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dc.contributor.authorÇınar, Çiğdem Kekik
dc.contributor.authorBeşışık, Sevgi Kkalayoğlu
dc.contributor.authorOğuz, Fatma Savran
dc.contributor.authorOğuz, Süleyman Rüştü
dc.contributor.authorKıvanç, Demet
dc.contributor.authorSargın, Deniz
dc.date.accessioned2024-02-04T13:30:27Z
dc.date.available2024-02-04T13:30:27Z
dc.date.issued2022
dc.identifier.issn2651-4060
dc.identifier.urihttps://doi.org/10.26650/JARHS2022-1130823
dc.identifier.urihttps://search.trdizin.gov.tr/yayin/detay/1172500
dc.identifier.urihttp://hdl.handle.net/11446/4924
dc.description.abstractObjective: The minor histocompatibility antigens (mHAgs) are the epitopes composed of polymorphic essential peptides, and they create T cell response limited to a variety of class I and II HLA alleles. In recent years, there has been extensive research on the distribution of polymorphic regions in different populations. The incompatibility between recipient and donor, may initiate a strong cellular immune response despite HLA full-matched transplantation. We determined the frequency of minor antigens among hematopoietic stem cell transplantation (HSCT) recipients who underwent transplantation for various hematological diseases. Material and Methods: The study population included 200 healthy individuals, 150 HLA-typed patients who were candidates for allogeneic HSCT, and 20 recipients/donors with allogeneic transplants. Minor HAgs identified by using polymerase chain reaction (PCR) and sequence specific primer (SSP) methods. Results: When the allele frequencies and genotypes of the patients were compared with those of the healthy group, the difference was not significant regarding to immunogenic or non-immunogenic allele frequencies. The individuals with immunogenic homozygous H allele (HH genotype) were a few more in the healthy group, and this difference proved to be statistically significant. In fact, our study population Insufficient though the number was, based on the data received from 20 transplant patients and donors, GvHD was observed in 5 of 10 patients who had minor incompatibility. Conclusion: We assume that determining the mHAg frequencies in the healthy Turkish population and in patients with malignant hematological diseases will likely contribute to the understanding of the immune response.en_US
dc.language.isoengen_US
dc.relation.ispartofSabiaden_US
dc.identifier.doi10.26650/JARHS2022-1130823
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleCHARACTERIZATION OF MINOR HISTOCOMPATIBILITY ANTIGENS AND THEIR ROLE IN ALLOGENEIC HEMATOPOIETIC STEM CELL TRANSPLANTATION: SINGLE CENTER EXPERIENCE IN TURKIYEen_US
dc.typearticleen_US
dc.departmentDBÜen_US
dc.identifier.issue3en_US
dc.identifier.volume5en_US
dc.identifier.startpage130en_US
dc.identifier.endpage134en_US
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.department-tempİstanbul Üniversitesi, İstanbul Tıp Fakültesi, Tıbbi Biyoloji Anabilim Dalı, İstanbul, Türkiye İstanbul Üniversitesi, İstanbul Tıp Fakültesi, İç Hastalıkları Anabilim Dalı, Hematoloji Anabilim Dalı, İstanbul, Türkiye İstanbul Üniversitesi, İstanbul Tıp Fakültesi, Tıbbi Biyoloji Anabilim Dalı, İstanbul, Türkiye Demiroğlu Bilim Üniversitesi, Tıp Fakültesi, Tıbbi Biyoloji ve Genetik Anabilim Dalı, İstanbul, Türkiye İstanbul Üniversitesi, Sağlık Bilimleri Enstitüsü, Tıbbi Biyoloji Anabilim Dalı, İstanbul, Türkiye İstanbul Üniversitesi, İstanbul Tıp Fakültesi, İç Hastalıkları Anabilim Dalı, Hematoloji Anabilim Dalı, İstanbul, Türkiyeen_US
dc.identifier.trdizinid1172500en_US


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