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Biomedical subjects

G Biberfeld

Publications and source records attributed to G Biberfeld.

At least 199 records · Page 11Linked to original sources
PubMed1983

Characterization of malignant and non-neoplastic cell phenotypes in highly malignant non-Hodgkin lymphomas.

Malignant and non-neoplastic cells in 38 cases of highly malignant non-Hodgkin lymphomas: 3 centrocytic anaplastic, 18 centroblastic, 13 immunoblastic and 4 lymphoblastic (according to the Kiel classification) were immunophenotyped in cryosections and cell suspensions by means of monoclonal antibodies. Additionally, cell cycle analysis on cell suspensions was performed by DNA flow cytofluorometry. In 33 (87%) lymphomas the malignant cells expressed monoclonal surface immunoglobulin (Ig), which indicated B-cell origin of tumors. In 7 of the 19 B-cell lymphomas tested by the peroxidase-antiperoxidase method, cytoplasmic Ig was found. Four lymphomas were of T-cell and one of non-B/non-T-cell origin. In II B-cell and 2 lymphoblastic non-B-cell tumors, common acute lymphoblastic leukemia antigen (CALLA) was found. In 25 of 30 studied NHL the malignant cells expressed receptor for transferrin and in 19 of 28 cases a high percentage of cells in S-phase (greater than 10.85%) was found. Number and distribution as well as type of non-B-cells infiltrating B-cell-derived lymphomas varied considerably from case to case. Among these cells Leu 3+ (T helper/inducer) cells predominated. Leu 2+ (T suppressor/cytotoxic) and Leu 7+ (natural killer and killer) cells constituted less numerous groups. Correlation of cytodiagnostic analyses with clinical observations indicates that high content of infiltrating T cells may be a favorable prognostic feature in highly malignant B-cell lymphomas.

Adolescent↗
PubMed1983

Autoantibodies against the basal cell layer: an association with chronic hepatitis B.

The presence of antibodies against the basal cells of squamous epithelium (BCL-Ab) was studied by indirect immunofluorescence in Rumanian and Swedish carriers of hepatitis B surface antigen (HBsAg), in patients with acute viral hepatitis (AVH), chronic liver diseases (CLD), and various other diseases, and in apparently healthy subjects. Titers of BCL-Ab greater than or equal to 40 were found in 8% of 320 HBsAg carriers, in 20% of 292 patients with CLD associated with HBsAg, and in 2% of 816 patients with HBsAg-negative CLD. BCL-Ab were not found in 167 patients with AVH, nor in 1389 patients with various nonhepatic conditions, nor in 344 apparently healthy subjects. These data indicate an association of BCL-Ab with CLD predominantly of hepatitis B etiology. Possibly hepatitis B virus may induce a form of liver metaplasia with the expression of an antigen with a specificity in common with the regenerative layer of basal cells in the squamous epithelium.

Autoantibodies↗
PubMed1983

Mitogen-induced switching of immunoglobulin heavy-chain class secretion in chronic B-lymphocytic leukaemia and immunocytoma cell populations.

Lymphocytes from peripheral blood, bone marrow, and lymph nodes from six patients with chronic B-lymphoproliferative disease were studied. Two of the patients had a polymorphic immunocytoma with surface membrane immunoglobulin phenotype mu kappa. Four patients had chronic B-lymphocytic leukaemia (CLL) with the phenotypes mu kappa, mu delta kappa, mu lambda, and mu delta lambda, respectively. In no case did the monoclonal cell populations express gamma chains on the surface, and none produced monoclonal immunoglobulin in vivo. The malignant B lymphocytes were cultured in the presence of polyclonal B-cell activators. Immunoglobulin secretion was detected with the protein A plaque assay and with a modification of the reversed haemolysis-in-agar plaque assay. Immunoglobulin secretion was induced in four of the cell populations. In both the immunocytomas and in one of the CLL cell clones the heat-inactivated Staphylococcus aureus strain Cowan I induced secretion of IgG, as well as IgM, associated only with the same light chain as was expressed on the surface of the unstimulated cells. Thus, mitogens can induce immunoglobulin secretion in vitro in malignant B lymphocytes, and Cowan I bacteria also have the ability to induce a switch of immunoglobulin production from IgM to IgG in a fraction of the leukaemic cell populations.

Adult↗
PubMed1983

T-lymphocyte subpopulations in relation to immunosuppression in measles and varicella.

