Rheumatology 2000; 39: 1280-1285
© 2000 British Society for Rheumatology
Grand Rounds in Rheumatology |
Do B cells influence disease progression in chronic synovitis? Lessons from primary hypogammaglobulinaemia
Rheumatology Unit, GKT, Guys, Kings and St Thomas Hospitals, School of Medicine and Dentistry, London and
1 Rheumatology Unit, Norfolk & Norwich Hospital, Norwich, Norfolk, UK
Abstract
We describe a 62-yr-old male patient with primary hypogammaglobulinaemia (PH) who fulfilled the 1987 American Rheumatism Association/American College of Rheumatology revised diagnostic criteria for rheumatoid arthritis (RA) but, despite persistent symmetrical synovitis, did not develop erosions. Virology studies and blood and synovial fluid (SF) cultures were consistently negative; a search for crystals in the SF was unrevealing. Peripheral blood (PB) B cells were absent, whilst the PB CD3+ cell count was normal. The ratio of naive (CD45RA+) to memory (CD45R0+) cells was also normal (1:1) but the CD4:CD8 ratio was reversed. To our knowledge, this is the first report which combines the immunophenotypic analysis of the PB with that of the SF and synovial membrane (SM). This confirmed the absence of B cells and the reversed CD4:CD8 ratio. However, as in other chronic arthropathies, the SF and SM cellular infiltrate consisted almost exclusively of memory T cells, consistent with the preferential localization of this subset to inflamed tissues. This case indicates that synovitis can proceed persistently in the absence of B cells and that the migratory mechanisms of T cells are not altered. However, the case suggests that the absence of B cells and negativity for rheumatoid factor, combined with an increased presence of CD8+ (suppresser/cytotoxic) T cells in the joint, might contribute to the non-erosive nature of the synovitis.
KEY WORDS: Hypogammaglobulinaemia, Chronic arthritis.
Notes
Correspondence to: C. Pitzalis, Rheumatology Unit, 5th Floor, Thomas Guy House, Guy's Hospital, London SE1 9RT, UK.