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T Ritter

Publications and source records attributed to T Ritter.

6 recordsLinked to original sources
PubMed1992

Specificity and T cell receptor beta chain usage of a human collagen type II-reactive T cell clone derived from a healthy individual.

Collagen type II (CII) is a cartilage-specific matrix compound well known as an inducer of an experimental, T cell-dependent autoimmune arthritis, a disease which shows some similarities to human rheumatoid arthritis. Here we report on an HLA-DR7-restricted human CD4 T cell clone (TC9), which was isolated from a healthy donor and recognizes human CII. After screening CNBr fragments of CII and tryptic fragments derived thereof, the T cell epitope could be mapped to amino acid residues 271-285 of the triple helical region of CII that are located within CNBr fragment 11 [alpha 1 (II) CB11]. This epitope was confirmed by a synthetic peptide stimulatory for TC9. The T cell receptor beta chain of TC9 was cloned using the polymerase chain reaction; it comprises V beta 6.7 and contains besides J beta 2.3 and C beta 2 an as yet undescribed sequence for the D segment.

Adult↗
PubMed1990

[Changes in the general activation level in psychophysiologic studies--II. Values of auditory evoked potentials in relation to impression and perception and heart rate].

In psychophysiology all procedures used are accompanied with changes of general activation level (GAL) of the subjects. In our study these changes are characterized by self-assessment of the internal state and by the mean heart rate (HR) of each period. On the basis of these data group mean auditory evoked potentials (AEPs) were computed. The influence of the GAL on the N 110- and P 190-amplitudes of the AEPs was analysed. There was no effect on the P 190-amplitude whereas the N 110-amplitude shows distinct responses on changes in GAL. These amplitudes diminished when the subjects reported a change of internal state. The diminishing of N 110-amplitudes took place as well at an increase as at a decrease of the internal state factors. Comparing the HR and the N 110 of the AEPs we found an inverse U-shaped dependence. These results are discussed in comparison to the literature. Furthermore a model which could elucidate the observed findings is presented for a critical discussion.

Adult↗
PubMed1977

Fetal development in experimental uremia.

Uremic women on hemodialysis with metabolic bone disease (hyperparathyroidism, osteomalacia resulting from defective vitamin D metabolism) and anemia (erythropoietin deficiency) are known to give birth to infants without bone disease or anemia. Therefore, skeletal development (enchondral and desmal bone formation) and hepatic erythropoiesis were evaluated in fetuses of uremic rats. These fetuses failed to show defective mineralisation or evidence of bone disease. Bolus injection of high doses of exogenous PTH into the maternal or fetal organism did not affect fetal bone histology. In addition, no apparent defect of bone mineralisation or bone formation was found in fetuses of ricketic rats. Normal mineralisation in the offspring of uremic rats may be explained by fetal hyperphosphatemia and/or insensitivity of fetal (woven) bone mineralisation to vitamin D. Absence of fetal anemia (normal hematocrits, normal density of hematopoietic cells in the liver) in the presence of maternal anemia is presumably due to the insensitivity of fetal erythropoiesis to erythropoietin.

Animals↗