4.2 Article

HLA class II antigens associated with lupus nephritis in Italian SLE patients

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HUMAN IMMUNOLOGY
卷 64, 期 4, 页码 462-468

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ELSEVIER SCIENCE INC
DOI: 10.1016/S0198-8859(03)00017-X

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human leukocyte antigen; lupus nephritis; systemic lupus erythematosus

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Human leukocyte antigen DR2 (HLA-DR2), namely the allelic variant HLA-DR15, have been associated with lupus nephritis (LN) in Caucasians. The Study investigated the relationships between HLA class II alleles and lupus nephritis in Italian patients. Two hundred forty-four patients fulfilling the American Rheumatism Association criteria for systemic lupus erythematosus (SLE) were typed for HLA-DRB1*, -DQA1*, -DQB1*, and -DPB1* alleles by polymerase chain reaction-sequence-specific oligonucleotide and polymears chain reacrion-single-strand polymorphism; 71 patients had, renal damage assessed by renal biopsy. Glomerulonephritis was classified using WHO criteria. Significance was tested by X-2 on 2X2 tables. HLA-DQA1*,0101 was strongly associated with LN (OR = 2.72 [1.43-5.19]; p = 0.002), whereas HLA-DRB1*1501 was only marginally associated (OR = 1.94 [0.88-4.26]; p = not significant). HLA-DQA1*0102 demonstrated a significant protective effect (OR = 0.31 [0.14-0.86]; P = 0.002). On analyzing the distribution of HLA-DRB1*1501 bearing haplo- types in our SLE patients we found that the HLA-DRB 1 *1501 greatly enhanced the risk of developing LN conferred by the DQA1*0101 allele (OR = 65.96 [9-351326.25]), whereas DQA1*0102 suppressed the nephritogenic effect of DRB1*1501. At renal biopsy, 80% of DRB1 *15 positive patients were classified as having class IV LN with the remaining 2096 having class III LN. The figures were 19% and 21%, respectively, among the HLA-DR15 negative patients. In the Italian population HLA-DQA and HLA-DR alleles interact in conferring susceptibility to or protection against lupus nephritris, the diffuse proliferative glomerulonephritis (i.e., the most severe form of nephritis) is associated with the HLA-DR15 bearing haplotypes. Haman Immunology 64. 462-468 (2003). (C) American Society for Histocompatibility and Immunogenctics, 2003. Published by Elsevier Science Inc,

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