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Biomedical subjects

A Svejgaard

Publications and source records attributed to A Svejgaard.

At least 325 records · Page 18Linked to original sources

Typing for MLC determinants: methods and applications.

MLC typing of random individuals can be performed using a panel of inactivated HLA-D homozygous cells. Eight different HLA-D specificities are now internationally accepted. The evaluation of the results must take into account both the general responding capacity of the cell to be typed and the general stimulating capacity of the typing cells. An evaluation based on the 75th percentile is discussed in detail and some pitfalls are mentioned. Furthermore a description is given of primed lymphocyte typing (PLT), where cells primed in ordinary MLC cultures to one HLA-D determinant have the ability to respond in an accelerated way to similar HLA-D antigens when re-exposed to such cells in secondary cultures. In our experiments, an excellent correlation is found between these two ways of MLC typing provided that the cells used for priming are well characterized (i.e. HLA-D homozygous cells). Finally, some clinical applications of MLC typing are described, especially in connection with transplantation and association between HLA and various diseases.

Culture Techniques↗

Immunological in vitro parameters in patients with multiple sclerosis and in normal individuals.

The general immunological capacity of 40 patients with multiple sclerosis has been evaluated with lymphocyte transformation test including both mitogens (PHA and PWM) and antigens (PPD, Candida albicans, Staph. aureus and E. coli). Determination of T and B cells was performed by E-, EAC-rosetting and immunofluorescence for surface immunoglobulins. Compared with the results obtained in 42 normal individuals only minor differences were found.

Adult↗

Immunological studies in sarcoidosis: a comparison of disease activity and various immunological parameters.

We found it valuable to separate the heterogeneous types of sarcoidosis into more homogeneous groups on the basis of activity and duration of the disease. This view is supported in the present study by the finding of a marked depression of T-cell function in patients with chronic-active sarcoidosis. Patients with acute or chronic-inactive disease had only moderately depressed T-cell function as measured by tuberculin skin test and DNCB index. These results are in agreement with those of some previous investigations. The remainder of the abnormal findings, particularly low total number of circulation T lymphocytes, elevated serum IgG levels, and presence of autoantibodies, could not be correlated to disease activity, extent of the disease, or T-cell function. We have found no explanation for the presence of autoantibodies but suspect that they may be nonspecifically related to the disease process.

Adolescent↗

Developments in histocompatibility testing.

Recent progress in HLA typing involves new methods which allow typing for MLC (mixed lymphocyte culture) and Ia (immune associated) antigens. These antigens seem to play a major role in transplant rejection in HLA non-immunised patients. When the new typing methods eventually become applied in matching of kidneys it seems likely that the results of kidney transplantation will be significantly improved.

Antigens↗

The relation of HL-A antigens to liver histology in methotrexate-treated psoriatics.

A total of 45 patients with severe psoriasis vulgaris treated with Methylaminopterin NFN (Methotrexate Lederle) were HL-A typed in order to seek a possible correlation between HL-A antigens and the histological abnormalities in post-Methotrexate (MTX) liver biopsies. Highly significantly increased frequencies of w17 and TY (P less than 0.0001) were found, while HL-A13 Was only slightly increased. No statistically significant correlations were found between HL-A antigens and liver histology. HL-A typing does not seem to be of any predictive value in the pre-MTX screening of psoriatics in order to rule out patients with a high risk of liver damage during long-term MTX therapy.

Adult↗

HLA factors and immune function.

The HLA system is the major histocompatibility system (MHS) in man and contains a variety of closely linked genes, which control a large number of alloantigens, some complement components, and certain immune responses. The alloantigens are of three different kinds: (i) so-called "classical" or serologically detectable (SD) antigens which are present on all nucleated cells and controlled by genes of at least three different loci; (ii) MLC (= mixed lymphocyte culture = LD = lymphocyte dependent) antigens which are as yet only recognizable by in vitro culture assays; (iii) Ia (= immune-associated) antigens which (like MLC antigens) primarily are present on B lymphocytes and which can be detected serologically. Our knowledge of immune-response (Ir) determinants in man is as yet rather limited but by inference from studies of MHS in mice, guinea-pigs, and rhesus monkeys it is almost certain that HLA contains such genes. Immune response genes control in a dominant way the ability to respond specifically with IgG antibody production and cell-mediated immunity to certain specific antigens. Ir genes are closely linked to the MLC and Ia genes. They seem to be particularly important for immune responses involving T lymphocyte function (including T-B cell cooperation), and it seems likely that they code for "antibody-like", carrier-specific immune receptors on T cells. Evidence that HLA contains Ir determinants derives from the observations (i) that a variety of "immunopathic" disorders are associated with HLA factors; (ii) that ragweed hayfever seems to be inherited with certain HLA types within families; and (iii) that the occurrence of anti-adrenal antibodies is associated with HLA in Addison's disease. Autoimmune thyreoiditis is controlled by the MHS in mice and chickens, and in analogy, Graves' disease is associated with HLA in man.

Autoantibodies↗

Evidence for tryosine peptide homologies in the HLA antigens system.

The tetrameric HLA antigens are composed of two heavier chains which carry the alloantigenic determinants and two lighter chains identified as beta2-microglobulin. Although at least 40 different antisera are required to define the varying HLA specificities, it appears that these antigens may be closely related to each other and to the immunoglobulins. Through the use of a new electrophoretic technique, which is able to compare simultaneously the tyrosine peptides produced from radioiodinated cell surface proteins, this report gives evidence that HLA antigens of the three chromosomal loci may have similar amino-acid sequences. Since the retention of homologous tyrosine residues and a tendency for sequence preservation surrounding these residues are features of immunoglobulin structure, this may indicate that similarly conservative evolutionary mechanisms have been operative in the HLA allelelic proteins or that immunoglobulins and HLA antigens may indeed have a common evolutionary origin.

Antigen-Antibody Reactions↗

Cell-mediated immunity to a serologically defined (SD) HL-A antigen panel in kidney-transplanted patients.

The graft-directed, cell-mediated immunity in kidney-allografted patients was examined with a seriologically defined (SD), donor-unrelated panel of antigenic material in clinical steady state, soon after transplantation, and during acute rejection episodes. The SD antigens were selected from the panel on the basis of predictions hypothesized from the SD match of donor and recipient. The cell-mediated immunity was measured by the direct leukocyte migration agarose test (LMAT). Positive reactions in kidney-transplanted patients were induced particularly by one preparation (antigen 52) and were unpredictable on the basis of SD classification. The investigation shows that other antigenic determinants, different from SD antigens, probably play an important role as inducers of cell-mediated, graft-associated immunity in kidney-transplanted patients.

Adult↗

On the heterogeneity of linkage estimations between LA and four loci of the HL-A system,.

Three cases of crossing over between the LA and FOUR loci of HL-A system are presented in this note. Recombination fractions between those two loci are also calculated from familial data kindly provided by other European laboratories. It is suggested that differences found in maternal and paternal recombination frequency are due to the heterogeneity of estimates of each laboratory.

Child↗