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通过在肌肉细胞中表达病毒蛋白产生MHC I类限制性细胞毒性T淋巴细胞:非肌肉细胞的抗原呈递

Generation of MHC class I-restricted cytotoxic T lymphocytes by expression of a viral protein in muscle cells: antigen presentation by non-muscle cells.

作者信息

Ulmer J B, Deck R R, Dewitt C M, Donnhly J I, Liu M A

机构信息

Department of Virus and Cell Biology, Merck Research Laboratories, West Point, PA 19486, USA.

出版信息

Immunology. 1996 Sep;89(1):59-67. doi: 10.1046/j.1365-2567.1996.d01-718.x.

Abstract

Expression of reporter genes in muscle cells has been achieved by intramuscular (i.m.) injection of plasmid DNA expression vectors. We previously demonstrated that this technique is an effective means of immunization to elicit both antibodies capable of conferring homologous protection and cell-mediated immunity leading to cross-strain protection against influenza virus challenge in mice. These results suggested that expression of viral proteins by muscle cells can result in the generation of cellular immune responses, including cytotoxic T lymphocytes (CTL). However, because DNA has the potential to be internalized and expressed by other cell types, we sought to determine whether or not induction of CTL required synthesis of antigen in non-muscle cells and if not whether transfer of antigen to antigen-presenting cells from muscle cells may be involved. In the present study we demonstrate that transplantation of nucleoprotein (NP)-transfected myoblasts into syngeneic mice led to the generation of NP-specific antibodies and CTL and cross-strain protective immunity against a lethal challenge with influenza virus. Furthermore transplantation of NP-expressing myoblasts (H-2k) intraperitoneally into F1 hybrid mice (H-2d x H-2k) elicited NPCTL restricted by the MHC haplotype of both parental strains. These results indicate that NP expression by muscle cells after transplantation was sufficient to generate protective cell-mediated immunity and that induction of the CTL response was mediated at least in part, by transfer of antigen from the transplanted muscle cells to a host cell.

摘要

通过肌内(i.m.)注射质粒DNA表达载体已实现报告基因在肌肉细胞中的表达。我们之前证明,该技术是一种有效的免疫方法,可引发既能提供同源保护的抗体,又能引发细胞介导的免疫反应,从而在小鼠中对流感病毒攻击产生交叉株保护。这些结果表明,肌肉细胞表达病毒蛋白可导致细胞免疫反应的产生,包括细胞毒性T淋巴细胞(CTL)。然而,由于DNA有可能被其他细胞类型内化并表达,我们试图确定CTL的诱导是否需要在非肌肉细胞中合成抗原,如果不需要,那么抗原从肌肉细胞转移到抗原呈递细胞是否可能参与其中。在本研究中,我们证明将核蛋白(NP)转染的成肌细胞移植到同基因小鼠中会导致产生NP特异性抗体和CTL,并对流感病毒的致死性攻击产生交叉株保护性免疫。此外,将表达NP的成肌细胞(H-2k)腹腔内移植到F1杂交小鼠(H-2d×H-2k)中会引发受两个亲本品系MHC单倍型限制的NP CTL。这些结果表明,移植后肌肉细胞中的NP表达足以产生保护性细胞介导的免疫,并且CTL反应的诱导至少部分是由抗原从移植的肌肉细胞转移到宿主细胞介导的。

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