Patients with measles or varicella were studied during the acute phase (first week) of illness and, after recovery, by lymphocyte stimulation tests and determination of T-lymphocyte subpopulations, using the monoclonal antibodies Leu 2a and Leu 3a directed at the suppressor/cytotoxic and the helper T-cell subsets, respectively. Low proliferative responses to phytohemagglutinin were found during the acute phase of both diseases. The response to purified protein derivate of tuberculin was also low in all measles patients tested and in some of the varicella patients. In both infections increased spontaneous DNA synthesis was demonstrated. In the acute phase of measles there was T lymphocytopenia but no change of the ratio between T lymphocytes of helper and suppressor/cytotoxic cell phenotypes. In the acute phase of varicella the percentage and the absolute number of Leu 2-positive (suppressor/cytotoxic) T cells were increased. Measurement of the size of the lymphocytes indicated activation of this subset. Cryopreserved blood mononuclear cells from the acute phase of varicella could suppress the phytohemagglutinin response of autologous convalescent-phase cells. This was not seen when cells from measles patients were tested. The suppression of the lymphocyte stimulation response in varicella is probably in part caused by activation of suppressor cells, whereas the suppression of the stimulation response in measles seems to be due mainly to other mechanisms.

Adolescent↗
PubMed1983

Specific and non-specific B cell activation in measles and varicella.

Lymphocytes from eight patients with measles and six patients with varicella were studied during the acute phase (first week) of illness and after recovery for spontaneous and pokeweed mitogen (PWM)-induced production of immunoglobulins (Ig) and viral antibodies by an enzyme linked immunosorbent assay (ELISA). In both infections acute phase lymphocytes showed increased spontaneous in vitro IgM and IgG productions including IgM and IgG antibodies to the aetiological virus as well as IgG antibodies to unrelated viruses (varicella, measles, rubella and mumps) to which the patient had serum antibodies. PWM induced no further Ig synthesis in the acute phase. In the convalescent phase viral antibody production could be demonstrated only in PWM stimulated cultures. In four patients the spontaneous synthesis of antibodies to a non-aetiological virus seemed to precede the production of IgG antibodies to the aetiological virus. All patients showed an increase of ELISA determined serum antibodies to the aetiological virus from the acute to the convalescent phase. Three of seven measles patients also showed a minor but significant increase or decrease of serum IgG antibodies to varicella and one of six varicella patients a significant rise of serum IgG antibodies to measles. Thus both measles and varicella infections were associated with non-specific as well as specific B cell activation. The non-specific B cell activation may be induced by non-specific helper factors from activated T cells.

Adolescent↗
PubMed1982

T lymphocyte subpopulations defined by monoclonal antibodies and FC receptor binding in relation to immunosuppression in vaccine-induced rubella infection.

Lymphocyte stimulation tests and determination of T lymphocyte subpopulations were undertaken before and 7-11 days after rubella vaccination of healthy subjects. The proliferatory response of blood mononuclear cells to phytohemagglutinin (PHA) and purified protein derivate was suppressed after vaccination, as was the immunoglobulin production of pokeweed mitogen (PWM) stimulated cultures. After removal of phagocytic cells the response to PHA was still suppressed after vaccination in most cases, but when the cultures were depleted of non-T lymphocytes the suppression was no longer demonstrable. The proportion of T lymphocytes with receptors for the Fc part of IgG increased after vaccination, whereas there was no significant change of the T lymphocyte subpopulations identified with monoclonal antibodies directed at the suppressor/cytotoxic or helper T cell subsets.

Adolescent↗
PubMed1982

Radiosensitive t cell suppression in relation to the TG cell level in synovial fluid of patients with rheumatic disease.

Radiosensitive T cell suppression was studied in relation to the level of T cells with IgG-Fc receptor (TG cells) in synovial fluid and blood of nine patients with rheumatic diseases. Irradiation of T cells significantly decreased the proportion of TG cells in the blood of patients and healthy controls. The proportion of synovial TG cells was low in all patients before as well as after irradiation. Irradiation enhanced the helper effect of T cells on pokeweed-mitogen induced immunoglobulin production by allogeneic B cells. This increased helper effect was taken as an expression of decreased suppressor activity following irradiation. By this method suppressor activity was demonstrable in synovial T cells of six out of nine patients and in blood T cells of six out of eight patients and six out of eight healthy subjects. Thus the low level of synovial TG cells was in most patients not associated with a lack of radiosensitive synovial suppressor cell activity.

Adult↗
PubMed1982

T lymphocyte subpopulations defined by monoclonal antibodies in synovial fluid of patients with rheumatic disease.

