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Biomedical subjects

K Bendtzen

Publications and source records attributed to K Bendtzen.

At least 307 records · Page 17Linked to original sources

Mechanism of action of cyclosporin A. Effect on T-cell-binding of interleukin 1 and antagonizing effect of insulin.

Previous studies have shown that cyclosporin A (CyA) prevents the elaboration of the lymphokine leucocyte migration inhibitory factor (LIF). Since LIF production is interleukin 1 (IL-1)-dependent, we carried out experiments using partially and highly purified IL-1 preparations to study the effect of CyA. We found that (a) IL-1 was consistently depleted during a 1-h incubation with human blood T lymphocytes but not with B lymphocytes or erythrocytes; (b) the depletion could not be ascribed to pinocytosis, cell functions requiring active metabolism, or enzyme-mediated destruction of IL-1; (c) CyA, but not biologically inactive cyclosporin, antagonized the apparent absorption of IL-1; (d) T cells pre-exposed to CyA were rendered incapable of removing the monokine; and (e) CyA was capable of displacing IL-1 once absorbed by T cells. Because the putative binding of IL-1 showed saturability, reversibility (with CyA as a probe), and tissue specificity consistent with a known target for the monokine, we propose that IL-1 interacts with a receptor-like structure on T cells. Finally, we found that insulin interfered with the function of CyA at the very early macrophage-T-cell co-operative stage, even at physiological concentrations.

Absorption↗

Effects of leukotrienes on neutrophil migration, and on production and action of lymphokines.

The effect of the leukotrienes LTB4, LTC4 and LTD4 on the production of the lymphokine leukocyte migration inhibitory factor (LIF) from human peripheral blood mononuclear cells was tested. LTC4 and LTD4 failed to influence LIF production by cells stimulated by antigen or the polyclonal T cell activator, phytohemagglutinin (PHA). LTB4, at concentrations 10(-7) to 10(-6) M, showed significant inhibition of antigen-induced LIF production but was without effect when cells were stimulated by PHA. The cell levels of cyclic adenosine monophosphate (cAMP) were unaffected by 2.5 X 10(-7) M LTB4 in the absence or presence of theophylline. These results indicate that LTB4 acts on the early effector stage of the immune response without affecting the cellular cAMP content.

Antibody Formation↗

Lack of evidence for human lymphokines with thrombocyte aggregating activity. An in vitro study.

The ability of human lymphocytes to produce soluble mediator(s) with thrombocyte aggregating activity (TAA) was investigated in an in vitro technique. Isolated human mononuclear cells were stimulated with phytohaemagglutinin or purified protein derivative of tuberculin. The supernatants were investigated for lymphokine activity in a leucocyte migration inhibitory factor assay. Supernatants were then tested for their ability to aggregate human thrombocytes, and in contrast to the results of previous studies, we were not able to demonstrate any TAA. Most likely, lymphokines with TAA are not involved in the thrombotic processes seen in human cell-mediated immune inflammatory reactions.

Adenosine Diphosphate↗

Diagnosis of Hodgkin's disease hampered by an Epstein-Barr virus infection treated with acyclovir.

We report a case of Hodgkin's disease associated with Epstein-Barr virus (EBV) infection in a 75-year-old male. The patient was given a 5-day course of acyclovir to which he responded well, with partial resolution of the lymphoma and return to well-being. A biopsy from the lymphoma after acyclovir treatment showed a change in the histological picture with a reduction in the number of giant cells. Relationships between EBV infection and Hodgkin's lymphoma are discussed.

Acyclovir↗

A standardized human T-lymphocyte proliferation assay for detecting soluble accessory factors from monocytes. I. Monocyte and monokine requirements.

