Baker P J, Amsbaugh D F, Prescott B, Stashak P W
J Immunogenet. 1976 Aug;3(4):275-86. doi: 10.1111/j.1744-313x.1976.tb00584.x.
Recombinant-inbred strains of mice, as well as the progenitor strains from which they were derived, were evaluated with respect to the capacity of B cells to respond to an optimally immunogenic dose of Type III pneumococcal polysaccharide (SSS-III) and the amount of suppressor and amplifier T cell activity present. None of these functional activities was found to be linked to genes within the major histocompatibility (H-2) or the IgCH allotype complex, and several autosomal genes appeared to govern the expression of each of these characteristics.
对重组近交系小鼠及其亲本品系进行了评估,涉及B细胞对III型肺炎球菌多糖(SSS-III)最佳免疫原性剂量的反应能力以及存在的抑制性和辅助性T细胞活性水平。这些功能活性均未发现与主要组织相容性(H-2)或IgCH同种异型复合体内的基因相关,且有几个常染色体基因似乎控制着这些特征的表达。