Is recipient priming with graft foreign antigen a prerequisite for the blood transfusion effect?
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Biomedical subjects
Publications and source records attributed to C David.
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Adult rats are used to consume their diet within the space of 30 min. They are sacrified after fasting 2 hours or 30 to 90 min. after the end of meal. Blood sugars are determined. -- The administration of galactose (GAL group) at 40 p. 100 of the diet induces a high postprandial galactosemia (near 600 mg p. 100 ml) without glycemia change: the absorbed galactose is not converted into glucose. -- The consumption of glucose-galactose mixture (G-G group) don't induce postprandial hyperglycemia. However, galactosemia is about 250 mg p. 100 ml. In our conditions, glucose and galactose seem absorbed by two different systems. The galactose absorption would be favoured; otherwise, the absorbed glucose would be partly epimerized into galactose. Galatitolemia goes on 24 hours after the meal but it is not immediately modified by the galactose consumption. The galactosemia and galactitolemia variations are independent one of the others.
Nutritional balances are made with groups of 12 rats Wistar receiving well-balanced diets with 40 p. 100 of sucrose (T), or 40 p. 100 of lactose (L and P), or hydrolyzed lactose (LH and PH). Whey (L) and ultrafiltration permeate (P) are used in crude state or after enzymic industrial lactase hydrolysis (LH and PH). The animals consume diets during eight months. Faeces contain neither lactose nor galactose, but glucose in small quantities. In all urines occurs about 0,5 mg/day of glucose. The lactose diets (L and P) provoke a week lactosury (0,36 p. 100 of ingestion). Galactose and galactitol are abundant in urines: with lactose diets (L and P), the urinary excretion is equal to 4 p. 100 of ingested galactose. In urines of hydrolyzed lactose diets (LH and PH) the excretion reaches 26 p. 100 of ingestion. In this case the excretion is remarkably invariable from third day of eighth month: the urinary galactose corresponds to 23 p. 100 and galactitol to 3 p. 100 of consumed galactose. The urines of lactose diets (L and P) and hydrolyzed lactose diets (LH and PH) contain 100 and 300 mg/day of non sugar reducing substances respectively, i.e. 40 p. 100 of total urinary reducing power. The apparent retention of lactose (L and P) is 95,5 p. 100 and that of the hydrolyzed lactose (LH and PH) is 86 p. 100 after 8 months of experiment but it is estimated that digestive flora consumes 40 p. 100 of dietary lactose (L and P).
Three groups of 15 rats Wistar receive a well-balanced diet with 40 per cent of sucrose (T), lactose (P) or hydrolyzed lactose (PH) in the form of ultrafiltration permeate. After 160 days, no cataract is revealed in the T and P groups. In the PH group, 14 rats reached by cataracts in both eyes: it is slightly developed (PH 2), mildly developed (PH 3) or practically total (PH 4). The inositol disappearance, the high quantity of galactitol, the water and sodium increases are the factors observed before the lens opacification and are responsible for the cataract. Then, during the opacification, soluble proteins, potassium and hydratation of the lens decrease. Galactose 1-P is slowly formed before and during the lens opacification. The lens of the P group (lactose) differ from the control group (T) by the nature and the quantity of hexitols, only.
In the syngeneic mixed lymphocyte reaction, Ly 1 cells proliferate following stimulation with Ia-positive macrophage-like cells. The proliferation is accompanied by the release of interleukin 2 into the medium. Both the proliferation and interleukin 2 production are dependent on the expression of Ia antigenic determinants, as the addition of haplotype-specific anti-Ia antisera to the cultures inhibits both parameters.
Previous studies of the B5.C-H-2 bm12 (bm12) strain have demonstrated the presence of a mutation localized to the I-A subregion of the mouse H-2 major histocompatibility complex. This mutation has been shown to be responsible for defects in Ir-gene function in Ia and MLR determinants. A comparison of the molecular size of the bm12 mutant and the parental B6 Ia-antigen component polypeptides failed to demonstrate any differences in the alpha and beta polypeptides. Thus, no major structural additions for deletions are present in the Ia alpha and beta chain polypeptide or carbohydrate structure. A significant decrease in the amount of invariant (31K) polypeptide was, however, consistently observed in the bm12 Ia antigen preparations. Tryptic peptide comparisons of 14C B6 and 3H bm 12 alpha and beta polypeptides demonstrated a limited number of peptide differences in the bm 12 beta polypeptide but none in the bm12 alpha polypeptide. The significance of these biochemical mutations and altered biological phenomena are discussed in relation to a model of the immunological interaction sites on Ia antigens.
