Skip to main content
letter
. 2009 May;15(5):832–834. doi: 10.3201/eid1505.081091

Table. Results of genetic screening for single nucleotide polymorphisms known to be associated with sepsis severity in patient with Plasmodium malariae infection, France*.

Gene rs Wild type Heterozygous Homozygous
Pathogen detection
TLR2 5743708 X
TLR2 5743704 X
TLR4 4986790 X
TLR5 5744168 X
CD14 2569190 X
MD-2 –1625C/G X
FcγRIIa 1801274 X
MBL2 52 A/D X
MBL2 54 A/B X
MBL2 57 A/C X
MBL2 –550 H/L X
MBL2 –221 X/Y X
MBL2
+4 P/Q
X


TLR signaling
IRAK1 1059703 X
TIRAP 8177374 X
IκB 3138053 X
IκB
2233406

X

Inflammation
Lymphotoxin α 909253 X
TNF α 1800629 X
ACE 17236674 X
MIF 755622 X
IL-6 1800795 X
IL-10
1800896
X


Coagulation
PAI-1 1799768 X
Factor V 6025 X

*Except for MD-2 and MBL2, rs is the nomenclature used to describe the variants (initially described by den Dunnen and Antonarakis [4]). TLR, toll-like receptor; MBL2, mannose-binding lectin 2; IRAK-1, interleulin-1 receptor-associated kinase; TIRAP, toll interleukin-1 receptor-associated protein; IκB:, inhibitor of Nf-κB; TNF, tumor necrosis factor; ACE, angiotensin-converting enzyme; MIF, macrophage migration inhibitory factor; IL, interleukin; PAI-1, plaminogen activator inhibitor-1.