dc.contributor.author | Almasi, S | |
dc.contributor.author | Aliparasti, MR | |
dc.contributor.author | Naghili, B | |
dc.contributor.author | Yeganeh, K | |
dc.contributor.author | Rahnama, B | |
dc.contributor.author | Tavanafar, F | |
dc.contributor.author | Hazhir Karzar, B | |
dc.contributor.author | Amini Khiabani, S | |
dc.contributor.author | Naghili, A | |
dc.contributor.author | Babaloo, Z | |
dc.date.accessioned | 2018-08-26T08:34:11Z | |
dc.date.available | 2018-08-26T08:34:11Z | |
dc.date.issued | 2018 | |
dc.identifier.uri | http://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/52518 | |
dc.description.abstract | Leprosy, which is developed by the obligate intracellular Mycobacterium leprae (ML); has different manifestations, associated with the host immune responses. The protective immune response against ML includes T-cell-mediated immunity. The CTLA-4 has a great impact as a negative regulator of the immune response and maintenance of peripheral tolerance. This study analyzed the relationship between CTLA-4 + 49A/G gene polymorphism and clinical manifestation of leprosy disease and susceptibility among the Azeri population living Northwest Iran. One hundred and ninety-two leprosy patients and 185 healthy controls participated in the study. CTLA-4 + 49A/G genotyping was conducted via tetra-primer amplification refractory mutation system-polymerase chain reaction (T-ARMS-PCR) analysis. The allelic and genotypic frequencies of + 49A/G gene polymorphism were similar in controls and patients. However, older ages, older age of onset and over-representation in male were observed in lepromatous leprosy patient carriers of GG genotype. The current study demonstrates that although CTLA-4 + 49A/G polymorphism was not correlated with a higher genetic risk for leprosy, the presence of a GG genotype was associated with older ages, older age of onset and over-representation in male in Iranian Azeri population. é 2017 | |
dc.language.iso | English | |
dc.relation.ispartof | Infection, Genetics and Evolution | |
dc.subject | adenine | |
dc.subject | cytotoxic T lymphocyte antigen 4 | |
dc.subject | guanine | |
dc.subject | CTLA4 protein, human | |
dc.subject | cytotoxic T lymphocyte antigen 4 | |
dc.subject | adult | |
dc.subject | Article | |
dc.subject | Azeri (people) | |
dc.subject | controlled study | |
dc.subject | female | |
dc.subject | gene amplification | |
dc.subject | gene frequency | |
dc.subject | gene mutation | |
dc.subject | genetic polymorphism | |
dc.subject | genotype | |
dc.subject | human | |
dc.subject | Iran | |
dc.subject | leprosy | |
dc.subject | major clinical study | |
dc.subject | male | |
dc.subject | pathogenesis | |
dc.subject | priority journal | |
dc.subject | allele | |
dc.subject | Azerbaijan | |
dc.subject | case control study | |
dc.subject | genetic association study | |
dc.subject | genetic predisposition | |
dc.subject | genetics | |
dc.subject | leprosy | |
dc.subject | onset age | |
dc.subject | single nucleotide polymorphism | |
dc.subject | Age of Onset | |
dc.subject | Alleles | |
dc.subject | Azerbaijan | |
dc.subject | Case-Control Studies | |
dc.subject | CTLA-4 Antigen | |
dc.subject | Female | |
dc.subject | Gene Frequency | |
dc.subject | Genetic Association Studies | |
dc.subject | Genetic Predisposition to Disease | |
dc.subject | Genotype | |
dc.subject | Humans | |
dc.subject | Leprosy | |
dc.subject | Male | |
dc.subject | Polymorphism, Single Nucleotide | |
dc.title | Analysis of CTLA-4 + 49A/G gene polymorphism in cases with leprosy of Azerbaijan, Northwest Iran | |
dc.type | Review | |
dc.citation.volume | 57 | |
dc.citation.spage | 121 | |
dc.citation.epage | 127 | |
dc.citation.index | Scopus | |
dc.identifier.DOI | https://doi.org/10.1016/j.meegid.2017.11.001 | |