Polyarthritis in a patient with common variable immunodeficiency: a case
report
Kryštůfková O.1, Růžičková Š.1, Vlková M.2, Wiesnerová R.3, Gatterová J.1, Kramářová Z.1, Půtová I.1, Vencovský J.1
1Revmatologický ústav, Praha, 2Ústav klinické imunologie a alergologie FN, Brno, 3Revmatologická ambulance nemocnice, Kolín |
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Summary:
The authors present here a case report of 50-years old patient with common variable immunodeficiency
(CVID). She developed polyarticular arthritis that was coincident with multiple vaccinations (given from professional
reasons). CVID was diagnosed at the age of 42 years on the basis of recurrent pneumonias, urinary
tract infection, asymptomatic abscess in the small pelvis, and low levels of immunoglobulins: IgG (2.6 g/l) and
IgA (0.5 g/l). Further, she developed insufficient specific autoantibody response after vaccinations against
hepatitis A and enteroviruses infections (poliomyelitis). The regular replacement treatment with intravenous
immunoglobulins (IVIG) was initiated in a dose of 350-400 mg per kg and month. Severe polyarthritic syndrome
with clinical and radiological manifestations resembling rheumatoid arthritis (RA) developed at the
age of 46 years. Except for rheumatoid factor (RF), ACR criteria of RA were fulfilled. Ureaplasma polyarthritis
was considered and further excluded by therapeutical test with antibiotics. Efficacy of corticosteroids and
antimalarials was insufficient, and sulphasalazine had to be withdrawn due to gastrointestinal intolerance.
Since the disease activity was high (DAS = 6.95), methotrexate was added and good effect has been achieved
(DAS response = 3.73, actual DAS = 3.15). In this context, corticosteroid treatment could be finished. Despite
of full IVIG substitution during the 4-years of follow-up, recurrent infections of urinary tract appeared leading
to methotrexate withdrawal. It caused further polyarthritis outbreak for that methotrexate was again
added after 6 months. In this paper, putative contribution of vaccine administration to the onset of polyarthritis
is discussed, particularly, with respect to genetic predisposition in a patient with positive family history
of a father having RA and genotype HLA-DRB1*0101 and IL-1RN*2, both predisposing to autoimmune
diseases and severe course of polyarthritis. Furthermore, risks of opportunistic infections and possible intensification
of antibody immunodeficiency in patients with basal treatment of polyarthritis are discussed.
Key words:
common variable immunodeficiency, rheumatoid arthritis, vaccination, shared epitope methotrxate
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