Table II.

Primers used for reverse transcription-quantitative PCR.

Gene	Sequence, 5′→3′
GAPDH
Forward	TGACTTCAACAGCGACACCCA
Reverse	CACCCTGTTGCTGTAGCCAAA
CCL3
Forward	TGTTGCCAAACAGCCACAC
Reverse	CAGAGCAAACAATCACAAACACAC
CCL5
Forward	TCCCACAGGTACCATGAAGGTC
Reverse	GCAATGTAGGCAAAGCAGCAG
CCL17
Forward	CAGAGGGACCTGCACACAGA
Reverse	TTCAGCTTTCTAAGGGGAATGG
CCL19
Forward	ACCAGGCTTCCAGCTCCTCT
Reverse	ACCAGGCGGCTTTATTGGT
CCL21
Forward	GCCACACTCTTTCTCCTGCTTT
Reverse	ACTCTCCCTCCTCGGTCTCTCT
CCL22
Forward	GGTATTTGAACCTGTGGAATTGGAG
Reverse	CAGGCCCTGGATGACACTGA
CXCL10
Forward	TGCAAGCCAATTTTGTCCAC
Reverse	GACCTTTCCTTGCTAACTGCTTTC
CXCL11
Forward	GCTGTGATATTGTGTGCTACAGTTG
Reverse	TTGGGTACATTATGGAGGCTTTC
CXCL12
Forward	CCCTGCTTACCCGCAAAA
Reverse	CTTCAGAGGCAATCACAAAACC