The proportion of T lymphocytes reacting with monoclonal antibodies to suppressor or helper T cell subsets and the proportion of T lymphocytes with Fc receptors for IgG or IgM were determined in synovial fluid and blood of 16 patients with rheumatic diseases including rheumatoid arthritis (RA), psoriatic arthritis, ankylosing spondylitis and juvenile rheumatoid arthritis. The percentage of T cells reacting with monoclonal antibodies (Leu 2a or OKT 8) directed at the suppressor/cytotoxic T cell subpopulation, was significantly higher in synovial fluid than in blood of patients or healthy donors. Monoclonal antibodies (Leu 3a or OKT 4) with specificity for the helper T cell subpopulation, reacted with a lower percentage of synovial T cells than of blood T cells of patients or controls. This distribution pattern was found in patients with RA as well as in the other patients with chronic arthritis. The percentage of T cells with Fc-IgG receptors (TG cells) was much lower in synovial fluid than in blood of patients or controls. Thus, in synovial fluid the percentage of T cells reacting with monoclonal antibody to the suppressor/cytotoxic cell subset was fairly high (mean 45%) whereas the proportion of TG cells, considered to represent suppressor cells, was low (mean 4%).

Adult↗
PubMed1980

Immunosuppression and alterations of T-lymphocyte subpopulations after rubella vaccination.

Lymphocyte stimulation tests and determinations of T-lymphocyte subpopulations were undertaken in 11 subjects before and after rubella vaccination and in 11 controls. The lymphocyte stimulation response to phytohemagglutinin was suppressed 7 to 10 days after vaccination. The proportion of T lymphocytes with receptors for the Fc part of immunoglobulin G increased after vaccination, whereas there was no significant change in the proportion of T lymphocytes with immunoglobulin M-Fc receptors.

Adolescent↗
PubMed1980

Subpopulations of T lymphocytes in patients with ankylosing spondylitis.

Subpopulations of human blood T lymphocytes were determined in 20 patients with ankylosing spondylitis and in 20 healthy individuals. The proportion of T lymphocytes with receptors for the Fc portion of IgG (TG cells) was increased in 9 patients. The proportion of T lymphocytes bearing receptors for the fc portion of IgM (TM cells) was within the range found in healthy controls in all but 4 patients, who had a decreased level of TM cells.

Adult↗
PubMed1980

Suppressor T cells in mycosis fungoides and so-called premycotic eruptions.

The proportions of suppressor T cells (TG) and helper T cells (TM) were determined in 5 patients with Mycosis fungoides (MF), 4 patients with parapsoriasis en plaques/poikiloderma atrophicans vasculare and 3 patients with generalized chronic dermatitis. All the MF patients showed increased proportions of suppressor T cells, whereas the others did not differ from age- and sex-matched healthy controls.

Adult↗
PubMed1980

A T lymphocyte subpopulation in multiple sclerosis patients bearing Fc receptors for both IgG and IgM1.

Abnormally low proportions of total T lymphocytes were found in peripheral blood lymphocytes (PBL) of patients with multiple sclerosis (MS) accompanied by high proportions of T lymphocytes with Fc receptors (FcR) for IgG (T gamma cells). Seventy-five percent of the MS patients had greater than 40% T gamma in the T lymphocyte-enriched population. In 6 out of 16 cases, T mu were also elevated. This elevation, however, did not seem to correlated with disease stage. By mixed rosetting and direct observation with an indirect immunofluorescence test, 30 to 50% of the T gamma cells in MS PBL were also shown to bear FcR for IgM. This population bearing FcR for IgG and IgM, designated T gamma mu, was usually found to be 10% or less of the T gamma population in normal controls. The significance of this T gamma mu population for the MS disease process requires further evaluation.

Adult↗
PubMed1980

Identification of three FcR-positive T cell subsets (T gamma, T mu and T gamma mu) in the cerebrospinal fluid of multiple sclerosis patients.

Proportions of T cells and T cell subsets, as identified by their Fc receptors (FcR) for IgM and IgG (Tmu and T gamma), were determined in the peripheral blood lymphocyte (PBL) and cerebrospinal fluid (CSF) lymphocyte populations in patients with multiple sclerosis (MS). On average, MS patients had 79% total T cells (62% of which were T gamma, 66% Tmu) in CSF lymphocytes compared to 66% total T cells (30% T gamma, 63% Tmu) in PBL. Normal age- and sex-matched controls PBL had 74% total T cells (20% T gamma, 54% Tmu). By direct observation using an indirect immunofluorescence assay, 41% of the CSF T gamma cells in MS patients bore receptors for IgM; these cells were designated T gamma mu and, according to the double-marker analysis, did not seem to correlate with disease stage. In MS PBL, 20% of T gamma cells were T gamma mu compared to 9% in the control PBL T gamma population. Thus, MS patients had a higher proportion of total T cells, T gamma cells and T gamma mu cells in their CSF than in their peripheral blood and than those populations found in normal control blood. The significance of this T gamma mu population for the continuing disease state in MS is discussed.

Adult↗