PubMed HealthSearch

Biomedical subjects

W Müller-Ruchholtz

Publications and source records attributed to W Müller-Ruchholtz.

At least 199 records · Page 11Linked to original sources

Demonstration of cell-mediated immunological reactivity to transplantation antigens in uveo-retinal tissues.

Lymph node cells from inbred rats, sensitized against allotransplantation antigens, were tested for reactivity against uveo-retinal tissues, using a two-step leucocyte migration inhibition test: (1) These tissues induced positive reactions indicating the presence of transplantation antigens. (2) This was true for strong and weaker histoincompatibility systems. (3) Quantitatively, uveo-retinal tissues were somewhat less reactive than lymphocytes as antigen.

Animals

[Allogenic and xenogenic aortic segmental transplants in inbred rats angiographically demonstrable vascular changes (author's transl)].

In order to make a systematic study of the significance of immunological reactions in vascular grafts, segments of abdominal aorta (4-5 mm long) were grafted into inbred rats. Four experimental combinations were used: I. syngeneic (CDF leads to CDF), II. weakly allogeneic (LEW leads to CDF), III. strongly allogeneic (BD 5 leads to CDF), IV. xenogeneic (guinea pig leads to CDF). After 100 days the gaft was macroscopically evaluated, angiographed and measured. Whereas no alterations of the vascular wall were found in group I, the degree of aneurysm formation increased significantly corresponding to the degree of histoincompatibility in the other groups: group II showed little aneurysm formation (medicum size 1.27 fold), group III more pronounced (1.71 fold) and group IV very pronounced (3.9 fold) with partial thrombosis in 3/5 of the cases. These findings are interpreted, as functional and morphological consequences of the immunogenicity of the aorta tissue. The conclusion was reached that the degree of histoincompatibility should be more carefully considered, also in vascular grafting.

Animals

[Effect of D-penicillamine on the humoral primary response (author's transl)].

The influence of D-penicillamine (Pen) on the humoral primary response was studied systematically. Inbred rats are sensitized with erythrocytes of mice of one strain. Pen given at various schedules (dosage: 3 X 100 resp. 3 X 1000 mg/kg at 24 h intervals) showed no effect on antibody titer 7 days after sensitization. When Pen is given before the antigen the slope of the titer after day 7 is accelerated. Compared to experiments with alkylating drugs and antimetabolites in the same model Pen does not show immunosuppressive potency.

Animals

Presence and kinetics of sensitized cells in different tissue compartments.

The question was studied as to whether lymph nodes (LN), spleen (SP) and bone marrow (BM) contain different amounts of sensitized cells at various times after one or repeated immunizations. The following model was used: C57 mice were injected i.p. once, twice or three times with C3H cells. Between 3 and 20 days after the last immunization, LN, SP and BM cell suspensions were tested in vivo for their local cutaneous lymphocyte transfer reactivity in C3H mice and in vitro for their lymphocytotoxicity (partially after preincubation with anti-theta serum). In both test systems similar observations were made: after one sensitization, reactive cells were demonstrated first in the LN and then in the SP, but only during the next few days; BM cell reactivity appeared later. In the first few days after two sensitizations SP cells reacted strongly whereas LN and BM cells reacted weakly; later BM cell reactivity increased while the others decreased. After three sensitizations reactivity of the SP cells predominated during the entire period of observations; the BM cells showed less, the LN cells no reactivity. These findings suggest dependance of T cell-mediated reactivity on (1) the origin of the cells from LN, SP or BM, (2) the time of the harvesting from these tissues, and (3) the degree of sensitization.

Animals

Immunosuppressive activity of heterologous antimacrophage sera.

Antisera against rat macrophages were raised in rabbits and tested individually, serologically and in vivo, by injecting 1.5 ml/100 g into LEW rats 1 and 4 days following a graft of CDF rat skin. 1. Erythrocyte absorption reduced the mean lymphocytotoxic titer of antimacrophage sera from 1:16 to 1:1, but yielded strongly immunosuppressive sera. They extended the graft survival time from the normal rate of 11-14 days up to 217 days. 2. Additional absorption with lymphocytes reduced this activity significantly, but still yielded very active sera (graft survival up to 83 days). 3. After the procedure for serologically exhaustive absorption was repeated, an in vivo control for exhaustive absorption of anti-lymphocyte antibodies was performed. The results showed that the double-absorbed sera did not exhibit reduced immunosuppressive activity. 4. The above activity was found in 9/16 antisera. Seven antisera were inactive in vivo, though they showed similar in vitro activity with respect to their toxic titers against macrophages. These results confirm and extend our earlier functional and morphological studies on AMS. They are discussed in relationship to the controversial data from literature.

Absorption

[Recent details of the frequency and immunologic reactivity of sympathetic ophthalmia (author's transl)].

When giving details of the frequency of Sympathetic Ophthalmia a clear distinction must be made between this disorder and the Phacogenic Ophthalmia also affecting the second eye. The latter is found with lens damage, whereas genuine Sympathetic Ophthalmia in relation to enucleation, eye damage and eye opening surgery at Heidelberg University between 1937 and 1973 is less than 1%, a figure markedly below figures quoted in the earlier literature. In two out of three patients with recent genuine Sympathetic Ophthalmia we found an augmented stimulation index in the LTT with retina antigen, not choroid antigen, as compared to control groups. This can be regarded as due to an individually augmented immunologic reactivity towards eye specific tissue antigens.

Antigen-Antibody Reactions