Monocyte (M phi-) depleted human peripheral blood mononuclear cells exhibit reduced capacity to proliferate, when stimulated with low doses of phytohaemagglutinin (PHA). Stimulation with higher doses of the mitogen or addition of graded numbers of autologous M phi's potentiated the response proportionally, and 10% M phi's restored the response completely. Addition of only 0.1% M phi's was needed for potentiating the response significantly. Pretreatment of M phi's with Actinomycin-D or heating impaired the accessory effect, whereas x-irradiation had no effect. The presence of M phi's did not influence the viability of the proliferating lymphocytes. Crude supernatants from M phi-cultures, even at very low concentrations, partly restored the PHA response, as did preparations of highly purified human Interleukin-1.

Cell Communication↗

Lymphocyte function and chromosome aberrations in patients with early mycosis fungoides and parapsoriasis en plaques.

Thirteen patients with stage I or II mycosis fungoides (MF) and 10 patients with large-plaque parapsoriasis en plaques (PEP) were examined for immunologic and cytogenetic disturbances. Total lymphocyte counts and immunoglobulin concentrations in the blood were normal. In vitro lymphocyte responses to polyclonal activators and various antigens in standard concentrations were normal. However, titration of phytohemagglutinin and concanavalin A (ConA) disclosed significantly lowered responses to suboptimal concentrations in the patient group, most pronounced in patients with MF II. ConA-induced leukocyte migration inhibitory factor (LIF) production, tested in an indirect leukocyte migration inhibitory assay, was low in the patient group. Furthermore spontaneous LIF production in vitro and small amounts of serum LIF were demonstrated in a few patients. The chromosomal banding pattern, sister chromatid exchange, and break frequency were within normal limits except for 3 translocations in the MF group. It is concluded that even in early-stage MF a pathologic function of blood lymphocytes can be demonstrated, when sensitive methods are applied. The findings might be important for monitoring disease activity and effect of treatment.

Adult↗

Specific cellular immunity in acoustic neuroma patients.

An indirect leukocyte migration agarose technique to detect cell-mediated immunity was modified to obtain a specific assay for release of human leukocyte migration inhibitory factor. Acoustic neuroma patients exhibited a significant cellular immune response against acoustic neuroma extract (P less than .01) as well as perilymph from acoustic neuroma patients (P less than .01) when compared to healthy control persons. All 19 patients tested reacted to acoustic neuroma extract. Seven of 21 perilymph samples did not elicit migration inhibition. Crossover determination of antigenicity of two negative and four positive perilymph samples against three patients revealed highly reproducible results, uncorrelated to perilymph concentration of potassium and protein. Flow cytofluorometry did not reveal malignant DNA patterns in 10 acoustic neuromas examined. Immunofluorescence studies did not reveal autoantibodies against acoustic neuromas in sera from 11 patients. The responsible antigen(s), the mechanism of immunization, and the diagnostic implications remain to be determined.

Adult↗

Immunosuppressive actions of gold salts.

In rheumatoid arthritis both lymphocyte-mediated and antibody-mediated immune reactions are important for the inflammatory lesions. In vivo activated B lymphocytes/plasma cells, T lymphocytes and monocytes/macrophages (Mo) are intimately involved in the disease process. Several clinical observations suggest an immunosuppressive action of gold salts. In humans, gold salts interfere with a number of Mo functions in vitro, including cellular interactions between Mo and T lymphocytes. Some workers have shown that the activation of human T lymphocytes is inhibited by gold salts, most probably secondary to an inhibition of Mo-T cell cooperation. Recent experiments indicate that gold salts also affect the in vitro differentiation of human B lymphocytes in response to polyclonal activators. Both the gold atom and the SH group seem to be important for the immunosuppressive actions of gold salts.

Anti-Inflammatory Agents↗

Effects of cyclosporin A (CyA) and methylprednisolone (MP) on the immune response. II. Further studies of the monocyte - T cell interactions leading to lymphokine production.

