Table 6.

Association of genotype with severe acute GVHD

Genotypet testP
RIFNγIntron1-3/3 +2.09 .046 
RIFNγIntron1-3+ +0.76 .452 
RIFNγIntron1-2/2 −0.40 .692 
RIFNγIntron1-2+ −1.84 .073 
RIL-6−174GG +0.71 .480 
RIL-6−174G+ +1.59 .125 
RIL-10−1064i(12-16)+ +2.53 .014 
RTNFd3d3 +1.94 .059  
DIFNγIntron1-3/3 −0.34 .736 
DIFNγIntron1-3+ −0.36 .717 
DIFNγIntron1-2/2 +0.25 .804 
DIFNγIntron1-2+ +0.38 .703 
DIL-6−174GG −0.31 .761 
DIL-6−174G+ +0.91 .928 
Genotypet testP
RIFNγIntron1-3/3 +2.09 .046 
RIFNγIntron1-3+ +0.76 .452 
RIFNγIntron1-2/2 −0.40 .692 
RIFNγIntron1-2+ −1.84 .073 
RIL-6−174GG +0.71 .480 
RIL-6−174G+ +1.59 .125 
RIL-10−1064i(12-16)+ +2.53 .014 
RTNFd3d3 +1.94 .059  
DIFNγIntron1-3/3 −0.34 .736 
DIFNγIntron1-3+ −0.36 .717 
DIFNγIntron1-2/2 +0.25 .804 
DIFNγIntron1-2+ +0.38 .703 
DIL-6−174GG −0.31 .761 
DIL-6−174G+ +0.91 .928 

Univariable analysis of association of genotype with severe aGVHD (grades III-IV) versus nonsevere (0-II) by Kruskal-Wallis test. Recipient IFNγIntron1, IL-10−1064, and TNFd genotype associate with severe (grades III-IV) aGVHD.

R indicates recipient; D, donor.

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