"Clinical significance of psychotherapy for unipolar depression: A meta-analytic approach to social comparison": Correction to Nietzel et al.

Reports an error in "Clinical significance of psychotherapy for unipolar depression: A meta-analytic approach to social comparison" by Michael T. Nietzel, Robert L. Russell, Kelly A. Hemmings and Monica L. Gretter (Journal of Consulting and Clinical Psychology, 1987[Apr], Vol 55[2], 156-161). The data presented in Table 2 were incorrect because a row and a column were inadvertently omitted. The corrected Table 2 appears in the erratum. (The following abstract of the original article appeared in record 1987-28817-001.) This study used meta-analysis to study the clinical significance of psychotherapy for symptoms of unipolar depression. The following questions were addressed: How similar is the posttherapy adjustment of depressed adults to that of nondepressed adults? Is this adjustment maintained at follow-up? What dimensions of treatment, therapists, or design are associated with clinical significance? Using the Beck Depression Inventory (BDI), we calculated composite BDI norms from 28 published studies. Sixty effect sizes (from 31 outcome studies utilizing the BDI) were calculated. The results indicated that psychotherapy produces outcomes that have moderate clinical significance and that are well-maintained at follow-up, that individual therapy is associated with greater clinical significance than group treatment, and that type of therapy is not related to improvement. Alternative approaches for operationalizing clinical significance as the return of individuals to normal levels of functioning are discussed. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Variability in Immunohistochemical Detection of Programmed Death Ligand 1 (PD-L1) in Cancer Tissue Types

In normal cell physiology, programmed death 1 (PD-1) and its ligand, PD-L1, play an immunoregulatory role in T-cell activation, tolerance, and immune-mediated tissue damage. The PD-1/PD-L1 pathway also plays a critical role in immune escape of tumor cells and has been demonstrated to correlate with a poor prognosis of patients with several types of cancer. However, recent reports have revealed that the immunohistochemical (IHC) expression of the PD-L1 in tumor cells is not uniform for the use of different antibodies clones, with variable specificity, often doubtful topographical localization, and with a score not uniquely defined. The purpose of this study was to analyze the IHC expression of PD-L1 on a large series of several human tumors to correctly define its staining in different tumor tissues.     

Conjugated linoleic acid and oxidative stress

At the present time, conjugated linoleic acid (CLA) is the subject of a growing number of studies since it has been demonstrated to possess anticarcinogenic and antiatherogenic activities in experimental animal models and to increase in some pathological states in humans. In both situations, CLA has been claimed to be involved in oxidative stress, as an antioxidant in the first case and as a primary product of a free-radical attack on polyunsaturated fatty acids (PUFA) in the other. The controversial results are due mostly to a lack of a suitable methodology because the presence of conjugated dienes (CD) in lipid moiety has been taken for years as evidence of lipid peroxidation due to the occurrence of this structure in fatty acid hydroperoxides. We have recently developed a new methodology that consists of the extraction of fatty acids, including CD fatty acid hydroperoxides, by mild saponification and their separation and identification by high-performance liquid chromatography with diode array detector. Fatty acid analyses of liver homogenate, oxidized in vitro either with Fe-ADP or t-butyl hydroperoxide (t-ButylHP), of lamb and rats fed CLA at levels known to prevent carcinogenesis, showed that CLA and its metabolites steadily decreased during oxidative stress and that they are more prone to oxidation than their corresponding methylene-interrupted fatty acids. No significant antioxidant effect of CLA was detected in any model tested. However, CD fatty acid hydroperoxides increased in the t-ButylHP model but not in the Fe-ADP model, owing probably to the degradation of CD fatty acid hydroperoxides induced by this oxidative agent. In conclusion, CLA and its metabolites seem to behave, under oxidative stress, as regular PUFA. Thus, it is highly unlikely that the peculiar effects of CLA are directly related to interference in lipoperoxidative processes.     

