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J Dormont

Publications and source records attributed to J Dormont.

At least 91 records · Page 5Linked to original sources

[Primary antibody response in vitro of human blood lymphocytes].

A method for the induction of a primary in vitro antibody response toward a hapten, using human blood lymphocytes is presented. The stimulation of human lymphomonocytic cells with trinitrophenyl (TNP) conjugates of polyacrylamide beads elicits the production of IgM antibody forming cells specific for TNP, with a peak on day 7-day 9. The response is reproducible in its magnitude in the same individual. This model should facilitate clinical and fundamental studies of human antibody response.

Antibody Formation↗

The xenogeneic effect-- evidence for coparticipation of human monocytes and T lymphocytes in the restoration of nude mouse in vitro response to sheep red blood cells.

The restorative ability of human peripheral blood lymphocyte fractions on nude mouse spleen cell in vitro antibody response to SRBC was studied. Strongly adherent cells (monocytes) enhanced nude cell response, but not to the same extent as the optimal number (10(6)) of unfractionated human peripheral blood lymphocytes. T-depleted cells lost their ability to optimally restore the response, while T-enriched cells showed a definite restorative ability. The recombination of adherent cells with T-enriched cells produced an effect comparable to that of unfractionated cells, both in terms of magnitude and dose-response curve. These data suggest that both monocytes and T cells are necessary for an optimal xenogeneic effect in Mishell-Dutton cultures.

Animals↗

Delayed hypersensitivity to mono-azobenzene arsonate-N-acetyl-L-tyrosine. II. An operational model in the mouse.

Immunization of the mouse by free mono-ABA-Tyrosine (ABA-Tyr) in complete Freund's adjuvant leads to a specific sensitization. This can be assessed by increase in ear thickness after challenge with ABA-Protein conjugates. The intensity of the skin reaction is directly related to both the antigen dosage and the amount of BCG incorporated in the adjuvant. A close correlation has been shown between delayed skin reaction and "in vitro" lymphocyte proliferation in the presence of either ABA-Protein or free ABA-Tyr. In both "in vivo" and "in vitro" tests, sensitization is detectable from day 5 with a maximum on day 7. Contrasting with this strong cellular response, no antibody can be found. Thus, mouse sensitization with ABA-Tyr provides an operational model for pure cellular immunity. The extension of ABA-Tyr model to mouse may vacilitate the analysis of the involved cell populations.

Animals↗

Delayed hypersensitivity to mono-azobenzene-arsonate-N-acetyl-L-tyrosine. I. Induction of cellular sensitivity in the rat.

In the guinea pig, mono-ABA-Tyrosone (ABA-Tyr) has been extensively studied as a hapten capable of inducing delayed type hypersensitivity in the absence of circulating antibodies. This model has been extented to the rat, and cellular sensitivity has been assessed both "in vivo" (skin reaction) and "in vitro" (cellular proliferation and lymphocyte migration inhibition). All the reactions studied follow a reproducible pattern with maximal positivity between 4 and 13 days, and negative responses after 20 days. Circulating antibodies were not detectable at any period after immunization. In view of the original properties of ABA-Tyr, and of the advantage of the rat as an experimental animal, the proposed model can be expected to facilitate further studies on the cellular mechanisms of delayed hypersensitivity.

Animals↗

Effect of azathioprine on in vitro antibody response. Differential effect on B cells involved in thymus-dependent and independent responses.

The effect of azathioprine (Az) on the primary in vitro antibody response of mouse spleen cell cultures has been studied. The response towards T cell-dependent antigens is suppressed by low Az concentrations (50% inhibition by 10(-2) mug/ml and 100% suppression by 10(-1) mug/ml). The same pattern is observed when Az addition is delayed until day 2, but the suppression is absent or partial when Az is added on day 3. In the early period (day 0 to day 1) the effect of Az is reversible upon addition of an excess of purine nucleosides. In contrast, the response to a T cell-independent antigen (TNP-T4) is relatively insensitive to Az, since 100-fold higher drug concentrations are required to obtain an inhibition. With the assumption that T helper cells are likely to be highly sensitive to Az, the effect of low Az concentrations on the other two cell populations involved in T cell-dependent responses has been evaluated. Adherent cells appear unaffected. In contrast, the B-cell response is markedly sensitive to Az, as shown by the effect of Az on the response of nude mouse cells to a T cell-dependent antigen in the presence of T-cell products, either specific or non-specific. On the other hand, the B-cell response to mitogens is resistant to az. Thus, Az has a differential effect on B-cell response according to the thymus dependency of the antigen. This may suggest the existence of two pathways for B-cell activation or two different B-cell subpopulations.

Animals↗