Search PubMed⌕ Search

Biomedical subjects

R Berger

Publications and source records attributed to R Berger.

At least 685 records · Page 38Linked to original sources

Constitutional C-band pattern in patients with adenomatosis of the colon and rectum.

The pattern of polymorphism in the C-band-positive constitutive heterochromatin of chromosomes #1, #9, and #16 was studied in fibroblasts from 23 unrelated patients with adenomatosis of the colon and rectum and in peripheral lymphocytes from 78 control persons. The parameters of the heterochromatic regions analyzed were relative size, symmetry-asymmetry within homologous chromosome pairs, and frequency of inversions. The polyposis coli patients had a significantly higher frequency (p less than 0.05) of partial and total heterochromatin inversion on chromosome #9 than the control group (37.0% compared with 21.8%). In the other parameters studied, no significant differences were found between patients and controls.

Chromosome Banding↗

C-band heteromorphism in breast cancer patients.

The pattern of heteromorphism in the C-band-positive constitutive heterochromatin of human chromosomes #1, #9, and #16 was studied in peripheral lymphocytes of 54 breast cancer patients and 78 control individuals. The parameters of the heterochromatic regions analyzed were relative size, symmetry-asymmetry within homologous pairs, and prevalence of inversions. Significant differences between the two groups were found in C-band size of chromosomes #1, #9, and #16 and in incidence of inversions on chromosomes #1 and #9. Significant differences were noted between premenopausal and postmenopausal cancer patients in regard to inversions on chromosome #9 and between familial and sporadic patients in regard to C-band size on chromosome #16.

Adult↗

Etiologic diagnosis of bacterial nosocomial pneumonia in seriously ill patients.

We identified retrospectively 19 critically ill, intubated patients in whom tracheobronchial secretions had been cultured before antimicrobials were administered. Each of these patients had bacterial nosocomial pneumonia, as diagnosed by a positive bacterial culture from blood, pleural fluid, percutaneously aspirated lung material, special endobronchial brushings, and/or postmortem lung specimens. In 11 (58%) patients, the predominant organism in the tracheobronchial secretions was the same one identified in the diagnostic culture. However, in eight (42%) patients, the infecting bacteria were either not predominant or did not grow in the culture of respiratory secretions. We conclude that standard microbiologic studies of central tracheobronchial secretions are not always reliable for establishing the etiology of a bacterial nosocomial pneumonia in this type of patient.

Adult↗

[Rearrangement of the proto-oncogene c-myc in fresh cells from Burkitt's leukemia (L3)].

The presence of a rearrangement of the proto-oncogene c-myc was investigated in the DNA of fresh cells isolated from the blood of two patients with Burkitt's leukemia (L3), and from the node biopsy of a patient with Burkitt's lymphoma. Both samples from the L3 leukemia patients had the characteristic t(8;14) translocation, while the lymphoma specimen presented no abnormality of chromosome 8. Only one of the leukemic DNA's presented a rearranged c-myc pattern, with the breakpoint region located between the first and the second exon. The c-myc pattern of the two other patients appeared normal. The finding of a rearranged c-myc oncogene in fresh cells from a Burkitt's leukemia is direct evidence for the implication of c-myc in the disease whereas most of the rearrangements previously described have been found in cell lines established in culture.

Base Sequence↗

Cytogenetics of Burkitt's lymphoma-leukaemia: a review.

Two types of chromosomal abnormality have been found in Burkitt's lymphoma-leukaemia. Three specific translocations, t(8;14), t(8;22) and t(2;8), having in common 8q24 band involvement, are thought to be present in the overwhelming majority of cases. These stereotyped translocations have been shown in many cases to be related to DNA molecular rearrangements of the immunoglobulin genes and the c-myc oncogene. Secondary chromosomal abnormalities, some of them nonrandom, have also been described. Their possible relation to other oncogene involvement and to the Epstein-Barr virus genome is discussed.

Burkitt Lymphoma↗

Live varicella vaccine in healthy individuals.

Eight hundred healthy seronegative children and 32 adults were vaccinated with the Oka-strain live attenuated varicella vaccine (Varilrix), manufactured by Smith Kline-RIT, Belgium. The vaccine was safe (no side effects) in healthy individuals, highly immunogenic (dose-dependent induction of humoral antibodies and specific cell-mediated immune response), and highly protective against clinical varicella. The simultaneous administration of a measles-mumps-rubella vaccine together with the varicella vaccine is possible, although combination in the same syringe was less effective than simultaneous administration in different arms. Various observations suggest that the risk of contracting zoster in adulthood may well be reduced for varicella vaccinees. Based on our results, it is recommended that seronegative hospital staff be vaccinated. Furthermore, if the varicella vaccine should prove to be cost effective, large-scale immunization of healthy children may be indicated.

Antibodies, Viral↗

Delayed hypersensitivity skin test to detect susceptibility to varicella and zoster.

