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The following book on the IgG Subclass is made available by the permisssion of CLB Reagents (Netherlands). It is for your personal use and may not be reproduced without the permission of CLB Reagents. This material is for information use only and should not be construed as medical advice. We are not responsible for any misprints or error or ommissions. Certain charts ,graphs and table have been ommitted or changed in style (not content) to fit this web site. Please use this information as part of your discussion with your medical professional.

2    IgG subclasses and humoral immunity

2.1   Immunoglobulins and humoral immunity

The glycoprotein immunoglobulin G (IgG), a major effector molecule of the humoral immune response in man, accounts for about 75% of the total immunoglobulins in plasma of healthy individuals. The immunoglobulins of the other four classes,IgM, IgA, IgD and IgE, each of which has characteristic properties and functions, constitute the other 25% of the immunoglobulins (3). Antibodies of the IgG class express their predominant activity during a secondary antibody response. Thus, the appearance of specific IgG antibodies generally corresponds with the 'maturation' of the antibody response, which is switched on upon repeated contact with an antigen. In comparison to antibodies of  the IgM class, IgG antibodies have a relatively high affinity and persist in the circulation for a long time. The five classes of human immunoglobulins can be distinguished on the basis of the amino acid composition. This is also the basis for antigenic differences between these molecules and for immunological recognition by specific antisera/antibodies (4).

2.2   Molecular basis of immunoglobulin synthesis

The polypeptide chains of immunoglobulins are encoded by three non-linked cluster of autosomal genes, one cluster coding for heavy chains of all classes and subclasses, a second one for kappa-light chains and a third one for lambda light chains. These three gene clusters are called the H-, k-and y gene families respectively. In humans the H gene family is on chromosome 14, the k gene family is on chromosome 2 and the y gene family is on chromosome 22. Molecular genetic studies have revealed the arrangement of gene segments within the heavy chain and light chain families. Each heavy chain is encoded by 4 distinct types of gene segments, designated V(H)(variable),D(diversity), J(H) (joining) and C(H)(constant). The variable region of the heavy chain is encoded by the V(H')D and J(H) segments. The light chains are encoded by the 3 gene segments, V(L)'J(L) and C(L). The variable region of the light chains is encoded by the V(L) and J(L) segments.

The C gene segments of the heavy and light chains encode for the constant regions. Nine immunoglobulin heavy chain isotypes are  found in humans: IgM, IgG, IgE, IgG (isotypically comprising four different subclasses IgG1, IgG2, IgG3 and IgG4) and IgA (with subclasses IgA1 and IgA2).

The C(H) gene segments determine the class and/or subclass of the heavy chain, whereas the V(H)'D and J(H) regions determine the antigen-recognizing part of the immunoglobulin molecule. The heavy chain constant region genes lie 3' to the V(H)' D and J(H) genes. During the maturation of progenitor B cells to mature B cells an active heavy chain exon is formed by V(H),D,J(H) integration (recombined V(H) DJ(H) gene), followed by linkage to a certain C(H)-gene locus. This matrix is transcribed to mRNA and subsequently translated to an immunoglobulin heavy chain molecule The C(H) gene closest to the J(H) locus, the Cu gene (IgM), is the first isotype gene to be expressed. The other C(H) genes can subsequently be expressed by 'downstream' switching mechanisms with simultaneous deletion of the original isotypic C(H) genes.According to this model the order of the C region genes on the chromosome largely determines the immunoglobulin isotype in an immune response. However, this mechanism may be influenced by isotype-specific switch factors such as IL-4 and IL-5. The relative localization of the genes controlling the isotypes of the immunoglobulin classes and subclasses has the following 5' to 3'-oriented sequence on the DNA of chromosome 14 (figure 3):

Cu (IgM)-C(d)(IgD)-Cy3 (IgG3)-Cy1(IgG1)-pseudogene Ce1-Ca1 (IgA1) -pseudogene cy-cy2 (IgG2)-Cy4 (IgG4-Ce(IgGE)-Ca2 (IgA2). By comparing the four IgG subclass genes, it becomes clear that the genes for IgG3 and IgG1 are close together, as are those for IgG2 and IgG4(5). The synthesis of each subclass is independently regulated. IgG1 and IgG3 levels generally rise more quickly than those of IgG2 and IgG4, possibly reflecting the occurrence of a successive 'downstream switch' in the immunoglobulin heavy chain constant region genes(6).

Gene deletions resulting in a complete deficiency, a total lack, of one or more IgG subclasses are very rare(7). In fact, most abnormalities are based upon regulatory defects,resulting in a decreased level (deficiency) rather than a total lack of one or more immunoglobulin (sub) classes. In some patients, an IgG2. Indeed, the genes encoding IgG2,IgG4 and the IgA subclasses are closely linked and this combined deficiency is due to a regulation defect of the 'downstream switch' in the heavy chain loci. This may result in a Maturation arrest in the immune response. It is likely that the expression of the immunoglobulins whose genes are located downstream in the C(H) region (especially IgG4 and IgE) requires more help from T helper 2 cells in comparison with upstream isotypes (IgG1 and IgG3) (8,9,10). IgG4 and also IgG2 deficiencies are found in imunodeficiency states characterised by a predominant T cell defect, such as in ataxia telangiectasia, AIDS and immune reconstitution after bone marrow transplantation (see section 4).

The observation that IgG subclass-limited responses occur suggests that the repertoire of V genes, as expressed in antibody diversity, differs between some subclasses.

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