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Table 4 Gene-expression changes in pathogen recognition

From: Genome-wide transcription profiling of human sepsis: a systematic review

 

Pathogen recognition

Signal transduction

Johnson[27, 28]

Increase expression in toll-like receptor (TLR) pathway genes.

Increased expression in pathways genes associated with NF-k B, STAT, JAK and MAPKs.

Talwar[8]

Increase expression in TLR pathway genes.

Increased expression in genes associated with STAT, JAK and MAPKs pathways.

Calvano[10]

Increase expression in TLR pathway genes and CD14 genes.

Increased expression in genes associated with STAT, NF-k B, CREB, JAK and MAPKs pathways.

Prabhakar[9]

Increase expression in genes encoding for CD14 molecules.

Increased expression in genes associated with JAK pathway.

Prucha[14]

 

Increased expression in genes associated with MAPKs pathway.

Tang-1[15, 16]

 

Reduced expression in pathways genes associated with NF-k B and MAPKs pathways.

Tang-2[18]

Increase expression in TLR pathways genes.

Increased expression in genes associated with JAK, STAT and MAPKs pathways.

Cobb[20, 21]

 

Increased expression in genes associated with MAPKs pathway.

Wong[2326]

Increase expression in TLR pathways genes.

Increased expression in genes associated with NF-k B STAT and MAPKs pathways.

Payen[19]

Increase expression in TLR pathways genes in survivors.

Greater expression of genes associated with MAPKs pathway in non-survivors.

Pachot[22]

Increase expression in TLR pathways genes in survivors.

Greater expression of genes associated with MAPKs pathway in non-survivors.

  1. Abbreviations; NF-ĸB denotes nuclear factor kappa-B, MAPKs denotes mitogen activated protein kinase, JAK denotes Janus Kinase, STAT denotes transducer and activator of transcription protein, CREB denotes cAMP responsive element binding protein, TLR denotes toll-like receptor.