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Growing rats receive for 270 days well-balanced diets with 40 p. 100 of lactose or industrial hydrolyzed lactose. Whey and ultrafiltration permeate are used in crude state or after enzymic lactose hydrolysis. In lactose diets the ingesta and the food efficiency are considerably reduced as well as the growth. The water intake is greatly increased. The dry mater digestibility is not modified by the lactose after an experiment of 7 months. Hydrolyzed lactose provokes all these phenomena but with a weaker intensity. In a zootechnical point of view the lactose hydrolysis reduces the detrimental properties of lactose. After 270 days animals having received lactose show a high hypertrophy of small intestine and caecum tissues as well as a small renal hypertropy (dry matter/100 g of living weight). Hydrolyzed lactose involves the comparable modifications but with a less extent. Numerous facts attributed to lactose molecule are partially imputable to galactose molecule mainly the increase of water consumption. Only the growth of bone tissue (femur) is provoked by the lactose molecule itself and not to its components. When the diet is well-balanced the presence of whey proteins does not seem to modify the lactose effects.
As a first step in determining the genetic control of experimental autoimmune myasthenia gravis in mice, we tested the proliferative responses of lymph node cells to torpedo acetylcholine receptors (TAR). Studies with congenic and recombinant inbred strains of mice revealed that T-cell responses to TAR are controlled by an H-2 linked Ir gene, mapping in the I-A subregion of mouse major histocompatibility complex.
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The expression of immune response-associated (Ia) antigens on the surface of mouse strain GR (H-2dx) ascites leukemia (GRSL) cell lines was studied by cytotoxic tests, immunofluorescence, and immunoprecipitation assays. Ia expression varied among the three GRSL cells lines (GRSL 2, GRSL 14, and GRSL 15) studied by cytotoxic assay. GRSL 14 cells showed the strongest expression of Ia antigens among these three cell lines. A time-course study of tumor growth in mice revealed that Ia antigens on the tumor cells demonstrated the strongest expression 10 days after injection of GRSL cells into GR mice, and that subsequently it decreased until the death of the animal. Cells treated with neuraminidase exhibited more readily detectable Ia antigens, expecially in the late stages of leukemia, which suggested that Ia antigens had been masked by sialic acid. Immunoprecipitation studies revealed that Ia molecules on the leukemia cell had the same molecular weight as those on the normal lymphocytes. Immunofluorescence studies disclosed that Ia antigens were distributed diffusely on the surface of the tumor cells.
A three-stage sampling survey among farmers and their families living on farms in the department of Ille-et-Vilaine gave the following results: Among 490 persons examined 313 (64 per cent) showed a positive skin test and 105 (21 per cent) a positive serological reaction; 88 of the 105 patients ignored their health status, although 45 of these presented clinical symptoms (nine per cent). This survey is continuing in order to study the non-respondents and to better analyse the epidemiological situation at a farm level.
Fifteen cases of severe cranio-cerebral injuries (C.C.I.) with hemianopsia and rehabilitation problems are presented. The correlation between the side of the hemianopsia, dexterity, visual motor organization, intellectual functions and rehabilitation outcome are discussed.
Ia specificities 1-10 were detected on LPS-stimulated splenic lymphocytes and on Con A-stimulated spleen, lymph node, and thymus blasts by direct cytotoxic tests. Since Ia antigens are not readily detectable on resting thymocytes, our results suggest that T cells require some signal before they exhibit full expression of Ia specificities. Absorption-elution studies indicated that most of the Ia specificities detected on T and B cells may be identical. Ia antigens detected by homologous antisera gave much stronger reactions than those detected by cross-reacting antisera.
H-2 antigens are expressed in substantial amounts of murine blood platelets (for H-2 antigenic content 1 lymphocyte approximately 50 platelets) whereas Ia antigens are probably not expressed at all (minimal Ia antigenic content more than 35 times lower than for H-2). This property of blood platelets makes them very useful for the selective absorption of anti-H-2 antibodies from complex sera and for the preparation of specific anti-Ia antibodies from such sera. In 20 sera produced against the complete H-2 complex, 12 sera contained anti-Ia antibodies beside the expected anti-H-2 antibodies. In two sera, separation of the anti-Ia antibodies was easily obtained by absorption of the anti-H--2 antibodies on platelets. The analysis of one serum (C3H.Q X B10.D2) anti-C3H [(q X d) anti-k] showed that, in addition to be expected anti-H--2.23 and anti-Ia.2 antibodies, it contained at least three other Ia antibodies, separable by absorption on lymphocytes, which recognized three antigens--Ia.17, determined by the haplotypes k, f, s, r, j; Ia.18, determined by the haplotypes k, f, s; and Ia.19 determined by the haplotypes k and r. The genes are located in the I--A and/or I--B subregions of the H--2 complex.
Fifty infants and children were treated for staphylococcal infections complicated by bacteremia. Of these, 28 had serious underlying diseases, principally leukemia (15 cases). All were treated with intravenous antibiotics for a median duration of 12.7 days. Although 13 patients died (26%), the staphylococcal infection had apparently been eradicated in all but three (6%), one of whom died before treatment could be started. The relatively brief treatment periods required in even severely compromised leukemic patients and the survival of all but one of 22 previously healthy patients with staphylococcal bacteremia suggest that the prognosis is better than previously reported.
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