N. Pipitone et al., Do B cells influence disease progression in chronic synovitis? Lessons from primary hypogammaglobulinaemia, RHEUMATOLOG, 39(11), 2000, pp. 1280-1285
We describe a 62-yr-old male patient with primary hypogammaglobulinaemia (P
H) who fulfilled the 1987 American Rheumatism Association/American College
of Rheumatology revised diagnostic criteria for rheumatoid arthritis (RA) b
ut, despite persistent symmetrical synovitis, did not develop erosions. Vir
ology 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 (CD45RO(+)) cells was also normal (1:1
) but the CD4:CD8 ratio was reversed. To our knowledge, this is the first r
eport which combines the immunophenotypic analysis of the PB with that of t
he SF and synovial membrane (SM). This confirmed the absence of B cells and
the reversed CD4:CD8 ratio. However, as in other chronic arthropathies, th
e SF and SM cellular infiltrate consisted almost exclusively of memory T ce
lls, consistent with the preferential localization of this subset to inflam
ed 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 negati
vity for rheumatoid factor, combined with an increased presence of CD8(+) (
suppresser/cytotoxic) T cells in the joint, might contribute to the non-ero
sive nature of the synovitis.