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J Nemeskéri

Publications and source records attributed to J Nemeskéri.

6 recordsLinked to original sources

Genetic studies in a Hungarian isolate: Ivád.

A total of 675 individuals from the Hungarian isolate Ivád has been typed for 25 genetic polymorphisms. This sample was devided into three subgroups: 1. Full Ivádys (both spouses and their ancestors are members of the Ivád family; n = 330), 2. Half Ivádys (= either husband or wife and his or her, respectively, ancestors are from the Ivády family, the other partner from the outside population; n = 267), and 3. Non-Ivádys (married couples not belonging to the Ivády family; n = 78). The main concern of this paper is 1. to show to intra-Ivád variability of the distribution of various genetic parameters (allele frequencies, heterozygosity, gene diversity etc.) among these three groups, and 2. to analyze the impact of the different mating patterns of these groups on the genetic structure of the Ivád population. From the comparison of the Ivád gene frequencies with that of neighbouring populations (Pétervására and Erdökövesd) it is seen that drift or founder effects played some role. Within the Ivád population only few gene frequencies show a marked heterogeneity. As expected the average heterozygosity in Full Ivádys is somewhat lower than in Half Ivádys and Non-Ivádys, respectively. The pattern of genetic relationships of the various Ivád groups is in conformity with the demographic and historical facts of this village.

Alleles↗

HLA and T-lymphocyte function in old age.

The role of the major histocompatibility complex in the genetic control of reactivity of peripheral blood mononuclear cells (T lymphocytes) to lectins and allogeneic cells as a function of age was investigated. In randomly selected aged subjects the frequencies of HLA-A, B, and some C locus alleles did not differ significantly from those in the control group. However, some tendencies of haplotype frequency differences between young and aged subjects were found. Significant associations of impaired or preserved T-lymphocyte function could be detected in connection with some HLA-A (A3, A11) antigens only. The tendency of some phenotypic HLA-A and B or C and B antigen associations to be in correlation with impaired or preserved T-lymphocyte reactivity in old age seemed to be independent of their age-related frequency differences. In family studies of a partially inbred Hungarian population, differences were found in the rate of diminution of allogeneic reactivity in groups sharing different HLA haplotypes. Based on statistical analysis of these data, a genetic factor segregating with the MHC and taking part in the regulation of the age-dependent decline of T-lymphocyte reactivity can be postulated.

Adolescent↗