Aboud-Pirak E, Lubin I, Pirak M E, Canaan A, Lowell G H, Reisner Y
Department of Chemical Immunology, Weizmann Institute of Science, Rehovot, Israel.
Immunol Lett. 1995 May;46(1-2):9-14. doi: 10.1016/0165-2478(94)00005-c.
Normal strains of mice are rendered sensitive to small amounts (3-10 micrograms) of staphylococcal enterotoxin B (SEB) by transplanting bone marrow cells of SCID donor mice to lethally irradiated recipients. Four to 12 weeks post-transplantation, SEB induces 56-100% lethality. Transplantation of normal mouse bone marrow cells, either alone or with the SCID mouse selected bone marrow cells, does not confer SEB sensitivity. These data imply that either irradiation ablates certain cell population(s), that confer resistance to SEB in normal mice (populations that are absent in the SCID donor mice) or that the donor cells selectively repopulate recipients with SEB-sensitive cells. This model will help elucidate the cells, cytokines and the SEB peptide fragments responsible for SEB toxicity and will be useful in identifying promising vaccine candidates and in developing preventive medicines to protect against this potent toxin.
通过将重症联合免疫缺陷(SCID)供体小鼠的骨髓细胞移植到接受致死剂量照射的受体小鼠体内,可使正常品系小鼠对少量(3 - 10微克)的葡萄球菌肠毒素B(SEB)敏感。移植后4至12周,SEB可诱导56%至100%的致死率。单独移植正常小鼠骨髓细胞或与SCID小鼠筛选的骨髓细胞一起移植,均不会使小鼠产生对SEB的敏感性。这些数据表明,要么是照射消除了某些在正常小鼠中赋予对SEB抗性的细胞群体(这些群体在SCID供体小鼠中不存在),要么是供体细胞选择性地用对SEB敏感的细胞重新填充受体。该模型将有助于阐明负责SEB毒性的细胞、细胞因子和SEB肽片段,并将有助于识别有前景的疫苗候选物以及开发预防药物以抵御这种强效毒素。