Yount W J, Kunkel H G, Litwin S D
J Exp Med. 1967 Jan 1;125(1):177-90. doi: 10.1084/jem.125.1.177.
Further delineation of the antigens characteristic of the Vi or gamma(2c) subgroup of gamma-globulin was carried out utilizing a number of rabbit and primate antisera. Two genetic antigens characteristic of this subgroup, Gm(b) and Gm(g), were also detected by precipitation techniques with certain of the antisera. These were clearly differentiated from antigens common to all proteins of this subgroup. The concentration, of Vi protein in normal and pathological sera from several population groups was measured quantitatively utilizing a variety of immunological procedures. All sera studied showed measurable levels. The mean value for Caucasian sera was 1.06 mg/ml, representing approximately 8% of gammaG-globulin. This agreed closely with a figure of 8.4% for the incidence of myeloma proteins of the Vi subgroup among all gammaG-myeloma proteins in Caucasians. A relationship was found between the Vi subgroup concentration and the specific genetic type of a given individual. Measurements of the Gm(b) genetic determinants, which are found solely in Vi-type proteins, brought forward this relationship. Gm(b+) individuals showed higher concentrations of Vi-type gamma-globulin than those who were Gm(b-), and this difference was statistically significant for both the homozygous and heterozygous states. It appeared that the structural genes for Gm(b+) polypeptide chains showed a greater synthetic capacity than those for Gm(b-) types. The possible significance of such effects in governing the relative composition of the antibody population in a given individual is discussed.
利用多种兔和灵长类抗血清,对γ球蛋白Vi或γ(2c)亚组特有的抗原进行了进一步的描述。通过某些抗血清的沉淀技术,还检测到了该亚组特有的两种遗传抗原Gm(b)和Gm(g)。这些抗原与该亚组所有蛋白质共有的抗原明显不同。利用多种免疫学方法,对来自几个群体的正常和病理血清中Vi蛋白的浓度进行了定量测定。所有研究的血清都显示出可测量的水平。白种人血清的平均值为1.06毫克/毫升,约占γG球蛋白的8%。这与白种人所有γG骨髓瘤蛋白中Vi亚组骨髓瘤蛋白的发生率8.4%非常接近。发现Vi亚组浓度与特定个体的特定遗传类型之间存在关联。对仅在Vi型蛋白中发现的Gm(b)遗传决定簇的测量揭示了这种关联。Gm(b+)个体比Gm(b-)个体显示出更高浓度的Vi型γ球蛋白,并且这种差异在纯合子和杂合子状态下均具有统计学意义。似乎Gm(b+)多肽链的结构基因比Gm(b-)类型的结构基因具有更大的合成能力。讨论了这种效应在控制给定个体中抗体群体相对组成方面的可能意义。