Toll-like receptor 4 polymorphisms and aspergillosis in stem-cell transplantation

被引:340
作者
Bochud, Pierre-Yves [1 ,2 ]
Chien, Jason W. [5 ]
Marr, Kieren A. [1 ,5 ]
Leisenring, Wendy M. [1 ,5 ]
Upton, Arlo [1 ]
Janer, Marta [2 ]
Rodrigues, Stephanie D. [2 ]
Li, Sarah [2 ]
Hansen, John A. [3 ,5 ]
Zhao, Lue Ping [4 ]
Aderem, Alan [2 ]
Boeckh, Michael [1 ,5 ]
机构
[1] Fred Hutchinson Canc Res Ctr, Vaccine & Infect Dis Inst, Program Infect Dis, Seattle, WA 98109 USA
[2] Fred Hutchinson Canc Res Ctr, Inst Syst Biol, Seattle, WA 98109 USA
[3] Fred Hutchinson Canc Res Ctr, Div Clin Res, Seattle, WA 98109 USA
[4] Fred Hutchinson Canc Res Ctr, Div Publ Hlth Sci, Seattle, WA 98109 USA
[5] Univ Washington, Dept Med, Seattle, WA 98195 USA
基金
瑞士国家科学基金会; 美国国家卫生研究院;
关键词
D O I
10.1056/NEJMoa0802629
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Toll-like receptors (TLRs) are essential components of the immune response to fungal pathogens. We examined the role of TLR polymorphisms in conferring a risk of invasive aspergillosis among recipients of allogeneic hematopoietic-cell transplants. Methods: We analyzed 20 single-nucleotide polymorphisms (SNPs) in the toll-like receptor 2 gene (TLR2), the toll-like receptor 3 gene (TLR3), the toll-like receptor 4 gene (TLR4), and the toll-like receptor 9 gene (TLR9) in a cohort of 336 recipients of hematopoietic-cell transplants and their unrelated donors. The risk of invasive aspergillosis was assessed with the use of multivariate Cox regression analysis. The analysis was replicated in a validation study involving 103 case patients and 263 matched controls who received hematopoietic-cell transplants from related and unrelated donors. Results: In the discovery study, two donor TLR4 haplotypes (S3 and S4) increased the risk of invasive aspergillosis (adjusted hazard ratio for S3, 2.20; 95% confidence interval [CI], 1.14 to 4.25; P=0.02; adjusted hazard ratio for S4, 6.16; 95% CI, 1.97 to 19.26; P=0.002). The haplotype S4 was present in carriers of two SNPs in strong linkage disequilibrium (1063 A/G [D299G] and 1363 C/T [T399I]) that influence TLR4 function. In the validation study, donor haplotype S4 also increased the risk of invasive aspergillosis (adjusted odds ratio, 2.49; 95% CI, 1.15 to 5.41; P=0.02); the association was present in unrelated recipients of hematopoietic-cell transplants (odds ratio, 5.00; 95% CI, 1.04 to 24.01; P=0.04) but not in related recipients (odds ratio, 2.29; 95% CI, 0.93 to 5.68; P=0.07). In the discovery study, seropositivity for cytomegalovirus (CMV) in donors or recipients, donor positivity for S4, or both, as compared with negative results for CMV and S4, were associated with an increase in the 3-year probability of invasive aspergillosis (12% vs. 1%, P=0.02) and death that was not related to relapse (35% vs. 22%, P=0.02). Conclusions: This study suggests an association between the donor TLR4 haplotype S4 and the risk of invasive aspergillosis among recipients of hematopoietic-cell transplants from unrelated donors.
引用
收藏
页码:1766 / 1777
页数:12
相关论文
共 44 条
[1]   Human toll-like receptor 4 mutations but not CD14 polymorphisms are associated with an increased risk of gram-negative infections [J].
Agnese, DM ;
Calvano, JE ;
Hahm, SJ ;
Coyle, SM ;
Corbett, SA ;
Calvano, SE ;
Lowry, SF .
JOURNAL OF INFECTIOUS DISEASES, 2002, 186 (10) :1522-1525
[2]   Pathogen recognition and innate immunity [J].
Akira, S ;
Uematsu, S ;
Takeuchi, O .
CELL, 2006, 124 (04) :783-801
[3]   TLR4 mutations are associated with endotoxin hyporesponsiveness in humans [J].
Arbour, NC ;
Lorenz, E ;
Schutte, BC ;
Zabner, J ;
Kline, JN ;
Jones, M ;
Frees, K ;
Watt, JL ;
Schwartz, DA .
NATURE GENETICS, 2000, 25 (02) :187-+
[4]   Defining opportunistic invasive fungal infections in immunocompromised patients with cancer and hematopoietic stem cell transplants: An international consensus [J].
Ascioglu, S ;
Rex, JH ;
de Pauw, B ;
Bennett, JE ;
Bille, J ;
Crokaert, F ;
Denning, DW ;
Donnelly, JP ;
Edwards, JE ;
Erjavec, Z ;
Fiere, D ;
Lortholary, O ;
Maertens, J ;
Meis, JF ;
Patterson, TF ;
Ritter, J ;
Selleslag, D ;
Shah, PM ;
Stevens, DA ;
Walsh, TJ .
CLINICAL INFECTIOUS DISEASES, 2002, 34 (01) :7-14
[5]   TLRs govern neutrophil activity in aspergillosis [J].
Bellocchio, S ;
Moretti, S ;
Perruccio, K ;
Fallarino, F ;
Bozza, S ;
Montagnoli, C ;
Mosci, P ;
Lipford, GB ;
Pitzurra, L ;
Romani, L .
JOURNAL OF IMMUNOLOGY, 2004, 173 (12) :7406-7415
[6]   Inferences, questions and possibilities in toll-like receptor signalling [J].
Beutler, B .
NATURE, 2004, 430 (6996) :257-263
[7]   Innate immunogenetics: a tool for exploring new frontiers of host defence [J].
Bochud, Pierre-Yves ;
Bochud, Murielle ;
Telenti, Amalio ;
Calandra, Thierry .
LANCET INFECTIOUS DISEASES, 2007, 7 (08) :531-542
[8]   Polymorphisms in Toll-like receptor 9 influence the clinical course of HIV-1 infection [J].
Bochud, Pierre-Yves ;
Hersberger, Martin ;
Taffe, Patrick ;
Bochud, Murielle ;
Stein, Catherine M. ;
Rodrigues, Stephanie D. ;
Calandra, Thierry ;
Francioli, Patrick ;
Telenti, Amalio ;
Speck, Roberto F. ;
Aderem, Alan .
AIDS, 2007, 21 (04) :441-446
[9]   Aspergillus fumigatus antigens activate innate immune cells via toll-like receptors 2 and 4 [J].
Braedel, S ;
Radsak, M ;
Einsele, H ;
Latgé, JP ;
Michan, A ;
Loeffler, J ;
Haddad, Z ;
Grigoleit, U ;
Schild, H ;
Hebart, H .
BRITISH JOURNAL OF HAEMATOLOGY, 2004, 125 (03) :392-399
[10]  
*CAS W RES U, 2005, SAGE STAT AN GEN EP