Lipid and fatty acid composition of different fractions from rat urinary transitional epithelium

The phospholipid composition of rat urinary transitional epithelium (TE) and the fatty acid composition of microsomal, mitochondrial, cytosolic, and plasma membrane (PM) subcellular fractions were investigated. PM marker enzymes and electron microscopy analysis were used to characterize the PM fraction, which showed a distinctive lipid composition compared to the general profile of PM from different sources. The levels of cholesterol and sphingomyelin were not enriched in the PM fraction; on the other hand, the increased amounts of glycosphingolipids and phosphatidylserine, and the decreased level of phosphatidylcholine followed the general features of a PM profile. This differential PM lipid composition may reflect the unique morphology of this mammal TE, consisting of concave plaques with an asymmetrical membrane unit. The distribution of the double bond across the PM indicated a higher unsaturation of the inner relative to the outer part of the PM hemileaflet. In addition, the presence of 20∶3n−9 nonessential fatty acid in a normal TE may represent a characteristic fatty acid metabolism of this epithelium. The authors wish to dedicate this work to the memory of the late Professors Benito Monis, who participated in the generation of this research and whose working hypothesis remains a source of fruitful inspiration.     

Vacuum Plasma Spray Deposition of Titanium Particle/Glass-Ceramic Matrix Biocomposites

The vacuum plasma spray technique (VPS) has been successfully employed to coat Ti-6A1-4V substrates with bioactive glasses and Ti-particle/glass-ceramic matrix biocomposites. The composites were prepared by sintering, under an Ar flow, green bars of bioactive glass powders and 30% volume Ti particles. The bioactive glasses have the two following compositions: SCB (48.8SiO₂−48.8CaO−2.4B₂O₃) and TSCB (46.6SiO₂−48.7CaO−2.5B₂O₃−2.2TiO₂) (mol%). The VPS bioactive coatings were characterized by means of scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), X-ray diffraction (XRD), and mechanical tests (Vickers indentations and tensile and shear tests). Their bioactivity was tested by soaking the samples in a simulated body fluid (SBF) and by analyzing the growth of hydroxylapatite (HA) by SEM, EDS, and XRD. Leaching tests of Ca, Si, and P in SBF were made by inductively coupled plasma-atomic emission spectroscopy (ICP-AES, Perkin-Elmer 5000) to study the in vitro bioactivity of the samples versus time. Each coating was found to be bioactive and well bonded to the substrate; the composites showed better mechanical properties than the pure glass matrices and the hydroxylapatite coatings deposited by the same VPS technique.     

Synthetic peptides as substrate for assaying the proteolytic activity of Lactobacillus helveticus

Four Lactobacillus helveticus strains were studied for proteolytic capacity and general aminopeptidase (AP) and X-Pro dipeptidyl aminopeptidase (DAP) activity. The rate of hydrolysis and the activity against synthetic substrates with N-terminal residues of Arg, Lys, Leu, Glu or Pro, varied markedly among the strains. The X-Pro DAP activity was consistently high. The crude cell-wall and cytoplasm extracts from strain Lb. helveticus ISLC59 were analysed thoroughly for their proteolysis ability by using four synthetic peptide substrates, including alpha(s)1-CN(f1-23). Peptides formed during in vitro hydrolysis of the synthetic substrates by cell wall and cytoplasm preparations were identified by LC-ESI/MS. In doing so, it was possible to infer a prevalent endopeptidase activity splitting Lys7-His8 and Gln13-Glu14 bonds in the cytoplasm, and to deduce a secondary activity, which hydrolysed Glu14-Val15, Leu16-Asn17, Glu18-Asn19 and Lys3-His4 bonds lacking in the cell-wall. The presence of exopeptidases, as mainly AP, DAP, and carboxypeptidase (CPase) was deduced from the formation of several N- and C-terminally truncated peptides sets. The AP activity was higher in the cell-wall layer, where CPase activity was absent. The in vitro assays with cell extracts of the Lb. helveticus ISLC59 strain revealed extensive exopeptidase and endopeptidase activities. In several cases, the hydrolytic system of Lb. helveticus that splits in vitro alpha(s)1-CN(f1-23) peptide bonds was similar to that of Lactococcus lactis. The effects were also compared with those occurring in vivo in hard cheese such as Grana Padano.     

Increasing the antibacterial effect of lysozyme by immobilization on multi-walled carbon nanotubes

We report a facile strategy to obtain multiwalled carbon nanotubes (MWCNTs) functionalized with covalently bonded lysozyme. The functionalization procedure has been investigated by means of several techniques, including thermogravimetry, Raman spectroscopy, transmission electron microscopy, and cyclic voltammetry. A functionalization of about 1 lysozyme molecule every 4000 carbon atoms is obtained. The modified lysozyme-CNTs nanocomposite shows a significant increase of the antibacterial activity towards the Gram-positive S. aureus if compared with lysozyme in solution.