Psoriasis: Physiopathology and immunogenetics

被引:11
作者
Ammar, M. [1 ]
Souissi-Bouchlaka, C. [1 ]
Gati, A. [1 ]
Zaraa, I. [2 ]
Bouhaha, R. [1 ]
Kouidhi, S. [1 ]
Ben Ammar-Gaied, A. [1 ]
Doss, N. [3 ]
Mokni, M. [2 ]
Marrakchi, R. [1 ]
机构
[1] Univ El Manar II, Fac Sci Tunis, Lab Genet Immunol & Pathol Humaines, Tunis 2092, Tunisia
[2] Hop Rabta, Serv Dermatol, Tunis 1007, Tunisia
[3] Hop Mil Tunis, Serv Dermatol, Tunis, Tunisia
来源
PATHOLOGIE BIOLOGIE | 2014年 / 62卷 / 01期
关键词
Psoriasis; Genetic; Immunopathology; Physiopathology; TH17; PSORS1; NECROSIS-FACTOR-ALPHA; SUSCEPTIBILITY LOCUS PSORS1; EPIDERMAL-GROWTH-FACTOR; HUMAN-LEUKOCYTE ANTIGEN; GENOME-WIDE SEARCH; FAMILIAL PSORIASIS; T-CELLS; HLA-C; INTERFERON-GAMMA; TRANSGENIC MICE;
D O I
10.1016/j.patbio.2013.07.014
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Psoriasis is a multifactorial disease that involves genetic, immunological and environmental factors. During the last decade, several studies by genome scan on families or cases/controls helped to highlight more than ten loci "PSORS" located on different chromosomes and containing several candidate genes. Psoriasis appears as a genetic disease that follows the mixed model with the involvement of a major gene (PSORS1) and a set of minor genes with a variable penetrance depending on the locus. Genetic data have focused on the involvement of the immune system in the pathogenesis of psoriasis. It is now accepted that psoriasis is an immunological disease involving the response profiles TH1 and TH17. Much remains to be done to better elucidate the mechanisms involved in the genesis of psoriatic lesions to find new therapeutic targets. (C) 2013 Published by Elsevier Masson SAS.
引用
收藏
页码:10 / 23
页数:14
相关论文
共 133 条
  • [1] Corneodesmosin expression in psoriasis vulgaris differs from normal skin and other inflammatory skin disorders
    Allen, M
    Ishida-Yamamoto, A
    McGrath, J
    Davison, S
    Iizuka, H
    Simon, M
    Guerrin, M
    Hayday, A
    Vaughan, R
    Serre, G
    Trembath, R
    Barker, J
    [J]. LABORATORY INVESTIGATION, 2001, 81 (07) : 969 - 976
  • [2] Genome-wide linkage scan for psoriasis susceptibility loci in multiplex Tunisian families
    Ammar, M.
    Bouchlaka-Souissi, C.
    Helms, C. A.
    Zaraa, I.
    Jordan, C. T.
    Anbunathan, H.
    Bouhaha, R.
    Kouidhi, S.
    Doss, N.
    Dhaoui, R.
    Ben Osman, A.
    El Gaied, A. Ben Ammar
    Marrakchi, R.
    Mokni, M.
    Bowcock, A. M.
    [J]. BRITISH JOURNAL OF DERMATOLOGY, 2013, 168 (03) : 583 - 587
  • [3] HUMAN KERATINOCYTES ARE A MAJOR SOURCE OF CUTANEOUS PLATELET-DERIVED GROWTH-FACTOR
    ANSEL, JC
    TIESMAN, JP
    OLERUD, JE
    KRUEGER, JG
    KRANE, JF
    TARA, DC
    SHIPLEY, GD
    GILBERTSON, D
    USUI, ML
    HART, CE
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (02) : 671 - 678
  • [4] Arnold R, 1999, J IMMUNOL, V162, P7140
  • [5] Interleukin-10 promoter polymorphism in psoriasis
    Asadullah, K
    Eskdale, J
    Wiese, A
    Gallagher, G
    Friedrich, M
    Sterry, W
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2001, 116 (06) : 975 - 978
  • [6] SPECIFIC NUCLEOTIDE-SEQUENCE OF HLA-C IS STRONGLY ASSOCIATED WITH PSORIASIS-VULGARIS
    ASAHINA, A
    AKAZAKI, S
    NAKAGAWA, H
    KUWATA, S
    TOKUNAGA, K
    ISHIBASHI, Y
    JUJI, T
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1991, 97 (02) : 254 - 258
  • [7] Psoriasis susceptibility locus on 18p revealed by genome scan in Finnish families not associated with PSORS1
    Asumalahti, K
    Laitinen, T
    Lahermo, P
    Suomela, S
    Itkonen-Vatjus, R
    Jansen, C
    Karvonen, J
    Karvonen, SL
    Reunala, T
    Snellman, E
    Uurasmaa, T
    Saarialho-Kere, U
    Kere, J
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2003, 121 (04) : 735 - 740
  • [8] A candidate gene for psoriasis near HLA-C, HCR (Pg8), is highly polymorphic with a disease-associated susceptibility allele
    Asumalahti, K
    Laitinen, T
    Itkonen-Vatjus, R
    Lokki, ML
    Suomela, S
    Snellman, E
    Saarialho-Kere, U
    Kere, J
    [J]. HUMAN MOLECULAR GENETICS, 2000, 9 (10) : 1533 - 1542
  • [9] Intraepidermal lymphocytes in psoriatic lesions are activated GMP-17(TIA-1)+CD8+CD3+CTLs as determined by phenotypic analysis
    Austin, LM
    Coven, TR
    Bhardwaj, N
    Steinman, R
    Krueger, JG
    [J]. JOURNAL OF CUTANEOUS PATHOLOGY, 1998, 25 (02) : 79 - 88
  • [10] BAKER BS, 1988, TRANSPLANT P, V20, P72