Contribution of TAP genes to genetic predisposition for diffuse panbronchiolitis

Tissue Antigens

Volumn 53, Issue 4 I, 1999, Pages 366-373

  Keicho, N ^a   Tokunaga, K ^b   Nakata, K ^c   Taguchi, Y ^d   Azuma, A ^e   Tanabe, K ^a   Matsushita, M ^b   Emi, M ^e   Ohishi, N ^a   Kudoh, S ^e  

^a UNIVERSITY OF TOKYO   (Japan)

^b UNIVERSITY OF TOKYO   (Japan)

^c TORANOMON HOSPITAL   (Japan)

^d TENRI HOSPITAL   (Japan)

^e NIPPON MEDICAL SCHOOL   (Japan)

Author keywords

Association study; Diffuse panbronchiolitis; LMP2; TAP1; TAP2

Indexed keywords

HLA ANTIGEN CLASS 1; HLA B ANTIGEN;

AMINO ACID SUBSTITUTION; ARTICLE; ASIAN; BRONCHIOLITIS; CHROMOSOME 6; CONTROLLED STUDY; DISEASE ASSOCIATION; EXON; GENE LINKAGE DISEQUILIBRIUM; GENETIC PREDISPOSITION; HUMAN; MAJOR CLINICAL STUDY; PATHOGENESIS; PRIORITY JOURNAL;

ALLELES; ATP-BINDING CASSETTE TRANSPORTERS; BRONCHIOLITIS; CYSTEINE ENDOPEPTIDASES; GENETIC PREDISPOSITION TO DISEASE; HLA-B ANTIGENS; HUMANS; JAPAN; POLYMORPHISM, GENETIC; PROTEINS;

EID: 0032739595     PISSN: 00012815     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0039.1999.530407.x     Document Type: Article

References (33)

