Immunogenetics basis of human systemic lupus erythematosus;Bases immunogenetiques du lupus systemique chez l'homme

Revue de Medecine Interne

Volumn 19, Issue 10, 1998, Pages 726-730

  Michel, M ^a   Meyer, O ^b   Frances C ^c   Tournier Lasserve, E ^a   Piette, J C ^c  

^a INSERM   (France)

^b BICHAT HOSPITAL   (France)

^c PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

Author keywords

Candidate genes; Chromosome 1; Immunogenetic; Multiplex families; Systemic lupus erythematosus

Indexed keywords

ANTIPHOSPHOLIPID SYNDROME; ARTICLE; AUTOIMMUNE DISEASE; CHROMOSOME 1; GENETIC SUSCEPTIBILITY; HUMAN; IMMUNOGENETICS; MAJOR CLINICAL STUDY; MAJOR HISTOCOMPATIBILITY COMPLEX; SYSTEMIC LUPUS ERYTHEMATOSUS; ANIMAL; COMPARATIVE STUDY; DIZYGOTIC TWINS; GENE; GENETIC POLYMORPHISM; GENETIC PREDISPOSITION; GENETICS; IMMUNOLOGY; MONOZYGOTIC TWINS; MOUSE; REVIEW; TWINS;

AUTOANTIBODY; COMPLEMENT; FC RECEPTOR; HLA ANTIGEN;

ANIMALS; ANTIPHOSPHOLIPID SYNDROME; AUTOANTIBODIES; CHROMOSOMES, HUMAN, PAIR 1; COMPLEMENT SYSTEM PROTEINS; DISEASES IN TWINS; GENES; GENETIC PREDISPOSITION TO DISEASE; HLA ANTIGENS; HUMANS; LUPUS ERYTHEMATOSUS, SYSTEMIC; MAJOR HISTOCOMPATIBILITY COMPLEX; MICE; POLYMORPHISM, GENETIC; RECEPTORS, FC; TWINS, DIZYGOTIC; TWINS, MONOZYGOTIC;

EID: 0032419773     PISSN: 02488663     EISSN: None     Source Type: Journal    
DOI: 10.1016/s0248-8663(98)80708-x     Document Type: Article

References (27)

