Tsuji M, Eyster C L, O'Brien R L, Born W K, Bapna M, Reichel M, Nussenzweig R S, Zavala F
Department of Medical and Molecular Parasitology, New York University School of Medicine, NY 10010, USA.
Int Immunol. 1996 Mar;8(3):359-66. doi: 10.1093/intimm/8.3.359.
Six murine T cell clones expressing gamma delta TCR were generated from malaria immunized, alpha beta T cell-deficient mice. Phenotypic characterization of these clones has revealed that, in contrast to conventional alpha beta T cells, there is a considerable degree of heterogeneity among these gamma delta clones with regard to their surface markers and their lymphokine profile. One clone was found to display significant anti-parasite activity in vivo upon adoptive transfer. We attempted to determine whether the protective clone differs in one or more key characteristics from the non-protective clones. Although no obvious pattern peculiar to the protective gamma delta clone was observed, it appears that more than one parameter may, in combination, define a distinct protective phenotype, and thus explain the functional difference between the protective and non-protective gamma delta clones.
从经疟疾免疫的αβ T细胞缺陷小鼠中产生了六个表达γδ TCR的小鼠T细胞克隆。对这些克隆的表型特征分析表明,与传统的αβ T细胞不同,这些γδ克隆在表面标志物和淋巴因子谱方面存在相当程度的异质性。发现一个克隆在过继转移后在体内表现出显著的抗寄生虫活性。我们试图确定保护性克隆在一个或多个关键特征上是否与非保护性克隆不同。虽然未观察到保护性γδ克隆特有的明显模式,但似乎多个参数可能共同定义一种独特的保护表型,从而解释保护性和非保护性γδ克隆之间的功能差异。