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1.
Int J Immunogenet ; 42(5): 329-35, 2015 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-26211915

RESUMO

Human platelet antigens (HPA) are immunogenic structures that result from single nucleotide polymorphisms (SNPs) leading to single amino acid substitutions. This study sought to determine the allele and genotype frequencies of HPA-1, HPA-2, HPA-3, HPA-4, HPA-5 and HPA-15 in platelet donors from the state of Rio Grande do Sul (RS), Brazil, and compare their allele frequencies to those observed in other populations. HPA genotyping was performed by PCR-SSP method. The study sample comprised 201 platelet donors (167 Caucasians and 34 non-Caucasians). Allele 'a' was that most commonly found for HPA-1 to 5 in both groups. The HPA-15ab genotype predominated over homozygous genotypes of this system. Fisher's exact test revealed statistically significant differences for the HPA-5 system, with a greater prevalence of the HPA-5b allele in non-Caucasians. The neighbour-joining method and principal components analysis revealed genetic proximity between our Caucasian group and European populations. We conclude that the allele frequencies of HPA-1 to 5 and HPA-15 found in our Caucasian sample are similar to those reported for European populations. These findings corroborate the ethnic makeup of the population of RS. The higher frequency of the HPA-5b allele found in the non-Caucasian group of our sample suggests the possibility of allosensitization in patients who receive platelet transfusions from genetically incompatible donors.


Assuntos
Antígenos/genética , Doadores de Sangue , Plaquetas/metabolismo , Técnicas de Genotipagem/métodos , Adulto , Brasil , Feminino , Frequência do Gene/genética , Loci Gênicos , Genótipo , Humanos , Masculino , Filogenia , Análise de Componente Principal
2.
Tissue Antigens ; 84(5): 479-83, 2014 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-25329634

RESUMO

The human leukocyte antigen (HLA) system has a major role in the regulation of the immune response as it is involved in the defense against pathogens. Evidence for association with tuberculosis (TB) is more consistent for class II than for class I HLA genes. TB is important among indigenous peoples in South America, not only because of its historical role in regional depopulation, but also because it is still widespread. The aim of this study was to evaluate the association of HLA class II alleles, haplotypes and genotypes and tuberculin skin test response (TST) in 76 individuals of the Aché population. Poisson Regression was employed to assess risk genotypes. DRB1*04, DQA1*03 and DQB1*03:02 were associated with TST response in this population.


Assuntos
Alelos , Antígeno HLA-DR4/genética , Haplótipos , Indígenas Sul-Americanos , Tuberculose/genética , Brasil , Feminino , Cadeias alfa de HLA-DQ/genética , Cadeias beta de HLA-DQ/genética , Cadeias HLA-DRB1/genética , Humanos , Masculino , Teste Tuberculínico
3.
Int J Tuberc Lung Dis ; 18(8): 952-7, 2014 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-25199010

RESUMO

SETTING: Cytokines play an important role in anti-tuberculosis immune response, combined with antigen-presenting cells and lymphocytes. Immune response gene polymorphisms have been reported to be associated with tuberculosis (TB) susceptibility in some but not all studies. OBJECTIVE: To evaluate the association of immune response genes with susceptibility to tuberculin skin test (TST) reactivity and/or TB. DESIGN: Fourteen single nucleotide polymorphisms were genotyped in 96 individuals of the Aché, a native Paraguayan population, by allelic discrimination using real-time polymerase chain reaction. Univariate and multivariate Poisson regression were employed to assess risk genotypes. RESULTS: A higher prevalence of purified protein derivative reactivity was associated with the TNF-α CCA/TCG haplotype (PR 1.298, 95%CI 1.059-1.589) and with the IL-10 AT/CC diplotype (PR 1.181, 95% CI 1.024-1.362), and the presence of the IL-8 rs4073 T allele was associated with protection against TB (PR 0.482, 95%CI 0.273-0.851). CONCLUSIONS: These results suggest that polymorphisms in genes associated with immune response are involved in TST reactivity and susceptibility to TB in the Aché population.


Assuntos
Interleucina-10/genética , Interleucina-8/genética , Tuberculose/epidemiologia , Fator de Necrose Tumoral alfa/genética , Adulto , Estudos de Casos e Controles , Feminino , Predisposição Genética para Doença , Genótipo , Humanos , Indígenas Sul-Americanos/genética , Masculino , Pessoa de Meia-Idade , Análise Multivariada , Paraguai , Distribuição de Poisson , Polimorfismo de Nucleotídeo Único , Reação em Cadeia da Polimerase em Tempo Real , Análise de Regressão , Teste Tuberculínico , Tuberculose/genética , Tuberculose/imunologia , Adulto Jovem
4.
Tissue Antigens ; 82(3): 177-85, 2013 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-24032724

RESUMO

Native American populations generally have a higher prevalence of infectious diseases than non-Native populations and this fact can induce different pressures in their immune system. We investigated the patterns of population differentiation (FST ) of 32 polymorphisms related to adaptive immune response in four Native American populations (Aché, Guarani-Kaiowá, Guarani-Ñandeva and Kaingang), and the results were compared with the three major world population data [Yoruba of Ibadan, Nigeria (YRI), Utah residents with northern and Western Europe ancestry (CEU) and Han Chinese of Beijing, China (CHB)] available in the HapMap database. The Aché clearly differentiated from the other Amerindians, but when all Native Americans were compared with the samples of other ethnic groups the lowest difference (0.08) was found with CHB (Asians), the second lowest (0.15) with YRI (Africans) and the most marked with CEU (European-derived). The considerable intra and interethnic differences found can be explained both in terms of diverse evolutionary distances and more recent environmental pathogen exposures; and they should be appropriately considered prior to any specific public health action.


Assuntos
Citocinas/genética , Imunidade Inata , Indígenas Sul-Americanos , Polimorfismo de Nucleotídeo Único , Dinâmica Populacional , Povo Asiático , Evolução Biológica , População Negra , Brasil/etnologia , Citocinas/imunologia , Bases de Dados Genéticas , Projeto HapMap , Humanos , Antígenos de Histocompatibilidade Menor , Proteínas Nucleares/genética , Proteínas Nucleares/imunologia , Filogeografia , Proteína Tirosina Fosfatase não Receptora Tipo 22/genética , Proteína Tirosina Fosfatase não Receptora Tipo 22/imunologia , Receptores de Calcitriol/genética , Receptores de Calcitriol/imunologia , Receptores Purinérgicos P2X7/genética , Receptores Purinérgicos P2X7/imunologia , População Branca
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