1. Kotzin BL. Systemic lupus erythematosus. Cell. 85:1996;303-306.
2. Drake CG, Kotzin BL. Genetic and immunological mechanisms in the pathogenesis of systemic lupus erythematosus. Cur Opin Immunol. 4:1992;733-740.
3. Arnett FC Jr. The genetics of human lupus. Wallace DJ, Hahn BH. 5th edition Dubois's lupus erythematosus. 1997;77-117 Williams and Wilkins, Baltimore.
4. Deapen D, Escalante A, Weinrib L, Horwitz D, Bachman B, Roy-Burman P, et al. A revised estimate of twin concordance in systemic lupus erythematosus. Arthritis Rheum. 35:1992;311-318.
5. Drake CG, Rozzo SJ, Hirschfeld HF, Smarnworawong NP, Palmer ED, Kotzin BL. Analysis of the New-Zealand black contribution to lupus-like renal disease. Multiple genes that operate in a threshold manner. J Immunol. 154:1995;2441-2447.
6. Reveille JD, Anderson KL, Schrohenloher RE, Acton RT, Barger BO. Restriction fragment length polymorphism analysis of HLA-DR, DQ, DP and C4 alleles in caucasians with systemic lupus erythematosus. J Rheumatol. 18:1991;14-18.
7. Colten HR. Complement deficiences. Ann Rev Immunol. 10:1992;809-834.
8. Botto M, Dell'Agnola C, Bygrave AE, Thompson EM, Cook HT, Petry F, et al. Homozygous C1q deficiency causes glomerulonephritis associated with multiple apoptotic bodies. Nature Genet. 19:1998;56-59.
9. Sullivan KE, Wooten C, Schmeckpeper BJ, Goldman D, Petri MA. A promoter polymorphism of tumor necrosis factor alpha associated with systemic lupus eythematosus in African-Americans. Arthritis Rheum. 40:1997;2207-2211.
10. Liossis STC, Ding XZ, Dennis GJ, Tsokos GC. Altered pattern of TCR/CD3-mediated protein-tyrosin phosphorylation in T cells from patients with systemic lupus erythematosus. J Clin Invest. 101:1998;1448-1457.
11. Wu J, Wilson J, He J, Schur PH, Mountz JD. Fas ligand mutation in a patients with systemic lupus erythematosus and lymphoproliferative disease. J Clin Invest. 98:1996;1107-1113.
12. Salmon JE, Millard S, Schachter LA, Arnett FC, Ginzler EM, Gourley MF, et al. FcγRIIA alleles are heritable risk factors for lupus nephritis in African-Americans. J Clin Invest. 97:1996;1348-1354.
13. Duits AJ, Bootsma H, Derksen RHWM, Spronk PE, Kater L, Kallenberg CGM, et al. Skewed distribution of IgG Fc receptor IIA (CD32) polymorphism is associated with renal disease in systemic lupus erythematosus patients. Arthritis Rheum. 39:1995;1832-1836.
14. Wu J, Edberg CJ, Redecha PB, Bansal VM, Guyre P, Coleman K, et al. A novel polymorphism of FcγRIIIA (CD16) alters receptor function and predisposes to autoimmune disease. J Clin Invest. 100:1997;1059-1070.
15. Vyse TJ, Todd JA. Genetic analysis of autoimmune disease. Cell. 85:1996;311-318.
16. Tsao BP, Cantor RM, Kalunian KC, Chen CJ, Badsha H, Singh R, et al. Evidence for linkage of a candidate chromosome 1 region to human systemic lupus erythematosus. J Clin Invest. 99:1997;725-731.
17. Tsao BP, Cantor RM, Badsha H, Grossman JM, Kalunian KC, Hartung K, et al. A susceptibility gene for SLE maps to a 5 cM region of chromosome 1q [Abstract]. Arthritis Rheum. 40:1997;315. (Suppl).
18. Krahe R, Julkunen H, Mannila H, Lokki H, Ollikainen V, Ignatius J, et al. Exclusion of three candidate susceptibility regions in human chromosomes 1q31-q42, 5q23-q32, and 9p22-p21 for systemic lupus erythematosus (SLE) in a Finnish founder population [Abstract]. Am J Human Genet. 61:1997;A281. (Suppl).
19. Pablos JL, Carreira PE, Martin-Villa JM, Montalvo G, Arnaiz-Villena A, Gomez-Reino JJ. Polymorphism of the heat-shock protein gene HSP 70-2 in systemic lupus erythematosus. Br J Rheumatol. 34:1995;721-723.
20. Yang PM, Olsen NJ, Siminovitch KA, Olee T, Kozin F, Carson DA, et al. Possible deletion of a developmentally regulated heavy-chain variable region gene in autoimmune diseases. Proc Natl Acad Sci USA. 87:1990;7907-7911.
21. Tebib JG, Alcocer-Varela J, Alarcon-Segovia D, Schur PH. Association beteen a Tcell receptor restriction fragment length polymorphism and systemic lupus erythematosus. J Clin Invest. 86:1990;1961-1967.
22. Mehrian R, Quismorio FP Jr, Strassmann G, Stimmler MM, Horwitz DA, Kitridou RC, et al. Synergitic effect between IL-10 and bcl-2 genotypes in determining susceptibility to systemic lupus erythematosus. Arthritis Rheum. 41:1998;596-602.
23. Piette JC, Wechsler B, Frances C, Papo T, Godeau P. Exclusion criteria for the primary antiphospholipid syndrome. J Rheumatol. 20:1993;1802-1804.
24. Goldberg SN, Conti-Kelly AM, Greco TP. A family study of anticardiolipin antibodies and associated clinical conditions. Am J Med. 95:1995;473-479.
25. Sebastiani GD, Galeazzi M, Morozzi G. The immunogenetics of the antiphospholipid syndrome, anticardiolipin antibodies, and lupus anticoagulant. Semin Arthritis Rheum. 25:1996;414-420.
26. Brousse V, Piette JC. Genetic aspects of the primary antiphospholipid syndrome. Nouv Rev Fr Hématol. 37:1995;65-67. Suppl II.
27. Piette JC, Michel M, Tincani A, Cervera C, Shoenfeld Y, Crassard I, et al. Characterization of familial antiphospholipid syndrome: a European Antiphospholipid Forum Project [Abstract]. Lupus. 1998;. à paraître.