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Biomedical subjects

F M Ubeira

Publications and source records attributed to F M Ubeira.

60 records · Page 4Linked to original sources

Modulation of the anti-phosphorylcholine immune response during Trichinella spiralis infections in mice.

The nematode Trichinella spiralis is able to modulate the antibody response, as measured by the plaque-forming cell (PFC) technique, to three thymus-dependent (TD) antigens: (1) a heterologous antigen unrelated to the parasite (sheep red blood cells (SRBC]; (2) an antigenic fraction, rich in phosphorylcholine (PC), obtained from T. spiralis (FCp1) and (3) a heterologous antigen unrelated to the parasite, but sharing the PC epitope with the FCp1 fraction (PC-KLH). During the life-cycle of the parasite in BCF1 mice, two opposing immunomodulating activities occur: (1) an immuno-potentiating activity in mice infected during the intestinal and larval migratory stages, for all three antigens, and (2) a carrier-specific immunosuppressive response in mice infected and immunized with the FCp1 fraction during the muscle phase of the life-cycle. The anti-PC PFC response of these mice is dependent on the infection dose and decreases from day 35 post-infection (p.i.) until at least day 85 p.i. The factor responsible for the stimulating effect observed during this stage is the presence of migratory larvae in the host. All the foregoing seems to indicate that T. spiralis can use specific suppression mechanisms to aid in its own survival.

Animals↗

Effect of clofibrate and hydrocortisone on intestinal trichinellosis in mice.

These investigations show the immunosuppressive effects of Clofibrate (CPIB) and hydrocortisone on the intestinal cycle of Trichinella nelsoni. They demonstrate an effect of CPIB similar to that of hydrocortisone in the establishment of the muscular and intestinal phase of this parasite. A higher retention rate of intestinal adult worms was observed in hydrocortisone-treated mice. These facts are consistent with the idea that CPIB can act on diverse immune cells, involving both thymus-dependent and thymus-independent antigens.

Animals↗

Differences in the enzymatic profile in human lymphoid tumors.

In order to evaluate the utility of enzyme galleries in the differential diagnosis of human lymphoid malignancies, we have determined ninety-three cytosolic enzymic activities in four human lymphomas (Hodgkin's disease, nodular esclerosing type; immunoblastic sarcoma, B-cell type; plasmacytoid lymphocytic lymphoma and prolymphocytoid transformation of B-chronic lymphocytic leukemia), using a semiquantitative colorimetric method. We found 27 discriminative enzymes among the samples. These enzymes were: one esterase (C4); two oxidases (beta-glucuronidase and alpha-fucosidase); twenty two arylamidases and two dehydrogenases). Our preliminary results seem to indicate that this methodology may be an important complement to the pathological and immunological studies in the diagnosis of the lymphoproliferative disorders.

Clinical Enzyme Tests↗

Effect of clofibrate on the growth-kinetics of the murine P 1798(sc) lymphoma.

Clofibrate (CPIB) is a drug applied as an antilipidaemic agent in mammals. In this work we have tested its efficacy in vivo on the growth kinetics of P 1798(sc) lymphoma transplanted to recipient (BALB/c x AKR)F1 mice. Our results show a facilitation of the tumour growth rate in treated recipients. This fact may be related to an effect of the agent on the recipient which produces a decrease in the immune response as was confirmed on testing CPIB on thymus-dependent antigens in haemolytic plaque assays.

Animals↗

[Analysis of the escape of tumor P1798(SC) from immunologic control in hybrid mice (Balb/c X AKR)F1 (BAF1)].

Expression of tumoral antigens and their masking by sialic acids were studied. Tumour with greater content in sialic acid [P1798(sc)] can surpass the histocompatibility barrier. Furthermore, removal of sialic acid residues from membrane by neuramidase treatment results in a retarded or inhibited tumoral growth. These results suggest an antigenic masking by sialic acids. On the other hand, in the anti-P1798(sc) humoral response are involved two antigens, at least, also expressed by syngeneic hepatocytes and thymocytes, as demonstrated by cytotoxicity assays.

Animals↗