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1.
Genet. mol. biol ; 21(3): 301-5, Sept. 1998. tab
Article in English | LILACS | ID: lil-238900

ABSTRACT

Uma análise do perfil dos antígenos HLA de classe II numa amostra da populaçäo de Säo Paulo é descrita neste trabalho. Os dados foram obtidos através de técnicas de amplificaçäo gênica utilizando-se iniciadores seqüências-específicos para HLA-DRB (PCR-SSP) ou amplificaçäo gênica seguida de hibridaçäo com oligonucleotídeos específicos (PCR-SSOP) para HLA-DQA e DQB. Foram calculadas as freqüências gênicas e as freqüências haplotípicas DRB-DQB e DQA-DQB e a populaçäo mostrou estar em equilíbrio genético de acordo com a lei de Hardy-Weinberg. Finalmente, comparamos também os dados obtidos com os da populaçäo de Porto Velho, Rondônia, salientando a importância da obtençäo de dados regionais para os controles quando se estuda este complexo sistema genético.


Subject(s)
Humans , Chromosomes, Human , HLA Antigens , Gene Amplification , Genetics, Population , Immunogenetics , Polymorphism, Genetic , Polymerase Chain Reaction
2.
Braz. j. med. biol. res ; 31(5): 665-70, May 1998. ilus, tab
Article in English | LILACS | ID: lil-212405

ABSTRACT

Six hundred million people are at risk of infection by Schistosoma mansoni, MHC haplotypes have been reported to segregate with susceptibility to schistosomiasis in murine models. In humans, a major gene related to susceptibility/resistance to infection by S. mansoni (SM1) and displaying the mean fecal egg count as phenotype was detected by segregation analysis. This gene displayed a codominant mode of inheritance with an estimated frequency of 0.20-0.25 for the deleterious allele and accounted for more than 50 percent of the variance of infection levels. To determine if the SM1 gene segregates with the human MHC chromosomal region, we performed a linkage study by the lod score method. We typed for HLA-A, B, C, DR and DQ antigens in 11 informative families from an endemic area for schistosomiasis in Bahia, Brazil, by the microlymphocytotoxicity technique. HLA-DR typing by the polymerase chain reaction with sequence-specific primers (PCR-SSP) and HLA-DQ were confirmed by PCR-sequence-specific oligonucleotide probes (PCR-SSOP). The lod scores for the different theta values obtained clearly indicate that there is no physical linkage between HLA and SM1 genes. Thus, susceptibility or resistance to schistosomiasis, as defined by mean fecal egg count, is not primarily dependent on the host's HLA profile. However, if the HLA molecule plays an important role in specific immune responses to S. mansoni, this may involve the development of the different clinical aspects of the disease such as granuloma formation and development of hepatosplenomegaly.


Subject(s)
Humans , Animals , Haplotypes , Major Histocompatibility Complex , Schistosomiasis/genetics , Disease Susceptibility/genetics , DNA Primers , Histocompatibility Antigens , Histocompatibility Testing , Pedigree , Polymerase Chain Reaction/methods , Schistosoma mansoni/genetics , Schistosomiasis/immunology
3.
Braz. j. med. biol. res ; 25(1): 39-47, 1992. tab
Article in English | LILACS | ID: lil-108998

ABSTRACT

Antigen, gene and haplotype frequencies are imnportant data for population analysis, poaternity exclusion testing, genetic studies, and for organ transplantation selection. We have studied the class I histocompatibility antigens of 617 unrelated individuals from the city of Säo Paulo, Brazil, to determine antigen and gene frequencies of HLA-A and 28 HLA-B antigens. Estimated haplotype frequencies were also determined, as well as the genetic distances of this population from European Caucasian and Negro populations. A previously unknown linkage disequilibrium was detected for A23-B49 and a clear trend towards antigen frequencies intermediate between Caucasoid and Negro populations was observed


Subject(s)
Adult , Humans , Antigens, CD , Histocompatibility Antigens , Black People , Bone Marrow Transplantation , Brazil , White People , Gene Frequency , Heart Transplantation , Kidney Transplantation , Major Histocompatibility Complex
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