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Biomedical subjects

J Henry

Publications and source records attributed to J Henry.

At least 163 records · Page 9Linked to original sources
PubMed1984

Tumoricidal response following perfusion over immobilized protein A: identification of immunoglobulin oligomers in serum after perfusion and their partial characterization.

Previously, we showed that perfusion of plasma from hosts bearing breast adenocarcinoma over immobilized staphylococcal protein A resulted in objective tumor regressions. In the present study, sera perfused in vitro over immobilized staphylococcal protein A were analyzed by physicochemical and immunochemical methods to characterize newly formed products. Sera from normal and breast adenocarcinoma-bearing dogs showed increased levels of C1q-binding IgG after perfusion over a strain of staphylococcus that is protein A rich (Cowan I), but not protein A deficient (Woods 46). C1q binding levels were also increased in normal and tumor-bearing canine or human sera which were perfused over purified protein A immobilized in collodion charcoal (PACC), and this increase was localized in sucrose density gradient fractions ranging from 7S to 19S. Polyacrylamide gel electrophoresis analysis of the high-molecular-weight fraction in postperfusion canine sera, isolated by G-200 fractionation and immunoaffinity chromatography, showed predominantly heavy and light immunoglobulin chains of canine IgG. Furthermore, protein A was released from PACC after perfusion with serum or solutions containing IgG or albumin from humans, dogs, and chickens. After serum perfusion over PACC, protein A was identified in the effluent by additional studies as follows: (a) polyacrylamide gel electrophoresis analysis showed that eluted 125I-protein A comigrated with the protein A marker; (b) postperfusion C1q-binding complexes, isolated by gel filtration under dissociating conditions and affinity chromatography on IgG-Sepharose showed a single precipitin band with normal human (protein A reactive) but not chicken (protein A unreactive) serum. Protein A released from PACC which appeared in postperfusion sera was associated with immunoglobulins in macromolecular complexes since (a) eluted 125I-protein A was largely (NH4)2SO4 and polyethylene glycol precipitable, whereas free protein A was not, and it sedimented in sucrose density gradient fractions distributed beyond the 7S marker, compared to free protein A which localized below 7S; (b) radiolabeled protein A eluting from PACC after serum perfusion showed 8-fold greater binding to C1q-coated tubes compared to free protein A; and (c) increased C1q-binding IgG in postperfusion sucrose density gradient fractions corresponded to the appearance of protein A in parallel gradient fractions.(ABSTRACT TRUNCATED AT 400 WORDS)

Adenocarcinoma↗
PubMed1983

Protein kinases in normal human blood cells.

Protein kinases active on basic and acidic artificial substrates were investigated in normal human erythrocytes, platelets, polymorphonuclear and mononuclear cells. These two types of protein kinases were partially purified by affinity chromatography, then assayed for their enzymatic activity using [gamma-32P]ATP or GTP as phosphoryl donor. Partially purified kinases active on acidic substrates were subjected to high-performance liquid chromatography (HPLC). Protein kinases active on basic substrates were analyzed by cellulose acetate electrophoresis of crude cellular extracts and the influence of 3'5' cyclic AMP was studied. Three forms of casein-phosvitin kinases could be distinguished according to their molecular weight (165 K, 38 K, and 31 K). The 165 K species, in contrast to the light species, can use GTP instead of ATP as phosphoryl donor and corresponds to the "so-called" casein kinase 2. This form is very sensitive to proteolysis and, when partial purification is performed without the addition of various antiproteolytic agents, it is degraded into 120-135 K and 105-115 K active species; this artefactual degradative process is especially active in platelet extracts. As many as eight different active bands of histone and protamine kinases can be separated by cellulose acetate electrophoresis, several of them being stimulated by cyclic AMP. Isozymic patterns of protein kinases, levels of activity on the different substrates, and utilization of ATP and GTP were found to be specific for each cell type. These results suggest the possibility of using protein kinases as markers for cell differentiation.

Blood Cells↗
PubMed1983

Postoperative axillary lymphoscintigraphy in the management of breast cancer.

Postoperative axillary lymphoscintigrams have been performed according to a technique of two-staged injection in 313 patients who had undergone a radical mastectomy with axillary dissection for breast cancer. Total absence of visualization of residual nodes suggests that dissection could be said to be complete in only 35.8% of the investigated patients, or because of metastatic disease causing blockage. The visualized residual nodes in patients represent a risk of developing nodal relapse, especially with positive pathological demonstration of axillary node invasion and without nodal irradiation. On the other hand, when the investigation showed the interruption of the lymphatic pathways of the arm, patients developed upper limb edemas more frequently. It is concluded that this simple and non traumatic technique is of value in order to assess the immediate postoperative axillary nodal status, and that it may influence the treatment of the patients.

Axilla↗
PubMed1982

Morphometrics of the avian lung. 1. The domestic fowl (Gallus gallus variant domesticus).

The lungs of 5 domestic fowls have been analysed electron microscopically by standard morphometric methods. The anatomical diffusing capacity has been calculated from the relevant parameters. The blood-gas barrier consisted essentially of endothelium, basal lamina, and a very thin squamous epithelial cell. Granular cells are absent and interstitial tissue is minimal. The following measurements are mean values applying to both lungs together, in the fixed state: lung volume, 25.0 cm3; total intrapulmonary blood volume, 6.9 cm3; volume of the exchange tissue, 11.6 cm3; pulmonary capillary blood volume, 3.51 cm3; pulmonary capillary haematocrit, 62.7%; total intrapulmonary air volume, 16.61 cm3; air capillary volume, 6.68 cm3; surface area of the blood-gas barrier, 2.08 m2; surface area of the barrier per unit volume of exchange tissue, 179.5 mm2/mm3; arithmetic mean thickness of the tissue barrier, 1.20 micrometers; harmonic mean thickness of the tissue barrier, 0.314 micrometers; harmonic mean thickness of the plasma layer, 0.342 micrometers. The values of the maximum and minimum morphometric diffusing capacities for the lung (DL02 m) were respectively 3.55 and 1.50 ml O2/min/mm Hg; those for the membrane (Dmo2 m) were 13.61 and 12.01 ml O2/min/mm Hg.

Animals↗
PubMed1982

Experience of telecobalt therapy in operable breast cancer at J. Bordet Institute (1969-1975).

Between 1969 and 1975, postoperative radiotherapy was performed at the J. Bordet Institute on 787 stage I-III operable breast cancer patients. Crude 10 years survival rates are respectively 61% for stage I, 59% for stage II and 30% for stage III. The results have been analysed according to clinical characteristics of significant prognostic value and according to the technical conditions of treatment. The status of the axillary nodes appears to be the most important prognostic factor. Radiotherapy to the thoracic wall and lymph drainage areas has varied little throughout the whole period with the dose to the internal mammary chain being the only parameter which varied significantly. Loco-regional recurrences occurred only in 5, 2% of patients without distant metastases appearing previously or during the following year (2.4 for stage I patients). Severe sequelae were seen in only a very few cases. Survival appears significantly correlated with an adequate dose of irradiation to mammary node chain.

Breast Neoplasms↗