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Abstracts (complete list) - Wissenschaft Online

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Stephan Borte, Uwe Gerd Liebert, Michael Borte, Ulrich Sack<br />

Long-term cell-mediated immunity following vaccination with<br />

live, attenuated measles-mumps-rubella-vaccine in children<br />

with juvenile idiopathic arthritis under treatment with lowdose<br />

Methotrexate and/or tumour necrosis factor α receptor<br />

antagonist<br />

Juvenile idiopathic arthritis (JIA) represents a heterogeneous group of disorders<br />

characterized by chronic inflammatory arthritis and turns out to be the commonest<br />

rheumatic disease seen in childhood worldwide. The multidisciplinary management of<br />

JIA is founded on anti-inflammatory and immunomodulating drugs. However, infection<br />

is one of the leading causes of morbidity and mortality in JIA. The risks of serious<br />

adverse events following vaccination and the immunogenicity of vaccines at all have<br />

been a matter of controversy and there is some reluctance to vaccination that need to<br />

be enlightened. We intended to display the course of humoral and cell-mediated<br />

immunity to measles-mumps-rubella-vaccination (MMR) in healthy children and<br />

adolescents and to evaluate potential influences of low-dose Methotrexate therapy and<br />

Etanercept treatment in JIA on success of immunisation and maintenance of long-term<br />

immunity. Therefore, production of IFNγ by T memory cells upon in vitro stimulation<br />

with measles, mumps and rubella antigens and seroprevalence of virus-specific IgG<br />

antibodies were investigated in PBMC and plasma from 16 healthy children and 16<br />

children with JIA, being treated with low-dose Methotrexate or in combination with<br />

Etanercept. Our results indicate that MMR-vaccination induced immunity in childhood is<br />

characterized by steady decline of humoral immunity and development of long-term cellmediated<br />

immunity. Low-dose MTX therapy following <strong>complete</strong>d MMR-vaccination was<br />

proved not to hamper Th1-like cell-mediated immunity in vitro. Furthermore, neither<br />

low-dose MTX nor Etanercept treatment during the course of vaccination showed to<br />

markedly interfere with intended outcome of immunisation and generation of long-term<br />

cell-mediated immunity to MMR. No cases of serious adverse events following MMRvaccination<br />

were observed. In conclusion, these results argue for MMR-vaccination in<br />

children with JIA using live, attenuated vaccines to ensure protection from infection and<br />

to prevent morbidity and mortality related to this diseases.

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