The immunosuppressive drugs cyclosporin A (CyA) and methylprednisolone (MP) abolished the elaboration of the lymphokine leukocyte migration inhibitory factor (LIF) by mononuclear cells challenged by recall antigen. Suppression in both cases was reversible upon removal of the drugs, and participation of T suppressor cells of their mediators could not be demonstrated. The CyA-induced effect was exerted in the early stage of lymphocyte activation (less than 60 min), whereas MP still inhibited LIF release when added 60 min after the antigen. In contrast to earlier findings that the drugs failed to affect the release of T cell-activating factor (TAF) and lymphocyte-activating factor (LAF) from macrophages (M-phi's) stimulated by phorbol myristate acetate. MP (but not CyA) markedly reduced TAF production by M-phi's incubated with tuberculin. M-phireover, partially purified TAF and LAF both restored LIF production in the presence of CyA (but not MP), an effect not mimicked by the T cell product T cell growth factor. However, suppression by both drugs was abrogated by exogenous cGMP. Hence, CyA seems to obstruct the interaction between TAF/LAF and the immune T cell, whereas MP affects antigen-induced T cell activation at the Mo level as well as the level of lymphokine production and/or release. The effects of both drugs seem related to intracellular events involving cGMP.

Adult↗

Studies on the active site of human leukocytic pyrogen.

Leukocytic pyrogen, a polypeptide produced by phagocytic mononuclear cells, is thought to be the endogenous mediator of fever. In addition to its effects on thermoregulation, leukocytic pyrogen has been shown to induce synthesis of acute-phase proteins, increase lymphocyte blastogenesis to mitogens, and cause release of neutrophil-specific granule contents. Despite its important role in biologic responses, little is known concerning the structure-function relationship of the molecule. In the present studies several protein-modifying conditions were used in order to examine specific amino acid participation at the active site. Because the state of purity of leukocytic pyrogen may be critical during certain reaction conditions, highly purified preparations were used. Experiments suggest that the active site requires the gamma-carboxyl group of glutamic acid and that blocking arginine reduces both the pyrogenic and neutrophil releasing properties of the molecule. Other studies demonstrate that the pyrogenicity of human leukocytic pyrogen is not due to serine esterase or carboxypeptidase B activity and that the 15,000-dalton molecule may be a glycoprotein. These experiments provide further evidence that the lymphocyte-activating and neutrophil-granule-releasing properties of human leukocytic pyrogen require the same active site which produces fever.

Arginine↗

Effects of cyclosporin A (CyA) and methylprednisolone (MP) on the immune response. I. T-cell-activating factor abrogates CyA- but not MP-induced suppression of antigen-induced lymphokine production.

The influence of cyclosporin A (CyA) and methylprednisolone (MP) on the elaboration of the human lymphokine, leukocyte migration inhibitory factor (LIF) was investigated. Both CyA and MP at pharmacological concentrations inhibited the release of LIF from immune lymphocytes challenged by recall antigen. By contrast, the release of LIF in response to polyclonal activation by phytohaemagglutinin A was not affected by CyA or by MP. CyA and MP had no effect on the production of the monokine, T-lymphocyte-activating factor (TAF) by stimulated blood monocytes. However, addition of partially purified TAF to antigen-stimulated lymphocytes completely abrogated the inhibitory effect of CyA, but not that of MP. Thus, CyA and MP affect antigen-induced production of LIF by immune lymphocytes by different mechanisms.

Adult↗

Effect of cyclosporin A (CyA) on the immune response. CyA competitively inhibits the function of monocyte/macrophage-derived T-lymphocyte-activating factor(s).

The mechanism of action of the immunosuppressive drug, cyclosporin A (CyA), was analyzed with respect to antigen-induced production of the human lymphokine, leukocyte migration inhibitory factor (LIF). Mononuclear cells as well as purified T-cells did not elaborate LIF in the presence of pharmacological concentrations of CyA. CyA-induced immunosuppression was competitively reversed by addition of the partially purified monokines, T-cell-activating factor (TAF) and lymphocyte-activating factor (LAF). CyA did not affect T-cell priming with antigens. The drug failed to abolish LIF production if added 60 min after challenge of T-cells with recall antigen in the presence of TAF. Furthermore, addition of TAF within 15 min to CyA-treated T-cells resulted in unaltered LIF production. These results suggest that CyA suppresses the early stage of the immune response by competing with the function of TAF/LAF on the immune T-cell.

Adult↗