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HLA-B allele frequency in 182 males (n=653) 

HLA-B allele frequency in 182 males (n=653) 

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Renal transplantation is the most successful treatment option for chronic renal failure patients. But success of this depends on HLA antigen matching between the renal recipient & donor. This study is the first report from Karnataka state of South India to find out distribution of HLA-A and B antigens in live renal transplant recipients and donors...

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... B*51 (8.8%), and B*44 (7.6%) were in the list of most frequent allele. [9] This showed some similarity with our results like HLA-A*02, A*11, HLA-B*35, DRB1*07 were found to be most frequent in our study. Kankonkar et al., identified HLA-A*02 (19.25%), ...
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Background: The understanding of transplant acceptance or rejection derives directly from knowing human leukocyte antigen (HLA) involved in the immune response. The HLA of the major histocompatibility complex contains a numerous family of genes located on the short arm of the chromosome number 6 and divided majorly into two classes, Class I (HLA‑A, B, and C) and Class II (HLA‑DR, DQ, and DP). The detection and detailed information of these histocompatibility genes are essential for the better outcome of organ transplants. Aims and Objectives: The aim of the present study is to analyze the frequencies of HLA‑A, B, and DRB1 in chronic kidney disease (CKD) patients and their prospective donors as well as to see the prevalence of heterogenicity. Materials and Methods: A total of 264 patients diagnosed with CKD and 333 potential donors were studied retrospectively in the present study. All these cases were analyzed for HLA‑A, B, and DRB1 loci typing by PCR‑SSOP method based on the Luminex platform. Results: We identified 15 different alleles of HLA‑A, 29 of HLA‑B, and 13 of HLA‑DRB1 amongst studied samples. Out of these identified HLA alleles, HLA‑A*02, HLA‑B*35, and HLA‑DRB1*15 were more frequent as compared to others. The results showed significant heterogenicity in the identified HLA‑A, B, and DRB1alleles. Conclusion: The result highlights the diversity of HLA‑A, B, and DRB1 alleles and is valuable as a reference for organ transplantations. Further, these findings can also guide in better donor selection and hence improved transplant outcome. In addition, this information could be a starting point for the development of an indigenous transplant assay kit