Cancer Therapy & Research Center at the University of Texas Health Science Center at San Antonio, 2040 Babcock Road, Suite 201, San Antonio, TX 78229, USA.
J Immunol Methods. 2010 Apr 15;355(1-2):86-90. doi: 10.1016/j.jim.2010.01.013. Epub 2010 Feb 8.
Cytotoxic T cells (CTLs) are an important component of adaptive immunity. The study of antigen-specific CTLs in vivo is desirable yet difficult. Identification of the class I-restricted peptide used by CTLs for target recognition is often required for detailed studies, but is generally not known for most antigens. Toxoplasma gondii is a medically important, obligate intracellular parasite and is often used as a model for studies of parasite immunology. No class I-restricted peptides for CTLs are known. We show here a new and convenient method to detect T. gondii-specific CTLs in vivo. We engineered T. gondii tachyzoites to express the model antigen ovalbumin, for which many useful reagents and transgenic mice are available. Using ovalbumin-transgenic T. gondii tachyzoites, antigen-specific CTLs were detected in vivo, and at much earlier time points post-infection than previously reported. This new method has several additional advantages over current methods to detect T. gondii-specific CTLs.
细胞毒性 T 细胞 (CTL) 是适应性免疫的重要组成部分。在体内研究抗原特异性 CTL 是理想的,但却很困难。通常情况下,对于大多数抗原,都不知道 CTL 用于靶标识别的 I 类限制肽。刚地弓形虫是一种重要的医学病原体,是一种专性细胞内寄生虫,通常被用作寄生虫免疫学研究的模型。目前还不知道 CTL 的 I 类限制肽。我们在此展示了一种新的、方便的方法来检测体内的刚地弓形虫特异性 CTL。我们设计了刚地弓形虫速殖子来表达模型抗原卵清蛋白,对于这种抗原,有许多有用的试剂和转基因小鼠可供使用。使用卵清蛋白转基因刚地弓形虫速殖子,在体内检测到了抗原特异性 CTL,并且比以前报道的更早的感染后时间点。与目前检测刚地弓形虫特异性 CTL 的方法相比,这种新方法具有几个额外的优势。