Analysis of the 8.1 ancestral MHC haplotype in severe, pneumonia-related sepsis

被引:6
作者
Istvan Aladzsity [1 ]
Madach, Krisztina [2 ]
Szilagyi, Agnes [1 ,3 ,4 ]
Janos Gal [2 ]
Istvan Penzes [2 ]
Zoltan Prohaszka [1 ,3 ,4 ]
George Fust [1 ]
机构
[1] Semmelweis Univ, Res Lab, Dept Internal Med 3, H-1125 Budapest, Hungary
[2] Semmelweis Univ, Dept Anesthesiol & Intens Therapy, H-1125 Budapest, Hungary
[3] Semmelweis Univ, Res Grp Inflammat Biol & Immunogenom, H-1089 Budapest, Hungary
[4] Hungarian Acad Sci, H-1089 Budapest, Hungary
基金
匈牙利科学研究基金会;
关键词
Pneumonia; Sepsis; Septic shock; 8.1 ancestral haplotype; COPD; INFLUENCES IMMUNOLOGICAL PARAMETERS; COMMUNITY-ACQUIRED PNEUMONIA; SEPTIC SHOCK; GENETIC POLYMORPHISMS; ASSOCIATION; MORTALITY; SUSCEPTIBILITY; GUIDELINES; MANAGEMENT; DIAGNOSIS;
D O I
10.1016/j.clim.2011.02.013
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The most frequent Caucasian MHC haplotype, AH8.1 - associated with numerous immunopathological differences and certain autoimmune diseases - was recently linked to the delayed onset of bacterial colonization in cystic fibrosis. Based on this observation, we hypothesized that the carriers of AH8.1 have lower risk for a worse outcome in sepsis. AH8.1 carrier state was determined in 207 Caucasian patients with severe, pneumonia-related sepsis. Our data showed that in patients without chronic obstructive pulmonary disease (COPD), septic shock - a serious consequence of the bacterial infection - occurred significantly less frequently (OR=0.3383; 95% CI=0.1141-0.995; p=0.043) in carriers of AH8.1, than in non-carriers. According to the multivariate logistic regression analysis, this haplotype had an independent protective role against septic shock in all patients (OR=0.315; 95% CI=0.100-0.992; p=0.048), particularly in COPD-free patients (OR=0.117; 95% CI=0.025-0.554; p=0.007). These results indicate that AH8.1 may confer protection against the progression of bacterial infection, and this could explain, at least partially, its high frequency in the Caucasian population. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:282 / 289
页数:8
相关论文
共 37 条
  • [31] Real-time PCR quantification of human complement C4A and C4B genes
    Szilagyi, A
    Blasko, B
    Szilassy, D
    Fust, G
    Sasvari-Szekely, M
    Ronai, Z
    [J]. BMC GENETICS, 2006, 7 (1)
  • [32] The 8.1 ancestral MHC haplotype is strongly associated with colorectal cancer risk
    Toth, Eva Katalin
    Kocsis, Judit
    Madaras, Balazs
    Biro, Adrienn
    Pocsai, Zsuzsa
    Fust, George
    Blasko, Bernadett
    Karadi, Istvan
    Adany, Roza
    Laki, Judit
    [J]. INTERNATIONAL JOURNAL OF CANCER, 2007, 121 (08) : 1744 - 1748
  • [33] Heat shock protein 70 gene polymorphisms in Mexican patients with spondyloarthropathies
    Vargas-Alarcón, G
    Londoño, JD
    Hernández-Pacheco, G
    Gamboa, R
    Castillo, E
    Pacheco-Tena, C
    Cardiel, MH
    Granados, J
    [J]. ANNALS OF THE RHEUMATIC DISEASES, 2002, 61 (01) : 48 - 51
  • [34] Septic shock and respiratory failure in community-acquired pneumonia have different TNF polymorphism associations
    Waterer, GW
    Quasney, MW
    Cantor, RM
    Wunderink, RG
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2001, 163 (07) : 1599 - 1604
  • [35] Heat shock protein 70-2+1267 AA homozygotes have an increased risk of septic shock in adults with community-acquired pneumonia
    Waterer, GW
    ElBahlawan, L
    Quasney, MW
    Zhang, Q
    Kessler, LA
    Wunderink, RG
    [J]. CRITICAL CARE MEDICINE, 2003, 31 (05) : 1367 - 1372
  • [36] WATERER GW, EXPERT REV RESP MED, V4, P229
  • [37] High incidence of ancestral HLA haplotype 8.1 and monoclonal incomplete DH-JH immunoglobulin heavy chain gene rearrangement in persistent polyclonal B-cell lymphocytosis
    Wolowiec, Dariusz
    Nowak, Jacek
    Majewski, Miroslaw
    Haus, Olga
    Duszenko, Ewa
    Stella-Holowiecka, Beata
    Mika-Witkowska, Renata
    Makuch-Lasica, Hanna
    Nowak, Grazyna
    Krawcewicz, Andzelika
    Kuliczkowski, Kazimierz
    Warzocha, Krzysztof
    [J]. ANNALS OF HEMATOLOGY, 2008, 87 (07) : 597 - 598