A crude varicella skin-test antigen corresponding to an inactivated partly-purified high-titre varicella Oka-strain vaccine was prepared at Smith Kline-RIT. It was used for a delayed hypersensitivity skin test in 60 healthy adults for determination of their immune status. The findings were analysed according to the presence or absence of humoral antibodies to varicella-zoster virus (VZV), and of a specific cell-mediated immune (CMI) response as measured by the VZV-specific lymphocyte transformation test. The immune status to varicella could be determined in all subjects provided that the amount of antigenic material in the skin-test antigen was sufficiently high. The 2 tests for the CMI response, the delayed hypersensitivity skin test and the lymphocyte transformation test, gave concordant results in both seropositive and seronegative individuals. The inactivated skin-test antigen cannot replace vaccination with the live varicella vaccine since it is unable to induce seroconversion in seronegatives or an antibody booster response in seropositives. Furthermore, seropositive and seronegative subjects showing a negative response to the varicella-zoster-specific lymphocyte transformation test remained negative 2 weeks after the injection of the skin-test antigen.

Antibodies, Viral↗

Restoration of varicella-zoster virus cell-mediated immune response after varicella booster vaccination.

In older age groups, an increasing proportion of healthy adults with a positive varicella history have lost their capacity for a cell-mediated immune (CMI) response to varicella-zoster virus (VZV) antigen despite the presence of virus-specific humoral antibodies. While it remains a matter of speculation whether this decline is connected with a predisposition to herpes zoster, it is known that a second zoster attack is rare in immunocompetent individuals. In order to determine whether the VZV-specific CMI response can be restored through varicella vaccination, the immune status of a group with naturally occurring herpes zoster was compared with that of a group of vaccinated subjects. Twenty zoster patients were tested for VZV antibody and VZV-specific CMI within the first 4 days of the disease. Antibodies were present in normal or moderately high titres (mean: 2,900). Lymphocyte reactivity to VZV antigen was negative or weakly positive in 17 of the 20 patients. After 6 weeks, antibody titres rose significantly (mean: 36,000) and the lymphocyte response was highly positive in 11, weakly positive in 6, and remained negative in 3 patients. Thirty-three healthy adults ranging in age from 55-65 years with a negative VZV-specific CMI, but positive VZV antibodies (mean: 190), were immunized with the Oka-strain varicella vaccine (Varilrix). After 6 weeks, the mean antibody titre had only increased slightly (mean: 400). However, a positive VZV-specific CMI response occurred in 28 out of 33 subjects, while 5 remained negative. Therefore, conversion from a negative to a positive CMI response can be achieved by varicella vaccination of seropositive subjects. This raises the question whether booster vaccination of CMI-negative subjects could prevent zoster.

Adult↗

[Possibilities and limits in the detection of nosocomial rotavirus infections].

During an epidemiological survey on rotavirus gastroenteritis in the area of Berne (Switzerland) different virus types were analyzed according to their genome segment pattern. Nosocomial rotavirus infections among pediatric patients were carefully investigated. Possible limitations of such studies are discussed in details.

Child↗

Production of erythropoietin by cloned malignant murine erythroid cells.

A specific immunological assay was used to demonstrate that the erythropoietic factor produced by the recently described FMuLV-induced murine erythroleukemic cell line IW32 is an authentic erythropoietin (epo). Several independent virus-induced erythroleukemic and myeloblastic cell lines were tested for epo production. Among six erythroleukemic cell lines induced by FMuLV, another (NN10) was shown to produce epo by biological and immunological assays. Four Friend-virus-induced erythroleukemias and four FMuLV-induced myeloblastic cells were negative. The amounts of epo produced were similar in IW32 and NN10 supernatants after 48 h in culture. The in vitro bioassay gave the highest levels (up to 1000 mU/ml), the in vivo bioassay the lowest, and the radioimmunoassay gave intermediate results. NN10 and IW32 cell lines have been induced by two different FMuLV and were shown to be independent by cytogenetic studies. The molecular weights of IW32 and NN10 epo were close to the molecular weight of mouse plasma epo but elution profiles suggested that some differences might exist between these epos. Cloned IW32 and NN10 cells were shown to retain both the ability for erythroid differentiation after incubation with chemical inducers and the ability to produce epo. This demonstrates that malignant erythroid cells were the source of epo production in these cell lines.

Animals↗

[Rearrangement of the c-myc proto-oncogene locus in a cell line of T-lymphoblastic origin].

A molecular rearrangement of the proto-oncogene c-myc located downstream of the exon III 3' end has been found in a cell line derived from KE37 cell line established from an acute T-lymphoblastic leukemia. This rearrangement resulted from a chromosomal translocation t(8; 14)(q24; q11). Since the 14q11 chromosomal band has been found to be involved in several T-cell leukemias and lymphomas, the importance of the rearrangement of c-myc discovered in the KE37 cell line lies in the possibility of analyzing chromosome 14 DNA near the breakpoint involved in the translocation.

Cell Line↗

[Acute myeloblastic leukemia with involvement of the basophilic cell line and anomalies of the short arm of chromosome 12 (12p)].

Among 16 leukemia patients with abnormalities of the short arm of chromosome 12 (12p) were found 5 patients with an increased number of marrow basophils and a special M2 cytological feature. This new correlation between 12p abnormalities and M2-baso phenotype is presented. The localisation of c-k ras 2 genes at the same 12p site suggests a possible mutation of this c-oncogene.

Basophils↗