HLA-B17 and the HLA-A1, B17 haplotype in acute myelogenous leukemia

التفاصيل البيبلوغرافية
العنوان: HLA-B17 and the HLA-A1, B17 haplotype in acute myelogenous leukemia
المؤلفون: Robert Cooper, Eugene R. Heise, Edward J. Parrish
المصدر: Tissue antigens. 14(2)
سنة النشر: 1979
مصطلحات موضوعية: Adult, Male, Myeloid, Adolescent, Immunology, Remission, Spontaneous, Human leukocyte antigen, Haploidy, Major histocompatibility complex, Biochemistry, Myelogenous, Antigen, HLA Antigens, Genetics, Immunology and Allergy, Medicine, Humans, Prospective Studies, Aged, biology, business.industry, Haplotype, General Medicine, Middle Aged, medicine.disease, Prognosis, Leukemia, Exact test, Leukemia, Myeloid, Acute, medicine.anatomical_structure, Phenotype, biology.protein, Female, business
الوصف: Seventy-nine Caucasians with acute myelogenous leukemia (AML) were genotyped to determine whether AML, the induction of remission or patient survival were associated with particular HLA phenotypes or haplotypes. HLA-B17 and B27 were increased in AML patients over 40 years of age. Combined analysis of four independent studies indicates that HLA-B17 is significantly but weakly associated with AML, relative risk = 1.48 (.01 less than P less than .025). The A1, B17 and Aw24, Bw35 haplotypes occurred more frequently in the AML group as compared to racial and geographic controls (uncorrected P = 0.0068 and 0.0098, respectively Fisher's Exact Test). Induction of remission occurred less frequently in patients with the B17 phenotype as compared to patients lacking this antigen (P = 0.047). Patient survival was associated with remission status (P = 0.002) but was not significantly associated with particular HLA phenotypes or haplotypes. These results indicate that a gene or genes in the HLA-B region of the major histocompatibility complex can influence susceptibility to AML and also the response to chemotherapy.
تدمد: 0001-2815
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06f01554af48bd22bad4472ae3ceb154Test
https://pubmed.ncbi.nlm.nih.gov/291140Test
حقوق: CLOSED
رقم الانضمام: edsair.doi.dedup.....06f01554af48bd22bad4472ae3ceb154
قاعدة البيانات: OpenAIRE