Limits...
B lymphocyte involvement in ankylosing spondylitis: the heavy chain variable segment gene repertoire of B lymphocytes from germinal center-like foci in the synovial membrane indicates antigen selection.

Voswinkel J, Weisgerber K, Pfreundschuh M, Gause A - Arthritis Res. (2001)

Bottom Line: In contrast to RA, neither VH6 genes nor the autoimmunity-prone VH4-34 were seen, whereas another autoimmunity-prone gene, V3-23, was predominantly used (11%).CDR3 were shorter and more variable in length than in RA.Comparable with RA and reactive arthritis, there is a biased repertoire of selected VH genes, whereas the panel of represented genes is different and less clonal expansion was observed.

View Article: PubMed Central - HTML - PubMed

Affiliation: Department of Rheumatology, Universitätsklinikum Lübeck, Lübeck, Germany. Jvoswinkel@aol.com

ABSTRACT
The synovial membrane (SM) of affected joints in ankylosing spondylitis (AS) is infiltrated by germinal center-like aggregates (foci) of lymphocytes similar to rheumatoid arthritis (RA). We characterized the rearranged heavy chain variable segment (VH) genes in the SM for gene usage and the mutational pattern to elucidate the B lymphocyte involvement in AS. Cryosections from an AS-derived SM were stained for B and T lymphocytes. B cells were isolated from different areas of a focus. The rearranged VH genes were amplified by semi-nested polymerase chain reaction (PCR) using oligonucleotides specific for the six different VH families and heavy chain joining segments (JHs). PCR products were cloned and sequenced.Fifty-nine of 70 different heavy chain gene rearrangements were potentially functional. Most of the rearranged genes were mutated (range, 1-15%). Thirty of 70 products had a mutational pattern typical for antigen selection. Most of the rearranged VH genes belonged to the VH3 family (54%), consistent with data from healthy donors and patients with RA, while VH4 genes, in contrast to RA, were identified less frequently (10%) and VH5 genes were over-represented (11%). In contrast to RA, neither VH6 genes nor the autoimmunity-prone VH4-34 were seen, whereas another autoimmunity-prone gene, V3-23, was predominantly used (11%). One VH1-derived and one VH3-derived B cell clone were expanded. CDR3 were shorter and more variable in length than in RA. Comparable with RA and reactive arthritis, there is a biased repertoire of selected VH genes, whereas the panel of represented genes is different and less clonal expansion was observed.

Show MeSH

Related in: MedlinePlus

The synovial focus. Double-immunohistological staining (anti-CD20 alkaline phosphatase-anti-alkaline phosphatase and anti-CD3 streptavidin biotin horseradish peroxidase reaction) of 8 μm sections from frozen SM obtained by total joint replacement of an AS patient's right hip (B cells, red staining; T cells, brown staining).
© Copyright Policy
Related In: Results  -  Collection


getmorefigures.php?uid=PMC30712&req=5

Figure 1: The synovial focus. Double-immunohistological staining (anti-CD20 alkaline phosphatase-anti-alkaline phosphatase and anti-CD3 streptavidin biotin horseradish peroxidase reaction) of 8 μm sections from frozen SM obtained by total joint replacement of an AS patient's right hip (B cells, red staining; T cells, brown staining).

Mentions: The SM of inflamed peripheral joints in AS (Fig. 1) in certain cases resembles RA with intense mononuclear cell infiltration forming foci similar to germinal centers (GC) that contain B and T lymphocytes as well as plasma cells [2,3]. Recent immunohistologic analysis of five AS SMs demonstrated B cell rich infiltrates in two cases, whereas no B cells were detected in the three others [4].


B lymphocyte involvement in ankylosing spondylitis: the heavy chain variable segment gene repertoire of B lymphocytes from germinal center-like foci in the synovial membrane indicates antigen selection.

Voswinkel J, Weisgerber K, Pfreundschuh M, Gause A - Arthritis Res. (2001)

The synovial focus. Double-immunohistological staining (anti-CD20 alkaline phosphatase-anti-alkaline phosphatase and anti-CD3 streptavidin biotin horseradish peroxidase reaction) of 8 μm sections from frozen SM obtained by total joint replacement of an AS patient's right hip (B cells, red staining; T cells, brown staining).
© Copyright Policy
Related In: Results  -  Collection

Show All Figures
getmorefigures.php?uid=PMC30712&req=5

Figure 1: The synovial focus. Double-immunohistological staining (anti-CD20 alkaline phosphatase-anti-alkaline phosphatase and anti-CD3 streptavidin biotin horseradish peroxidase reaction) of 8 μm sections from frozen SM obtained by total joint replacement of an AS patient's right hip (B cells, red staining; T cells, brown staining).
Mentions: The SM of inflamed peripheral joints in AS (Fig. 1) in certain cases resembles RA with intense mononuclear cell infiltration forming foci similar to germinal centers (GC) that contain B and T lymphocytes as well as plasma cells [2,3]. Recent immunohistologic analysis of five AS SMs demonstrated B cell rich infiltrates in two cases, whereas no B cells were detected in the three others [4].

Bottom Line: In contrast to RA, neither VH6 genes nor the autoimmunity-prone VH4-34 were seen, whereas another autoimmunity-prone gene, V3-23, was predominantly used (11%).CDR3 were shorter and more variable in length than in RA.Comparable with RA and reactive arthritis, there is a biased repertoire of selected VH genes, whereas the panel of represented genes is different and less clonal expansion was observed.

View Article: PubMed Central - HTML - PubMed

Affiliation: Department of Rheumatology, Universitätsklinikum Lübeck, Lübeck, Germany. Jvoswinkel@aol.com

ABSTRACT
The synovial membrane (SM) of affected joints in ankylosing spondylitis (AS) is infiltrated by germinal center-like aggregates (foci) of lymphocytes similar to rheumatoid arthritis (RA). We characterized the rearranged heavy chain variable segment (VH) genes in the SM for gene usage and the mutational pattern to elucidate the B lymphocyte involvement in AS. Cryosections from an AS-derived SM were stained for B and T lymphocytes. B cells were isolated from different areas of a focus. The rearranged VH genes were amplified by semi-nested polymerase chain reaction (PCR) using oligonucleotides specific for the six different VH families and heavy chain joining segments (JHs). PCR products were cloned and sequenced.Fifty-nine of 70 different heavy chain gene rearrangements were potentially functional. Most of the rearranged genes were mutated (range, 1-15%). Thirty of 70 products had a mutational pattern typical for antigen selection. Most of the rearranged VH genes belonged to the VH3 family (54%), consistent with data from healthy donors and patients with RA, while VH4 genes, in contrast to RA, were identified less frequently (10%) and VH5 genes were over-represented (11%). In contrast to RA, neither VH6 genes nor the autoimmunity-prone VH4-34 were seen, whereas another autoimmunity-prone gene, V3-23, was predominantly used (11%). One VH1-derived and one VH3-derived B cell clone were expanded. CDR3 were shorter and more variable in length than in RA. Comparable with RA and reactive arthritis, there is a biased repertoire of selected VH genes, whereas the panel of represented genes is different and less clonal expansion was observed.

Show MeSH
Related in: MedlinePlus