染性病毒。使用重组痘苗病毒载体致敏靶细胞的进一步研究证实了这些克隆对病毒糖蛋白的特异性。这些研究还证明了BALB/c系中存在一群对水疱性口炎病毒糖蛋白具有特异性的II类限制性CTL。为了确定所识别的决定簇,使用了天然存在的变异病毒和为逃避单克隆抗体中和作用而选择的突变病毒;根据靶细胞裂解模式,定义了三组被克隆识别的表位。因此,在缺乏对水疱性口炎病毒产生CTL反应所需的I类MHC抗原的情况下,dm2小鼠产生了具有CD4+表型的CTL,这些CTL识别病毒糖蛋白上的不同表位,并以II类MHC限制的、抗原特异性方式裂解细胞。

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