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Interaction between the Immune System and
Tumor Cells: Cutaneous Disorders as a
Consequence of Autoimmunity and
Immunosuppression
M. LAIMER, C. M. LANSCHUETZER, AND H. HINTNER
Department of Dermatology, Paracelsus Private Medical University, Salzburg, Austria
ABSTRACT : The interaction between the immune system and tumor cells is dis-
cussed with regard to examples of lymphoproliferative disorders associated
with autoimmune phenomena, immunosuppression favoring tumorigenic in-
fections, and a new therapeutic modality whereby a drug-induced Th1 immune
response leads to complete regression of skin tumors.
KEYWORDS : autoimmunity; lymphoproliferative disorders; skin tumors;
immunosuppression
AUTOIMMUNITY
Pemphigus diseases are characterized by blistering, erosions, acantholysis, and
autoantibodies against structural proteins of desmosomes (FIG . 1).1,2 The qualitative
and quantitative pathogenic significance of pemphigus autoantibodies has been
demonstrated by antibody transfer and knockout mice experiments. Although shar-
ing several aspects with classical pemphigus, paraneoplastic pemphigus (PNP) is a
distinct, heterogeneous autoimmune syndrome associated with severe ulceration of
mucosae and polymorphous skin lesions with a mononuclear infiltrate, occuring
within the context of mainly hematological malignancies (non-Hodgkins lymphoma,
chronic lymphocytic lymphoma, Castleman`s disease, etc.). There is evidence that
the pathogenic mechanism in PNP comprises both humoral and cellular autoimmu-
nity: Autoantibodies directed against desmogleins (Dsg1 and Dsg3) and intracellular
proteins of the plakin family (desmoplakins I and II, BP230, envoplakin, periplakin)
may emerge from autoreactive clones of lymphoma cells, or reflect a cross-reactive
antitumor response (molecular mimicry) or a dys
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