. Author manuscript; available in PMC: 2009 Nov 11.

Published in final edited form as: J Immunol. 2009 Apr 1;182(7):4459–4470. doi: 10.4049/jimmunol.0801450

TABLE III.

Real-time PCR confirmation of differentially expressed apoptosis genes^a

Accession No.	Gene Symbol	Gene Name	p Value for Comparison of HIV-1-Infected Individuals vs Controls (Quantitative PCR)	Ratio of Signal between HIV-1-Infected Individuals and Controls
N98591	IL6	IL-6	0.0004	166.40
W92812	PPBP	Proplatelet basic protein (chemokine (C-X-C motif) ligand 7)	0.0010	3.58
AA425102	CCL2	Chemokine (C-C motif) ligand 2	0.0001	12.85
NM_002984	CCL4	Chemokine (C-C motif) ligand 4	0.0050	5.99
AA457705	IER3	Immediate early response 3	0.0071	3.06
H77597	MT1H	Metallothionein 1H	0.0002	8.58
H53340	MT1G	Metallothionein 1G	0.0008	5.09
T49159	PAI2	Serine (or cysteine) proteinase inhibitor, clade B (OVA), member 2	0.0043	6.88
W02699	CD153	CD30L	0.0004	0.38
AA167728	SIVA	CD27-binding (Siva) protein	0.0180	0.48
AI952615	p21	CDKN1A/Waf1/Cip1/Sdi1	0.0220	1.54

Differentially expressed apoptosis genes validated by real-time PCR are shown. The accessions, gene symbols, gene names, p values, and fold ratios for apoptosis genes differentially expressed between HIV-1 and control monocytes (all but CCL4 and p21 were also identified as significant by microarray analysis) were confirmed for significance by real-time PCR analysis and are indicated.