Durandy Anne, Revy Patrick, Imai Kohsuke, Fischer Alain
INSERM U429, Hôpital Necker-Enfants Malades, Paris, France.
Immunol Rev. 2005 Feb;203:67-79. doi: 10.1111/j.0105-2896.2005.00222.x.
Hyper-immunoglobulin M (IgM) syndromes are primary immunodeficiencies characterized by normal or elevated serum IgM levels with the absence of other isotypes, pinpointing to a defect in the Ig class switch recombination (CSR). The delineation of hyper-IgM syndromes made it possible to better define the mechanisms underlying the two major events of antibody maturation in humans, CSR and introduction of somatic hypermutation (SHM) in the variable region of immunoglobulins. The description of the activation-induced cytidine deaminase (AID) deficiency, characterized by a defect in both CSR and SHM, demonstrated for the first time that this molecule acts as a master player in the antigen-induced Ig gene-modification events responsible for both CSR and SHM. However, deleterious mutations located in the C-terminus lead to a CSR defect without affecting SHM, providing evidence for a role of AID in CSR distinct from the cytidine deaminase activity, likely by binding to a specific CSR cofactor. Molecular causes of two other hyper-IgM conditions have not yet been defined. However, they may be caused by either a defect in AID targeting on S regions or a CSR-specific DNA-repair defect. The mechanism of action of AID remains somewhat debated, but the observation that uracil-DNA-glycosylase deficiency leads to a severe hyper-IgM syndrome strongly argues in favor of a DNA-editing activity of AID.
高免疫球蛋白M(IgM)综合征是原发性免疫缺陷病,其特征是血清IgM水平正常或升高,而其他同种型缺乏,这表明免疫球蛋白类别转换重组(CSR)存在缺陷。高IgM综合征的明确使得更好地定义人类抗体成熟的两个主要事件——CSR和免疫球蛋白可变区体细胞超突变(SHM)的潜在机制成为可能。激活诱导的胞苷脱氨酶(AID)缺陷的描述,其特征是CSR和SHM均有缺陷,首次证明该分子在负责CSR和SHM的抗原诱导的Ig基因修饰事件中起主要作用。然而,位于C末端的有害突变导致CSR缺陷而不影响SHM,这为AID在CSR中的作用提供了证据,该作用不同于胞苷脱氨酶活性,可能是通过与特定的CSR辅因子结合。另外两种高IgM病症的分子原因尚未明确。然而,它们可能是由AID靶向S区域的缺陷或CSR特异性DNA修复缺陷引起的。AID的作用机制仍存在一定争议,但尿嘧啶-DNA-糖基化酶缺陷导致严重的高IgM综合征这一观察结果有力地支持了AID的DNA编辑活性。