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Biomedical subjects

R A Knight

Publications and source records attributed to R A Knight.

At least 145 records · Page 8Linked to original sources

Concurrent and predictive validity of components of disordered thinking in schizophrenia.

Although the various manifestations of disordered thought have played a central role in diagnostic and theoretical considerations of schizophrenia, such symptoms have not been found specific to schizophrenia, and at best have shown weak relations to outcome. As part of a 7-year followup study of a sample of young, acute, psychotic inpatients, we explored the hypothesis that despite these poor results there might be particular components of disordered thought that might have prognostic utility and be able to discriminate narrowly defined schizophrenics. Using extant symptom scales as our models, we constructed five internally consistent scales of disordered thought from behavioral ratings made using the Psychotic Inpatient Profile--Poverty of Speech, Attentional Impairment, Incoherence, Delusions, and Hallucinations. We tested the ability of these scales to predict various aspects of outcome adaptation including outcome diagnosis. In general, the Attentional Impairment scale demonstrated the best prognostic utility, predicting poorer outcome in several domains. Paradoxically, patients diagnosed by Research Diagnostic Criteria (RDC) as definite schizophrenic at outcome had been rated as showing less attentional impairment than probable and nonschizophrenics. An examination of the pattern of correlations between Attentional Impairment and performance on cognitive tasks suggested that attentional difficulties may be related to different underlying cognitive processes in those diagnosed schizophrenic and nonschizophrenic at outcome by RDC.

Adult↗

Human immune responses to herpes simplex virus, varicella-zoster and cytomegalovirus in vitro.

The cell principally responsible for lymphocyte proliferation to herpes simplex virus (HSV), varicella-zoster (VZ) and cytomegalovirus (CMV) has been shown to be a T cell of helper phenotype. Lymphocytes from a proportion of proliferation-positive normal individuals produced anti-viral antibody in vitro. Although in some cases, and at some time-points, the antibody was specific for the priming virus, in others, antibodies to more than one virus were detected. Similarly, some T-cell clones proliferated specifically to the priming virus, whereas others were not specific for the virus used in the priming culture. Two clones helped the production of HSV-specific antibody, one by autologous, the other by both autologous and allogeneic non-T cells.

Antibodies, Viral↗

Isolation of two phospholipases A2 from Mojave rattlesnake (Crotalus scutulatus scutulatus) venom and variation of immunologically related venom proteins in different populations.

Two phospholipases A2 of mol. wt 14,500 (P1) and 14,400 (P2) and pI 9.2 and 7.4 respectively were isolated from Crotalus scutulatus scutulatus venom. The two isoenzymes cross-reacted immunologically with phospholipase A2 from C. adamanteus and C, atrox, but not with Mojave toxin, excluding them as the basic subunit of the Mojave toxin complex. C. s. scutulatus venoms from Arizona had two common bands recognized by anti-P2 which were absent in most C. s. scutulatus venoms from Texas, suggesting two genetically different populations east and west of the Continental Divide.

Animals↗

Null cell immunoregulation in SLE.

Fresh normal T cells do not lyse MDA-157 target cells. Normal null cells, cultured for 4 days with MDA-157 stimulators, and then mixed overnight with fresh normal T cells, induce cytotoxicity on MDA-157 targets and suppressor activity in the T-cell acceptor population. With the same normal acceptor T cells, MDA-157 activated null cells from 13/18 patients with Systemic Lupus Erythematosus (SLE), unlike activated cells from a disease control population, induce little or no T-cell cytotoxicity or suppression. These results provide further evidence for abnormal null cell function in SLE.

Cells, Cultured↗

Electrophoretic variants of Mojave rattlesnake (Crotalus scutulatus scutulatus) venoms and migration differences of Mojave toxin.

Mojave toxin was found in comparable quantities in venoms from Mojave rattlesnakes captured in the Big Bend region of Texas and southeastern Arizona. Toxicities in mice were also comparable. Electrophoretic profiles of venom differed significantly between the two groups, suggesting two genetic divergent groups. Immunotransfer revealed several electrophoretic variants of Mojave toxin among the Texas snake venoms, all of which migrated slower than Mojave toxin of venoms from the Arizona snakes.

