Hammarström L, Granström M, Oxelius V, Persson M A, Smith C I
Clin Exp Immunol. 1984 Mar;55(3):593-601.
IgM, IgG, IgA and IgE class and IgG and IgA subclass levels were determined in 18 IgG2 deficient and six IgG3 deficient donors. IgG2 deficiency was associated with concomitant IgG4, IgA (in particular IgA2) and IgE deficiency. This pattern is compatible with a regulation defect of the downstream switch in the heavy chain locus on chromosome 14. IgG3 subclass deficiency was not associated with further deficiencies. Specific anti-teichoic acid antibodies were lacking in most IgG2 deficient donors supporting the notion that anti-teichoic acid antibodies are normally of this subclass. This was also confirmed in a subclass-specific ELISA using sera from normal donors although substantial amounts of specific IgG1 antibodies were also noted. Two IgG2 deficient donors had normal IgG titres (IgG1 in the subclass specific ELISA) and the lack of IgG1 anti-teichoic acid antibodies in most IgG2 deficient donors may suggest a lack of maturation of the appropriate idiotype. IgG antibodies to alpha-toxin, a pure protein, were within the lower normal range in a large proportion of IgG2 deficient donors but largely normal in the IgG3 deficient donors.
在18名IgG2缺陷和6名IgG3缺陷的供体中测定了IgM、IgG、IgA和IgE类以及IgG和IgA亚类水平。IgG2缺陷与IgG4、IgA(尤其是IgA2)和IgE缺陷同时存在有关。这种模式与14号染色体上重链基因座下游开关的调节缺陷相符。IgG3亚类缺陷与其他缺陷无关。大多数IgG2缺陷的供体缺乏特异性抗磷壁酸抗体,这支持了抗磷壁酸抗体通常属于该亚类的观点。在使用正常供体血清的亚类特异性ELISA中也证实了这一点,尽管也注意到大量特异性IgG1抗体。两名IgG2缺陷的供体具有正常的IgG滴度(在亚类特异性ELISA中为IgG1),大多数IgG2缺陷的供体缺乏IgG1抗磷壁酸抗体可能表明缺乏适当独特型的成熟。针对纯蛋白α毒素的IgG抗体在大部分IgG2缺陷的供体中处于正常范围下限,但在IgG3缺陷的供体中大多正常。