1. Homma H, Yamanaka A, Tanimoto S et al. Diffuse panbronchiolitis: a disease of the transitional zone of the lung. Chest 1983: 83: 63-9.
2. Corne J. Diffuse panbronchiolitis: a new Japanese export? Lancet 1996: 348: 1465-6.
3. Suzuki M, Usui K, Tatmura N et al. Familial cases of diffuse panbronchiolitis. Jpn J Thorac Dis 1981: 19: 645-51.
4. Chu YC, Yeh SZ, Chen CL, Chen CY, Chang CY, Chiang CD. Diffuse panbronchiolitis: report of a case. J Formosan Med Assoc 1992: 91: 912-5.
5. Kim YW, Han SK, Shim YS et al. The first report of diffuse panbronchiolitis in Korea: five case reports. Intern Med 1992: 31 : 695-701.
6. Hu H, Liu Y-N. The first case of diffuse panbronchiolitis reported in China. Ther Res 1996: 17: 339-44.
7. Tsang KWT, Ooi CGC, Ip MSM et al. Clinical profiles of Chinese patients with diffuse panbronchiolitis. Thorax 1998: 53: 274-80.
8. Poletti V, Patelli M, Poletti G, Bertanti T. Spiga L. Diffuse panbronchiolitis observed in an Italian. Chest 1990: 98: 515-516.
9. Fitzgerald JE, King Jr TE, Lynch DA, Tuder RM, Schwarz MI. Diffuse panbronchiolitis in the United States. Am J Respir Crit Care Med 1996: 154: 497-503.
10. Kudoh S, Uetake T, Hagiwara K, Hirayama M, Kimura H, Sugiyama Y. Clinical effect of low dose long term erythromycin chemotherapy of diffuse panbronchiolitis. Jpn J Thorac Dis 1987: 25: 632-42.
11. Kudoh S, Azuma A, Yamamoto M, Izumi T, Ando M. Improvement of survival in patients with diffuse panbronchiolitis treated with low-dose erythromycin. Am J Respir Crit Care Med 1998: 157: 1829-32.
12. Koyama H, Geddes DM. Erythromycin and diffuse panbronchiolitis. Thorax 1997: 52: 915-8.
13. Tomlinson IPM, Bodmer WF. The HLA system and the analysis of multifactorial genetic disease. Trends Genet 1995: 11: 493-8.
14. Sugiyama Y, Kudoh S, Maeda H, Suzaki H, Takaku F. Analysis of HLA antigens in patients with diffuse panbronchiolitis. Am Rev Respir Dis 1990: 141: 1459-62.
15. Tokunaga K, Ishikawa Y, Ogawa A et al. Sequence-based association analysis of HLA class I and II alleles in Japanese supports conservation of common haplotypes. Immunogenetics 1997: 46: 199-205.
16. Keicho N, Tokunaga K, Nakata K et al. Contribution of HLA genes to genetic predisposition in diffuse panbronchiolitis. Am J Respir Crit Care Med 1998: 158: 8-16-50.
17. Elliott T. Transporter associated with antigen processing. Adv Immunol 1997: 65: 47-109.
18. Hughes AL. Evolution of the proteasome components. Immunogenetics 1997: 46: 82-92.
19. Coakley G, Lanchbury JS. MHC-encoded TAP genes in rheumatic diseases. Br J Rheumatol 1996: 35: 501-5.
20. Donato L, de la Salle H, Hanau D et al. Association of HLA class I antigen deficiency related to a TAP2 gene mutation with familial bronchiectasis. J Pediatr 1995: 127: 895-900.
21. Teisserenc H, Schmitt W, Blake N et al. A case of primary immunodeficiency due to a defect of the major histocompatibility gene complex class I processing and presentation pathway. Immunol Letters 1997: 57: 183-7.
22. Sugiyama Y, Kudoh S, Kitamura S. A case of bare lymphocyte syndrome with clinical manifestations of diffuse bronchiolitis. Jpn J Thorac Dis 1989: 27: 980-3.
23. Wang L, Hirayasu K, Ishizawa M, Kobayashi Y. Purification of genomic DNA from human whole blood by isopropanol-fractionation with concentrated NaI and SDS, Nucleic Acids Res 1994: 22: 1774-5.
24. Powis SH, Tonks S, Mockridge I, Kelly AP, Bodmer JG, Trowsdale J. Alleles and haplotypes of the MHC-encoded ABC transporters TAP1 and TAP2. Immunogenetics 1993: 37: 373-80.
25. Beck S, Kelly A, Radley E, Khurshid F, Alderton RP, Trowsdale J. DNA sequence analysis of 66 kb of the human MHC class II region encoding a cluster of genes for antigen processing, J Mol Biol 1992: 228: 433-41.
26. Deng GY, Muir A, Maclaren NK, She J-X. Association of LMP2 and LMP7 genes within the major histocompatibility complex with insulin-dependent diabetes mellitus: population and family studies. Am J Hum Genet 1995: 56: 528-34.
27. Maruya E, Ishikawa Y, Lin L et al. New polymorphisms within human TAP2 in the ATP-binding domain and profiles of TAP polymorphism in Japanese. MHC 1997: 3: 1-8.
28. Kuwata S, Yanagisawa M, Saeki H et al. Lack of primary association between transporter associated with antigen processing genes and atopic dermatitis. J Allergy Clin Immunol 1995: 96: 1051-60.
29. Powis SJ, Deverson EV, Coadwell WJ et al. Effect of polymorphism of an MHC-linked transporter on the peptides assembled in a class I molecule. Nature 1992: 357: 211-5.
30. Heemels MT, Schumacher TN, Wonigeit K et al. Peptide translocation by variants of the transporter associated with antigen processing. Science 1993: 262: 2059-63.
31. Obst R, Armandola EA, Nijenhuis M, Momburg F, Hämmerling GJ. TAP polymorphism does not influence transport of peptide variants in mice and humans. Eur J Immunol 1995: 25: 2170-6.
32. Ortmann B, Copeman J, Lehner PJ et al. A critical role for tapasin in the assembly and function of multimeric MHC Class I-TAP complexes. Science 1997: 277: 1306-9.
33. Furukawa H, Murata S, Yabe T et al. Splice acceptor site mutation of the transporter associated with antigen processing 1 gene in human histocompatibility leukocyte antigen class I deficiency. J Clin Invest 1999: in press.