Animals↗

Inappropriate peripheral blood lymphocyte responses to herpes viruses in patients with Behçet's syndrome.

Specific antibody production and the proliferative response of peripheral blood lymphocytes (PBLs) to a variety of viruses, including herpes simplex virus-type-1 (HSV-1) and varicella zoster (VZ), were studied in 7 patients with Behçet's syndrome. None of the patients produced an antibody response against HSV-1 or VZ. Furthermore, none of the patients showed a proliferative response to VZ, and three of them also failed to mount a response to HSV-1. These results suggest that the PBLs of patients with Behçet's syndrome make an inappropriately poor antibody and proliferative response when stimulated by HSV-1 and VZ.

Adult↗

Specific allogeneic help by T lymphocytes from patients with systemic lupus erythematosus.

Unfractionated mononuclear cells from patients with systemic lupus erythematosus (SLE) immunized with influenza vaccines do not produce a secondary in vitro anti-influenza antibody response when challenged with virus antigen. Irradiated T lymphocytes from normal, disease control and from SLE donors whether vaccinated or not, help allogeneic normal non-T cells to produce specific anti-influenza antibody in vitro. Irradiated normal T cells, however, do not help allogeneic non-T cells from SLE donors. Non-irradiated T cells from 40% of the SLE patients, irrespective of whether or not they had been vaccinated, also provide specific help for MLC incompatible normal non-T cells in the influenza antibody response. This non-restricted interaction was not seen using non-irradiated T cells from any normal or disease control donor. No anti-DNA antibodies were produced in virus stimulated cultures of non-irradiated or irradiated SLE T cells with allogeneic normal non-T cells.

Antibodies, Antinuclear↗

Immunological reactivity to a new glutaraldehyde tanned bovine pericardial heart valve.

The presence of pericardial specific antibodies directed against prosthetic bovine tissue heart valves was quantified by use of an indirect immunofluorescence technique. Serum samples containing antibodies displayed bright fluorescence when tagged with a secondary layer conjugated to FITC. Specific antibody production was undetectable in dogs or sheep who had undergone heart valve replacement (mitral or tricuspid) with a new unicusp prosthesis (Meadox Medicals Inc., NJ), as long as 17 mos following implantation. Similarly, anti-pericardial IgG was not detected in the serum of patients grafted with an analogous commercially available tissue heart valve, although in one patient the presence of low affinity IgM was suggested. This study documents the low immunological reactivity of this new tissue heart valve. Clinically valvular dysfunction due to an immunological response is not expected.

Animals↗

Recognition of marrow elements by natural killer cells: are NK cells involved in haemopoietic regulation?

NK cells from young normal mice are cytolytic in vitro for a virus-induced tumour cell line, YAC-1. Cytotoxicity is inhibited by the addition of unlabelled homologous YAC-1 cells and by regenerating bone marrow cells from the spleens of lethally irradiated, bone-marrow-grafted mice. Quiescent marrow from syngeneic and allogeneic mice produces little or no competition. This suggests that NK cells recognize, and may regulate, marrow progenitor cells.

Animals↗

Defective autologous and allogeneic mixed lymphocyte reactions in hairy cell leukaemia.

The autologous and allogeneic mixed lymphocyte reactions were measured using peripheral blood cells from 13 patients with hairy cell leukaemia (HCL), six of whom had been splenectomized when first studied. T cells from five patients responded to autologous stimulation, and one of these had received splenectomy. Significant alloreactivity was observed in nine patients, of whom three were splenectomized. An absent autologous reaction was associated with ratios of OKT4:OKT8 positive cells less than 1.5, and such ratios were more often observed after splenectomy. Non-T cells from 10 of 11 patients stimulated allogeneic normal T cells. The amounts of HLA-DR antigens on hairy cells were similar to those on normal peripheral blood non-T cells. These data suggest that the defects of response in HCL reflect abnormalities at the responder T cell level. Such defects may contribute to the defective host defence frequently observed in HCL.

Antibodies, Monoclonal↗

Trichuris odocoileus sp. n. (Nematoda: Trichuridae) from white-tailed deer, Odocoileus virginianus, in southeastern U.S., and a key to trichurids in North American ruminants.

