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Biomedical subjects

P Kilian

Publications and source records attributed to P Kilian.

5 recordsLinked to original sources

Failure of IL-1 receptor antagonist and monoclonal anti-IL-1 receptor antibody to inhibit antigen-specific immune responses in vivo.

rIL-1R antagonist (rIL-1ra) and 35F5, a neutralizing mAb, have been shown to inhibit the ability of IL-1 alpha and IL-1 beta to bind to type I but not type II murine receptors. Additionally, IL-1ra and 35F5 inhibit a variety of inflammatory responses in vitro and in vivo. In the present report we have evaluated the activity of human IL-1ra and 35F5 in murine Ag-specific cell-mediated and humoral immune response models. Administration of IL-1ra, either twice daily or as a continuous infusion, did not inhibit the cytolytic T lymphocyte response to allogeneic splenocytes. The CTL response was also not inhibited by daily administration of 35F5. The delayed type hypersensitivity response to oxazolone was similarly refractory to administration of IL-1ra and 35F5. In the humoral immune response models, neither the splenic plaque response to SRBC nor the IgG or IgM response to TNP-keyhole limpet hemocyanin was inhibited by treatment with IL-1ra or 35F5. These data suggest that signaling through the type I IL-1R is not required for these Ag-specific immune responses.

Animals

Differentiation capacity of human non-small-cell lung cancer cell lines after exposure to phorbol ester.

Three cell lines of squamous-cell carcinoma and 3 of large-cell carcinoma origin were investigated for the expression of differentiation markers and functional parameters (proliferation, morphology, cornified envelope formation, involucrin staining, transglutaminase activity, adhesiveness and migration) under normal cell culture conditions and after treatment with the tumor promoter phorbol-12-myristate-13-acetate (PMA). Although all original tumors had been described as poorly differentiated by histological grading, we found significant heterogeneity in the expression of differentiation markers in cell culture. A systematic grading of the cell lines became possible only after PMA stimulation. PMA generally increased expression of differentiation markers in cell lines of comparably low grades of differentiation, as indicated by dose-dependent inhibition of proliferation and cloning efficiency, induction of squamous markers, and decreased adhesiveness and cell motility. In contrast, cell lines of apparently higher differentiation by these criteria showed little response to PMA. The results presented show that the assessment of differentiation capacity by comparison of differentiation markers under normal cell culture and PMA-stimulated conditions in established NSCLC cell lines allows for a refined cell culture grading, which might advance the classification and characterization of such cell lines which, otherwise, appear to be very heterogeneous. It may also help to correlate cellular functions with various states of differentiation in vitro.

Biomarkers, Tumor

Visualization of cytokine and virus receptors common to the immune and central nervous system.

Interleukin 1 (IL-1) and the human retrovirus HTLV-III/LAV represent two distinct molecular and biological constituents that are apparently shared by both the immune and central nervous systems. IL-1 is a cytokine produced principally by monocytes of the immune system and glial cells of brain in situ or in vitro. HTLV-III/LAV represents a unique class of human retrovirus which is the recognized etiological vector of acquired immunodeficiency syndrome (AIDS) which exhibits cellular tropism to helper T lymphocytes or brain by the interactions with an entry protein previously described as the T4 antigen. Autoradiography was used to examine the specific binding distribution of 125I-IL-1 alpha and anti-T4 antibody to rat and squirrel monkey brain sections, respectively. Representative data shows unique neuroanatomical distributions of the IL-1 binding protein (receptor) and the T4 antigen in brain. The autoradiographic study provides a qualitative and quantitative analysis of shared receptors between the immune and nervous systems and offers potential for the discovery of new biological or pathological interactions of these common physiological constituents.

Animals