Anti-MALT1 monoclonal antibody, clone 50

NF-kappa B is an important transcription factor in the immune system, and aberrant NF-kappa B activity contributes to malignant diseases and autoimmunity. In T cells, NF-kappa B is activated upon TCR stimulation, and signal transduction to NF-kappa B activation is triggered by a cascade of phosphorylation events. However, fine tuning and termination of TCR signaling are only partially understood. Phosphatases oppose the role of kinases by removing phosphate moieties. The catalytic activity of the protein phosphatase PP2A has been implicated in the regulation of NF-kappa B. PP2A acts in trimeric complexes in which the catalytic subunit is promiscuous and the regulatory subunit confers substrate specificity. To understand and eventually target NF-kappa Bspecific PP2A functions it is essential to define the regulatory PP2A subunit involved. So far, the regulatory PP2A subunit that mediates NF-kappa B suppression in T cells remained undefined. By performing a siRNA screen in Jurkat T cells harboring a NF-kappa B-responsive luciferase reporter, we identified the PP2A regulatory subunit B56 gamma as negative regulator of NF-kappa B in TCR signaling. B56 gamma was strongly up-regulated upon primary human T cell activation, and B56 gamma silencing induced increased I kappa B kinase (IKK) and I kappa B alpha phosphorylation upon TCR stimulation. B56 gamma silencing enhanced NF-kappa B activity, resulting in increased NF-kappa B target gene expression including the T cell cytokine IL-2. In addition, T cell proliferation was increased upon B56 gamma silencing. These data help to understand the physiology of PP2A function in T cells and the pathophysiology of diseases involving PP2A and NF-kappa B.

An 80-year-old man presented with the accumulation of pleural fluid in the right thoracic cavity. Serum electrophoresis revealed an M-component and immunofixation confirmed IgM/.. The level of IgM was 1,526 mg/dL. Imaging studies showed an infiltrative condition of the ipsilateral lung parenchyma. The fluid contained abundant neoplastic cells with the morphological and immunophenotypic features of plasma cells, which expressed IgM/. monoclonal immunoglobulins on the cell surface and in the cytoplasm. The karyotype was 48,XY,+3, add(9)(p13),+12,add(14)(q32),del(16)(q22),-18,+mar,and a series of fluorescence in situ hybridization studies demonstrated that the add(14) chromosome represented der(14) t(14;18)(q32;q21), at which the MALT1-immunoglobulin heavy-chain (IGH) fusion gene was localized. A long-distance polymerase chain reaction amplified the fragment encompassing the two genes, showing that the junction occurred at the J6 segment of IGH and 3.7-kb upstream of the MALT1 breakpoint cluster. We propose that this case represents an extreme form of the plasmacytic differentiation of extranodal marginal zone lymphoma that developed in the lung.