A new species of Trichuris from the cecum of white-tailed deer, Odocoileus virginianus, from the southeastern United States, is characterized herein. Males had spicules 2.20 to 3.05 mm long with bluntly rounded tips, an ejaculatory duct equal to or slightly longer than the vas deferens, and a spinous spicular sheath with an expansion near its center. Females had a spinous vulva, usually not everted, a loop in the oviduct just before it opened into the uterus, and a slightly curved posterior portion. Trichuris odocoileus was differentiated from T. lani , a species described in Russia which is most like T. odocoileus, by 1) possessing a spicular sheath with a central expansion, 2) greater size with longer ejaculatory duct and vas deferens, 3) slightly larger eggs, and 4) the unique loop in the oviduct. Trichuris odocoileus constitutes the 6th species of Trichuris recovered from North American ruminants. A key is provided to facilitate differentiation of the six species.

Animals↗

Intranuclear incorporation of thymic low molecular weight RNA by murine bone marrow immunoblasts and inhibition of plasma cell formation by a derivative of rifampicin.

An in vitro culture system for the proliferation of IgG-forming plasma cells from mouse bone marrow cultures has previously been described. The present study attempts to elucidate the mode of action of thymic RNA in these cultures. Autoradiography after using radiolabeled thymic RNA showed that radioactive material was mainly incorporated into the nuclei of IgG-forming plasma cells. No radiolabeled thymic RNA was incorporated into the cells except immunoblasts. The incorporated thymic RNA was acid insoluble and digested by RNase, but resistant to DNase and pronase. Radioactivity in the nucleotide pool after the cells were cultured with radiolabeled thymic RNA was negligible, indicating that reutilization of degraded RNA did not occur in the nuclei of the plasma cells. Moreover, the incorporation of radiolabeled thymic RNA by the cells was not prevented by excess unlabeled nucleosides. Escherichia coli transfer RNA, L-cell RNA and synthetic polynucleotide poly(A-U) were incorporated but were distributed in a different manner in the cells. A derivative of rifampicin, 2'5'-dimethyl N(4') benzyl-N(4')[desmethyl]rifampicin (AF/ABDMP), a possible inhibitor of RNA-dependent DNA polymerases, suppressed both the incorporation of thymic RNA and the differentiation of immunoblasts. AF/ABDMP suppressed DNA synthesis by bone marrow cultures to the same level as those pretreated with anti-mouse B-cell antibodies and complement. DNA dependent RNA polymerase activity was observed in the supernatant of bone marrow cultures stimulated by normal syngeneic thymic RNA and human gammaglobulin as antigen. These results imply a possible relationship between B-cell differentiation and RNA-dependent DNA polymerases.

Animals↗

Inhibition of proliferative and suppressor responses in the autologous mixed lymphocyte reaction by serum from patients with systemic lupus erythematosus.

Serum from patients with systemic lupus erythematosus (SLE) prevents the proliferative response of normal T cells when stimulated by autologous or allogeneic non-T cells. The abrogation of proliferation in an autologous mixed lymphocyte reaction (AMLR) with SLE serum is associated with a lack of suppressor T cell generation. Fractionation of SLE sera on sucrose gradients reveals an 18-12 S peak of Raji cell binding material. Fractions with an S value of </=12 S show inhibitory activity in an AMLR.

Adult↗

Effects of activated T cells on natural killing.

Two populations of human blood lymphocytes--one forming rosettes with sheep erythrocytes, the other non-rosetting--are cytolytic in vitro for several long term cultured tumour-derived cell lines. A particular breast cancer-derived target cell (MDA-157) is only killed by the non-rosetting effector. Rosetting cells from normal donors infected or immunized with influenza virus augment cytolytic activity on MDA-157 targets by non-rosetting effector cells. Similar augmenting activity can be induced by incubating the rosetting population with sources of immune (gamma), but not leucocyte (alpha) interferon in vitro. This augmentation of cytolytic activity does not require compatibility at the major histocompatibility locus between the augmenting and effector populations.

Antibody-Dependent Cell Cytotoxicity↗