Laboratory of Marine Biochemistry, Department of Bioscience and Biotechnology, Graduate School of Bioresource and Bioenvironmental Sciences, Kyushu University, Fukuoka 812-8581, Japan.
Department of Applied Aquabiology, National Fisheries University, Shimonoseki, Yamaguchi 759-6595, Japan.
Dev Comp Immunol. 2014 May;44(1):111-5. doi: 10.1016/j.dci.2013.12.008. Epub 2013 Dec 14.
Although many recent studies have suggested that CD4(+) helper T cell (Th-cell) functions are well conserved among teleost fishes and mammals, there is little evidence that CD4(+) Th-cells in fish are actually involved in both humoral and cell-mediated immunity during a secondary immune response. In the present study, adoptive transfer using clonal ginbuna crucian carp and crucian carp hematopoietic necrosis virus (CHNV) was used to investigate the functions of CD4(+) cells during humoral and cell-mediated immunity. With regard to humoral immunity, transplanting CHNV-sensitized donor cells, containing CD4(+) cells, into naive fish induced more rapid and stronger antibody production than by transplanting non-sensitized donor cells or sensitized donor cells lacking CD4(+) cells. During cell-mediated immunity, no significant differences were found in recipients that received sensitized cells regardless of whether the donor cells contained CD4(+) cells, although recipients that received both sensitized donor cells (with and without CD4(+) cells) exhibited more efficient cell-mediated cytotoxicity than those that received non-sensitized donor cells. These findings suggest that inducing a secondary antibody response requires CD4(+) cell help, and secondary cell-mediated immunity can be induced both by CD4(+) cells and leukocytes other than CD4(+) cells.
尽管许多最近的研究表明,CD4(+)辅助 T 细胞(Th 细胞)的功能在硬骨鱼类和哺乳动物中得到了很好的保留,但几乎没有证据表明鱼类中的 CD4(+)Th 细胞实际上参与了二次免疫应答中的体液免疫和细胞介导免疫。在本研究中,使用克隆锦鲤和锦鲤造血坏死病毒(CHNV)的过继转移来研究 CD4(+)细胞在体液免疫和细胞介导免疫中的功能。在体液免疫方面,将含有 CD4(+)细胞的 CHNV 致敏供体细胞移植到无敏鱼体内,诱导的抗体产生比移植非致敏供体细胞或缺乏 CD4(+)细胞的致敏供体细胞更快、更强。在细胞介导免疫方面,无论供体细胞是否含有 CD4(+)细胞,接受致敏细胞的受者之间没有发现显著差异,尽管接受致敏供体细胞(有和没有 CD4(+)细胞)的受者表现出比接受非致敏供体细胞更高的细胞介导细胞毒性。这些发现表明,诱导二次抗体反应需要 CD4(+)细胞的帮助,二次细胞介导免疫既可以由 CD4(+)细胞诱导,也可以由除 CD4(+)细胞以外的白细胞诱导。