In paraneoplastic neurological syndromes (PNS), ectopic expression of
onconeural antigens by the tumor triggers an immune response that not
only reacts with the tumor but also with the same antigens expressed in
the nervous system. This immune response inhibits tumor growth. However,
the price of tumor control is high, as PNS are devastating neurological
syndromes leaving most of the patients severely disabled within a few
months. One of the most frequently involved tumors is small cell lung
cancer (SCLC), and approximately 50% of patients with PNS and SCLC have
high-titer antibodies against the onconeural Hu-antigens (anti-Hu).
Previous studies have clearly demonstrated that anti-Hu antibodies do
not play a pathogenic role in Hu-PNS and tumor control, but rather are a
useful diagnostic marker. Therefore, a role for the cellular immune
system in the pathogenesis of PNS is hypothesized. In this thesis the
role of T cells in PNS was investigated by studying CSF and blood of
Hu-PNS patients. This role of T cells was confirmed by (i) 4-fold higher
T lymphocyte numbers in CSF of Hu-PNS patients compared to controls;
(ii) association of Hu-PNS with HLA-DQ2 and HLA-DR3; and (iii)
neurological improvement or stabilization upon treatment with hCG.
However, the presence of HuD-specific CD8+ T cells in CSF could not be
demonstrated. Therefore, more research is required to either confirm or
reject a role for T lymphocytes in Hu-PNS.
http://repub.eur.nl/res/pub/30676/111005_Graaf%2C%20Marieke%20Theodora%20de.pdf
http://repub.eur.nl/res/pub/30676/111005_Graaf%2C%20Marieke%20Theodora%20de.pdf
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