Polymorphism of antigen processing (TAP, LMP) and HLA class II genes in celiac disease

Human Immunology

Volumn 40, Issue 1, 1994, Pages 8-16

  Djilali Saiah, Idriss ^a   Caillat Zucman, Sophie ^a   Schmitz, Jacques ^a   Laise Chaves Vieira, Maria ^a   Bach, Jean François ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

HLA ANTIGEN CLASS 2;

ADOLESCENT; ADULT; ARTICLE; CELIAC DISEASE; CHILD; CONTROLLED STUDY; FEMALE; GENETIC POLYMORPHISM; GENETIC PREDISPOSITION; GENETIC RISK; HISTOCOMPATIBILITY; HUMAN; INFANT; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; PROTEIN PROCESSING;

ADOLESCENT; ADULT; BASE SEQUENCE; CELIAC DISEASE; CHILD; CHILD, PRESCHOOL; FEMALE; FRANCE; GENES, MHC CLASS II; HISTOCOMPATIBILITY ANTIGENS CLASS II; HUMAN; INFANT; MALE; MOLECULAR SEQUENCE DATA; POLYMORPHISM (GENETICS); PROTEINS;

EID: 0028200674     PISSN: 01988859     EISSN: None     Source Type: Journal    
DOI: 10.1016/0198-8859(94)90015-9     Document Type: Article

References (55)

1. Celiac sprue
2. Hal DW3 associated with celiac disease
3. Evidence that celiac disease is primarily associated with a D locus allelic specificity
4. Celiac disease
5. HLA class II frequencies in celiac disease patients in the west of Ireland
6. Restriction fragment length polymorphism in HLA class II genes of Latin American Caucasian celiac disease patients
7. ∗0201) heterodimer
8. HLA class II alleles associated with celiac disease susceptibility in a Southern European population
9. Evidence for a primary association of celiac disease to a particular HLA-DQ α/β heterodimer
10. Oligotyping of celiac multiplex families with the 11th International Histocompatibility Workshop reagents
11. T lymphocyte recognition of a celiac disease-associated cis- or trans-encoded HLA-DQ ⋏/β heterodimer
12. ∗0501, β 10201) restricted T cells isolated from the small intestinal mucosa of celiac disease patients
13. HLA-DR3 and DR7-negative celiac disease
14. HLA-DR and -DQ genotype of celiac disease patients serologically typed to be non-DR3 or non-DR5/7
15. Reassessment of HLA association with celiac disease in special reference to the DP association
16. Genetic markers in Australian Caucasian subjects with coeliac disease
17. A combination of a particular HLA-DPβ allele and an HLA-DQ heterodimer confers susceptibility to coeliac disease
18. Structural analysis of the HLA-DR, -DQ, and -DP alleles on the celiac disease-associated HLA-DR3 (DRw17) haplotype
19. Celiac disease is associated with an extended HLA-DR3 haplotype which includes HLA-DPw1
20. A family study confirms that the HLA-DP associations with celiac disease are the result of an extended HLA-DR3 haplotype
21. HLA-DP polymorphism in Northern Italian celiac patients
22. A locus telomeric to HLA-DPB encodes susceptibility to coeliac disease
23. Sequences encoded in the class II region of the MHC related to the ‘ABC’ superfamily of transporters
24. MHC class II region encoded proteins related to the multidrug resistance family of transmbrane transporters
25. A gene in the human major histocompatibility complex region controlling the class I antigen presentation pathway
26. Transport protein genes in the murine MHC: possible implications for antigen processing
27. A proteasome-related gene between the two ABC-transporter loci in the class II region of the human MHC
28. Second proteasome-related gene in the human MHC class II region
29. Proteasomes are regulated by interferon gamma: implications for antigen processing
30. Proteasome subunits encoded in the MHC are not generally required for the processing of peptides bound by MHC class I molecules
31. Two putative subunits of a peptide pump encoded in the human major histocompatibility complex class II region
32. Restored expression of major histocompatibility class I molecules by gene transfer of a putative peptide transporter
33. Ham-2 corrects the class I antigen processing defect in RMA-S cells
34. Presentation of viral antigen by MHC class I molecules is dependent on a putative peptide transport heterodimer
35. Assembly and function of the two ABC transporter proteins encoded in the human major histocompatibility complex
36. Round table discussion diagnosis criteria in coeliac disease
37. A simple and efficient non-organic procedure for the isolation of genomic DNA from blood
38. Selection of unrelated donors for bone marrow transplantation is improved by HLA class II genotyping with oligonucleotide hybridization
39. Age-dependent HLA genetic heterogeneity of type 1 insulin dependent diabetes mellitus
40. Polymorphism in a second ABC transporter gene located within the class II region of the human major histocompatibility complex
41. Allelic variants of the human putative peptide transporter involved in antigen processing
42. Genomic polymorphism, recombination, and linkage disequilibrium in human major histocompatibility complex-encoded antigen-processing genes
43. Molecular basis of human leukocyte antigen class II disease association
44. Gliadin uptake in human enterocytes: differences between coeliac patients in remission and control individuals
45. ∗0501 allele are essential for the onset of DQw2-positive and DQw2-negative coeliac disease
46. An extended HLA-D region haplotype associated with celiac disease
47. ∗0201
48. Effect of polymorphism of an MHC-linked transporter on the peptides assembled in a class I molecule
49. Presentation of numerous viral pepties to mouse major histocompatibility complex (MHC) class I-restricted T lymphocytes is mediated by the human MHC-encoded transporter or by a hybrid mouse-human transporter
50. Linkage disequilibrium between TAP2 variants and HLA class II alleles: no primary association between TAP2 variants and insulin-dependent diabetes mellitus
51. Protection from insulin-dependent diabetes mellitus is linked to a peptide transporter gene
52. Alleles and haplotypes of the MHC-encoded ABC transporters TAP1 and TAP2
53. Haplotypic variation of the transporter associated with antigen processing (TAP) genes and their extension of HLA class II region haplotypes
54. TAP1 and TAP2 polymorphism in coeliac disease
55. MHC class II deletion mutant expresses normal levels of transgene encoded class II molecules that have abnormal conformation and impaired antigen presentation ability